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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/6430" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/6430</id>
  <updated>2026-10-08T16:29:57Z</updated>
  <dc:date>2026-10-08T16:29:57Z</dc:date>
  <entry>
    <title>Genetic basis of HIV-1 resistance and susceptibility: An approach to understand correlation between human genes and HIV-1 infection</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/6601" />
    <author>
      <name>Kumar, Vijay</name>
    </author>
    <author>
      <name>Prakash, O</name>
    </author>
    <author>
      <name>Manpreet, S</name>
    </author>
    <author>
      <name>Sumedh, G</name>
    </author>
    <author>
      <name>Medhi, B</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/6601</id>
    <updated>2009-11-17T16:30:33Z</updated>
    <published>2006-09-01T00:00:00Z</published>
    <summary type="text">Title: Genetic basis of HIV-1 resistance and susceptibility: An approach to understand correlation between human genes and HIV-1 infection
Authors: Kumar, Vijay; Prakash, O; Manpreet, S; Sumedh, G; Medhi, B
Abstract: HIV infection is the serious medical and public health issue of&#xD;
present generation. By 2005, it has already infected a cumulative total of more&#xD;
than sixty million people worldwide and the number of HIV positive cases are&#xD;
rising day by day. India is currently estimated to have about 5.1 million&#xD;
infected persons with HIV-1 or AIDS (second only to South Africa) and this&#xD;
number could increase to 24 million in the next ten years. This pandemic&#xD;
situation of the AIDS stimulated a plethora of longitudinal cohort studies&#xD;
which are designed to document medical heterogeneity as well as to mitigate the&#xD;
factors that regulate the HIV-1 infection, disease progression and the immune&#xD;
defenses. In recent years these genetic studies have led to the discovery of&#xD;
various MHC and non MHC encoded genes, which directly or indirectly influence&#xD;
the susceptibility and resistance to HIV infection and AIDS.&#xD;
&#xD;
These&lt;i style=""&gt; &lt;/i&gt;genes&#xD;
and their mutated&lt;i style=""&gt; &lt;/i&gt;forms and their&#xD;
products which play a major role in determining the susceptibility or&#xD;
resistance to HIV-1 infection and AIDS. These genes have been categorized into&#xD;
MHC or non MHC encoded genes. The MHC encoded genes which determine HIV&#xD;
resistance or susceptibility are &lt;i style=""&gt;HLA-B57,&#xD;
HLA-B58, HLA-B27, HLA-Bw4&lt;/i&gt; and &lt;i style=""&gt;HLA-A11&lt;/i&gt;&#xD;
in Southeast Asians. On the other hand, non MHC encoded genes &lt;i style=""&gt;are CCR5, CCR2, RANTES, CXCL12, CXCR6,&#xD;
CCL3L1, Interleukin-10 (IL-10),&lt;/i&gt; and &lt;i style=""&gt;interferon&#xD;
gamma&lt;/i&gt;. The site specific mutations in these genes determine the&#xD;
susceptibility or resistance to HIV-1 infection and AIDS. In future the study&#xD;
of host genes in relation to HIV-1 infection may provide the researchers to&#xD;
develop newer chemotherapeutic approaches to prevent or cure HIV-1 infection&#xD;
effectively.
Page(s): 683-692</summary>
    <dc:date>2006-09-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>&lt;smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="place"&gt;&lt;smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="country-region"&gt; Efficient protocols for &lt;i style=""&gt;in vitro&lt;/i&gt; regeneration of &lt;i style=""&gt;Pennisetum glaucum &lt;/i&gt;(L) Br. &lt;/smarttagtype&gt;&lt;/smarttagtype&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/6600" />
    <author>
      <name>Arockiasamy, S</name>
    </author>
    <author>
      <name>Rani, S Sahaya</name>
    </author>
    <author>
      <name>Ignacimuthu, S</name>
    </author>
    <author>
      <name>Melchias, G</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/6600</id>
    <updated>2009-11-17T16:30:34Z</updated>
    <published>2006-09-01T00:00:00Z</published>
    <summary type="text">Title: &lt;smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="place"&gt;&lt;smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="country-region"&gt; Efficient protocols for &lt;i style=""&gt;in vitro&lt;/i&gt; regeneration of &lt;i style=""&gt;Pennisetum glaucum &lt;/i&gt;(L) Br. &lt;/smarttagtype&gt;&lt;/smarttagtype&gt;
Authors: Arockiasamy, S; Rani, S Sahaya; Ignacimuthu, S; Melchias, G
Abstract: A system was developed for &lt;i&gt;in vitro&lt;/i&gt; regeneration of &lt;i style=""&gt;Pennisetum glaucum&lt;/i&gt; through organogenesis&#xD;
and somatic embryogenesis. Mature embryo and leaf base explants of &lt;i style=""&gt;Pennisetum glaucum &lt;/i&gt;(L) Br. cv HH B60 (Poaceae) were&#xD;
cultured on Murashige and Skoog agar medium supplemented with 11.3 µ&lt;i&gt;M&lt;/i&gt; of&#xD;
2,4-D for callus induction. Embryogenic calli were induced within eight weeks.&#xD;
Percentage of callus induction and somatic embryogenesis was significantly&#xD;
higher in mature embryo than leaf base explants. Maximum shoot regeneration was&#xD;
obtained via organogenesis on MS medium supplemented with 4.43 µ&lt;i&gt;M &lt;/i&gt;of BAP&#xD;
and 4.64 µ&lt;i&gt;M&lt;/i&gt; of kinetin from the calli of both the explants. The&#xD;
frequency of plant regeneration through somatic embryogenesis was comparatively&#xD;
lower than organogenesis. Regeneration frequency was higher in mature embryo&#xD;
explants than leaf base explants. The shoots regenerated via organogenesis were&#xD;
elongated and rooted efficiently on MS medium supplemented with IBA (0.49 µ&lt;i&gt;M&lt;/i&gt;).&#xD;
The rooted plantlets were hardened and transferred to soil.
Page(s): 757-761</summary>
    <dc:date>2006-09-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Cumulative antioxidant defense against oxidative challenge in galactose-induced cataractogenesis in Wistar rats</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/6599" />
    <author>
      <name>Raju, T N</name>
    </author>
    <author>
      <name>Kumar, C Sanat</name>
    </author>
    <author>
      <name>Kanth, V Rajani</name>
    </author>
    <author>
      <name>Ramana, B Venkata</name>
    </author>
    <author>
      <name>Reddy, P Uma Maheswara</name>
    </author>
    <author>
      <name>Suryanarayana, P</name>
    </author>
    <author>
      <name>Reddy, G Bhanuprakash</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/6599</id>
    <updated>2009-11-20T16:30:34Z</updated>
    <published>2006-09-01T00:00:00Z</published>
    <summary type="text">Title: Cumulative antioxidant defense against oxidative challenge in galactose-induced cataractogenesis in Wistar rats
Authors: Raju, T N; Kumar, C Sanat; Kanth, V Rajani; Ramana, B Venkata; Reddy, P Uma Maheswara; Suryanarayana, P; Reddy, G Bhanuprakash
Abstract: Natural dietary&#xD;
ingredients are known for their antioxidant activity. Of such, curcumin, the&#xD;
active principle of turmeric, at 0.01% in the diet proved as pro-oxidative in&#xD;
galactose-induced cataract &lt;i style=""&gt;in vivo&lt;/i&gt;.&#xD;
The purpose of this study was to investigate the effect of vitamin E (VE), a&#xD;
well-known antioxidant, in combination with curcumin on the onset and&#xD;
maturation of galactose induced cataract. Periodic slit-lamp microscope&#xD;
examination indicated that in combination with vitamin-E, 0.01% curcumin (G-IV)&#xD;
delayed the onset and maturation of galactose-induced cataract. Biochemical&#xD;
analyses revealed that combined treatment of 0.01% curcumin and vitamin-E diet&#xD;
exhibited an efficient antioxidant effect, as it inhibited lipid peroxidation&#xD;
and contributed to a distinct rise in reduced glutathione content. The results&#xD;
indicate that natural dietary ingredients are effective in combination rather&#xD;
than the individual administration as they are complementing each other in reducing&#xD;
the risk of galactose induced cataract.
Page(s): 733-739</summary>
    <dc:date>2006-09-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Immunostimulatory effect of &lt;i style=""&gt;Tinospora cordifolia&lt;/i&gt; Miers leaf extract in &lt;i style=""&gt;Oreochromis mossambicus&lt;/i&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/6598" />
    <author>
      <name>Sudhakaran, D Samuel</name>
    </author>
    <author>
      <name>Srirekha, P</name>
    </author>
    <author>
      <name>Devasree, L D</name>
    </author>
    <author>
      <name>Premsingh, S</name>
    </author>
    <author>
      <name>Michael, R Dinakaran</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/6598</id>
    <updated>2009-11-18T16:30:43Z</updated>
    <published>2006-09-01T00:00:00Z</published>
    <summary type="text">Title: Immunostimulatory effect of &lt;i style=""&gt;Tinospora cordifolia&lt;/i&gt; Miers leaf extract in &lt;i style=""&gt;Oreochromis mossambicus&lt;/i&gt;
Authors: Sudhakaran, D Samuel; Srirekha, P; Devasree, L D; Premsingh, S; Michael, R Dinakaran
Abstract: Immunostimulatory effect of leaf&#xD;
extract of &lt;i style=""&gt;T. cordifolia&lt;/i&gt; on (i)&#xD;
specific immunity (antibody response), (ii) non-specific immunity (neutrophil&#xD;
activity) and (iii) disease resistance against &lt;i style=""&gt;Aeromonas hydrophila&lt;/i&gt; was investigated in&#xD;
&lt;i style=""&gt;O. mossambicus&lt;/i&gt;. Ethanol and petroleum&#xD;
ether extracts of the leaves were used. Both ethanol and petroleum ether&#xD;
extracts administered at doses of 0.8, 8 or 80 mg/kg body weight, prolonged the&#xD;
peak primary antibody titres upto one to three weeks. Ethanol extract at the&#xD;
dose of 8 mg/kg and petroleum ether extract at the doses of 0.8 or 8 mg/kg&#xD;
enhanced the secondary antibody response. All the doses of ethanol extract&#xD;
significantly enhanced neutrophil activity. Fish injected with petroleum ether&#xD;
or ethanol extract at a dose of 8 mg/kg were protected against experimental&#xD;
infection with virulent&#xD;
&lt;i style=""&gt;A. hydrophila&lt;/i&gt;. The results indicates&#xD;
the potential of &lt;i style=""&gt;T. cordifolia&lt;/i&gt; leaf&#xD;
extracts for use as an immunoprophylactic to prevent diseases in finfish&#xD;
aquaculture.
Page(s): 726-732</summary>
    <dc:date>2006-09-01T00:00:00Z</dc:date>
  </entry>
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