Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Maxim Leonidovich Filipenko"'
Autor:
Roza Pavlovna Tiis, Ludmila Pavlovna Osipova, Daria Veniaminovna Lichman, Elena Nikolaevna Voronina, Maxim Leonidovich Filipenko
Publikováno v:
BMC Genetics, Vol 21, Iss S1, Pp 1-7 (2020)
Abstract Background N-acetyltransferase 2 plays a crucial role in the metabolism of a wide range of xenobiotics, including many drugs, carcinogens, and other chemicals in the human environment. The article presents for the first time data on the freq
Externí odkaz:
https://doaj.org/article/57aad86877244246933f939b738ee691
Autor:
Ulyana A. Boyarskikh, L. F. Gulyaeva, A. M. Avdalyan, A. A. Kechin, E. A. Khrapov, D. G. Lazareva, N. E. Kushlinskii, A. Melkonyan, A. Arakelyan, Maxim Leonidovich Filipenko
Publikováno v:
Frontiers in Oncology, Vol 10 (2020)
Objective: Mutations in TP53 lead to loss of function (LOF) or gain of function (GOF) of the corresponding protein p53 and produce a different effect on the tumor. Our goal was to determine the spectrum of somatic TP53 variants in BRCA1/2 associated
Externí odkaz:
https://doaj.org/article/6212bc92777a484e94d370ba926d020e
Autor:
Maria Alexandrovna Gordukova, Ilya Anatolievich Korsunsky, Yulia Vladimirovna Chursinova, Maria Mikhailovna Byakhova, Igor Petrovich Oskorbin, Andrey Petrovich Prodeus, Maxim Leonidovich Filipenko
Publikováno v:
Медицинская иммунология, Vol 0, Iss 0 (2019)
In this work we used a reference population of newborns and sampled dried blood spots on Guthrie cards of 2,739 individual samples to determine the reference interval of TRECs and KRECs values in order to diagnose primary immunodeficiency due to neon
Externí odkaz:
https://doaj.org/article/2762d74a4b6d431393b83041d6f98b8a
Autor:
Ekaterina Alekseevna Sokolova, Irina Arkadievna Bondar, Olesya Yurievna Shabelnikova, Olga Vladimirovna Pyankova, Maxim Leonidovich Filipenko
Publikováno v:
PLoS ONE, Vol 10, Iss 5, p e0124662 (2015)
The genes ABCC8 and KCNJ11 have received intense focus in type 2 diabetes mellitus (T2DM) research over the past two decades. It has been hypothesized that the p.E23K (KCNJ11) mutation in the 11p15.1 region may play an important role in the developme
Externí odkaz:
https://doaj.org/article/20bfdb2910b646f5814abed7ecee7eea
Autor:
Ekaterina Alekseevna Sokolova, Nadezhda Alekseevna Malkova, Denis Sergeevich Korobko, Aleksey Sergeevich Rozhdestvenskii, Anastasia Vladimirovna Kakulya, Elena Vladimirovna Khanokh, Roman Andreevich Delov, Fedor Alekseevich Platonov, Tatyana Yegorovna Popova, Elena Gennadievna Aref' eva, Natalia Nikolaevna Zagorskaya, Valentina Mikhailovna Alifirova, Marina Andreevna Titova, Inna Vadimovna Smagina, Svetlana Alksandrovna El' chaninova, Anna Valentinovna Popovtseva, Valery Pavlovich Puzyrev, Olga Georgievna Kulakova, Ekaterina Yur'evna Tsareva, Olga Olegovna Favorova, Sergei Gennadievich Shchur, Natalia Yurievna Lashch, Natalia Fyodorovna Popova, Ekaterina Valerievna Popova, Evgenii Ivanovich Gusev, Aleksey Nikolaevich Boyko, Yurii Sergeevich Aulchenko, Maxim Leonidovich Filipenko
Publikováno v:
PLoS ONE, Vol 8, Iss 4, p e61032 (2013)
Multiple sclerosis (MS) is a serious, incurable neurological disease. In 2009, the ANZgene studies detected the suggestive association of located upstream of CD40 gene in chromosome 20q13 (p = 1.3×10(-7)). Identification of the causal variant(s) in
Externí odkaz:
https://doaj.org/article/5420b759ae6745f08f4391af5e65c07c
Autor:
Ulyana A. Boyarskikh, L. F. Gulyaeva, A. M. Avdalyan, A. A. Kechin, E. A. Khrapov, D. G. Lazareva, N. E. Kushlinskii, A. Melkonyan, A. Arakelyan, Maxim Leonidovich Filipenko
Publikováno v:
Frontiers in Oncology, Vol 10 (2020)
Frontiers in Oncology
Frontiers in Oncology
Objective: Mutations in TP53 lead to loss of function (LOF) or gain of function (GOF) of the corresponding protein p53 and produce a different effect on the tumor. Our goal was to determine the spectrum of somatic TP53 variants in BRCA1/2 associated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5303e0ffaea3533b9a88878049420258
https://pubmed.ncbi.nlm.nih.gov/32766142
https://pubmed.ncbi.nlm.nih.gov/32766142
Autor:
Gulmira Nigmetzhanovna, Kulmambetova, Meruert Kuatbekovna, Imanbekova, Andrey Alexeevich, Logvinenko, Adilbek Temirzhanovich, Sukashev, Maxim Leonidovich, Filipenko, Erlan Mirhaidarovich, Ramanculov
Publikováno v:
Asian Pacific journal of cancer prevention : APJCP. 15(18)
Gastritis and gastric cancer are the most common diseases in the Kazakh population. Polymorphisms in genes coding of cytokines have been played important role with gastric disease risk. The risk alleles of cytokines in patients with gastritis can pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7ac4008cc09680453f8e47487099519b
https://pubmed.ncbi.nlm.nih.gov/25292060
https://pubmed.ncbi.nlm.nih.gov/25292060