Zobrazeno 1 - 10
of 255
pro vyhledávání: '"Ek, Khusnutdinova"'
Publikováno v:
Europe PubMed Central
Schizophrenia affects about 1% of the population. Its etiology is not fully understood. Environmental conditions certainly contribute to the development of schizophrenia, but the determining factor is genetic predisposition: the coefficient of herita
Autor:
Ri, Khusainova, Natalia Balinova, Ia, Kutuev, Spitsina NKh, Vl, Akhmetova, Rr, Valiev, Va, Spitsyn, Ek, Khusnutdinova
Publikováno v:
Europe PubMed Central
Eight Alu insertions at the NBC27, TPA25, NBC148, NBC123, ACE, APOA1, NBC51, and PV92 locus were examined in three subethnic groups of Kalmyks (Torgouds, Derbets, and Buzava). In general, the pattern of allele frequencies in Kalmyks was consistent wi
Autor:
Elena Lebedeva, Vp, Sakovich, Ri, Khusainova, Ia, Kutuev, Rr, Valiev, Nn, Khusnutdinova, Ek, Khusnutdinova
Publikováno v:
Europe PubMed Central
The distribution of allele and genotype frequencies of the Alu-insertion polymorphism of the angiotensin-converting enzyme (ACE) gene and missence mutations leading to the substitution of arginine to cysteine in positions 112 and 158 of apolipoprotei
Autor:
Ma, Bermisheva, Ia, Kutuev, Viktor Spitsyn, Villems R, Az, Batyrova, Korshunova TIu, Ek, Khusnutdinova
Publikováno v:
Europe PubMed Central
Mitochondrial DNA (mtDNA) variation was studied in population of Oroks (n = 61), the indigenous inhabitants of Eastern Siberia. Most of the mtDNA types examined fell into five haplogroups (C, D, G, M10, and Y) typical of Eastern Eurasian populations.
Autor:
Ri, Fatkhlislamova, Im, Khidiatova, Ek, Khusnutdinova, Sn, Popova, Petr Slominsky, Sa, Limborskaia
Publikováno v:
Europe PubMed Central
Distribution of CTG repetitive sequences in the myotonic dystrophy (MD) gene was analyzed in ten populations of the Volga-Ural region, including Tatars, Chuvashes, Maris, Udmurts, Mordovians, Komis, and four ethnogeographical groups of Bashkirs. A to
Publikováno v:
Europe PubMed Central
A comparative study of two techniques for the PCR genotyping of highly polymorphic tandem repeats was carried out by the example of a triplet repeat in the myotonin protein kinase gene. Sequencing denaturing gels were shown to yield more precise resu
Autor:
Ov, Beliaeva, Ev, Shabrova, Mi, Prosniak, Viktor Spitsyn, Ek, Khusnutdinova, Ai, Mikulich, Sa, Limborskaia
Publikováno v:
Europe PubMed Central
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::1af0d7178ad6e34f5a85a3614fb180b6
http://europepmc.org/abstract/med/9454062
http://europepmc.org/abstract/med/9454062
Autor:
Ds, Prokofyeva, Et, Mingajeva, Nv, Bogdanova, Rr, Faiskhanova, Dd, Sakaeva, Thilo Dörk, Ek, Khusnutdinova
Publikováno v:
Europe PubMed Central
Ovarian cancer is one of the most insidious of tumors among gynecological cancers in the world. BRCA1 and BRCA2 mutations are associated with high risk of ovarian cancer; however, they are causative only in a fraction of cases. The search for new gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::c561eaf1e57e1b38d9a4f30897760367
http://europepmc.org/abstract/med/29369605
http://europepmc.org/abstract/med/29369605
Autor:
Lu, Dzhemileva, Ol, Posukh, Na, Barashkov, Sa, Fedorova, Fm, Teryutin, Vl, Akhmetova, Im, Khidiyatova, Ri, Khusainova, Semen Lobov, Ek, Khusnutdinova
Publikováno v:
Europe PubMed Central
Acta Naturae
Acta Naturae
The mutations in theGJB2(Сх26) gene make the biggest contribution to hereditary hearing loss. The spectrum and prevalence of theGJB2gene mutations are specific to populations of different ethnic origins. For severalGJB2 mutations, their origin from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::b54c97c8511656088398b5e97411c630
http://europepmc.org/abstract/med/22649694
http://europepmc.org/abstract/med/22649694
Autor:
Im, Khidiiatova, Ri, Fatkhlislamova, Rv, Magzhanov, Sn, Popova, Petr Slominsky, Sa, Limborskaia, Ek, Khusnutdinova
Publikováno v:
Europe PubMed Central
The CTG repeat of the myotonic dystrophy (MD) gene was analyzed in 62 MD patients and 54 healthy members of their families. A CTG repeat expansion was revealed in 57 (92%) patients and in 12 relatives who did not express clinical signs of MD. Family
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::74999786a62ff7855fc2977477fbb5ad
http://europepmc.org/abstract/med/11094756
http://europepmc.org/abstract/med/11094756