Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Elena A Sazhenova"'
Autor:
Stanislav A. Vasilyev, Oksana Yu. Vasilyeva, Bismark Oppong-Peprah, Victoria V. Demeneva, Andrey S. Zuev, Elena A. Sazhenova, Tatiana V. Nikitina, Ekaterina N. Tolmacheva
Publikováno v:
RUDN Journal of Medicine, Vol 27, Iss 4, Pp 515-531 (2023)
Relevance. Abnormal epigenetic regulation of genes responsible for the development of the embryo and placenta is associated with many pregnancy pathologies. Aim. The aim of this work was to analyze the prevalence of abnormal methylation of the PRDM16
Externí odkaz:
https://doaj.org/article/1cd2e0681a16440aaac46dc6989c1e51
Autor:
Ekaterina N. Tolmacheva, Stanislav A. Vasilyev, Tatiana V. Nikitina, Ekaterina S. Lytkina, Elena A. Sazhenova, Daria I. Zhigalina, Oksana Yu. Vasilyeva, Anton V. Markov, Victoria V. Demeneva, Liubov A. Tashireva, Anna A. Kashevarova, Igor N. Lebedev
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-12 (2022)
Abstract The presence of an extra chromosome in the embryo karyotype often dramatically affects the fate of pregnancy. Trisomy 16 is the most common aneuploidy in first-trimester miscarriages. The present study identified changes in DNA methylation i
Externí odkaz:
https://doaj.org/article/a6b1dc2f7da74380aeced43e7be00328
Autor:
Elizaveta A. Fonova, Ekaterina N. Tolmacheva, Anna A. Kashevarova, Elena A. Sazhenova, Tatyana V. Nikitina, Maria E. Lopatkina, Oksana Yu. Vasilyeva, Aleksei А. Zarubin, Tatyana N. Aleksandrova, Sergey Yu. Yuriev, Nikolay A. Skryabin, Vadim A. Stepanov, Igor N. Lebedev
Publikováno v:
Cytogenetic and genome research. 162(3)
Skewed X-chromosome inactivation (sXCI) can be a marker of lethal genetic variants on the X chromosome in a woman since sXCI modifies the pathological phenotype. The aim of this study was to search for CNVs in women with miscarriages and sXCI. XCI wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57691888aeaf2d4fa83013d140bc85e3
https://pubmed.ncbi.nlm.nih.gov/35636401
https://pubmed.ncbi.nlm.nih.gov/35636401
Autor:
Ekaterina N. Tolmacheva, Stanislav A. Vasilyev, Tatiana V. Nikitina, Ekaterina S. Lytkina, Elena A. Sazhenova, Daria I. Zhigalina, Oksana Yu. Vasilyeva, Anton V. Markov, Victoria V. Demeneva, Liubov A. Tashireva, Anna A. Kashevarova, Igor N. Lebedev
Publikováno v:
Scientific Reports
Scientific Reports, Vol 12, Iss 1, Pp 1-12 (2022)
Scientific Reports [Еlectronic resource]. 2022. Vol. 12. P. 1166 (1-12)
Scientific Reports, Vol 12, Iss 1, Pp 1-12 (2022)
Scientific Reports [Еlectronic resource]. 2022. Vol. 12. P. 1166 (1-12)
The presence of an extra chromosome in the embryo karyotype often dramatically affects the fate of pregnancy. Trisomy 16 is the most common aneuploidy in first-trimester miscarriages. The present study identified changes in DNA methylation in chorion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14ada9fd795a3cd25bab29c437c2a38b
https://pubmed.ncbi.nlm.nih.gov/35064135
https://pubmed.ncbi.nlm.nih.gov/35064135
Comparative Cytogenetic Analysis of Spontaneous Abortions in Recurrent and Sporadic Pregnancy Losses
Autor:
Ekaterina N Tolmacheva, Tatiana N Nemtseva, S. A. Vasilyev, N. N. Sukhanova, Igor N. Lebedev, A. A. Kashevarova, Sergey Y Yuriev, T.V. Nikitina, Elena A Sazhenova, Nikolay A. Skryabin
Publikováno v:
Biomedicine Hub
Background: The majority of miscarriages are sporadic; however, 1-5% of couples experience recurrent pregnancy loss (RPL). Approximately 50-60% of miscarriages result from chromosomal abnormalities. Currently, there are conflicting reports regarding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c161378c852cbd0df638f6b824898bf
https://pubmed.ncbi.nlm.nih.gov/31988885
https://pubmed.ncbi.nlm.nih.gov/31988885