Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Yerlan M Ramanculov"'
Autor:
Barshagul T Baikara, Elena V Zholdybayeva, Saule E Rakhimova, Nazym B Nigmatullina, Kuvat T Momynaliev, Yerlan M Ramanculov
Publikováno v:
PLoS ONE, Vol 10, Iss 7, p e0132010 (2015)
Alport syndrome is a genetic condition that results in hematuria, progressive renal impairment, hearing loss, and occasionally lenticonus and retinopathy. Approximately 80% of Alport syndrome cases are caused by X-linked mutations in the COL4A5 gene
Externí odkaz:
https://doaj.org/article/22f624b1f7b5482784fd7c21111028ff
Autor:
Kuvat Momynaliev, Yerlan M. Ramanculov, Elena Zholdybayeva, Saule Rakhimova, Barshagul T. Baikara, Nazym B. Nigmatullina
Publikováno v:
PLoS ONE
PLoS ONE, Vol 10, Iss 7, p e0132010 (2015)
PLoS ONE, Vol 10, Iss 7, p e0132010 (2015)
Alport syndrome is a genetic condition that results in hematuria, progressive renal impairment, hearing loss, and occasionally lenticonus and retinopathy. Approximately 80% of Alport syndrome cases are caused by X-linked mutations in the COL4A5 gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33427689337fe3eeb4be201177b7c730
http://europepmc.org/articles/PMC4500592
http://europepmc.org/articles/PMC4500592
Autor:
Elena Zholdybayeva, Olga Visternichan, Pavel Tarlykov, Yerlan M. Ramanculov, Akbota Aitkulova, Gulmira N. Kulmambetova, Yerkebulan A. Talzhanov, Dana Taizhanova, Aisha N. Iskakova, Aliya U. Dzholdasbekova
Publikováno v:
Human Genomics
Background After coronary stenting, the risk of developing restenosis is from 20 to 35 %. The aim of the present study is to investigate the association of genetic variation in candidate genes in patients diagnosed with restenosis in the Kazakh popul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83f067c30489a12404430076355e0b4c