2017
DOI: 10.2174/1874294701710010046
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Genetic Fidelity Testing Using SSR Marker Assay Confirms Trueness to Type of Micropropagated Coconut (Cocos nucifera L.) Plantlets Derived from Unfertilized Ovaries

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Cited by 24 publications
(19 citation statements)
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References 29 publications
(29 reference statements)
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“…The in vitro propagation technique of direct organogenesis is the most popular method of reproduction because it can produce large amounts of seedlings that are identical to the mother plant. The results of the study were in line with the previous reports that the in vitro propagation sugarcane varieties GT54-C9 (Alla et al 2017), Albizia procera (Mohammad et al 2016), Gloriosa superba L. (Yadav et al 2013), Mulberry (Saha et al 2016), and Coconut (Bandupriya et al 2017).…”
Section: Genetic Stability Of Sugarcane Varieties During Subculturessupporting
confidence: 90%
“…The in vitro propagation technique of direct organogenesis is the most popular method of reproduction because it can produce large amounts of seedlings that are identical to the mother plant. The results of the study were in line with the previous reports that the in vitro propagation sugarcane varieties GT54-C9 (Alla et al 2017), Albizia procera (Mohammad et al 2016), Gloriosa superba L. (Yadav et al 2013), Mulberry (Saha et al 2016), and Coconut (Bandupriya et al 2017).…”
Section: Genetic Stability Of Sugarcane Varieties During Subculturessupporting
confidence: 90%
“…Ovary derived calli were raised using the method described by Bandupriya et al (2017) with the modifi cation that, instead of CRI 72 medium, modifi ed Eeuwens Y 3 medium (Eeuwens, 1976) was used. Welldeveloped embryogenic calli (Figure 1a) from the third or fourth cycle of sub-culturing were used for cryopreservation studies.…”
Section: Initiation and Multiplication Of Embryogenic Callus Through mentioning
confidence: 99%
“…Each alginate bead was cultured for regeneration in a small glass vial containing 15 mL somatic embryo induction medium [modifi ed Eeuwens Y 3 medium containing 95.0 μM 2,4-D and 2.7 gL -1 Glutamine (3G)] for 4 wk. Plant regeneration protocol described by Bandupriya et al (2017) was followed for the regeneration of plantlets.…”
Section: Plant Regenerationmentioning
confidence: 99%
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