Wie-yen Young

发表

Type I hair cell regeneration induced by Math1 gene transfer following neomycin ototoxicity in rat vestibular sensory epithelium

W. Guo, W. Guo, Shi-ming Yang, 2012, Acta oto-laryngologica.

Effects of DAPT and Atoh1 Overexpression on Hair Cell Production and Hair Bundle Orientation in Cultured Organ of Corti from Neonatal Rats

Li-dong Zhao, N. Wu, Hui-zhan Liu, 2011, PloS one.

Chondrocyte‐specific Smad4 gene conditional knockout results in hearing loss and inner ear malformation in mice

Ji-shuai Zhang, X. Yang, Wei-Wei Guo, 2009, Developmental dynamics : an official publication of the American Association of Anatomists.

Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family.

Hui Zhao, Ronghua Li, Qiuju Wang, 2004, American journal of human genetics.

[Mutation screening of MITF gene in patients with Waardenburg syndrome type 2].

J. Chen, B. Han, Guo-jian Wang, 2008, Yi chuan = Hereditas.

Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss

Hui Zhao, Xiaoming Li, Ronghua Li, 2005, Nucleic acids research.

Smad5 haploinsufficiency leads to hair cell and hearing loss

Wei-Wei Guo, Xiao Yang, Shi-ming Yang, 2009, Developmental neurobiology.

Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation

Hui Zhao, Qiuju Wang, J. Greinwald, 2005, American journal of medical genetics. Part A.

The role of Smad4 in vestibular development in mice

Wei-Wei Guo, Guan Yang, Xiao Yang, 2011, International Journal of Developmental Neuroscience.

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

Ronghua Li, Yaping Qian, D. Kang, 2006, Biochemical and biophysical research communications.

Mutations at position 7445 in the precursor of mitochondrial tRNA(Ser(UCN)) gene in three maternal Chinese pedigrees with sensorineural hearing loss.

J. Chen, B. Han, Guo-jian Wang, 2008, Mitochondrion.

Math1 gene transfer based on the delivery system of quaternized chitosan/Na-carboxymethyl-beta-cyclodextrin nanoparticles.

N. Wu, Wei-Wei Guo, Li-dong Zhao, 2010, Journal of nanoscience and nanotechnology.

Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss.

D. Kang, P. Dai, M. Guan, 2007, Biochemical and biophysical research communications.

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

Yaping Qian, J. Greinwald, J. Mo, 2005, American journal of medical genetics. Part A.

Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation.

Qiuju Wang, Yaping Qian, M. Guan, 2004, Biochemical and biophysical research communications.

Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss.

Ronghua Li, Qiuju Wang, Yaping Qian, 2005, Biochemical and biophysical research communications.

Regeneration of Stereocilia of Hair Cells by Forced Atoh1 Expression in the Adult Mammalian Cochlea

Hui-zhan Liu, Wei-Wei Guo, Shi-ming Yang, 2012, PloS one.

Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation.

Ronghua Li, Qiuju Wang, Yaping Qian, 2006, Biochemical and biophysical research communications.

Variants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness‐associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss

Ronghua Li, Yaping Qian, P. Dai, 2006, American journal of medical genetics. Part A.

Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation.

Ning Li, Min-Xin Guan, Qiuju Wang, 2005, Biochemical and biophysical research communications.

Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss

Hui Zhao, Xiaoming Li, Ronghua Li, 2005, Nucleic acids research.

The mitochondrial tRNA(Ala) T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing loss.

Yaping Qian, Yongyi Yuan, P. Dai, 2007, Biochemical and biophysical research communications.

Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese families.

Yaping Qian, Yongyi Yuan, P. Dai, 2006, Biochemical and biophysical research communications.