Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Olga E. Talantova"'
Autor:
Olga E. Talantova, Alla S. Koltsova, Andrei V. Tikhonov, Anna A. Pendina, Olga V. Malysheva, Olga A. Tarasenko, Elena S. Vashukova, Elena S. Shabanova, Arina V. Golubeva, Olga G. Chiryaeva, Andrey S. Glotov, Olesya N. Bespalova, Olga A. Efimova
Publikováno v:
Genes, Vol 14, Iss 4, p 913 (2023)
We report on the case of prenatal detection of trisomy 2 in placental biopsy and further algorithm of genetic counseling and testing. A 29-year-old woman with first-trimester biochemical markers refused chorionic villus sampling and preferred targete
Externí odkaz:
https://doaj.org/article/a34bdd5ca80744849bca12e403a367aa
Reproductive History of a Woman With 8p and 18p Genetic Imbalance and Minor Phenotypic Abnormalities
Autor:
Anna A. Pendina, Yulia V. Shilenkova, Olga E. Talantova, Olga A. Efimova, Olga G. Chiryaeva, Olga V. Malysheva, Vera S. Dudkina, Lubov' I. Petrova, Elena A. Serebryakova, Elena S. Shabanova, Irina D. Mekina, Evgeniia M. Komarova, Alla S. Koltsova, Andrei V. Tikhonov, Tatyana G. Tral, Gulrukhsor Kh. Tolibova, Natalia S. Osinovskaya, Mikhail I. Krapivin, Anastasiia V. Petrovskaia-Kaminskaia, Taisia S. Korchak, Tatyana E. Ivashchenko, Oleg S. Glotov, Olga V. Romanova, Anton E. Shikov, Stanislav P. Urazov, Viktoriya V. Tsay, Yurii A. Eismont, Sergei G. Scherbak, Yanina M. Sagurova, Elena S. Vashukova, Polina Y. Kozyulina, Natalya M. Dvoynova, Andrey S. Glotov, Vladislav S. Baranov, Alexander M. Gzgzyan, Igor Yu. Kogan
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
We report on the phenotype and the reproductive history of an adult female patient with an unbalanced karyotype: 8p23 and 18p11.3 terminal deletions and 8p22 duplication. The indication for karyotyping of the 28-year-old patient was a structural rear
Externí odkaz:
https://doaj.org/article/fda4cd6f8aaa4cae9b31415d767f293f
Autor:
Mikhail I. Krapivin, Andrei V. Tikhonov, Olga A. Efimova, Anna A. Pendina, Anna A. Smirnova, Olga G. Chiryaeva, Olga E. Talantova, Lubov’ I. Petrova, Vera S. Dudkina, Vladislav S. Baranov
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 12, p 6622 (2021)
The present study investigates telomere length (TL) in dividing chorionic cytotrophoblast cells from karyotypically normal and abnormal first trimester miscarriages and ongoing pregnancies. Using Q-FISH, we measured relative TLs in the metaphase chro
Externí odkaz:
https://doaj.org/article/c7bc01461f714421a08a394ea3d191c0
Autor:
Yulia V. Shilenkova, Anna A. Pendina, Irina D. Mekina, Olga A. Efimova, Evgeniia M. Komarova, Elena A. Lesik, Mariia A. Ishchuk, Elena M. Fedorova, Olga G. Chiryaeva, Lubov’ I. Petrova, Vera S. Dudkina, Olga E. Talantova, Alexander M. Gzgzyan, Igor Yu. Kogan
Publikováno v:
Genes, Vol 12, Iss 1, p 18 (2020)
We studied the impact of age and the serum anti-Müllerian hormone (AMH)/follicle-stimulating hormone (FSH) levels on the number of cumulus–oocyte complexes (COCs) retrieved from female reciprocal and Robertsonian translocation carriers after contr
Externí odkaz:
https://doaj.org/article/a07d566ecd334f60a78acc21120339c4
Autor:
Vera S. Dudkina, Polina Y. Kozyulina, Lubov’ I. Petrova, T. E. Ivashchenko, Andrey S. Glotov, Olga E. Talantova, A. L. Koroteev, Vladislav S Baranov, Anna A. Pendina, Andrei V. Tikhonov, N. M. Dvoynova, Olga G. Chiryaeva, Elena S Vashukova, Olga A. Efimova
Publikováno v:
Russian Journal of Genetics. 55:1208-1213
In recent years, noninvasive prenatal testing (NIPT) for fetal chromosomal abnormalities has come into wide use. NIPT allows detection of fetal chromosomal abnormalities without invasive sampling of fetal material: by analyzing cell-free fetal DNA in
Autor:
Yuliia G. Lezhnina, Olga A. Efimova, Olga G. Chiryaeva, Mikhail I. Krapivin, Vladislav S Baranov, Anna A. Pendina, Anastasiia V. Petrovskaia-Kaminskaia, Tatiana V. Kuznetzova, Vera S. Dudkina, Alla S. Koltsova, Lyubov I. Petrova, Andrei V. Tikhonov, Olga E. Talantova
Publikováno v:
Экологическая генетика, Vol 17, Iss 3, Pp 111-117 (2019)
Background: Incorrect epigenetic modifications of the human genome may result in epigenetic disorders, thus, highlighting the necessity of studying chromosome epigenetic patterns in human development. Aim of the study: A comparative analysis of acety
Autor:
Dmitrii Ivanov, Natalia Dvoynova, Olesya N. Bespalova, Olga A Tarasenko, N. R. Maksimova, Polina Y. Kozyulina, T. E. Ivashchenko, Alexander Koroteev, Igor Yu. Kogan, Elena S Vashukova, Anastasia Chentsova, Elena A. Serebryakova, Olga E. Talantova, Aitalina Sukhomyasova, Alisa Morshneva, Andrey S. Glotov, Vladislav S Baranov
Publikováno v:
Genes, Vol 12, Iss 743, p 743 (2021)
Genes
Volume 12
Issue 5
Genes
Volume 12
Issue 5
Clinical tests based on whole-genome sequencing are generally focused on a single task approach, testing one or several parameters, although whole-genome sequencing (WGS) provides us with large data sets that can be used for many supportive analyses.
Autor:
Elena M. Fedorova, Yulia V. Shilenkova, Igor Yu. Kogan, Olga E. Talantova, Alexander M. Gzgzyan, Mariia A. Ishchuk, Lubov’ I. Petrova, Anna A. Pendina, Elena A. Lesik, Evgeniia M. Komarova, Irina D. Mekina, Olga G. Chiryaeva, Olga A. Efimova, Vera S. Dudkina
Publikováno v:
Genes
Volume 12
Issue 1
Genes, Vol 12, Iss 18, p 18 (2021)
Volume 12
Issue 1
Genes, Vol 12, Iss 18, p 18 (2021)
We studied the impact of age and the serum anti-Mü
llerian hormone (AMH)/follicle-stimulating hormone (FSH) levels on the number of cumulus&ndash
oocyte complexes (COCs) retrieved from female reciprocal and Robertsonian translocation ca
llerian hormone (AMH)/follicle-stimulating hormone (FSH) levels on the number of cumulus&ndash
oocyte complexes (COCs) retrieved from female reciprocal and Robertsonian translocation ca
Autor:
Anastasiia V. Petrovskaia-Kaminskaia, Andrei V. Tikhonov, V. S. Baranov, Polina M. Navodnikova, Mikhail I. Krapivin, Olga A. Efimova, Olga E. Talantova, Anna A. Pendina, Oleg S. Glotov, Vladimir V. Kopat
Publikováno v:
Cytogenetic and Genome Research. 156:150-157
5-hydroxymethylcytosine (5hmC) is an oxidative derivative of 5-methylcytosine (5mC). Recent studies have revealed a sharp difference in the levels of 5hmC in 2 opposite DNA strands of a given chromosome and a chromosome-wide cell-to-cell variability