GJB2, SLC26A4, and mitochondrialDNA12S rRNAhot-spots in 156 subjects with non-syndromic hearing loss in Tengzhou, China

Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China

(2015) Yi Jiang et al.   PLoS One

A rapid method for simultaneous multi-gene mutation screening in children with nonsyndromic hearing loss

(2014) Wan Du et al.   GENOMICS

Interleukin 1B rs16944 G>A polymorphism was associated with a decreased risk of esophageal cancer in a Chinese population

(2013) Liang Zheng et al.   CLINICAL BIOCHEMISTRY

MiR-196a2 rs11614913 T>C polymorphism and risk of esophageal cancer in a Chinese population

(2013) Jishu Wei et al.   HUMAN IMMUNOLOGY

Genetic mutations in nonsyndromic deafness patients of Chinese minority and han ethnicities in Yunnan, China

(2013) Feng Xin et al.   Journal of Translational Medicine

Genome-wide association study validation identifies novel loci for atherosclerotic cardiovascular disease

(2012) X. CHEN et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Matrix metalloproteinases in type 2 diabetes and non-diabetic controls: effects of short-term and chronic hyperglycaemia

(2011) Krzysztof C. Lewandowski et al.   Archives of Medical Science

Urinary matrix metalloproteinase-8 and -9 activities in type 2 diabetic subjects: A marker of incipient diabetic nephropathy?

(2010) Nynke J. van der Zijl et al.   CLINICAL BIOCHEMISTRY

Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss

(2010) Jianxin Lu et al.   MITOCHONDRION

Genetic Structure of the Han Chinese Population Revealed by Genome-wide SNP Variation

(2009) Jieming Chen et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Genetic polymorphism c.1562C>T of the MMP-9 is associated with macroangiopathy in type 2 diabetes mellitus

(2009) Ying Wang et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

GJB2 mutation spectrum in 2063 Chinese patients with nonsyndromic hearing impairment

(2009) Pu Dai et al.   Journal of Translational Medicine

GJB2,SLC26A4and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects

(2008) Yu-Fen Guo et al.   ACTA OTO-LARYNGOLOGICA

SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss

(2008) Pu Dai et al.   GENETICS IN MEDICINE

Molecular analysis of the GJB2, GJB6 and SLC26A4 genes in Korean deafness patients

(2008) K.Y. Lee et al.   INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY