EGLN2 and RNF150 genetic variants are associated with chronic obstructive pulmonary disease risk in the Chinese population
Yipeng Ding,1,* Huan Niu,1,* Hua Yang,2 Pei Sun,1 Yu Chen,3 Mengling Duan,1 Dongchuan Xu,1 Junxue Xu,3 Tianbo Jin2,4 1Department of Emergency, People’s Hospital of Hainan Province, Haikou, Hainan, People’s Republic of China; 2School of Life Sciences, Northwest University, Xi&am...
Main Authors: | Ding YP, Niu H, Yang H, Sun P, Chen Y, Duan ML, Xu DC, Xu JX, Jin TB |
---|---|
Format: | Article |
Language: | English |
Published: |
Dove Medical Press
2015-01-01
|
Series: | International Journal of COPD |
Online Access: | http://www.dovepress.com/egln2-and-rnf150-genetic-variants-are-associated-with-chronic-obstruct-peer-reviewed-article-COPD |
Similar Items
-
Genetic Analysis of EGLN1 C127S Variant in Taiwanese Parkinson’s Disease
by: Han-Lin Chiang, et al.
Published: (2020-01-01) -
Association of genetic polymorphisms with chronic obstructive pulmonary disease in the Hainan population: a case-control study
by: Ding YP, et al.
Published: (2014-12-01) -
Suppression of glioma progression by Egln3.
by: Vicki A Sciorra, et al.
Published: (2012-01-01) -
Variants of the Low Oxygen Sensors EGLN1 and HIF-1AN Associated with Acute Mountain Sickness
by: Enhao Zhang, et al.
Published: (2014-11-01) -
Clinical observation of a patient with TMEM127 and EGLN1 gene variants, pheochromocytoma and pancreatic tumor
by: M. Yu. Yukina, et al.
Published: (2021-05-01)