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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/31464" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/31464</id>
  <updated>2026-10-12T22:11:29Z</updated>
  <dc:date>2026-10-12T22:11:29Z</dc:date>
  <entry>
    <title>Micropropagation of &lt;i style="mso-bidi-font-style:normal"&gt;Valeriana wallichii&lt;/i&gt; DC. (&lt;span style="font-size:13.0pt;mso-ansi-language:EN" lang="EN"&gt;Indian Valerian) through nodes &lt;/span&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/31487" />
    <author>
      <name>Singh, Sandeep</name>
    </author>
    <author>
      <name>Purohit, Vijay K</name>
    </author>
    <author>
      <name>Prasad, P</name>
    </author>
    <author>
      <name>Nautiyal, A R</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/31487</id>
    <updated>2016-07-20T06:04:29Z</updated>
    <published>2015-01-01T00:00:00Z</published>
    <summary type="text">Title: Micropropagation of &lt;i style="mso-bidi-font-style:normal"&gt;Valeriana wallichii&lt;/i&gt; DC. (&lt;span style="font-size:13.0pt;mso-ansi-language:EN" lang="EN"&gt;Indian Valerian) through nodes &lt;/span&gt;
Authors: Singh, Sandeep; Purohit, Vijay K; Prasad, P; Nautiyal, A R
Abstract: &lt;i style="mso-bidi-font-style:normal"&gt;In vitro &lt;/i&gt;&lt;span style="letter-spacing:-.1pt;mso-bidi-font-style:italic" lang="EN-GB"&gt;propagation&lt;i style="mso-bidi-font-style:normal"&gt;&#xD;
&lt;/i&gt;&lt;span style="letter-spacing:-.1pt;mso-bidi-font-style:&#xD;
italic" lang="EN-GB"&gt;method was developed for obtaining large number of plantlets of &lt;i style="mso-bidi-font-style:normal"&gt;Valeriana&#xD;
wallichii &lt;/i&gt;&lt;span style="letter-spacing:-.1pt;mso-bidi-font-style:&#xD;
italic" lang="EN-GB"&gt;DC. (Valerianaceae),&#xD;
an indigenous high value medicinal and aromatic plant species of Indian&#xD;
Himalayan region, using nodes of &lt;i&gt;in vitro&lt;/i&gt; grown seedlings. High frequency shoot proliferation was induced in&#xD;
explants cultured on Murashige and Skoog (MS) medium supplemented with&#xD;
different concentrations of 6-benzyladenine (BA), kinetin (Kn), adenine&#xD;
sulphate (AS) and thidiazuron (TDZ). Amongst all the tested cytokinins, 3.0 μM&#xD;
BA was found to be the most effective and an average of 12.0 shoots per nodal&#xD;
explant were formed after 15 d of culture. Higher concentration of TDZ&#xD;
(3.0 μM) was found least effective among all&#xD;
the cytokinins used for shoot induction. Rooting (100 %) was observed in&#xD;
PGR-free Murashige and Skoog medium after 12 d of&#xD;
incubation of microshoots. Well rooted plantlets (30-d-old) were successfully&#xD;
transplanted and established in mixture of soil and sand (3:1) under partially&#xD;
shade conditions.&#xD;
&#xD;
&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
Page(s): 127-130</summary>
    <dc:date>2015-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>&lt;span style="font-size:13.0pt;color:black;letter-spacing:-.4pt;mso-bidi-font-weight: bold" lang="EN-GB"&gt;Camptothecine and methoxy camptothecine from&lt;span style="font-size:13.0pt;mso-bidi-font-size:15.0pt;color:black;mso-bidi-font-weight: bold" lang="EN-GB"&gt; callus cultures of &lt;i style="mso-bidi-font-style:normal"&gt;Miquelia dentata &lt;/i&gt;Bedd.— A rare plant of the Western Ghats of India &lt;/span&gt;&lt;/span&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/31486" />
    <author>
      <name>Thriveni, H N</name>
    </author>
    <author>
      <name>Ravikanth, G</name>
    </author>
    <author>
      <name>Vasudeva, R</name>
    </author>
    <author>
      <name>Ganeshaiah, K N</name>
    </author>
    <author>
      <name>Shaanker, R Uma</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/31486</id>
    <updated>2016-07-20T06:03:22Z</updated>
    <published>2015-05-11T11:27:50Z</published>
    <summary type="text">Title: &lt;span style="font-size:13.0pt;color:black;letter-spacing:-.4pt;mso-bidi-font-weight: bold" lang="EN-GB"&gt;Camptothecine and methoxy camptothecine from&lt;span style="font-size:13.0pt;mso-bidi-font-size:15.0pt;color:black;mso-bidi-font-weight: bold" lang="EN-GB"&gt; callus cultures of &lt;i style="mso-bidi-font-style:normal"&gt;Miquelia dentata &lt;/i&gt;Bedd.— A rare plant of the Western Ghats of India &lt;/span&gt;&lt;/span&gt;
Authors: Thriveni, H N; Ravikanth, G; Vasudeva, R; Ganeshaiah, K N; Shaanker, R Uma
Abstract: &lt;i style="mso-bidi-font-style:normal"&gt;Miquelia&#xD;
dentata &lt;/i&gt;&lt;span style="font-size:9.0pt;mso-bidi-font-style:&#xD;
italic" lang="EN-GB"&gt;Bedd. (Family: Icacianceae)&#xD;
is a small climbing shrub producing anti-cancer alkaloid, camptothecine (CPT).&#xD;
The plant occurs sparsely in the southern parts of the forest&#xD;
of Western Ghats, India. Callus&#xD;
cultures of the plant were established using leaf explants on Murashige and&#xD;
Skoog medium supplemented with several plant growth regulators. The highest&#xD;
callus growth was obtained in the medium with 1.0 mg/L each of indole&#xD;
butyric acid (IBA) and benzyl adenine purine (BAP). The calli cultures produced CPT (5.4 µg/mg of the dry&#xD;
wt) and traces of methoxy camptothecine (MCPT).&#xD;
&#xD;
&lt;/span&gt;
Page(s): 123-126</summary>
    <dc:date>2015-05-11T11:27:50Z</dc:date>
  </entry>
  <entry>
    <title>Development of duplex RT-PCR for detection of &lt;i&gt;Konjac mosaic virus&lt;/i&gt; and Spathiphyllum chlorotic vein banding virus in taro and peace lily</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/31485" />
    <author>
      <name>Manikonda, Padmavathi</name>
    </author>
    <author>
      <name>Puthankalam, Srinivas Kalanghad</name>
    </author>
    <author>
      <name>Masarapu, Hema</name>
    </author>
    <author>
      <name>Pothur, Sreenivasulu</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/31485</id>
    <updated>2016-07-20T06:01:58Z</updated>
    <published>2015-01-01T00:00:00Z</published>
    <summary type="text">Title: Development of duplex RT-PCR for detection of &lt;i&gt;Konjac mosaic virus&lt;/i&gt; and Spathiphyllum chlorotic vein banding virus in taro and peace lily
Authors: Manikonda, Padmavathi; Puthankalam, Srinivas Kalanghad; Masarapu, Hema; Pothur, Sreenivasulu
Abstract: &lt;i&gt;Konjac mosaic virus&lt;/i&gt; (KoMV) and &lt;span style="mso-bidi-font-style:italic"&gt;Spathiphyllum&#xD;
chlorotic vein banding virus (SCVbV) infecting aroids in Andhra Pradesh,&#xD;
India have recently been reported as distinct potyviruses. Primers were&#xD;
designed based on their partial genome sequence (GenBank A/C EU979524, GQ421462) to detect above&#xD;
viruses by &#xD;
duplex-reverse transcription-polymerase chain reaction (duplex RT-PCR). Using&#xD;
this method, the two viruses were individually detected in limited number of&#xD;
filed/nursery collected &lt;i&gt;Colocasia esculenta &lt;/i&gt;(taro) and &lt;i&gt;Spathiphyllum&lt;/i&gt;&#xD;
spp. (peace lily). No &#xD;
co-infections with two viruses were traced among the screened samples. However,&#xD;
they were simultaneously detected in the simulated leaf samples of taro and&#xD;
peace lily (1:1, w/w).&#xD;
&#xD;
&lt;/span&gt;
Page(s): 120-122</summary>
    <dc:date>2015-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Expression analysis of BAX and GHR genes between parthenogenetic and  IVF embryos in caprine</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/31484" />
    <author>
      <name>Singh, Renu</name>
    </author>
    <author>
      <name>Kumar, Kuldeep</name>
    </author>
    <author>
      <name>Kumar, Manish</name>
    </author>
    <author>
      <name>Agarwal, Pranjali</name>
    </author>
    <author>
      <name>Mahapatra, P S</name>
    </author>
    <author>
      <name>Bag, Sadhan</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/31484</id>
    <updated>2016-07-20T05:57:53Z</updated>
    <published>2015-01-01T00:00:00Z</published>
    <summary type="text">Title: Expression analysis of BAX and GHR genes between parthenogenetic and  IVF embryos in caprine
Authors: Singh, Renu; Kumar, Kuldeep; Kumar, Manish; Agarwal, Pranjali; Mahapatra, P S; Bag, Sadhan
Abstract: The present study was carried out to compare&#xD;
the expression of proapoptotic (BAX) and growth hormone receptor genes (GHR)&#xD;
between diploid parthenogenetic and IVF (&lt;i&gt;in vitro&lt;/i&gt; fertilization) derived&#xD;
preimplantation embryos in caprine. For the study, a group of oocytes were&#xD;
fertilized with freshly collected goat semen for production of IVF derived&#xD;
embryos. While another group of oocytes were activated using 7% ethanol in mSOF&#xD;
(modified synthetic oviductal fluid) for 5 min, followed by 4 h incubation with&#xD;
2 mM 6-DMAP (6-dimethyl amino purine) in mSOF for production of diploid&#xD;
parthenogenetic embryos. After treatment, the oocytes were further cultured in&#xD;
mSOF medium for embryo development. Total RNA was isolated from morula stage&#xD;
diploid parthenogenetic and IVF embryos and cDNA was synthesized. The relative expression of BAX and GHR genes was&#xD;
analysed using real time PCR. The relative expression of BAX gene showed&#xD;
18.12-fold up regulation (P˂0.05), whereas GHR gene showed 0.15-fold down&#xD;
regulation (P˂0.05) in diploid parthenogenetic as compared to IVF derived&#xD;
embryos. The present study suggests marked variation in expression of&#xD;
proapoptotic as well as growth related genes in parthenogenetic embryos, which&#xD;
might be the reason for their improper development.&lt;b style="mso-bidi-font-weight:&#xD;
normal"&gt; &lt;/b&gt;
Page(s): 117-119</summary>
    <dc:date>2015-01-01T00:00:00Z</dc:date>
  </entry>
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