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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/23021</link>
    <description />
    <pubDate>Sat, 10 Oct 2026 21:25:46 GMT</pubDate>
    <dc:date>2026-10-10T21:25:46Z</dc:date>
    <item>
      <title>Comparative evaluation of whole blood D-Dimer test to plasma D - Dimer test for diagnosis of disseminated intravascular coagulation</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/23118</link>
      <description>Title: Comparative evaluation of whole blood D-Dimer test to plasma D - Dimer test for diagnosis of disseminated intravascular coagulation
Authors: Gupta, P K; Gupta, M; Chatterjee, T; Saxena, R
Abstract: Three rapid D-dimer test methods were&#xD;
compared for the diagnosis of acute disseminated intravascular coagulation (DIC).These&#xD;
were (a) SimpliRED, an autologous red cell agglutination assay. (b) DIMERTEST&#xD;
latex agglutination assay, containing monoclonal antibody DD - 3B6 / 22&lt;sup&gt;6&lt;/sup&gt;,&#xD;
and (c) D - DI latex agglutination assay containing mouse anti-human D-dimer monoclonal&#xD;
antibodies. The D-DI latex method having higher sensitivity (100%) and&#xD;
specificity (81%) in clinically acute DIC was postulated as the gold standard&#xD;
and compared with the other two methods. The results suggest that D-DI latex&#xD;
agglutination assay containing mouse anti-human D-Dimer monoclonal antibodies&#xD;
are the better assay methods amongst all the three kits analyzed. It is advisable&#xD;
to look for the nature of the antibody used to coat the latex particles in plasma&#xD;
based kits. In emergency setting RBC kits may be of some use as rapid diagnosis&#xD;
is advantageous.
Page(s): 382-384</description>
      <pubDate>Fri, 01 Apr 2005 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/23118</guid>
      <dc:date>2005-04-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Regeneration of plantlets from &lt;i&gt;in vitro &lt;/i&gt;raised leaf explants of &lt;i&gt;Cleisostoma  racimeferum &lt;/i&gt;Lindl</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/23117</link>
      <description>Title: Regeneration of plantlets from &lt;i&gt;in vitro &lt;/i&gt;raised leaf explants of &lt;i&gt;Cleisostoma  racimeferum &lt;/i&gt;Lindl
Authors: Temjensangba; Deb, Chitta Ranjan
Abstract: Protocorm like bodies (PLBs), callus and&#xD;
shoot buds developed in culture from &lt;i&gt;in vitro &lt;/i&gt;raised foliar explants of &lt;i&gt;Cleisostoma&#xD;
racimeferum. &lt;/i&gt;Among the different basal media, better result was obtained on&#xD;
MS medium containing sucrose (3%) and BA (2 μ&lt;i&gt;M&lt;/i&gt;) with ~80% frequency&#xD;
after 40 days of culture. Young leaves (15 week old) produced better PLBs. Whole&#xD;
leaf placed vertically upside-up orientation can regenerate PLBs and shoot buds&#xD;
(80%). PLBs and shoot buds formed on entire surface of the leaves. Cultures on&#xD;
BA and NAA (2 and 2 μ&lt;i&gt;M&lt;/i&gt; respectively in combination) stimulated callus mediated&#xD;
regeneration (68%). The rooted plantlets regenerated within 8-10 week from PLBs&#xD;
and shoot buds on MS medium containing IAA and kinetin (2 μ&lt;i&gt;M&lt;/i&gt; each in&#xD;
combination). BA containing medium triggered multiple shoot bud formation, while&#xD;
NAA alone or in combination with other growth regulators was inhibitory.&#xD;
Incorporation of activated charcoal (0.01 %) in the medium stimulated formation&#xD;
of repetitive PLBs and multiple shoot buds. Rooted plants were ready for harvest&#xD;
after 20-22 week of initiation of culture. About 65% of the potted plants&#xD;
survived after 3 months in the poly house.
Page(s): 377-381</description>
      <pubDate>Fri, 01 Apr 2005 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/23117</guid>
      <dc:date>2005-04-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>&lt;i&gt;In vitro &lt;/i&gt;studies of &lt;i&gt;Bacopa monnieri—&lt;/i&gt;An&lt;i&gt; &lt;/i&gt;important medicinal plant with reference to its biochemical variations</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/23116</link>
      <description>Title: &lt;i&gt;In vitro &lt;/i&gt;studies of &lt;i&gt;Bacopa monnieri—&lt;/i&gt;An&lt;i&gt; &lt;/i&gt;important medicinal plant with reference to its biochemical variations
Authors: Mohapatra, H P; Rath, S P
Abstract: Micropropagation of &lt;i&gt;Bacopa monnieri &lt;/i&gt;was&#xD;
achieved on MS and B5 medium supplemented with BAP and NAA using leaf explants&#xD;
and nodal segments. Best results were found on MS medium in both the explants&#xD;
with BAP (2.0 mg/l) showing higher percentage of regeneration. Besides that the&#xD;
biochemical parameters, like chlorophyll, carbohydrate, protein, of leaves both&#xD;
&lt;i&gt;in vivo &lt;/i&gt;and &lt;i&gt;in vitro &lt;/i&gt;have also been carried out in order to&#xD;
establish the sustainability of plants.
Page(s): 373-376</description>
      <pubDate>Fri, 01 Apr 2005 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/23116</guid>
      <dc:date>2005-04-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Isolation and characterization of a green tissue-specific promoter from pigeonpea [&lt;i&gt;Cajanus cajan &lt;/i&gt;(L.) Millsp.]</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/23115</link>
      <description>Title: Isolation and characterization of a green tissue-specific promoter from pigeonpea [&lt;i&gt;Cajanus cajan &lt;/i&gt;(L.) Millsp.]
Authors: Panguluri, S K; Sridhar, J; Jagadish, B; Sharma, P C; Kumar, P A
Abstract: Expression of &lt;i&gt;rbcS &lt;/i&gt;genes encoding&#xD;
small subunit of rubisco, most abundant protein in green tissue, is regulated&#xD;
by at least three parameters-tissue type, light conditions and stage of&#xD;
development. One of the green tissue-specific promoters of &lt;i&gt;rbcS &lt;/i&gt;gene&#xD;
family was isolated from pigeonpea by PCR. Expression of &lt;i&gt;uidA &lt;/i&gt;gene&#xD;
encoding β-glucuronidase in the transgenic tobacco plants under the control of&#xD;
pigeonpea &lt;i&gt;rbcS &lt;/i&gt;promoter, clearly showed that this promoter was as strong&#xD;
as pea &lt;i&gt;rbcS3A&lt;/i&gt; promoter characterized earlier. Study of the sequence similarity&#xD;
with pea &lt;i&gt;rbcS3A &lt;/i&gt;promoter, especially the region (boxes I and III) that&#xD;
is required for &lt;i&gt;rbcS3A &lt;/i&gt;expression, showed more than 50% divergence. In&#xD;
contrast, pigeonpea promoter sequence isolated in the present study was more similar&#xD;
to that of spinach and rice &lt;i&gt;rbcS &lt;/i&gt;promoters.
Page(s): 369-372</description>
      <pubDate>Fri, 01 Apr 2005 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/23115</guid>
      <dc:date>2005-04-01T00:00:00Z</dc:date>
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