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Frontiers in Molecular Neuroscience|August 14, 2023
cdh23 affects congenital hearing loss through regulating purine metabolismShu Yang, Bing-Lin Xie, Xiao-Ping Dong, et al.
Journal of the National Comprehensive Cancer Network : JNCCN|August 3, 2021
Comparing Patient-Controlled Analgesia Versus Non-PCA Hydromorphone Titration for Severe Cancer Pain: A Randomized Phase III TrialRongbo Lin, Sunzhi Lin, Shuitu Feng, et al.
Gene|August 19, 2007
Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigreesJianfu Chen, Li Yang, Aifen Yang, et al.
American Journal of Human Genetics|July 11, 2006
Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutationsMin-Xin Guan, Qingfeng Yan, Xiaoming Li, et al.
Mitochondrion|January 27, 2010
Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing lossJianxin Lu, Zhiyuan Li, Yi Zhu, et al.
Clinical Psychopharmacology and Neuroscience : the Official Scientific Journal of the Korean College of Neuropsychopharmacology|November 25, 2015
Risk Factors for Anxiety in Major Depressive Disorder PatientsLi-Min Xin, Lin Chen, Zhen-Peng Ji, et al.
Cancer Letters|April 28, 2018
Tumor suppressive microRNA-124a inhibits stemness and enhances gefitinib sensitivity of non-small cell lung cancer cells by targeting ubiquitin-specific protease 14Fei Yu, Ji-Bin Liu, Zhi-Jun Wu, et al.
Oncology Letters|December 15, 2018
Prognostic implications of decreased microRNA-101-3p expression in patients with non-small cell lung cancerHai-Min Lu, Wan-Wan Yi, Yu-Shui Ma, et al.
Nature Communications|October 1, 2022
Exportin 4 depletion leads to nuclear accumulation of a subset of circular RNAsLiang Chen, Yucong Wang, Jiamei Lin, et al.
Plos Genetics|March 26, 2015
Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndromeMariella Simon, Elodie M Richard, Xinjian Wang, et al.
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