Поиск

Автор

Ключевое слово

Коллекция

Дополнительно:

Период публикации

Научный руководитель

Оппонент

По вашему запросу найдено документов: 432

Страница 1 из 44

The role of pathogenic germline mutations of BRCA1/2, NBS1, and CHEK2 genes in gastric cancer development within the Volga-Ural region of Russia

Nurgalieva, A.Kh., Petrova, Sabina G., Gallyamova, Lilia F., Ekomasova, Natalia V., Sakaeva, Dina D., Fedorova, Yulia Yu, Dzhaubermezov, Murat A., Abdeev, Rustem R., Rakhimov, Radmir R., Khusnutdinova, Elza K., Prokofyeva, Darya S. (2025)

of this study was to compare the prevalence of mutations in the BRCA1 (c.68_69delAG, c.4035delA, c.5266dupC, c

Опыт лечения BRCA-ассоциированного рака молочной железы. BRCA-история одной семьи

Experience in treating brca-associated breast cancer. The brca-history of a family

Sultanbaev, A.V., Menshikov, K.V., Nasretdinov, A.F., Izmailov, A.A., Musin, S.I., Menshikova, I.A., Chashchin, A.V., Sultanbaeva, N.I., Султанбаев, А. В., Меньшиков, К. В., Насретдинов, А. Ф., Измайлов, А. А., Мусин, Ш. И., Меньшикова, И. А., Чащин, А. В., Султанбаева, Н. И. (2021)

of malignant neoplasms in the identified healthy relatives with BRCA1 c.5382insC mutation. © 2021 Alexander V

A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

Coignard, J., Lush, M., Beesley, J., O’Mara, T.A., Dennis, J, Tyrer, J.P., Barnes, D.R., McGuffog, L., Leslie, G., Bolla, M.K., Adank, M.A., Kiiski, J.I., Nevanlinna, H., team of authors (2021)

Breast cancer (BC) risk for BRCA1 and BRCA2 mutation carriers varies by genetic and familial

Erratum: Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (Nature communications (2021) 12 1 (1078))

Breast cancer (BC) risk for BRCA1 and BRCA2 mutation carriers varies by genetic and familial

АНАЛИЗ МУТАЦИИ В ГЕНАХ BRCA1 И RCA2 У ПАЦИЕНТОК С РАКОМ МОЛОЧНОЙ ЖЕЛЕЗЫ В ЭКСПЕРИМЕНТЕ

ANALYSIS OF BRCA1 AND BRCA2 GENES MUTATIONS IN BREAST CANCER PATIENTS IN AN EXPERIMENT

САПТАРОВА, Л.М., КОГИНА, Э. Н., ХАСАНШИНА, Л.М., ГАЛИМОВ, Ш. Н., SAPTAROVA, L.M., COGINA, E.N., KHASANSHINA, L.M., GALIMOV, SH.N. (2020)

ANALYSIS OF BRCA1 AND BRCA2 GENES MUTATIONS IN BREAST CANCER PATIENTS IN AN EXPERIMENT

MUTATIONAL LANDSCAPE OF PROSTATE TUMORS REVEALED BY WHOLE-EXOME SEQUENCING

Gilyazova, I.R., Yankina, M.A., Kunsbaeva, G.B., Klimentova, E.A., Izmaylov, A.A., V.N. Pavlov, Khusnutdinova, E.K. (2016)

are presented. DNA was isolated from the peripheral blood as well as healthy and tumor prostate tissue from each

НАСЛЕДСТВЕННЫЙ РАК ЯИЧНИКОВ: ВКЛАД ИЗМЕНЕНИЙ ГЕНОВ-КАНДИДАТОВ В ПАТОГЕНЕЗ ЗАБОЛЕВАНИЯ

THE HEREDITARY OVARIAN CANCER: ROLE OF CANDIDATE GENES IN DISEASE PATHOGENESIS

Фаисханова, Р.Р., Прокофьева, Д.С., Хуснутдинова, Э.К., Сакаева, Д.Д., Гордиев, М.Г., Faiskhanova, R.R., Prokofieva, D.S., Khusnutdinova, E.K., Sakaeva, D.D., Gordiev, M.G. (2019)

BRCA1/BRCA2 MUTATIONS

LYNCH SYNDROME GERMLINE MUTATIONS IN BREAST CANCER: NEXT GENERATION SEQUENCING CASE-CONTROL STUDY OF 1,263 PARTICIPANTS

NIKITIN, A.G., CHUDAKOVA, D.A., ENIKEEV, R.F., GORDIEV, M.G., SAKAEVA, D., DRUZHKOV, M., SHIGAPOVA, L.H., BROVKINA, O.I., SHAGIMARDANOVA, E.I., GUSEV, O.A. (2020)

that LS-mutations are present in patients with hereditary BC more frequently than in healthy donors

Whole Exome Sequencing Study Suggests an Impact of FANCA, CDH1 and VEGFA Genes on Diffuse Gastric Cancer Development

Nurgalieva, A., Galliamova, L., Ekomasova, N., Yankina, M., Sakaeva, D., Valiev, R., Prokofyeva, D., Dzhaubermezov, M., Fedorova, Y., Khusnutdinov, S., Khusnutdinova, E. (2023)

sequencing (WES) was performed on 18 DNA samples from adenocarcinoma specimens and non-tumor-bearing healthy

Скрининг рака молочной железы у носителей герминальных мутаций. Обзор литературы

Breast cancer screening in germline mutation carriers. A literature review

Breast cancer screening in germline mutation carriers. A literature review

Страница 1 из 44