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Стрельников Владимир Викторович
Стрельников Владимир Викторович
Медико-генетический научный центр РАМН
Нет подтвержденного адреса электронной почты
Название
Процитировано
Процитировано
Год
DNA methylation in the promoter regions of the laminin family genes in normal and breast carcinoma tissues
OA Simonova, EB Kuznetsova, EV Poddubskaya, TV Kekeeva, ...
Molecular Biology 49 (4), 598-607, 2015
652015
Системы генетических и эпигенетических маркеров в диагностике онкологических заболеваний
МА Пальцев, ДВ Залетаев
Медицина 384, 2009
602009
Геномика-медицине
ВИ Иванова, МВ Асеев, ОВ Бабенко, ВС Баранов, ЕВ Баранова, ...
Академкнига, 2005
492005
Methylation of the BIN1 gene promoter CpG island associated with breast and prostate cancer
EB Kuznetsova, TV Kekeeva, SS Larin, VV Zemlyakova, AV Khomyakova, ...
Journal of carcinogenesis 6 (1), 9, 2007
402007
Clinical relevance of somatic mutations in main driver genes detected in gastric cancer patients by next-generation DNA sequencing
MV Nemtsova, AI Kalinkin, EB Kuznetsova, IV Bure, EA Alekseeva, ...
Scientific reports 10 (1), 1-11, 2020
362020
Diagnostics of epigenetic alterations in hereditary and oncological disorders
DV Zaletaev, MV Nemtsova, VV Strelnikov, OV Babenko, EV Vasil'ev, ...
Molecular Biology 38 (2), 174-182, 2004
34*2004
Abnormal methylation of several tumor suppressor genes in sporadic breast cancer
VV Zemlyakova, AI Zhevlova, VV Strelnikov, LN Lyubchenko, ...
Molecular Biology 37 (4), 591-597, 2003
33*2003
The cancer-retina antigen recoverin as a potential biomarker for renal tumors
MO Golovastova, LV Tsoy, AV Bocharnikova, DO Korolev, ...
Tumor Biology 37 (7), 9899-9907, 2016
322016
Genome-wide methylotyping resolves breast cancer epigenetic heterogeneity and suggests novel therapeutic perspectives
AS Tanas, VO Sigin, AI Kalinkin, NV Litviakov, EM Slonimskaya, ...
Epigenomics 11 (6), 605-617, 2019
302019
A simple multiplex FRAXA, FRAXE, and FRAXF PCR assay convenient for wide screening programs
V Strelnikov, M Nemtsova, G Chesnokova, N Kuleshov, D Zaletayev
Human mutation 13 (2), 166-169, 1999
301999
Маркеры метилирования в диагностике онкологических заболеваний
ДВ Залетаев, ВВ Стрельников, МВ Немцова, ОВ Бабенко, ...
Медицинская генетика 9 (1), 15-21, 2010
22*2010
Rapid and affordable genome-wide bisulfite DNA sequencing by XmaI-reduced representation bisulfite sequencing
AS Tanas, ME Borisova, EB Kuznetsova, VV Rudenko, KO Karandasheva, ...
Epigenomics 9 (6), 833-847, 2017
212017
Novel markers of gene methylation and expression in breast cancer
EB Kuznetsova, TV Kekeeva, SS Larin, VV Zemlyakova, OV Babenko, ...
Molecular Biology 41 (4), 562-570, 2007
21*2007
Stargardt disease-associated mutation spectrum of a Russian Federation cohort
IV Zolnikova, VV Strelnikov, NA Skvortsova, AS Tanas, D Barh, ...
European Journal of Medical Genetics 60 (2), 140-147, 2017
202017
DNA methylation markers panel can improve prediction of response to neoadjuvant chemotherapy in luminal B breast cancer
VO Sigin, AI Kalinkin, EB Kuznetsova, OA Simonova, GG Chesnokova, ...
Scientific reports 10 (1), 1-9, 2020
172020
Novel tools for unbiased DNA differential methylation screening
AS Tanas, VV Shkarupo, EB Kuznetsova, DV Zaletayev, VV Strelnikov
Epigenomics 2 (2), 325-333, 2010
172010
Comparison of aberrant methylation of CpG islands in the p16/CDKN2A and p14/ARF promoters in non-small cell lung cancer and acute lymphoblastic leukemia
VV Zemlyakova, VV Strel'nikov, IB Zborovskaya, OV Balukova, ...
Molecular Biology 38 (6), 821-827, 2004
17*2004
Diagnosis of Martin-Bell syndrome based on an analysis of the structural-functional changes in the 5'-untranslated region of the FMR1 gene].
VV Strel'nikov, MV Nemtsova, GG Chesnokova, NP Kuleshov, ...
Molekuliarnaia biologiia 33 (2), 330, 1999
17*1999
RB1 and CDKN2A functional defects resulting in retinoblastoma
OV Babenko, VV Zemlyakova, SV Saakyan, AF Brovkina, VV Strelnikov, ...
Molecular Biology 36 (5), 625-630, 2002
162002
Genetic screening of Russian Usher syndrome patients toward selection for gene therapy
ME Ivanova, VN Trubilin, DS Atarshchikov, AM Demchinsky, VV Strelnikov, ...
Ophthalmic Genetics 39 (6), 706-713, 2018
142018
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