Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Yu. S. Fedotova"'
Publikováno v:
Vestnik otorinolaringologii. 81(4)
The objective of the present study was to elucidate the causes responsible for a cough in the pregnant women. It involved 92 patients including 23 ones presenting with bronchial asthma and 69 having no manifestations of asthma in their medical histor
Autor:
S. P. Sosnikhina, A. V. Lovtsyus, Natalia Tsvetkova, Yu. F. Bogdanov, Oxana Kolomiets, O. A. Tikholiz, O. S. Sapronova, E. I. Mikhailova, Yu. S. Fedotova
Publikováno v:
Russian Journal of Genetics. 43:1193-1200
The cytological phenotype was studied in a desynaptic form isolated from a population of rye cultivar Vyatka. The primary defect of desynaptic plants was identified as nonhomologous (heterologous) chromosome synapsis, which was observed by electron m
Autor:
Yu. S. Fedotova, Yu. F. Bogdanov, O. A. Tikholiz, G. A. Kirillova, V. G. Smirnov, E. I. Mikhailova, S. P. Sosnikhina, T. F. Mazurova
Publikováno v:
Russian Journal of Genetics. 38:156-164
The cytological expression of spontaneous mutation sy2 isolated from a population of weedy rye was examined. It was demonstrated that the primary defect of meiosis in the mutant plants is nonhomologous synapsis, which occurs simultaneously with the h
Autor:
G. A. Kirillova, O. A. Tikholiz, S. P. Sosnikhina, Yu. S. Fedotova, V. G. Smirnov, E. I. Mikhailova, Oxana Kolomiets, Yu. F. Bogdanov
Publikováno v:
Russian Journal of Genetics. 37:71-79
Analysis of manifestation and inheritance of a new mutation inducing irregular synapsis in rye showed that abnormal phenotype is determined by a recessive allele of the sy19 gene. In the homozygotes for this mutation, even at the light microscopic le
Autor:
S. P. Sosnikhina, V. G. Smirnov, E. I. Mikhailova, Yu. S. Fedotova, Yu. F. Bogdanov, J.H. de Jong, S. Ya. Dadashev
Publikováno v:
Genome. 41:284-288
A novel type of aberration in synaptonemal complex (SC) assembly was found in electron micrographs of surface spread midprophase I nuclei from pollen mother cell preparations of rye. The plants with the mutant phenotype were selected from the fifth-
Autor:
Yu F. Bogdanov, Yu S. Fedotova, S.P. Sosnikhina, V.G. Smirnov, S. Ya Dadashev, E.I. Mikhailova, J.H. de Jong
Publikováno v:
Genome. 41:284-288
Publikováno v:
Rossiiskaya rinologiya. 23:22
Autor:
Yu. S. Fedotova, V. G. Smirnov, S. A. Sosnikhina, E. I. Mikhailova, Yu. F. Bogdanov, S. A. Gadzhiyeva
Publikováno v:
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik. 88(8)
We studied the expression and inheritance of two spontaneous mutations found in different populations of rye Secale cereale L. that cause high univalent frequency in meiosis and low fertility. Both mutations were inherited as monogenic recessives. Fo
Autor:
Yu. F. Bogdanov, V. G. Smirnov, S. P. Sosnikhina, E. I. Mikhailova, Yu. S. Fedotova, Oxana Kolomiets
Publikováno v:
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik. 84(7-8)
A mutant form of weedy rye characterized by male and female sterility and having a hereditary block in the chromosome synapsis has been found and described. Genetic analysis has shown the synapsis block to be determined by the recessive allele of a g
Publikováno v:
Genome. 32:816-823
The process of synaptonemal complex degradation during diplotene was studied in spreads of rye microsporocytes stained with silver nitrate at pH 3.5–4.5 and 6.0–8.0. Two different patterns of the synaptonemal complex degradation process have been