Juyang Cao

Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA^Ser(UCN) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside‐induced and nonsyndromic hearing loss

Huijun Yuan, Yaping Qian, Yanjun Xu et al. · American Journal of Medical Genetics Part A · 2005 · 85 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: Implication for early detection and prevention of deafness

Pu Dai, Xin Liu, Dongyi Han et al. · Biochemical and Biophysical Research Communications · 2005 · 59 citations

Life Sciences, Genetics, Molecular Genetics +17

Correlation of Cochlear Blood Supply with Mitochondrial DNA Common Deletion in Presbyacusis

Pu Dai, Yang Wei–yan, Sichang Jiang et al. · Acta Oto-Laryngologica · 2004 · 56 citations

Life Sciences, Genetics, Molecular Biology +17

[Large-scale screening of mtDNA A1555G mutation in China and its significance in prevention of aminoglycoside antibiotic induced deafness].

Xin Liu, Pu Dai, Deliang Huang et al. · PubMed · 2006 · 18 citations

Medicine, Genetics, Molecular Genetics +17

Nonsense mutations in the PAX3 gene cause Waardenburg syndrome type I in two Chinese patients

Shuzhi Yang, Juyang Cao, Ruining Zhang et al. · Chinese Medical Journal · 2007 · 13 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14