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НАСЛЕДСТВЕННЫЙ РАК ЯИЧНИКОВ: ВКЛАД ИЗМЕНЕНИЙ ГЕНОВ-КАНДИДАТОВ В ПАТОГЕНЕЗ ЗАБОЛЕВАНИЯ
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.
(BRCA1, BRCA2, TP53, BARD1, CHEK2, RAD51, PALB2). Описаны основные типы мутаций при BRCA
Genetic changes in the FH gene cause vagal paraganglioma
Snezhkina A.V., Pavlov V.S., Kalinin D.V., Pudova E.A., Krasnov G.S., Ayupova A.F., Kobelyatskaya A.A., Dmitriev A.A., Atiakshin D.A., Fedorova M.S., Kudryavtseva A.V.
with mutations in the SDHx genes. However, data regarding the genetics of VPGL are limited. Herein, we report a
Germline variants associated with breast cancer in Khakass women of North Asia
Gervas, Polina A., Molokov, Aleksey, Zarubin, Aleksei, Topolnitskiy, Evgenii B., Shefer, Nikolay A., Pisareva, Lubov, Choynzonov, Evgeny L., Cherdyntseva, Nadezhda V.
Introduction Variants in the BRCA1/2 genes are responsible for familial breast cancer. Numerous
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))
Coignard, J., Lush, M., Beesley, J., Andrieu, N., Antoniou, A.C., Fabienne Lesueur, Noura Mebirouk, Nadine Andrieu, Joe Dennis, Daniel R. Barnes, Lesley McGuffog, Goska Leslie, Manjeet K. Bolla, Daniel Barrowdale, Debra Frost, Paul D. P. Pharoah, Qin Wang, Douglas F. Easton, Antonis C. Antoniou, Irene L. Andrulis, Hoda Anton-Culver, Argyrios Ziogas, Jacques Simard, Volker Arndt, Hermann Brenner, Norbert Arnold, Jacopo Azzollini, Siranoush Manoukian, Bermisheva, Marina, Khusnutdinova, Elza, Blomqvist, Carl, Białkowska, Katarzyna, Jakubowska, Anna
Breast cancer (BC) risk for BRCA1 and BRCA2 mutation carriers varies by genetic and familial
Predictors of Multiple Primary Malignancies: Literature Review
germline mutations
Massive parallel sequencing for diagnostic genetic testing of BRCA genes - A single center experience
Ermolenko N., Boyarskikh U., Kechin A., Mazitova A., Khrapov E., Petrova V., Lazarev A., Kushlinskii N., Filipenko M.
genetics testing. We developed and tested an amplicon-based method for resequencing the BRCA1 and BRCA2
Прогнозирование риска развития и особенностей течения рака молочной железы на основании разработанного скринингового метода выявления мутаций в генах BRCA и показателей интратуморального иммунного ответа
Курстак, Ирина Андреевна
рак молочной железы, рак яичников, полимеразная цепная реакция, мутация генов, BRCA, методика
Prospects of PARP Inhibitors in Treatment of BRCA-Mutated Pancreatic Cancer: a Literature Review
Prospects of PARP Inhibitors in Treatment of BRCA-Mutated Pancreatic Cancer: a Literature Review
New variants in the BRCA1 gene in Buryat Mongol breast cancer patients: Report from two families
Cherdyntseva, Nadezhda V., Voropaeva, Elena, Denisov, Evgeny V., Pisareva, Lubov, Malinovskaya, Elena, Maksimov, Vladimir, Voevoda, Michail, Perinov, Dmitriy, Panferova, Yelena, Gervas, Polina A., Cherdyntsev, Evgeny S., Choynzonov, Evgeny L.
BACKGROUND: The BRCA1 mutations that are endemic to the Slavic population of Russia have not been
Exome sequencing study of Russian breast cancer patients suggests a predisposing role for USP39
Kuligina, E.S., Sokolenko, A.P., Bizin, I.V., Romanko, A.A., Zagorodnev, K.A., Anisimova, M.O., Krylova, D.D., Anisimova, E.I., Mantseva, M.A., Varma, A.K., Hasan, S.K., Ni, V.I., Koloskov, A.V., Suspitsin, E.N., Venina, A.R., Aleksakhina, S.N., Sokolova, T.N., Milanović, A.M., Schürmann, P., Prokofyeva, D.S., Bermisheva, M.A., Khusnutdinova, E.K., Bogdanova, N., Dörk, T., Imyanitov, E.N.
predisposition, who lacked Slavic founder mutations in BRCA1, BRCA2, CHEK2, and NBS1 genes. Results

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