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Impairment of homologous chromosome synapsis in meiosis in rye Secale cereale L. caused by a recessive mutation of the sy18 gene. / Sosnikhina, S. P.; Mikhailova, E. I.; Tsvetkova, N. V.; Voylokov, A. V.; Lovtsyus, A. V.; Iordanskaya, I. V.; Kolomiets, O. L.; Bogdanov, Yu F.

In: Russian Journal of Genetics, Vol. 45, No. 11, 01.11.2009, p. 1385-1393.

Research output: Contribution to journal › Article › peer-review

Harvard

Sosnikhina, SP, Mikhailova, EI, Tsvetkova, NV, Voylokov, AV, Lovtsyus, AV, Iordanskaya, IV, Kolomiets, OL & Bogdanov, YF 2009, 'Impairment of homologous chromosome synapsis in meiosis in rye Secale cereale L. caused by a recessive mutation of the sy18 gene', Russian Journal of Genetics, vol. 45, no. 11, pp. 1385-1393. https://doi.org/10.1134/S1022795409110131

APA

Sosnikhina, S. P., Mikhailova, E. I., Tsvetkova, N. V., Voylokov, A. V., Lovtsyus, A. V., Iordanskaya, I. V., Kolomiets, O. L., & Bogdanov, Y. F. (2009). Impairment of homologous chromosome synapsis in meiosis in rye Secale cereale L. caused by a recessive mutation of the sy18 gene. Russian Journal of Genetics, 45(11), 1385-1393. https://doi.org/10.1134/S1022795409110131

Vancouver

Sosnikhina SP, Mikhailova EI, Tsvetkova NV, Voylokov AV, Lovtsyus AV, Iordanskaya IV et al. Impairment of homologous chromosome synapsis in meiosis in rye Secale cereale L. caused by a recessive mutation of the sy18 gene. Russian Journal of Genetics. 2009 Nov 1;45(11):1385-1393. https://doi.org/10.1134/S1022795409110131

Author

Sosnikhina, S. P. ; Mikhailova, E. I. ; Tsvetkova, N. V. ; Voylokov, A. V. ; Lovtsyus, A. V. ; Iordanskaya, I. V. ; Kolomiets, O. L. ; Bogdanov, Yu F. / Impairment of homologous chromosome synapsis in meiosis in rye Secale cereale L. caused by a recessive mutation of the sy18 gene. In: Russian Journal of Genetics. 2009 ; Vol. 45, No. 11. pp. 1385-1393.

BibTeX

@article{67c39df651314419bcab664ddf96b033,
title = "Impairment of homologous chromosome synapsis in meiosis in rye Secale cereale L. caused by a recessive mutation of the sy18 gene",
abstract = "Expression and inheritance of the sy18 mutation causing impairment of synapsis homology were studied. It was established that the abnormal phenotype is determined by a recessive allele of the sy18 gene. Univalents and multivalents are observed in homozygotes for this mutant allele. According to the electron microscopic analysis of synaptonemal complexes in mutants, homologous synapsis occurs together with nonhomologous synapsis. The sy18 gene was found to have no allelism with asynaptic genes sy1 and sy9 and with genes sy10 and sy19 causing, like sy18, disturbances in synapsis homology.",
author = "Sosnikhina, {S. P.} and Mikhailova, {E. I.} and Tsvetkova, {N. V.} and Voylokov, {A. V.} and Lovtsyus, {A. V.} and Iordanskaya, {I. V.} and Kolomiets, {O. L.} and Bogdanov, {Yu F.}",
year = "2009",
month = nov,
day = "1",
doi = "10.1134/S1022795409110131",
language = "English",
volume = "45",
pages = "1385--1393",
journal = "Russian Journal of Genetics",
issn = "1022-7954",
publisher = "МАИК {"}Наука/Интерпериодика{"}",
number = "11",

}

RIS

TY - JOUR

T1 - Impairment of homologous chromosome synapsis in meiosis in rye Secale cereale L. caused by a recessive mutation of the sy18 gene

AU - Sosnikhina, S. P.

AU - Mikhailova, E. I.

AU - Tsvetkova, N. V.

AU - Voylokov, A. V.

AU - Lovtsyus, A. V.

AU - Iordanskaya, I. V.

AU - Kolomiets, O. L.

AU - Bogdanov, Yu F.

PY - 2009/11/1

Y1 - 2009/11/1

N2 - Expression and inheritance of the sy18 mutation causing impairment of synapsis homology were studied. It was established that the abnormal phenotype is determined by a recessive allele of the sy18 gene. Univalents and multivalents are observed in homozygotes for this mutant allele. According to the electron microscopic analysis of synaptonemal complexes in mutants, homologous synapsis occurs together with nonhomologous synapsis. The sy18 gene was found to have no allelism with asynaptic genes sy1 and sy9 and with genes sy10 and sy19 causing, like sy18, disturbances in synapsis homology.

AB - Expression and inheritance of the sy18 mutation causing impairment of synapsis homology were studied. It was established that the abnormal phenotype is determined by a recessive allele of the sy18 gene. Univalents and multivalents are observed in homozygotes for this mutant allele. According to the electron microscopic analysis of synaptonemal complexes in mutants, homologous synapsis occurs together with nonhomologous synapsis. The sy18 gene was found to have no allelism with asynaptic genes sy1 and sy9 and with genes sy10 and sy19 causing, like sy18, disturbances in synapsis homology.

UR - http://www.scopus.com/inward/record.url?scp=76149110443&partnerID=8YFLogxK

U2 - 10.1134/S1022795409110131

DO - 10.1134/S1022795409110131

M3 - Article

AN - SCOPUS:76149110443

VL - 45

SP - 1385

EP - 1393

JO - Russian Journal of Genetics

JF - Russian Journal of Genetics

SN - 1022-7954

IS - 11

ER -

ID: 36101838