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Genetic Testing and Molecular Biomarkers|July 29, 2010
Analysis of a large-scale screening of mitochondrial DNA m.1555A>G mutation in 2417 deaf-mute students in northwest of ChinaYu-Fen Guo, Xiao-Wen Liu, Bai-Cheng Xu, et al.
Veterinary Microbiology|May 14, 2020
A porcine alveolar macrophage cell line stably expressing CD163 demonstrates virus replication and cytokine secretion characteristics similar to primary alveolar macrophages following PRRSV infectionYu-Lin Xu, Shao-Peng Wu, Yun-Gang Li, et al.
International Journal of Pediatric Otorhinolaryngology|February 19, 2011
Newborn hearing concurrent gene screening can improve care for hearing loss: a study on 14,913 Chinese newbornsQiu-Ju Wang, Ya-Li Zhao, Shao-Qi Rao, et al.
Acta Oto-Laryngologica|January 30, 2015
Identification of a novel mutation of PJVK in the Chinese non-syndromic hearing loss population with low prevalence of the PJVK mutationsQiu-Jing Zhang, Lan Lan, Na Li, et al.
Journal of Fish Biology|March 17, 2023
Effect of Bacillus amyloliquefaciens LSG2-8 on the intestinal barrier function of Amur minnow (Rhynchocypris lagowskii)Meng-Nan Yu, Wen-Li Zhu, Si-Bu Wang, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|August 23, 2008
[Correlation between phonetically balanced maximum and pure tone auditory threshold among 106 auditory neuropathy patients]Lan Lan, Dong-Yi Han, Wei Shi, et al.
International Journal of Pediatric Otorhinolaryngology|May 21, 2010
Identification of two novel mutations, c.232T>C and c.2006A>T, in SLC26A4 in a Chinese family associated with enlarged vestibular aqueductYu-Fen Guo, Yan-Li Wang, Bai-Cheng Xu, et al.
Chinese Medical Journal|April 12, 2016
Clinical Study on 136 Children with Sudden Sensorineural Hearing LossFeng-Jiao Li, Da-Yong Wang, Hong-Yang Wang, et al.
BMC Medical Genetics|May 28, 2010
Screening mutations of OTOF gene in Chinese patients with auditory neuropathy, including a familial case of temperature-sensitive auditory neuropathyDa-Yong Wang, Yi-Chen Wang, Dominique Weil, et al.
Chinese Medical Journal|March 18, 2017
Clinical Auditory Phenotypes Associated with GATA3 Gene Mutations in Familial Hypoparathyroidism-deafness-renal Dysplasia SyndromeLi Wang, Qiong-Fen Lin, Hong-Yang Wang, et al.
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