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Cited by 16 publications
(7 citation statements)
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“…It has antioxidant properties, promotes the development of normal tissues (vessels and grains of birch and pine), while the activity of peroxidase and polyphenol oxidase is 3, 7 and 2.3 times higher, respectively, in woods containing parenchymal cells. Therefore, DLPA inhibited the formation of proembryogenic undifferentiated cells, but promoted the development of various stages of somatic embryoids and seedlings [6,10] In the process of a long-term subculturing of suspensions of proembryogenic cells and embryoids due to somaclonal variability, it was not possible to get rid of chlorophyll deficiency, i.e. the presence of white cotyledons in germinating seedlings resulted from embryogenesis.…”
Section: Discussionmentioning
confidence: 99%
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“…It has antioxidant properties, promotes the development of normal tissues (vessels and grains of birch and pine), while the activity of peroxidase and polyphenol oxidase is 3, 7 and 2.3 times higher, respectively, in woods containing parenchymal cells. Therefore, DLPA inhibited the formation of proembryogenic undifferentiated cells, but promoted the development of various stages of somatic embryoids and seedlings [6,10] In the process of a long-term subculturing of suspensions of proembryogenic cells and embryoids due to somaclonal variability, it was not possible to get rid of chlorophyll deficiency, i.e. the presence of white cotyledons in germinating seedlings resulted from embryogenesis.…”
Section: Discussionmentioning
confidence: 99%
“…Suspension culture with small globular embryoids (<0.2 mm) (about 1000 pcs. of 0.05-0.2 mm in size in 10 ml of suspension) was equally added to culture vessels, in which different variants of nutrient media with the base, contained fourfold diluted mineral elements and vitamins of PG medium [10], and 10 g/l of sucrose were added. The variants of media differed in the presence or absence of growth regulators and biologically active substances.…”
Section: Methodsmentioning
confidence: 99%
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“…The plant samples were propagated by micrografting. They were cultured for four weeks on a hormone-free PG medium, at a 16-hour photoperiod; the temperature was +25-27 o C [11]. Afterwards, plant containing culture bottles were in the cold storage without internal lighting at 10-12°C for 6 months.…”
Section: Methodsmentioning
confidence: 99%