Zobrazeno 1 - 9
of 9
pro vyhledávání: '"N. S. Osinovskaya"'
Autor:
Arseny S. Molotkov, Natalya Yu. Shved, Olga V. Malysheva, N. S. Osinovskaya, Vladislav S Baranov, Maria I. Yarmolinskaya
Publikováno v:
Journal of obstetrics and women's diseases. 70:31-40
BACKGROUND: Uterine leiomyoma and endometriosis are the most common gynecological diseases in women of reproductive age. A number of data indicate that there are common elements in the pathogenesis of these hyperproliferative conditions. This article
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46edba86d0184a3c53c88873cf92ac9a
https://doi.org/10.17816/jowd64892
https://doi.org/10.17816/jowd64892
Autor:
N. Yu. Shved, Maria I. Yarmolinskaya, Vladislav S Baranov, Arseniy S. Molotkov, Olga V. Malysheva, N. S. Osinovskaya, O. S. Kopteva, Yu. S. Krylova
Publikováno v:
Cell and Tissue Biology. 14:129-138
Endometriosis is a widespread disorder in which a tissue morphologically and physiologically similar to endometrium is observed outside the uterine cavity. Earlier, we identified a number of genes that are overexpressed in ectopic endometrium compare
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13c1f2cdbe92626c3b4701602d8cff47
https://doi.org/10.1134/s1990519x20020066
https://doi.org/10.1134/s1990519x20020066
Autor:
N. Yu. Shved, N. S. Osinovskaya, Olga V. Malysheva, Elena S Vashukova, V. S. Baranov, T. E. Ivashchenko, Alexander V. Predeus, Maria I. Yarmolinskaya, N. Ganbarli, Andrey S. Glotov, Maria M. Danilova
Publikováno v:
Russian Journal of Genetics. 54:1358-1365
Here, we determined basic differentially expressed genes in endometrial lesions compared to eutopic endometrium of the patients with endometriosis (EM). Endometrial biopsy and tissue sampling were performed in ten women with pelvic EM and nine contro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::022874aa7cf3de4b4c87ddf0e9b36ba5
https://doi.org/10.1134/s1022795418110133
https://doi.org/10.1134/s1022795418110133
Publikováno v:
Problemy reproduktsii. 26:73
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a45a2d021747ef747e84c897624b1ecb
https://doi.org/10.17116/repro20202601173
https://doi.org/10.17116/repro20202601173
Autor:
I. Yu. Sultanov, Eric P. Hoffman, T. E. Ivashchenko, N. S. Osinovskaya, Svetlana Ghimbovschi, A. K. Dolinskii, V. F. Bezhenar, Vladislav S Baranov
Publikováno v:
Russian Journal of Genetics. 49:1245-1249
Uterine leiomyoma (UL) is a benign and most common tumor that affects 20–45% of women of fertile age. In this study, we analyzed the MED12 gene second exon nucleotide sequence from 15 DNA samples extracted from LM of 15 subjects with uterine leiomy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43e9d67236db54a1168e8a9ddb6a0f52
https://doi.org/10.1134/s1022795413120089
https://doi.org/10.1134/s1022795413120089
Autor:
N. S. Osinovskaya, T. E. Ivashchenko, A. K. Dolinskii, I. Yu. Sultanov, S. Ghimbovschi, E. Hoffman, V. F. Bezhenar’, V. S. Baranov
Publikováno v:
Генетика. 49:1426-1431
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffa04b9939ca540ee2e04522eeefb56e
https://doi.org/10.7868/s0016675813120084
https://doi.org/10.7868/s0016675813120084
Publikováno v:
Journal of obstetrics and women's diseases. 61:104-108
Miscarriage is one of the major problems of modern reproduction. Total frequency of micarrieges is estimated as 15–27 % of total pregnancies. Recurrent Miscarriage (RM) (three or more spontaneous abortions) is responsible for almost 20 % of total m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e682e00aa26175ac9aca4f30682d8a7
https://doi.org/10.17816/jowd613104-108
https://doi.org/10.17816/jowd613104-108
Autor:
V. G. Vakharlovsky, A. V. Mikhailov, V. S. Baranov, V. M. Lebedev, T. K. Kascheeva, N. Yu. Shwed, V. N. Gorbunova, T. V. Kuznetzova, T. E. Ivaschenko, N. S. Osinovskaya
Publikováno v:
Prenatal diagnosis. 12(7)
From a total of 490 cystic fibrosis (CF) high-risk families under supervision (mostly Russian Slavs from the European part of the country), DNA data including both direct screening for some CF gene (CFTR) mutations (delF508, G551D and 1677delTA) and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34919b9b71c0d029727d9230b8d65c40
https://pubmed.ncbi.nlm.nih.gov/1354866
https://pubmed.ncbi.nlm.nih.gov/1354866
Publikováno v:
Scopus-Elsevier
In 96 patients with congenital adrenal hyperplasia (CAH) and 50 healthy donors from northwestern Russia the distribution of the HLA-DQA1 alleles and the mutation spectrum and frequency at the CYP21B gene were examined. In the patients with nonclassic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aadb9bab61d41cbdb1717cb850ffcd33
http://www.scopus.com/inward/record.url?eid=2-s2.0-2342618790&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-2342618790&partnerID=MN8TOARS
