Zobrazeno 1 - 10
of 16
pro vyhledávání: '"D I, Zhigalina"'
Autor:
N. A. Skryabin, S. A. Vasilyev, T. V. Nikitina, D. I. Zhigalina, R. R. Savchenko, N. P. Babushkina, M. E. Lopatkina, A. A. Kashevarova, I. N. Lebedev
Publikováno v:
Вавиловский журнал генетики и селекции, Vol 23, Iss 2, Pp 244-249 (2019)
Recurrent pregnancy loss (RPL) is a severe reproductive pathology with a significant component of unexplained etiology. Extended homozygous regions as a possible etiological factor for RPL were sought in the genomes of embryos. Twenty-two paired firs
Externí odkaz:
https://doaj.org/article/baac6f4e959c4f66ba4e0f71b76dcf5c
Publikováno v:
Russian Journal of Genetics. 58:1208-1215
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd36a08949b2ed166c2ab8a29e176603
https://doi.org/10.1134/s1022795422100088
https://doi.org/10.1134/s1022795422100088
Autor:
V. M. Sivokha, M.E. Lopatkina, S. A. Vasiliev, I. N. Lebedev, O. Y. Vasilieva, N.A. Skryabin, Elena O. Belyaeva, R. R. Savchenko, Lyudmila P. Nazarenko, D. I. Zhigalina
Publikováno v:
Russian Journal of Genetics. 56:739-746
Detection of translocations in subtelomeric regions of chromosomes is a serious diagnostic problem, because they are difficult to determine by conventional cytogenetics with G banding. The aim of this work was the development of the technology of DNA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ab24c44dc1a24acb18c98d4252ca711
https://doi.org/10.1134/s1022795420060150
https://doi.org/10.1134/s1022795420060150
Autor:
A.A. Malakhova, Alexei A. Zarubin, D. I. Zhigalina, I.Zh. Zhalsanova, A.O. Bueverov, E.V. Grigor'eva, R. R. Savchenko, Suren M. Zakian, A.E. Postrigan, O.Yu. Vasilyeva, N.A. Skryabin, A.A. Sivtsev, M.E. Lopatkina, N.A. Kolesnikov, T. V. Nikitina, P.O. Bogomolov
Publikováno v:
Stem Cell Research, Vol 57, Iss, Pp 102556-(2021)
Wilson’s disease is a rare autosomal recessive disorder of copper metabolism. The copper accumulation in the viscera appears due to the functional impairment of copper-transporting ATPase, which is encoded by the ATP7B gene. In this study, PBMCs of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::204c838ad42b7004955414b4aab2abd0
https://pubmed.ncbi.nlm.nih.gov/34736038
https://pubmed.ncbi.nlm.nih.gov/34736038
Autor:
I. N. Lebedev, A. A. Kashevarova, D. I. Zhigalina, R. R. Savchenko, M.E. Lopatkina, N.A. Skryabin, T. V. Nikitina, E. A. Sazhenova
Publikováno v:
Russian Journal of Genetics. 55:1214-1226
Using chromosome microarray analysis, 52 samples of placental tissues from first trimester human spontaneous abortions were examined. One hundred twenty copy number variations (CNVs) were identified, affecting one or more genes (total of 427 genes).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f3a07fda7affe68eec66232ddc71b18
https://doi.org/10.1134/s1022795419100065
https://doi.org/10.1134/s1022795419100065
Autor:
Lada A. Zatula, Anton V. Markov, S. A. Vasilyev, Oksana Yu Vasilyeva, Victoria V. Demeneva, Diana V. Sharysh, I. N. Lebedev, D. I. Zhigalina, E. N. Tolmacheva
Publikováno v:
MethodsX, Vol 8, Iss, Pp 101445-(2021)
MethodsX
MethodsX
The methylation index of the LINE-1 promoter is one of the most commonly used markers for assessing the global level of genome methylation in various human cells and tissues. We developed an NGS-based protocol for DNA methylation analysis of the LINE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10e1be5584c6aa07890e74f1caeb8d2c
http://www.sciencedirect.com/science/article/pii/S2215016121002387
http://www.sciencedirect.com/science/article/pii/S2215016121002387
Autor:
D. I. Zhigalina, Vasilissa A Lee, T. V. Nikitina, S. A. Vasilyev, Oksana Yu Vasilyeva, E. A. Sazhenova, I. N. Lebedev, E. N. Tolmacheva, Lada A. Zatula, Ekaterina S Serdyukova, A. A. Kashevarova, Anton V. Markov
Publikováno v:
J Assist Reprod Genet
Journal of assisted reproduction and genetics. 2021. Vol. 38, № 1. P. 139-149
Journal of assisted reproduction and genetics. 2021. Vol. 38, № 1. P. 139-149
Purpose High frequency of aneuploidy in meiosis and cleavage stage coincides with waves of epigenetic genome reprogramming that may indicate a possible association between epigenetic mechanisms and aneuploidy occurrence. This study aimed to assess th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74abec7acb75f9aa12b0fbde5c5e55f1
https://pubmed.ncbi.nlm.nih.gov/33170392
https://pubmed.ncbi.nlm.nih.gov/33170392
Autor:
O.Yu. Vasilyeva, Suren M. Zakian, D. I. Zhigalina, N.A. Skryabin, I. N. Lebedev, N.A. Kolesnikov, A.O. Bueverov, E.V. Grigor'eva, A.A. Sivtcev, A.A. Malakhova, P.O. Bogomolov
Publikováno v:
Stem Cell Research, Vol 47, Iss, Pp 101922-(2020)
Wilson’s disease is an inherited disorder associated with copper accumulation in the liver, brain and other vital organs. Wilson’s disease is caused by mutations in the ATP7B gene. Over 300 mutations of ATP7B have been described. Despite the dise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37256cc2d17110225d9909ae5ab5ca2e
https://pubmed.ncbi.nlm.nih.gov/32738633
https://pubmed.ncbi.nlm.nih.gov/32738633
Publikováno v:
Tsitologiia. 58(6)
In the present study, we have carried out a comparative analysis of molecular karyotypes of cell free DNA from blastocoele fluid, trophectoderm and inner cell mass of human blastocysts at the preimplantation stages of development, using the comparati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::81664df4f2e21da293a62537449bf9c1
https://pubmed.ncbi.nlm.nih.gov/30192122
https://pubmed.ncbi.nlm.nih.gov/30192122
Autor:
Igor N. Lebedev, I. D. Evtushenko, D. I. Zhigalina, T. V. Ivanova, A. A. Mel’nikov, E. I. Grigorovich, E. S. Zhabina, S. A. Vasil’ev, E. A. Sazhenova, T.V. Nikitina, E. N. Tolmacheva
Publikováno v:
Cell and Tissue Biology. 10:55-59
Sex ratio in first trimester of pregnancy is skewed due to preferential elimination of female embryos. It could be resulted from aberrant X-chromosome inactivation. X-chromosome inactivation was analyzed in extraembryonic tissues of miscarriages and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e89d20f8fa2c1d9f4500a51440280de9
https://doi.org/10.1134/s1990519x16010119
https://doi.org/10.1134/s1990519x16010119