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Toxicology in Vitro : an International Journal Published in Association with BIBRA|June 26, 2017
Comparative metabolism of DDAO benzoate in liver microsomes from various speciesHong-Ying Ma, Jia-Da Yang, Jie Hou, et al.
Human Molecular Genetics|January 25, 2023
A functional spectrum of PROKR2 mutations identified in isolated hypogonadotropic hypogonadismXinying Wang, Danna Chen, Yaguang Zhao, et al.
British Journal of Pharmacology|March 20, 2014
Oxytocin inhibits the activity of acid-sensing ion channels through the vasopressin, V1A receptor in primary sensory neuronsFang Qiu, Chun-Yu Qiu, Huilan Cai, et al.
Hormone Research in Paediatrics|July 7, 2022
SLIT2 Rare Sequencing Variants Identified in Idiopathic Hypogonadotropic HypogonadismJiayu Wu, Zhenghuan Fang, Xinying Wang, et al.
Biochemical and Biophysical Research Communications|August 24, 2013
Functional analysis of the distal region of the third intracellular loop of PROKR2Xiao-Tao Zhou, Dan-Na Chen, Zhi-Qun Xie, et al.
The Journal of Clinical Endocrinology and Metabolism|November 6, 2019
Phenotypic Spectrum of Idiopathic Hypogonadotropic Hypogonadism Patients With CHD7 Variants From a Large Chinese CohortJia-Da Li, Jiayu Wu, Yaguang Zhao, et al.
Scientific Reports|October 25, 2016
Insertion of a knockout-first cassette in Ampd1 gene leads to neonatal death by disruption of neighboring genes expressionYongcheng Pan, Lusi Zhang, Qiong Liu, et al.
Signal Transduction and Targeted Therapy|June 4, 2023
CNTNAP2 intracellular domain (CICD) generated by γ-secretase cleavage improves autism-related behaviorsJing Zhang, Fang Cai, Renbin Lu, et al.
Scientific Reports|January 29, 2016
Genetic and functional analysis of a Li Fraumeni syndrome family in ChinaHuaying Hu, Jingping Liu, Xinbin Liao, et al.
Human Genetics|October 4, 2011
Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type IIHua Zhang, Hongsheng Chen, Hunjin Luo, et al.
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