По вашему запросу найдено документов: 15

Страница 1 из 2

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)
The results of the whole-exome DNA sequencing of eight prostate adenocarcinoma patients
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)
of possible new candidate genes, associated with the increased risk of gastric cancer development. Whole exome
Dissecting and analyzing the Subclonal Mutations Associated with Poor Prognosis in Diffuse Glioma
Bai, Ming, Wang, Xiaolong, Zhang, Huixue, Wang, Jianjian, Lyaysan, Gaysina, Xu, Si, Tian, Kuo, Wang, Tianfeng, Li, Jie, Wang, Na, Lu, Xiaoyu, Zhang, Xiaoming, Wang, Lihua (2022)
(GBMs) and low-grade gliomas (LGGs) by using exome sequencing data from TCGA and observed both clonal
ASSOCIATION OF 22 POTENTIAL PATHOGENIC VARIANTS OF NEW CANDIDATE GENES AND THE RISK OF OVARIAN CANCER
Mingazheva, E.T., Prokofyeva, D.S., Valova, Ya.V., Andreeva, E.A., Nurgalieva, A.Kh., Valiev, R.R., Ekomasova, N.V., Faishanova, R.R., Romanova, A.R., Khusnutdinova, E.K. (2022)
involved in the disease. As a result of previous exome sequencing of DNA samples from breast cancer Germany
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. (2020)
of hereditary BC cases. This study aimed to identify missing genetic determinants of BC. Methods: Whole exome
МАЖОРНАЯ МУТАЦИЯ В ГЕНЕ SPAST У ПАЦИЕНТОВ С АУТОСОМНО-ДОМИНАНТНОЙ СПАСТИЧЕСКОЙ ПАРАПЛЕГИЕЙ ИЗ РЕСПУБЛИКИ БАШКОРТОСТАН
MAJOR MUTATION IN THE SPAST GENE IN PATIENTS WITH AUTOSOMAL DOMINANT SPASTIC PARAPLEGIA FROM THE REPUBLIC OF BASHKORTOSTAN
KHIDIYATOVA, I.M., AKHMETGALEYEVA, A.F., YANKINA, M.A., KHUSNUTDINOVA, E.K., SHAVALIEVA, V.V., SAIFULLINA, E.V., MAGZHANOV, R.V., IDRISOVA, R.F., ХИДИЯТОВА И.М., АХМЕТГАЛЕЕВА А.Ф., САЙФУЛЛИНА Е.В., ИДРИСОВА Р.Ф., ЯНКИНА М.А., ШАВАЛИЕВА В.В., МАГЖАНОВ Р.В., ХУСНУТДИНОВА Э.К. (2019)
NGS target exome sequencing
ГЕНЕТИЧЕСКИЕ ОСНОВЫ ПРЕДРАСПОЛОЖЕННОСТИ К ДЕПРЕССИВНЫМ РАССТРОЙСТВАМ
GENETIC BASIS OF DEPRESSIVE DISORDERS
ДАВЫДОВА, Ю.Д., ЕНИКЕЕВА, Р.Ф., КАЗАНЦЕВА, А.В., МУСТАФИН, Р.Н., РОМАНОВА, А.Р., МАЛЫХ, С.Б., ХУСНУТДИНОВА, Э.К., Davydova Yu.D., Enikeeva R.F., Kazantseva A.V., Mustafin R.N., Romanova A.R., Malykh S.B., Khusnutdinova E.K.2 (2019)
, GWAS) и полноэкзомных (Whole Exome Sequencing, WES) исследованиях, продемонстрировавших связь
Генетические проблемы ДНК-портретирования как части ДНК-фенотипирования: обзор
Genetic problems of DNA portrait as part of DNA phenotyping: A review
Chemeris, Alexey V., Khalikov, Airat A., Garafutdinov, Ravil R., Chemeris, Dmitry A., Sakhabutdinova, Assol R., Khaliullina, Aigul F., Galyautdinov, Rushan R., Sagidullin, Rafael H., Aminev, Farit G., Чемерис, А .В ., Халиков, А .А ., Гарафутдинов, Р .Р ., Чемерис, Д .А ., Сахабутдинова, А .Р ., Халиуллина, А .Ф ., Галяутдинов, Р .Р ., Сагидуллин, Р .Х ., Аминев, Ф .Г . (2024)
exome
The potential of miR-153 as aggressive prostate cancer biomarker
Gilyazova, Irina, Ivanova, Elizaveta, Sinelnikov, Mikhail, Pavlov, Valentin, Khusnutdinova, Elza, Khusnutdinova, Elza, Beilerli, Aferin, Mikhaleva, Ludmila, Liang, Yanchao (2023)
of miR-153 were identified using exome sequencing. Protein-protein interaction (PPI) networks, Kyoto
Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene
Barashkov, N.A., Konovalov, F.A., Borisova, T.V., Teryutin, F.M., Solovyev, A.V., Pshennikova, V.G., Sapojnikova, N.V., Vychuzhina, L.S., Romanov, G.P., Gotovtsev, N.N., Morozov, I.V., Bondar, A.A., Platonov, F.A., Burtseva, T.E., Khusnutdinova, E.K., Posukh, O.L., Fedorova, S.A. (2021)
the genetic cause of congenital cataract spread in this population, we performed whole-exome sequencing

Страница 1 из 2

Google Scholar
OpenDoar

Фасеты

Авторы
Ключевые слова
Год