<?xml version='1.0' encoding='utf-8' ?>



<rss version="2.0"
      xmlns:opensearch="http://a9.com/-/spec/opensearch/1.1/"
      xmlns:dc="http://purl.org/dc/elements/1.1/"
      xmlns:atom="http://www.w3.org/2005/Atom">
   <channel>
     <title><![CDATA[NUST Institutions Library Catalogue Search for '(su:&quot;MS Biomedical Sciences BMS      &quot;)']]></title>
     <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?q=ccl=%28su%3A%22MS%20Biomedical%20Sciences%20BMS%20%20%20%20%20%20%22%29&amp;format=rss</link>
     <atom:link rel="self" type="application/rss+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?q=ccl=%28su%3A%22MS%20Biomedical%20Sciences%20BMS%20%20%20%20%20%20%22%29&amp;sort_by=relevance_dsc&amp;format=atom"/>
     <description><![CDATA[ Search results for '(su:&quot;MS Biomedical Sciences BMS      &quot;)' at NUST Institutions Library Catalogue]]></description>
     <opensearch:totalResults>185</opensearch:totalResults>
     <opensearch:startIndex>0</opensearch:startIndex>
     
       <opensearch:itemsPerPage>50</opensearch:itemsPerPage>
     
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    SAIKOSAPONIN B3 PROTECTS AGAINST MPTP-INDUCED PARKINSON'S DISEASE BY PREVENTING MITOCHONDRIAL OXIDATIVE DAMAGE /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=525210</link>
        
       <description><![CDATA[









	   <p>By Shahzadi,Neelam . 
	   Islamabad : SMME - NUST, 2016
                        . 57 P. : ill. ;
                        , Hardcover,
                         30cm.. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=525210">Place Hold on <em>SAIKOSAPONIN B3 PROTECTS AGAINST MPTP-INDUCED PARKINSON'S DISEASE BY PREVENTING MITOCHONDRIAL OXIDATIVE DAMAGE /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=525210</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Doxorubicin &amp; Disulfiram-metabolite Loaded Nanocarriers for The Effective Combination Therapy Against Acute Myeloid Leukaemia /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607153</link>
        
       <description><![CDATA[









	   <p>By Tariq, Urooba . 
	   
                        . 150p.
                        
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607153">Place Hold on <em>Doxorubicin &amp; Disulfiram-metabolite Loaded Nanocarriers for The Effective Combination Therapy Against Acute Myeloid Leukaemia /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607153</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Nanoencapsulation of Ferrocene Incorporated Thiourea and Doxorubicin for Treatment of Acute Myeloid Leukemia /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607171</link>
        
       <description><![CDATA[









	   <p>By Idrees, Nimra . 
	   
                        . 102p.
                        
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607171">Place Hold on <em>Nanoencapsulation of Ferrocene Incorporated Thiourea and Doxorubicin for Treatment of Acute Myeloid Leukemia /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607171</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Detecting Musculoskeletal Co-contraction for Ankle Rehabilitation through Variational Mode Decomposition in sEMG /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607172</link>
        
       <description><![CDATA[









	   <p>By Yasmeen, Sania . 
	   
                        . 56p. 
                        
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607172">Place Hold on <em>Detecting Musculoskeletal Co-contraction for Ankle Rehabilitation through Variational Mode Decomposition in sEMG /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607172</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Elucidation of Therapeutic Potential of Caffeine Nanoparticles against Acute Myeloid Leukemia /


    Usama Sabir





</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607173</link>
        
       <description><![CDATA[









	   <p>By Sabir, Usama. 
	   
                        . 88p.
                        
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607173">Place Hold on <em>Elucidation of Therapeutic Potential of Caffeine Nanoparticles against Acute Myeloid Leukemia /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607173</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Evaluation of the anti-cancerous effect of ciprofloxacin loaded liposomes against leukemia in rat model /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607175</link>
        
       <description><![CDATA[









	   <p>By Fatima, Sahar. 
	   
                        . 86p.
                        
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607175">Place Hold on <em>Evaluation of the anti-cancerous effect of ciprofloxacin loaded liposomes against leukemia in rat model /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607175</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Potential Inhibition of Lactate Dehydrogenase by Oxamate in Enterococcus faecalis /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607176</link>
        
       <description><![CDATA[









	   <p>By Raza, Laiba Hareem . 
	   
                        . 72p.
                        
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607176">Place Hold on <em>Potential Inhibition of Lactate Dehydrogenase by Oxamate in Enterococcus faecalis /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607176</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Biomineralization of PET (Polyethylene terephthalate) plastic through Sporosarcina species for plastic waste management /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607196</link>
        
       <description><![CDATA[









	   <p>By Kamran Shahzad, Muhammad . 
	   
                        . 48p. ;
                        
                         30cm.. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607196">Place Hold on <em>Biomineralization of PET (Polyethylene terephthalate) plastic through Sporosarcina species for plastic waste management /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607196</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Role of Nucleobindin 1 in Clozapine-Induced Neuroprotection in MPTP-Treated Mice Models /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607207</link>
        
       <description><![CDATA[









	   <p>By Bhatti, Rohama Makmas . 
	   
                        . 64p.
                        
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607207">Place Hold on <em>Role of Nucleobindin 1 in Clozapine-Induced Neuroprotection in MPTP-Treated Mice Models /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607207</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Characterization of the Role of Neurexin-1 in MPTP Induced Parkinsonism in Mice Model /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607208</link>
        
       <description><![CDATA[









	   <p>By Naeem, Mahnoor . 
	   
                        . 62p.
                        
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607208">Place Hold on <em>Characterization of the Role of Neurexin-1 in MPTP Induced Parkinsonism in Mice Model /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607208</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Plug and play: nnUNet for the Auto-Segmentation of Head &amp; Neck Tumors and Lymph Nodes on 3D FDG PET/CT Scans /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607209</link>
        
       <description><![CDATA[









	   <p>By Basharat, Sonia . 
	   
                        . 35p.
                        
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607209">Place Hold on <em>Plug and play: nnUNet for the Auto-Segmentation of Head &amp; Neck Tumors and Lymph Nodes on 3D FDG PET/CT Scans /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607209</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Brain Tumor Segmentation using CT Hybrid






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607211</link>
        
       <description><![CDATA[









	   <p>By Siddiqah, Mariyam . 
	   
                        . 30p.
                        
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607211">Place Hold on <em>Brain Tumor Segmentation using CT Hybrid</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607211</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Effects of Cassia Angustifolia and Nigella Sativa for the prevention of Diabetic Neuropathy /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607244</link>
        
       <description><![CDATA[









	   <p>By Khan, Mahum. 
	   
                        . 81p.
                        
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607244">Place Hold on <em>Effects of Cassia Angustifolia and Nigella Sativa for the prevention of Diabetic Neuropathy /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607244</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Therapeutic Potential of Rutin-Bound Glucose Carbon Dots for Alzheimer’s Disease /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607245</link>
        
       <description><![CDATA[









	   <p>By Khan, Sana. 
	   
                        . 76p.
                        
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607245">Place Hold on <em>Therapeutic Potential of Rutin-Bound Glucose Carbon Dots for Alzheimer’s Disease /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607245</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Early Diagnosis of AD by Detecting Amyloid-Beta in the Retina of AD-Induced Mice Using IR Spectroscopy /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607248</link>
        
       <description><![CDATA[









	   <p>By Waheed, Zuha. 
	   
                        . 66p.
                        
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607248">Place Hold on <em>Early Diagnosis of AD by Detecting Amyloid-Beta in the Retina of AD-Induced Mice Using IR Spectroscopy /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607248</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Mental Workload on the Children in Multilingual Environment /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607250</link>
        
       <description><![CDATA[









	   <p>By Niazi, Anum . 
	   
                        . 56p.
                        
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607250">Place Hold on <em>Mental Workload on the Children in Multilingual Environment /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607250</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Isolation, Phytochemical Analysis and Antibacterial Activity of Rumex  acetosella Plant /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607252</link>
        
       <description><![CDATA[









	   <p>By Abbasi, Zoya Orangzeb . 
	   
                        . 62p.
                        
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607252">Place Hold on <em>Isolation, Phytochemical Analysis and Antibacterial Activity of Rumex  acetosella Plant /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607252</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Evaluating Antibacterial And Wound Healing Activity Of Rumex acetosella Leaves /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607253</link>
        
       <description><![CDATA[









	   <p>By  Fareed, Laraib. 
	   
                        . 60p. ;
                        
                         30cm.. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607253">Place Hold on <em>Evaluating Antibacterial And Wound Healing Activity Of Rumex acetosella Leaves /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607253</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Development and Characterization of Biomaterials for Biomedical Applications /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607289</link>
        
       <description><![CDATA[









	   <p>By Zahra, Fatima . 
	   
                        . 53p.
                        
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607289">Place Hold on <em>Development and Characterization of Biomaterials for Biomedical Applications /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607289</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Prevention of Diabetes-Associated Cognitive Impairment through the Administration of Herbal Products /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607295</link>
        
       <description><![CDATA[









	   <p>By  Riaz, Hibba. 
	   
                        . 67p. ;
                        
                         30cm.. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607295">Place Hold on <em>Prevention of Diabetes-Associated Cognitive Impairment through the Administration of Herbal Products /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607295</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Cannabinoid Extract Protects Against Valproic Acid Induced Autism Spectrum Disorder /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607315</link>
        
       <description><![CDATA[









	   <p>By  Ali, Faiza. 
	   
                        . 79p. ;
                        
                         30cm.. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607315">Place Hold on <em>Cannabinoid Extract Protects Against Valproic Acid Induced Autism Spectrum Disorder /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607315</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Synthesis and Characterization of pH-Sensitive Smart Patch for Anti- Hypertensive Drug /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607316</link>
        
       <description><![CDATA[









	   <p>By  Azhar, Maleeha. 
	   
                        . 64p. ;
                        
                         30cm.. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607316">Place Hold on <em>Synthesis and Characterization of pH-Sensitive Smart Patch for Anti- Hypertensive Drug /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607316</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Development and Characterization of DNA-based Kit for Cancer Diagnosis /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607318</link>
        
       <description><![CDATA[









	   <p>By  Fatima, Areej. 
	   
                        . 74p. ;
                        
                         30cm.. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607318">Place Hold on <em>Development and Characterization of DNA-based Kit for Cancer Diagnosis /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607318</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Animal and clinical study for Treatment of Asthma using Intranasal inhalation of Himalayan salt /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607328</link>
        
       <description><![CDATA[









	   <p>By Tariq, Ayesha . 
	   
                        . 56p.
                        
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607328">Place Hold on <em>Animal and clinical study for Treatment of Asthma using Intranasal inhalation of Himalayan salt /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607328</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Mobile Tablet Base Therapies for Cognitive Rehabilitation of Stroke Patients /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607362</link>
        
       <description><![CDATA[









	   <p>By  Shad, Amna. 
	   
                        . 66p. ;
                        
                         30cm.. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607362">Place Hold on <em>Mobile Tablet Base Therapies for Cognitive Rehabilitation of Stroke Patients /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607362</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Multimodal Segmentation of Brain tumor using BraTS dataset 2020 /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607365</link>
        
       <description><![CDATA[









	   <p>By Saeed, Aniqa . 
	   
                        . 60p. ;
                        
                        
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607365">Place Hold on <em>Multimodal Segmentation of Brain tumor using BraTS dataset 2020 /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607365</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Genetic Screening for the Prevalence of PRNP Mutations in Pakistan /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607437</link>
        
       <description><![CDATA[









	   <p>By Khalid, Minahil . 
	   
                        . 83p.
                        , Prion diseases are highly contagious, rapidly progressive, and extremely life-threatening
neuronal condition. CJD is the prime example of prion disease. Many cases of CJD have
been reported up till now. It can be acquired, inherited or sporadic in nature. sCJD
accounts for the highest prevalence globally i.e., 85% of the cases, gCJD encompasses
10-15% of the cases whereas iCJD cases include 1-2%. Its long incubation period (10-12
years) and short disease duration (3-12 months) makes it difficult to diagnose, which has
contributed to higher death toll since its occurrence. World organizations are strictly
monitoring CJD cases, in order to curtail the spread of this fatal disease but they are far
behind in eradicating it completely. Hence it is imperative to identify CJD sources to
reduce the number of cases. Therefore, this present research is the first initiative to assess
the prevalence of CJD in Pakistani population. Results of this study indicated absence of
mutation at codon 200 in the participants under study. Most prevalent genotype were
M129-E200 (71%) and V129-E200 (29%) whereas M129-K200 and V129-K200 were
absent in the participants. In parallel study a survey encompassing questions related to
cognitive impaired just like CJD was also carried out to assess public knowledge
regarding it. Results indicated that educated groups lacked knowledge in theoretical as
well as non-theoretical aspects of CJD. This study is highly significant as it provides
preliminary data on the susceptible cases of CJD and proof that the public knowledge
also corresponds to the data gathered by genetic screening
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607437">Place Hold on <em>Genetic Screening for the Prevalence of PRNP Mutations in Pakistan /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607437</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Assessment of APOE Genotype in Pakistani Population with Relevance to Rapidly Progressive Alzheimer’s Disease /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607439</link>
        
       <description><![CDATA[









	   <p>By Rasheed, Urwah. 
	   
                        . 68p.
                        , According to the statistics provided by World Health Organization (WHO), approximately
55 million people are suffering from dementia globally making it a major public health
concern. Alzheimer’s Disease (AD) is the most common cause of dementia constituting
60-70% of cases worldwide. There are various environmental and genetic risk factors that
contribute to the development of AD, among the genetic risk factors, APOE polymorphism
is the major risk factor for AD. There are three isoforms of APOE gene E2, E3, and E4.
The presence of different isoforms of APOE gene in different genotypical combinations
determine how susceptible is the person to developing AD in the future. AD affects the
patient’s quality of life severely and makes even basic chores undoable, therefore it is
imperative for people to be aware of the disease and stay clear of the myths surrounding it.
The present study is the first one to assess the presence of APOE genotype in Pakistani
population with relevance to AD, no study of this sort has been carried out in Pakistan
before. The results showed complete absence of E2 allele in the tested population size. The
most prevalent allele was E3 which was expressed in the form of E3E3 (95%) and E3E4
(5%) genotypes. E4/E4 genotype was also completely absent. In this study, a detailed
survey was also conducted to assess the knowledge of AD in Pakistani people. In certain
non-technical areas, the respondents exhibited good knowledge about the AD, but in the
technical aspects where risk factors, diagnostic criteria and treatment options related to the
disease were involved, the participants displayed poor knowledge, this shows that even the
educated people in Pakistan are unaware about the basic knowledge of the disease. It is
imperative to establish organizations that can create awareness among the masses regarding
AD which is exponentially increasing in Pakistan.
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607439">Place Hold on <em>Assessment of APOE Genotype in Pakistani Population with Relevance to Rapidly Progressive Alzheimer’s Disease /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607439</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Comparison of a Human Portable Blood Glucose Meter and Automated Chemistry Analyzer for Measurement of Blood Glucose Concentrations in Human Diabetic Patients /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607444</link>
        
       <description><![CDATA[









	   <p>By Asad-Ur-Rehman. 
	   
                        . 46p.
                        , Diabetes is the most prevalent chronic metabolic disorder in Pakistan which is
characterized by an increased Blood Glucose level. An accurate diagnosis of diabetes is
very essential for its early detection and treatment. Almost 90\% of the cases are of Type
II Diabetes and the patients are required to continuously monitor their Blood Glucose
level to maintain a near-normal range of Blood sugar. A practical way to monitor sugar
levels is using a portable Glucometer at home which is faster and more convenient for
diabetes patients. The purpose of this study is to compare Blood Glucose levels measured
using Oxidase Method and a Portable Glucometer with reference Hexokinase Method in
Type II Diabetes patients to determine if Glucometers can be used as a home-based selfmonitoring device. A cross-sectional study was conducted with a total of 150 Type II
Diabetes patients. Blood samples were collected from the capillary of fingers for a
portable Glucometer and from veins for Hexokinase and Oxidase Plasma methods after
overnight fasting of 8 hours. Independent t-test and Pearson Correlation were used to
check the significance of our results. There was no statistically significant difference in
Blood Glucose readings obtained from Oxidase Method (128.31 + 61.4, p = 0.947) and
Glucometer (122.53 + 59.6, p = 0.370) with Reference Hexokinase Method (128.78 +
61.2). A statistically significant positive correlation was observed in both methods with
reference Hexokinase Method. Glucometer readings positively correlate with
Hexokinase, showing that Glucometer can be used as a home-based self-monitoring
Blood Glucose Device. 
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607444">Place Hold on <em>Comparison of a Human Portable Blood Glucose Meter and Automated Chemistry Analyzer for Measurement of Blood Glucose Concentrations in Human Diabetic Patients /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607444</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Deploying Efficient Net (BNs) for grading Diabetic Retinopathy severity levels from fundus images /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607466</link>
        
       <description><![CDATA[









	   <p>By Batool, Summiya . 
	   
                        . 40p.
                        , One of the common and escalating endocrine illnesses is diabetes mellitus. Diabetic
retinopathy is a common eye problem in patients with diabetes. Diabetic retinopathy
(DR), a retinal condition, is acknowledged as an epidemic on a global scale. One-third of
the estimated 285 million persons with diabetes show symptoms of DR, and one-third of
them have DR that threatens their vision [1]. In addition, the figures are rising. By 2040,
288 million individuals are expected to have AMD, and by 2050, the number of people
with DR is projected to treble. The need for reliable diabetic retinopathy screening
systems became a critical issue recently due to the increase in the number of diabetic
patients. The severity of DR can be graded into five stages: normal, mild NPDR, moderate
NPDR, severe NPDR, and PDR. Early diagnosis and treatment of DR can be
accomplished by organizing large regular screening programs. Numerous Convolutional
neural network models are developed for the diagnosis of DR in fundus images using
deep learning methods. In Deep Learning (DL) one of the methods is a computer-aided
medical diagnosis for the detection of DR. There are many DL-based methods such as
restricted Boltzmann Machines, convolutional neural networks (CNNs), auto-encoder,
and sparse coding. On the other hand, it is thought-provoking to distinguish it initially not
display signs in the initial classes. The current models for diabetic retinopathy mayn’t
identify entire classes of DR. The utmost commonly used metrics like accuracy, f1-score,
precision, and recall; do not cogitate the standard of difference among labels, which
supports spotting all classes of DR. In our paper used Efficient Net BNs models. We
concluded evaluation scores using the F1-score, which is applicable for grading various
classes of DR established on the intensity levels. We have accomplished the F1- score of
0.88 and 0.84 using the simple preprocess, Gaussian smoothing filters, and deploying an
Efficient Net BNs network on DeepDRiD and EYE-PACS datasets.
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607466">Place Hold on <em>Deploying Efficient Net (BNs) for grading Diabetic Retinopathy severity levels from fundus images /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607466</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Synthesis, Characterization and Application Of Natural Nano Composites /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607469</link>
        
       <description><![CDATA[









	   <p>By Tariq, Faiza . 
	   
                        . 71p.
                        , The use of natural polymers in the creation of skin wound dressings has gained attentionfor its potential to speed up healing and protect against pathogens. In this study, theability of the Papaver somniferum plant to heal wounds in various forms, suchas pureplant extract, plant-derived silver nanoparticles, and their inclusion in a polyvinyl alcohol
hydrogel, was investigated. Characterization of the compounds was done usingUVspectrophotometry, X-ray diffraction, Fourier transform infrared spectroscopy, scanningelectron microscopy, and energy dispersive spectroscopy. Antimicrobial tests showedthat silver nanoparticles had a zone of inhibition of 12mm against Staphylococcus aureus, while the silver nanoparticle hydrogel had a zone of inhibition of 23mmagainst Klebsillapneumonia. The zone of inhibition by the plant extract was 11mmagainst
Staphylococcus aureus, while the plant extract gel had a zone of inhibition of 16mmagainst Staphylococcus aureus. The results suggest that the bio-composite patches createdfrom these materials have potential to work against both gram-positive andgram-negative bacteria. In a mouse model, the wound healing capacity was highest for thesilver nanoparticle gel, with a wound closure of 1.7mm. Histological analysis alsoshowed that the silver nanoparticle hydrogel had excellent wound repair properties. Overall, the study suggests that pure AgNPs and bio-composite hydrogel of AgNPs haveefficient and quick healing of wounds as compared to the plant extract and plant nanocomposites hydrogel.
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607469">Place Hold on <em>Synthesis, Characterization and Application Of Natural Nano Composites /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607469</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Effect of Etoposide loaded Nanoparticles in the Treatment of Advanced Liver Diseases /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607470</link>
        
       <description><![CDATA[









	   <p>By Iqbal, Zarqa . 
	   
                        . 76p.
                        , Advanced liver diseases (ALD) continue to pose significant health challenges due to their
high global prevalence and limited currently available curative options, besides liver
transplantation. Liver disease therapeutics include many substances that may have
insufficient effectiveness and severe adverse effects, such as Etoposide, having toxic
nature with low compatibility and solubility in an aqueous solution. Nanoparticle-based
therapeutics emerged as an efficient and safe treatment option to minimize side effects.
Etoposide used for ALD is more toxic with low biocompatibility and solubility in an
aqueous solution which makes it less efficient. The purpose of the study is to use
nanoparticle-based etoposide for the treatment of ALD by improving its biocompatibility
and solubility which makes this target-based therapy less toxic and more effective. Rat
models used in this study were introduced with CCL4 and Urethane co-administration to
develop liver cirrhosis. The thin film hydration method was used to synthesize etoposideencapsulated liposomal nanoparticles. The stability and stealth effect of liposomes were
enhanced by polyethylene glycol (PEG) coating. Etoposides and PEG-coated etoposide
liposomes were administered intravenously, into diseased rats. Results showed that
etoposide and PEG-coated liposomal encapsulation are highly effective as compared to
etoposide alone and blank nanoparticles and hence, be a substantial strategy for the
treatment of ALD through intravenous drug delivery system.
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607470">Place Hold on <em>Effect of Etoposide loaded Nanoparticles in the Treatment of Advanced Liver Diseases /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607470</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Formation of Ciprofloxacin Loaded Transethosomes to Check the Antibacterial Activity Against Skin Infections /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607484</link>
        
       <description><![CDATA[









	   <p>By Tariq, Huraira. 
	   
                        . 67p.
                        , One of the serious challenges in the treatment of infectious diseases is the presence of bacterial
infections in subcutaneous wound tissue. Staphylococcus epidermidis (S. epidermidis) and
Propionibacterium acne (P. acne) are resistant bacterial strains that cause severe disease in
humans when penetrating the deeper layer of skin. Antibacterial drugs with a nonspecific target
have more difficulty in penetrating the deeper layer of infected skin. Broad spectrum antibiotics
are best to treat the infection but are not commonly used because bacteria’s make resistance
against them. To overcome these issues, a combined strategy of broad-spectrum antibacterial
drug and nanoparticle was formulated for targeted delivery, enhanced penetration to the infection
site specifically. The ciprofloxacin was entrapped in transethosomes and formulation was
synthesized by using the cold method. Transethosomes are very small in size that can reach the
deeper layer of skin to give potential effects. In the layers of skin, ciprofloxacin works by
binding to the enzymes topoisomerase IV and DNA gyrase and inhibit the DNA replication in
bacteria. The antibacterial activity of ciprofloxacin loaded transethosomes against skin infections
was assessed using Staphylococcus epidermidis and Propionibacterium acne and the method
used was well diffusion method. The characterization of ciprofloxacin loaded transethosomes
was done through, zeta potential, particle size evaluation, and drug release efficiency. Loaded
transethosomes displayed substantially have more potential effect than ciprofloxacin alone. The
in-vitro studies show that ciprofloxacin loaded transethosomes boost the antibacterial activity of
ciprofloxacin against gram positive.
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607484">Place Hold on <em>Formation of Ciprofloxacin Loaded Transethosomes to Check the Antibacterial Activity Against Skin Infections /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607484</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Bone X-ray abnormality detection using MURA dataset /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607691</link>
        
       <description><![CDATA[









	   <p>By Batool, Sana. 
	   
                        . 40p.
                        , Musculoskeletal abnormalities along with bone fractures are a wide range of
abnormalities that account for most visits of patients to Emergency department of hospitals.
According to an estimate, more than 1.7 billion people are affected by musculoskeletal disorders
each year. Bone X-rays are the first line imaging modality for imaging of fractured bones.
Radiologists then undergo reporting of X-rays for detection of fractures and pathologies.
Classification of bone X-rays into normal and abnormal is a time-taking process and is also
subjected to variability between different radiologists. Therefore, the use of automatic classifiers
incorporating deep learning algorithms is currently in use in clinical diagnostics. MURA is a
large publicly available dataset released by the machine learning group of Stanford university.
MURA dataset consists of 40,895 multi-view images of upper limb that belong to seven regions
namely shoulder, humerus, elbow, forearm, wrist, hand, and fingers. In this study we propose the
use of the single DenseNet-169 model trained on complete dataset along with multiple preprocessing and data augmentation steps, based on Keras in TensorFlow. Training data was
divided into 80:20 for training and validation respectively, whereas, testing of model was done
on validation set. The results obtained through the proposed technique include 80% testing
accuracy. This validates the effectiveness of this method for bone fractures classification.
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607691">Place Hold on <em>Bone X-ray abnormality detection using MURA dataset /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607691</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Targeting Microtubule-associated Protein Tau (MAPT) Interactors for Novel Therapeutic Interventions for Rapidly Progressive Alzheimer’s Disease /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607697</link>
        
       <description><![CDATA[









	   <p>By Fatimah. 
	   
                        . 74p.
                        , Rapidly Progressive Alzheimer's disease (rpAD) is a disease characterized by rapid cognitive
loss. It progresses quickly over the course of weeks to months and sometimes may take up to
two to three years. It’s rare and difficult to diagnose although accurate diagnosis is extremely
crucial for its treatment. Recent evidence suggests Tau as a promising therapeutic agent for the
development of disease-modifying drugsfor rpAD due to the involvement of Tau abnormalities
in rpAD neurodegeneration. To determine whether Tau is a suitable therapeutic target, in silico
tools were used to analyse the interaction of proteins isolated by Tau IP. It is identified that
proteins interact with MAPT during the pathology of disease and play a role in progression of
rpAD. The specific interaction between the MAPT region belonging from the MTB domain
2MZ7 and its interactors Neuromodulin, Synaptophysin and RhoA were investigated using
molecular docking and visualization tools like PyRx, PyMOL, Discovery Studio, and LigPlot+
and binding energies and bonding between the amino acids was observed and evaluated.
Protein network analysis revealed an aberration towards apoptotic pathway and signaling
pathway. Furthermore, binding of different drug compounds including Methamphetamine,
Ascorbic acid and Doxorubicin were evaluated through docking in silico. Doxorubicin showed
the highest binding energy of -6.0 kcal/mol with 2MZ7. These drug compounds and their
interaction with 2MZ7 yielding high binding affinity shows that binding site of MAPT can be
blocked using Doxorubicin to prevent the interaction of pathological proteins that are involved
in the accelerated progression of rpAD. 
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607697">Place Hold on <em>Targeting Microtubule-associated Protein Tau (MAPT) Interactors for Novel Therapeutic Interventions for Rapidly Progressive Alzheimer’s Disease /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607697</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Targeting Dihydrolipoamide Dehydrogenase (DLD) Interactors for Novel Therapeutic Interventions for Alzheimer’s Disease /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607708</link>
        
       <description><![CDATA[









	   <p>By Choudhary, Jawaria . 
	   
                        . 72p.
                        , Alzheimer's disease is the one of the most common type of dementia, which affects millions of
people worldwide. Severe memory loss is a defining feature, with episodic memory being
particularly damaged in the initial stages. The majority of occurrences of Alzheimer's disease
are random, while risk is increased if specific susceptibility genes are inherited. Alzheimer's
disease is linked to a decline in energy metabolism, but it is unclear whether this decline
worsens or prevents the condition. The finding that genetically dihydrolipoamide
dehydrogenase (DLD) is associated to the late-onset AD serves as further evidence for the
significance of energy metabolism in AD. To determine if DLD is an appropriate therapeutic
target, in silico tools have been used in our study to analyse the interaction of DLD with
CAND1, LAMP1, and TPP1 using molecular docking and visualization tools like PyRx,
PyMOL, Discovery Studio, and Ligplot++. It was observed that binding sites of 5NHG are
surrounded by 68 amino acids, and CAND1 (1191-1200), LAMP1 (216-225), and TPP1 (546-
555) were able to interact with the amino acids inside the binding pocket of 5NHG. Protein
network analysis showed aberration towards apoptosis. In our study, we also evaluated the
binding of ascorbic acid, acetaminophen, and methamphetamine after docking experiment to
find therapeutic potential. Ascorbic acid and acetaminophen showed the highest binding energy
with 5NHG. The interaction of these drug compounds with 5NHG yielding high binding
affinity shows that these compounds can be used to block the binding sites on DLD to prevent
the interaction of pathological proteins with DLD that are involved in the up-regulation or
down-regulation of DLD in diseased state.
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607708">Place Hold on <em>Targeting Dihydrolipoamide Dehydrogenase (DLD) Interactors for Novel Therapeutic Interventions for Alzheimer’s Disease /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607708</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    LIPOSOMAL DOXORUBICIN FOR THE TREATMENT OF ADVANCED LIVER DISEASE /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607717</link>
        
       <description><![CDATA[









	   <p>By Khan, Faryal . 
	   
                        . 59p.
                        , Nanoscale materials are utilized as diagnostic instruments or to administer therapeutic substances
to specific targeted regions in a controlled manner in the fields of nanomedicine and nano drug
carriers, which are still relatively young but are quickly evolving. Nanoparticles can potentially
deliver medications more accurately because they are currently made from biocompatible
materials. The treatment of advanced liver disease has benefited greatly from nanomedicine in
previous decades. Nano-based drug delivery systems improve the effectiveness of medications.
Today, advanced liver disease is being treated with liposomal nanoparticles. Nano-based drug
delivery systems increase the efficacy of both new and existing treatments through a detailed
investigation of nanoparticle manufacturing and utilization.
One of the most often used anticancer medications is doxorubicin. Doxorubicin (DOX) is a
medication that is frequently used to treat HCC. Doxorubicin is a medicine that belongs to the
anthracyclines class and is commonly used to treat different types of cancers, including lymphomas,
leukemias, breast, ovary, thyroid, and lungs.
Doxorubicin interacts with nitrogen - containing bases of DNA and prevents the production of
macromolecules. This, in turn, prevents the action of the enzyme topoisomerase II (Top II), which
inhibits the replication process. Consequently, malignant cells are prevented from proliferating.
According to early research, doxorubicin's cardiotoxicity is reduced when it is encapsulated inside
liposomes.
Due to its cardiotoxicity, the &quot;thin film hydration approach&quot; was utilized to create doxorubicinencapsulated liposome nanoparticles, which were then used to treat advanced liver disease. The
liposome nanoparticles were coated with polyethylene glycol (PEG) to boost their stability and
provide a stealth effect. Pegylation improves steric repulsion and is therefore regarded as a superior
stabilizer for various kinds of nanoparticles. PEG adopts the drug's erosion-controlled release
mechanism, which led to continuous release. It is noted that a significant technique to treat NAFLD
is to encapsulate the doxorubicin drug within liposomes and modify these liposome nanoparticles
via PEG.
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607717">Place Hold on <em>LIPOSOMAL DOXORUBICIN FOR THE TREATMENT OF ADVANCED LIVER DISEASE /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607717</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Validation of Antibacterial Activity of Gossypol against Enterococcus faecalis /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607823</link>
        
       <description><![CDATA[









	   <p>By Rasool, Misbah . 
	   
                        . 54p.
                        , Antibiotic resistance is a growing concern today that affects the entire world, necessitating the
development of new antibacterial medications. Nosocomial infections pose a serious challenge for
patients and hinder effective treatment. The second most common cause of nosocomial infections
is Enterococcus faecalis, and it depends on the lactate dehydrogenase enzyme's capacity to
maintain redox balance for growth, resistance, and virulence. As demonstrated before by
computational technique, our study attempted to assess the antibacterial effect of Gossypol on
Enterococcus faecalis by inhibiting Lactate Dehydrogenase Enzyme. We used six different
stressors, including 0.01% SDS, 2.5mM H2O2, 8% Ethanol, 10% DMSO, 10% Glucose, and
0.25% HOCl, in addition to our inhibitor Gossypol. Gossypol was employed in the following
concentrations: 5, 10, 25, 50, 75, 100, 150, 200 micrograms per milliliter using a large test tube
method, absorbance on a UV-visible spectrophotometer, and on a microscale using a 96-well flatbottom plate with a Microplate reader. Between control (Culture Media) and vehicle control, which
is DMSO, there is no discernible difference. At higher dosages of Gossypol, such as 100 and 200
micrograms per milliliter, there is significant growth inhibition; nevertheless, 5, 10, 25, 50, 75, and
100 micrograms per milliliter show no significant inhibition. Minimum Inhibitory Concentration
is 100 microgram per milliliter. We used our six different stress factors with MIC value of
Gossypol. There is no discernible growth inhibition when Gossypol is employed in conjunction
with stress factors such 0.01% SDS, 2.5mM H2O2, and 0.25% HOCl. However, at 100
micrograms per milliliter at the fourth and fifth hours, glucose 10% exhibits a strong inhibitory
impact, though not by a great deal. Along with MIC value of Gossypol, 100 micrograms per
milliliter, 8% ethanol and 10% DMSO significantly slowed the development of the bacteria. The
lactate dehydrogenase enzyme in Enterococcus faecalis was effectively inhibited by gossypol.
Future in vivo studies are required to demonstrate the antibacterial activity of Gossypol in greater
detail, as well as to compare it to antibiotics as an adjunctive treatment.
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607823">Place Hold on <em>Validation of Antibacterial Activity of Gossypol against Enterococcus faecalis /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607823</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Prevalence of APP-associated novel polymorphism in Pakistani Population /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607828</link>
        
       <description><![CDATA[









	   <p>By Maryam, Ammara . 
	   
                        . 70p.
                        , Alzheimer’s disease is a prevalent neurodegenerative disease characterized by dementia occurs in
aged individuals. The report of prevalence of AD showed that AD and dementia patients are
estimated as 35.6 million in 2010 and this number can reach up to 66 million by 2030.
The present study is the first one to assess the presence of APP genotype in the Pakistani population
with relevance to AD, and structural analysis of wild type APP, 710 (V&gt;G) and 718 (I&gt;L), and
720 (L&gt;S) mutated APP with ligands (BACE1, ADAM10, and Nicastrin). No study of this sort
has been carried out in Pakistan before. The in silico results showed that mutated APP at 718 codon
interacts with serine residue of BACE1, and tyrosine residue with Nicastrin. Change in these
residues cause protein to undergo aberrant denaturing and results in generation of amyloids due to
differential binding of mutated APP protein with ligands in AD. SNP analysis showed the
prevalence of 718 (I&gt;L) mutation in 4% of studied population. Symptoms of 718 (I&gt;L), mutation
in APP are Hippocampus atrophy, dementia with remarkable oral tendency, and Amnesia. It is
imperative to establish organizations that can create awareness among the masses regarding AD
which is exponentially increasing in Pakistan.
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607828">Place Hold on <em>Prevalence of APP-associated novel polymorphism in Pakistani Population /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607828</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Post-Discharge symptoms and analysis for COVID-19 patients /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607924</link>
        
       <description><![CDATA[









	   <p>By Shahjehan, Ayesha . 
	   
                        . 65p.
                        , Coronavirus was initially recognized as human COVID by researchers in 1965. Different
strains of coronavirus appeared in the following years MERS, SARS-1. Thousands of cases were
reported in individuals that to led many casualties, in 2019.
New strains of coronavirus emerged, known as covid-19that started to spread from
Wuhan, China. It was labeled a worldwide epidemic by the World Health Organization (WHO)
in March 2020, the first since 2009. Patients with covid-19 experienced gentle to extreme
indications like fever, cough, weariness, shortness of breath, migraine, loose bowels, nausea, and
vomiting. As SARS cov-2 is a novel infection, initially the infected patients were treated in a
single room along with the utilization of antiviral medication, including oseltamivir, ribavirin,
and ganciclovir, lopinavir, and ritonavir to decrease the viral burden. Indications during the
contamination may not resolve unexpectedly grumble about persistent side effects, even a long
time after the disease. The research is based on observing the symptoms of COVID and postCOVID in patients who perform PCR tests at a hospital. Sample of 26 males and 34 females.
Services were taken and their symptoms were noted during and after the quarantine. During the
assessment of the covid-19 pandemic, it was seen that overall unexpected issues have gotten
even after the onset of intensive covid-19. The prolonged aftereffect stays unexplained. The
point of this examination is to represent the persistent symptoms in patients who were released
from the health center and to explore the related element of danger. The impact of the study is
fundamental in investigating the components and potential persistent post-COVID disorder. It
presents a system of procedures for prognosis and handling of patients with suspected or
affirmed persevering post-COVID conditions.
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=607924">Place Hold on <em>Post-Discharge symptoms and analysis for COVID-19 patients /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=607924</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    EXPLORING ASSOCIATED SIGNALLING PATHWAYS IN THE DEVELOPMENT OF SKIN CANCER AND NEUROLOGICAL DISORDERS /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608105</link>
        
       <description><![CDATA[









	   <p>By  Iftikhar, Musawira. 
	   
                        . 65p. ;
                        
                        
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=608105">Place Hold on <em>EXPLORING ASSOCIATED SIGNALLING PATHWAYS IN THE DEVELOPMENT OF SKIN CANCER AND NEUROLOGICAL DISORDERS /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608105</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    DECISION SUPPORT SYSTEM FOR BONE FRACTURE DETECTION USING IMAGE PROCESSING TECHNIQUES /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608107</link>
        
       <description><![CDATA[









	   <p>By FAROOQ ,NAJWA . 
	   
                        . 51p. ;
                        
                        
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=608107">Place Hold on <em>DECISION SUPPORT SYSTEM FOR BONE FRACTURE DETECTION USING IMAGE PROCESSING TECHNIQUES /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608107</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Computational Analysis for Prediction of Potential Inhibitors of Lactate Dehydrogenase Enzyme of E.faecalis /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608109</link>
        
       <description><![CDATA[









	   <p>By Matloob, Muhammad . 
	   
                        . 96p. ;
                        
                        
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=608109">Place Hold on <em>Computational Analysis for Prediction of Potential Inhibitors of Lactate Dehydrogenase Enzyme of E.faecalis /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608109</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Computational Analysis for Prediction of Potential Inhibitors of Lactate Dehydrogenase Enzyme of E.faecalis /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608110</link>
        
       <description><![CDATA[









	   <p>By Matloob, Muhammad . 
	   
                        . 96p. ;
                        
                        
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=608110">Place Hold on <em>Computational Analysis for Prediction of Potential Inhibitors of Lactate Dehydrogenase Enzyme of E.faecalis /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608110</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Indigenous Design and Development of an Industrial Electrochemical Polishing System for MDDC Production Line of Coronary Stents /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608111</link>
        
       <description><![CDATA[









	   <p>By Sehar, Zainab . 
	   
                        . 72p. ;
                        
                        
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=608111">Place Hold on <em>Indigenous Design and Development of an Industrial Electrochemical Polishing System for MDDC Production Line of Coronary Stents /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608111</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    SYNTHESIS AND CHARACTERIZATION OF PEG CAPPED TAMOXIFEN LOADED ZINCOXIDE NANOPARTICLES AND THEIRTHERAPUTIC APPLICATIONS /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608144</link>
        
       <description><![CDATA[









	   <p>By  MALIK , MAHNOOR. 
	   
                        . 54p. ;
                        
                        
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=608144">Place Hold on <em>SYNTHESIS AND CHARACTERIZATION OF PEG CAPPED TAMOXIFEN LOADED ZINCOXIDE NANOPARTICLES AND THEIRTHERAPUTIC APPLICATIONS /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608144</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Human Placental-Derived Extracellular Matrix Sheets as Scaffolds for Cell Growth in Cornea Transplantation: A Promising Approach in Regenerative medicine /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608258</link>
        
       <description><![CDATA[









	   <p>By Khan, Unaiza Ali . 
	   
                        . 121p.
                        , Eye is a sensory organ designed for human vision. Its intricate components work
together to make the process of sight possible. The cornea is a critical part of the eye
responsible for clear vision, and corneal diseases or injuries can lead to visual impairment
or blindness. However, the limited availability of suitable donor tissue poses a significant
challenge. There is a significant influence on the quality of life when the visual acuity is
reduced. In terms of the overall prevalence of blindness and visual impairment Pakistan
ranks third position, following the India and Bangladesh across all age groups, totaling
21.78 million. Placenta-derived extracellular matrix (ECM) sheets have become an
effective therapeutic approach due to their rich composition of bioactive molecules, growth
factors, and supportive microenvironment for tissue regeneration. The unique composition
of placental-derived ECM sheets can provide a favorable microenvironment for the growth
of corneal cell and promote the regeneration of corneal tissue. In this study amniotic
membrane sheets, have been prepared by decellularizing placental tissue and different
characterization techniques have been used for a thorough examination of the human
amniotic membrane. Scanning Electron Microscopy (SEM) reveals intricate surface
features, while Hematoxylin and Eosin (H&amp;E) staining provides insights into tissue
architecture. Fourier Transform Infrared Spectroscopy (FTIR) offers a detailed
examination of biochemical composition. Microbial activity testing provides valuable
information of the membrane's antimicrobial properties. A p-value &lt; 0.05 in the ANOVA
analysis indicated a significant difference in antimicrobial activity among the three
bacterial strains. The characterization approaches utilized in this study contribute to a betterxx
knowledge of the biological characteristics of the human amniotic membrane, paving the
path for advances in regenerative medicine and tissue engineering. In this study a human
placental-derived extracellular matrix (ECM) sheets have been used to investigate the
integration potential of the ECM sheets with host corneal tissue. The positive outcome was
associated with a noticeable reduction in size of corneal defect due to the application of
amniotic membrane transplant. The use of AM proved to be essential in reducing notable
subjective symptoms like pain, as well as clinical signs such as redness and the size of
corneal ulcers.
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=608258">Place Hold on <em>Human Placental-Derived Extracellular Matrix Sheets as Scaffolds for Cell Growth in Cornea Transplantation: A Promising Approach in Regenerative medicine /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608258</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Development of UV Stabilizing Biomedical Textile by LbL Coating of Tinuvin-622 Polymeric Nanoparticles /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608365</link>
        
       <description><![CDATA[









	   <p>By Saleem Akhtar, Hurria . 
	   
                        . 81p. ;
                        
                         33cm.. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=608365">Place Hold on <em>Development of UV Stabilizing Biomedical Textile by LbL Coating of Tinuvin-622 Polymeric Nanoparticles /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608365</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Essential Oil (Eo) Blend Loaded Solid Lipid Nanoparticles (Slns) As Novel Deodorant /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608367</link>
        
       <description><![CDATA[









	   <p>By Zahra Rehman, Zahra Rehman. 
	   
                        . 66p.
                        , Human odors have been of great concern to society. The generation of malodor on the skin surface
of modern humans is caused by the biotransformation of naturally secreted non-odorous precursor
molecules into volatile odorants by members of the commensal microbiome. Culture-based
microbiological studies revealed that the axillary microbiota consists primarily of Gram-positive
bacteria of the genera Staphylococcus, Corynebacterium, and Propionibacterium. Currently there
is need to study the selective suppression of the growth of microorganisms involved in diseases
and unpleasant odors may result in the establishment of a good symbiotic relationship between
microorganisms and humans. As the growth of axillary microbiota which causes odor can be
controlled by several ways including hygiene and antimicrobial skin friendly essential oils. Given
the limitations in currently available products, a deodorant/antiperspirant formulation that
effectively prevents body odor without producing skin sensitivity or perceived undesirable
consequences is required. Our work is the deodorant production which is made from all naturally
extracted products which includes the lipid which sources from whale fish and is completely
alcohol and toxins free. This deodorant is fabricated using lecithin, solid lipid nanoparticles,
natural essential oils, and fragrance which are incorporated in a gel. The gel phase contains
triethanolamine, TEA and Carbopol-940. TEA is used in safer limits for the polymerization of
Carbopol-940 to form a clear gel. The essential oils used possess antibacterial properties which are
effective against sweat bacteria. The deodorant is aluminium and parabens free as they contribute
to cancer development and hormonal imbalance. 
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=608367">Place Hold on <em>Essential Oil (Eo) Blend Loaded Solid Lipid Nanoparticles (Slns) As Novel Deodorant /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608367</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
     In-Vivo Evaluation Of Silymarin Encapsulated Liposomal Nanoparticles In Chronic Mild Stress (Cms) Model And Depression Induced Liver Disorders /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608369</link>
        
       <description><![CDATA[









	   <p>By Fatima, Misha. 
	   
                        . 77p.
                        , Depression is categorized as one of the most prevalent psychological disorders that affect personal
wellbeing and social life of individuals. Symptoms vary from anhedonia to suicide commitment.
The molecular mechanism behind is the low concentration of neurotransmitters serotonin,
dopamine and norepinephrine in central nervous system. These are primarily responsible for
regulating and alleviating mood. In the chronic mild stress (CMS) model of depression, silymarin,
a plant-derived polyphenolic flavonoid of Silybum marianum, elicited strong antidepressant-like
action. It increased the levels of monoamines, particularly 5-hydroxytryptamine (5-HT) in the
cortex and dopamine (DA) in the mice hippocampal region and prefrontal cortex. The objective of
the current research was to investigate silymarin's antidepressant potential in CMS-induced
depressive-like behavior in mice and to identify its potential mechanism(s) of action. The mice
were given silymarin and silymarin loaded liposomal nanoparticles (SLNPs) for two weeks after
following CMS protocol for 28 days (4 weeks). Animals were assessed for behavioral alterations,
including exploratory activity in an open field test, behavioral despair in a forced swim test, and
anxiety-like behaviors in an elevated plus maze test. There lies a close relationship between
depression and inflammatory liver diseases. Hence the effect of depression on liver has also been
checked. Silymarin is a commercially available hepatoprotective drug but due to its antioxidant
properties, research has been conducted to evaluate its neuroprotective effect and hence its
prescription as antidepressant drug. However, due to its poor solubility and bioavailability there is
delay in the onset of treatment outcomes in many individuals. Certain side effects and
contraindications are also important regimen opponents. In this study, Silymarin loaded liposomal
nanoparticles (SLNPs) are prepared, characterized, and realized for the depression treatment in
Chronic Mild Stress (CMS) mice model of depression and its treatment efficiency on symptoms
of inflammatory liver diseases in mice as well. It presented face construct and validity response.
As such the SLNPs present improvement in depression measurement parameters as compared to
the simple silymarin. The SLNPs also positively impacted the aggression, anhedonia and rearing
in mice, however simple silymarin treated mice did not show improvement in social and personal
behavior. As such SLNPs compensated for delayed onset of fluoxetine response.
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=608369">Place Hold on <em> In-Vivo Evaluation Of Silymarin Encapsulated Liposomal Nanoparticles In Chronic Mild Stress (Cms) Model And Depression Induced Liver Disorders /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=608369</guid>
     </item>
	 
   </channel>
</rss>





