Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Valeria I, Ni"'
Autor:
Ilya V. Bizin, Alexandr A. Bessonov, Mikhail A Maydin, Aldon J. Whitehead, Olga A Volynshchikova, Albina A Avanesyan, Elena I Anisimova, Valeria I. Ni, Alexandr M Scherbakov, Alexandr A. Romanko, Evgeny N. Imyanitov, Oleg B Tkachenko, Grigory A. Raskin, Alexandr O. Ivantsov, Maxim A Kleshchev, Tatiana V. Gorodnova, Ksenia Shelekhova, Robert V Broyde, Anna P. Sokolenko
Publikováno v:
Pathobiology. 87:367-374
Introduction: There is some evidence suggesting a link between BRCA1/2 germline mutations and increased risk of gastric cancer. Methods: Endoscopic screening for stomach malignancies was performed in 120 BRCA1 mutation carriers in order to evaluate t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d1504816132772956d8f73147c4d397
https://doi.org/10.1159/000511323
https://doi.org/10.1159/000511323
Autor:
Evgeny N. Suspitsin, Peter Schürmann, Ilya V. Bizin, Maria O. Anisimova, Darya Prokofyeva, Aigul R. Venina, Elza Khusnutdinova, Tatiana N. Sokolova, Natalia Bogdanova, Ashok K. Varma, Evgeny N. Imyanitov, Maria A. Mantseva, Ekaterina Sh Kuligina, Andrey V. Koloskov, Syed K. Hasan, Ana Marija Milanović, Svetlana N. Aleksakhina, Anna P. Sokolenko, Marina Bermisheva, Daria D. Krylova, Kirill A. Zagorodnev, Thilo Dörk, Valeria I. Ni, Alexandr A. Romanko, Elena I Anisimova
Publikováno v:
Breast Cancer Research and Treatment. 179:731-742
Germline variants in known breast cancer (BC) predisposing genes explain less than half of hereditary BC cases. This study aimed to identify missing genetic determinants of BC. Whole exome sequencing (WES) of lymphocyte DNA was performed for 49 Russi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d3f247c2393a564cdf3b15604b2bcbe
https://doi.org/10.1007/s10549-019-05492-6
https://doi.org/10.1007/s10549-019-05492-6
Autor:
Elena I Anisimova, Ilya V. Bizin, Anna P. Sokolenko, Alexey M. Belyaev, Alexandr A. Bessonov, Svetlana N. Aleksakhina, Elena L. Savonevich, Tatiana N. Sokolova, Tatiana V. Gorodnova, Elena V. Preobrazhenskaya, Ilya A. Stepanov, Petr Krivorotko, Aglaya G. Iyevleva, Valeria I. Ni, Alexandr V. Togo, Evgeny N. Imyanitov, Alexandr A. Romanko, Igor Berlev
Publikováno v:
Breast cancer research and treatment. 184(1)
The spectrum of BRCA1 and BRCA2 mutations in Slavic countries is characterized by a high prevalence of founder alleles. We analyzed a large data set of Russian breast cancer (BC) and ovarian cancer (OC) patients, who were subjected to founder mutatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::112fe7c2b5a5b8a73150bb04cfcd874a
https://pubmed.ncbi.nlm.nih.gov/32776218
https://pubmed.ncbi.nlm.nih.gov/32776218
Autor:
Albina A, Avanesyan, Anna P, Sokolenko, Alexandr O, Ivantsov, Maxim A, Kleshchev, Mikhail A, Maydin, Ilya V, Bizin, Grigory A, Raskin, Ksenia V, Shelekhova, Tatiana V, Gorodnova, Alexandr A, Bessonov, Elena I, Anisimova, Olga A, Volynshchikova, Alexandr A, Romanko, Valeria I, Ni, Robert V, Broyde, Oleg B, Tkachenko, Aldon J, Whitehead, Alexandr M, Scherbakov, Evgeny N, Imyanitov
Publikováno v:
Pathobiology : journal of immunopathology, molecular and cellular biology. 87(6)
There is some evidence suggesting a link between BRCA1/2 germline mutations and increased risk of gastric cancer.Endoscopic screening for stomach malignancies was performed in 120 BRCA1 mutation carriers in order to evaluate the probability of detect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::521cae034133bb4f4ca834ecc06d3716
https://pubmed.ncbi.nlm.nih.gov/33161400
https://pubmed.ncbi.nlm.nih.gov/33161400