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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
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
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)
(BC). In this study, we performed Targeted Next-Generation Sequencing of MMR pathway genes MLH1, MSH2
Osteogenesis Imperfecta: Search for Mutations in Patients from the Republic of Bashkortostan (Russia)
Nadyrshina, D., Zaripova, A., Tyurin, A., Minniakhmetov, I., Zakharova, E., Khusainova, R. (2022)
Next-generation sequencing (NGS)
MODERN APPROACHES TO DIFFERENTIATION OF LIVE AND DEAD BACTERIA USING SELECTIVE AMPLIFICATION OF NUCLEIC ACIDS
BAYMIEV, A.K., KULUEV, B.R., SHVETS, K.Y., YAMIDANOV, R.S., MATNIYAZOV, R.T., CHEMERIS, D.A., IVANENKOV, Y.A., CHEMERIS, A.V., ZUBOV, V.V., ALEKSEEV, Y.I., MAVZYUTOV, A.R. (2020)
to establish the viability of microorganisms by amplification of specific sequences of nucleic acids, both
ПОИСК ИЗМЕНЕНИЙ НУКЛЕОТИДНОЙ ПОСЛЕДОВАТЕЛЬНОСТИ ГЕНА РЕМОДЕЛИРОВАНИЯ ХРОМАТИНА PBRM1 У ПАЦИЕНТОВ СО СВЕТЛОКЛЕТОЧНЫМ РАКОМ ПОЧКИ
IDENTIFICATION OF ALTERATIONS IN THE NUCLEOTIDE SEQUENCE OF THE CHROMATIN REMODELING GENE PBRM1 IN CLEAR CELL RENAL CELL CARCINOMA PATIENTS
Klimentova E.A., Gilyazova I.R., Izmailov A.A., Sultanov I.M., Bermisheva M.A., V.N. Pavlov, Khusnutdinova E.K., КЛИМЕНТОВА, Е.А., ГИЛЯЗОВА, И.Р., ИЗМАЙЛОВ, А.А., СУЛТАНОВ, И.М., БЕРМИШЕВА, М.А., В.Н. Павлов, ХУСНУТДИНОВА, Э.К. (2018)
of ccRCC. The aim of our investigation is identification of changes in the nucleotide sequence
Interrelation of Telomeres with Transposable Elements in Aging
Mustafin, R. N. (2020)
and their binding sites, noncoding RNAs and their targets in protein-coding gene sequences evolutionarily originated
Fractional Levy stable motion: Finite difference iterative forecasting model
Liu, H., Song, W., Li, M., Kudreyko, A., Zio, E. (2020)
the influence of current and past trends in stochastic sequences on future trends. We find that the discussed

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