L. Mei

Yong Feng, L. Mei, Hongsheng Chen, 2020, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

Novel mutations in the SOX10 gene in the first two Chinese cases of type IV Waardenburg syndrome.

K. Xia, Zhengmao Hu, Yong Feng, 2011, Biochemical and biophysical research communications.

Novel mutations of PAX3, MITF, and SOX10 genes in Chinese patients with type I or type II Waardenburg syndrome.

K. Xia, Zhengmao Hu, Yong Feng, 2010, Biochemical and biophysical research communications.

LEF-1 Regulates Tyrosinase Gene Transcription In Vitro

Yong Feng, Zhijie Niu, L. Mei, 2015, PloS one.

A Model of Waardenburg Syndrome Using Patient-Derived iPSCs With a SOX10 Mutation Displays Compromised Maturation and Function of the Neural Crest That Involves Inner Ear Development

Yong Feng, L. Mei, Chufeng He, 2021, Frontiers in Cell and Developmental Biology.

Identification and functional analysis of a novel missense mutation of PAX3 associated with Waardenburg syndrome type I

Yong Feng, Zhijie Niu, L. Mei, 2020, European Archives of Oto-Rhino-Laryngology.

Wnt signaling pathway involvement in genotypic and phenotypic variations in Waardenburg syndrome type 2 with MITF mutations

Yong Feng, Zhijie Niu, L. Mei, 2018, Journal of Human Genetics.

Functional analysis of a nonstop mutation in MITF gene identified in a patient with Waardenburg syndrome type 2

Yong Feng, Zhijie Niu, L. Mei, 2017, Journal of Human Genetics.

Application of a New Genetic Deafness Microarray for Detecting Mutations in the Deaf in China

Q. Pan, Yong Feng, L. Mei, 2016, PloS one.

Next-generation sequencing-based mutation analysis of genes associated with enlarged vestibular aqueduct in Chinese families

Yong Feng, Shu-shan Sang, L. Mei, 2020, European Archives of Oto-Rhino-Laryngology.

New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing

D. Yan, Yong Feng, L. Mei, 2019, Neural plasticity.

A New Genetic Diagnostic for Enlarged Vestibular Aqueduct Based on Next-Generation Sequencing

Yong Feng, L. Mei, Hongsheng Chen, 2016, PloS one.

Establishment of an iPSC line (CSUXHi003-A) from a patient with Waardenburg syndrome type Ⅱ caused by a MITF mutation.

Yong Feng, L. Mei, Hongsheng Chen, 2021, Stem cell research.

Mechanism underlying synergic activation of Tyrosinase promoter by MITF and IRF4

Yong Feng, L. Mei, Chufeng He, 2017 .

Proband Whole-Exome Sequencing Identified Genes Responsible for Autosomal Recessive Non-Syndromic Hearing Loss in 33 Chinese Nuclear Families

Yong Feng, Jing Liu, Shu-shan Sang, 2019, Front. Genet..

Exome Sequencing Identifies a Novel CEACAM16 Mutation Associated with Autosomal Dominant Nonsyndromic Hearing Loss DFNA4B in a Chinese Family

J. Yu, X. Liu, Jianguo Zhang, 2014, Journal of Human Genetics.

Otological manifestations in branchiootorenal spectrum disorder: A systematic review and meta‐analysis

F. Acke, L. Mei, Chufeng He, 2021, Clinical genetics.

Exome sequencing identifies a novel missense mutation of WFS1 as the cause of non-syndromic low-frequency hearing loss in a Chinese family.

X. Liu, Zhengmao Hu, Yong Feng, 2017, International journal of pediatric otorhinolaryngology.

Clinical Characteristics and Prognosis of Sudden Sensorineural Hearing Loss in Post-irradiated Nasopharyngeal Carcinoma Survivors.

Yong Feng, L. Mei, Zhihai Xie, 2020, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

Effect of systemic lupus erythematosus and rheumatoid arthritis on sudden sensorineural hearing loss

Yong Feng, L. Mei, Qiancheng Jing, 2019, The Laryngoscope.

Multivariate analysis of prognostic factors for idiopathic sudden sensorineural hearing loss treated with adjuvant hyperbaric oxygen therapy

Yong Feng, L. Mei, Chufeng He, 2017, European Archives of Oto-Rhino-Laryngology.

A novel mutation in the SMPX gene associated with X-linked nonsyndromic sensorineural hearing loss in a Chinese family

Yong Feng, Shu-shan Sang, Zhijie Niu, 2018, Journal of Human Genetics.

Exome sequencing identifies POU4F3 as the causative gene for a large Chinese family with non-syndromic hearing loss

Y. Li, X. Liu, K. Xia, 2016, Journal of Human Genetics.

Mutations in TMEM43 cause autosomal dominant auditory neuropathy spectrum disorder via interaction with connexin-mediated passive conductance channels

W. Park, Eunyoung Yi, S. Blanton, 2020, bioRxiv.

Elmod3 knockout leads to progressive hearing loss and abnormalities in cochlear hair cell stereocilia.

X. Liu, D. Yan, Yong Feng, 2019, Human molecular genetics.

Reproductive guidance through prenatal diagnosis and genetic counseling for recessive hereditary hearing loss in high-risk families.

M. Li, Yong Feng, Shu-shan Sang, 2018, International journal of pediatric otorhinolaryngology.

A rapid improved multiplex ligation detection reaction method for the identification of gene mutations in hereditary hearing loss

Yong Feng, L. Mei, Hongsheng Chen, 2019, PloS one.

[An investigation of SLC26A4 gene mutation in nonsydromic hearing impairment in Hunan province of China].

Yong Feng, L. Mei, Hongsheng Chen, 2010, Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery.

Digenic mutations involving both the BSND and GJB2 genes detected in Bartter syndrome type IV.

L. Mei, Chufeng He, Lu Jiang, 2017, International journal of pediatric otorhinolaryngology.

ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss

X. Liu, M. Li, D. Yan, 2018, Human Genetics.

Gene localization in a Chinese family with autosomal dominant non-syndromic deafness

K. Xia, Zhengmao Hu, Yong Feng, 2011, Acta oto-laryngologica.

Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type II

K. Xia, Yong Feng, L. Mei, 2012, Human Genetics.

DDDT_A_214918 3199..3206

Yong Feng, L. Mei, Chufeng He, 2019 .

Short-term effects of intravenous batroxobin in treatment of sudden sensorineural hearing loss: a propensity score-matched study

L. Mei, Chufeng He, Xinzhang Cai, 2023, Frontiers in Neurology.

A nonsense TMEM43 variant leads to disruption of connexin-linked function and autosomal dominant auditory neuropathy spectrum disorder

W. Park, Eunyoung Yi, S. Blanton, 2021, Proceedings of the National Academy of Sciences.

Modeling of pigmentation disorders associated with MITF mutation in Waardenburg syndrome revealed an impaired melanogenesis pathway in iPS-derived melanocytes.

Yong Feng, L. Mei, Chufeng He, 2023, Pigment Cell & Melanoma Research.

Establishment of an iPSC line (CSUXHi004-A) from a patient with Waardenburg syndrome type I caused by a PAX3 splice mutation.

Yong Feng, Jing Liu, L. Mei, 2021, Stem cell research.

[Study of the anatomy related to cochlear implantation guided by HRCT].

Yong Feng, L. Mei, Chufeng He, 2011, Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery.

Gene regulation analysis of patient-derived iPSCs and its CRISPR-corrected control provides a new tool for studying perturbations of ELMOD3 c.512A>G mutation during the development of inherited hearing loss

Yong Feng, L. Mei, Jie Sun, 2023, PloS one.

ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss

X. Liu, M. Li, D. Yan, 2018, Human Genetics.

ABCC1 deficiency potentiated noise-induced hearing loss in mice by impairing cochlear antioxidant capacity

L. Mei, Xianlin Liu, Jie Ling, 2024, Redox biology.

PAX3 mutation suppress otic progenitors proliferation and induce apoptosis by inhibiting WNT1/β-catenin signaling pathway in WS1 patient iPSC-derived inner ear organoids.

Yong Feng, L. Mei, Chufeng He, 2024, Biochemical and biophysical research communications.