De-liang Huang

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.

The topographical relationships and anastomosis of the nerves in the human internal auditory canal

De-liang Huang, Guang-yong Tian, Da-chuan Xu, 2008, Surgical and Radiologic Anatomy.

Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss.

Yiping Shen, David T. Miller, O. Platt, 2009, Physiological genomics.

Identification of SLC26A4 c.919-2A>G compound heterozygosity in hearing-impaired patients to improve genetic counseling

Dong-yi Han, Yongyi Yuan, Shasha Huang, 2012, Journal of Translational Medicine.

Rapid screening for the mitochondrial DNA C1494T mutation in a deaf population in China using real-time quantitative PCR

Dong-yi Han, Yongyi Yuan, P. Dai, 2012, Acta oto-laryngologica.

A de novo GJB2 (connexin 26) mutation, R75W, in a Chinese pedigree with hearing loss and palmoplantar keratoderma

Yongyi Yuan, D. Kang, P. Dai, 2009, American journal of medical genetics. Part A.

Common Molecular Etiologies Are Rare in Nonsyndromic Tibetan Chinese Patients with Hearing Impairment

Yue-shuai Song, Guo-jian Wang, Yongyi Yuan, 2012, PloS one.

Identification of a MYO7A mutation in a large Chinese DFNA11 family and genotype–phenotype review for DFNA11

L. Lan, J. Guan, B. Han, 2018, Acta oto-laryngologica.

Surgical management of endolymphatic sac tumor: classification, outcomes and strategy. A single institution’s experience

N. Wu, P. Dai, Dongyi Han, 2022, European Archives of Oto-Rhino-Laryngology.

Molecular Etiology of Hearing Impairment in Inner Mongolia: mutations in SLC26A4 gene and relevant phenotype analysis

Bailin Wu, L. Wong, Yongyi Yuan, 2008, Journal of Translational Medicine.

Identification of SLC26A4 c.919-2A>G compound heterozygosity in hearing-impaired patients to improve genetic counseling

Yongyi Yuan, Shasha Huang, P. Dai, 2012, Journal of Translational Medicine.

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

David T. Miller, O. Platt, Bai-Lin Wu, 2008, Genetics in Medicine.

Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China

Y. You, Yongyi Yuan, D. Kang, 2009, Journal of Translational Medicine.

[Sequencing analysis of whole SLC26A4 gene related to IVS7-2A > G mutation in 1552 moderate to profound sensorineural hearing loss patients in China].

Yongyi Yuan, D. Kang, P. Dai, 2009, Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery.

[Sequencing of SLC26A4 exons 7 and 8 and hot spot mutation analysis in 1552 moderate to profound sensorineural hearing loss patients in China].

Yongyi Yuan, D. Kang, P. Dai, 2007, Zhonghua yi xue za zhi.

Surgical management of endolymphatic sac tumor: classification, outcomes and strategy. A single institution’s experience

N. Wu, P. Dai, Shi-ming Yang, 2022, European Archives of Oto-Rhino-Laryngology.

[Management of operative complications in acoustic neuroma surgery].

De-liang Huang, Wei-yan Yang, Shiming Yang, 2006, Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery.

Prevalence of the GJB2 IVS1+1G >A mutation in Chinese hearing loss patients with monoallelic pathogenic mutation in the coding region of GJB2

Guo-jian Wang, Yongyi Yuan, Shasha Huang, 2010, Journal of Translational Medicine.

The prevalence of the 235delC GJB2 mutation in a Chinese deaf population

B. Han, L. Wong, E. Schmitt, 2007, Genetics in Medicine.

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

P. Dai, Huijun Yuan, De-liang Huang, 2006, Zhonghua yi xue za zhi.

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.

[Features of nationwide distribution and frequency of a common gap junction beta-2 gene mutation in China].

B. Han, Guo-jian Wang, Yongyi Yuan, 2007, Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery.

[Frequency of SLC26A4 IVS7-2A > G mutation in patients with severe to profound hearing loss from different area and ethnic group in China].

B. Han, Yongyi Yuan, D. Kang, 2007, Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery.

Clinical characteristics, treatments, and prognosis of patients with multiple primary carcinoma of head and neck

Wen-ming Wu, De-liang Huang, Lin Ma, 2020, Chinese medical journal.