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Jing-Yu Liu

Showing results (101-110 of 130) with videos related to

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Iscience|February 14, 2024
Circadian disruption during fetal development promotes pathological cardiac remodeling in male miceYang Yu, Jing-Yu Liu, Hui-Jiao Yang, et al.
American Journal of Medical Genetics. Part A|August 8, 2006
A novel mutation in GDF5 causes autosomal dominant symphalangism in two Chinese familiesXu Wang, Fuying Xiao, Qinbo Yang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 28, 2018
Evaluation of MYORG mutations as a novel cause of primary familial brain calcificationYou Chen, Feng Fu, Si Chen, et al.
Nature Communications|May 10, 2020
Spider venom-derived peptide induces hyperalgesia in Na<sub>v</sub>1.7 knockout mice by activating Na<sub>v</sub>1.9 channelsXi Zhou, Tingbin Ma, Luyao Yang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 20, 2021
A Novel SPAST Mutation Results in Spastin Accumulation and Defects in Microtubule DynamicsRui Chen, Shiyue Du, Yanyi Yao, et al.
Journal of Ethnopharmacology|December 22, 2020
Kellerin from Ferula sinkiangensis exerts neuroprotective effects after focal cerebral ischemia in rats by inhibiting microglia-mediated inflammatory responsesYan Mi, Kun Jiao, Ji-Kai Xu, et al.
The Journal of Investigative Dermatology|August 16, 2020
Germline Mutation of PLCD1 Contributes to Human Multiple Pilomatricomas through Protein Kinase D/Extracellular Signal-Regulated Kinase1/2 Cascade and TRPV6Kai Liu, Junyu Luo, Tingbin Ma, et al.
Genetic Testing and Molecular Biomarkers|October 23, 2019
A Novel <i>CDH1</i> Mutation Causing Reduced E-Cadherin Dimerization Is Associated with Nonsyndromic Cleft Lip With or Without Cleft PalateShiyue Du, Yujie Yang, Ping Yi, et al.
The Journal of Biological Chemistry|February 18, 2017
Pathogenic mutations in retinitis pigmentosa 2 predominantly result in loss of RP2 protein stability in humans and zebrafishFei Liu, Yayun Qin, Shanshan Yu, et al.
Epilepsia|July 17, 2018
A PRRT2 variant in a Chinese family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures results in loss of interaction with STX1BHongying Ma, Shenglei Feng, Xuejun Deng, et al.
Pageof 13

Showing results (101-110 of 130) with videos related to

Sort By:
Pageof 13
Iscience|February 14, 2024
Circadian disruption during fetal development promotes pathological cardiac remodeling in male miceYang Yu, Jing-Yu Liu, Hui-Jiao Yang, et al.
American Journal of Medical Genetics. Part A|August 8, 2006
A novel mutation in GDF5 causes autosomal dominant symphalangism in two Chinese familiesXu Wang, Fuying Xiao, Qinbo Yang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 28, 2018
Evaluation of MYORG mutations as a novel cause of primary familial brain calcificationYou Chen, Feng Fu, Si Chen, et al.
Nature Communications|May 10, 2020
Spider venom-derived peptide induces hyperalgesia in Na<sub>v</sub>1.7 knockout mice by activating Na<sub>v</sub>1.9 channelsXi Zhou, Tingbin Ma, Luyao Yang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 20, 2021
A Novel SPAST Mutation Results in Spastin Accumulation and Defects in Microtubule DynamicsRui Chen, Shiyue Du, Yanyi Yao, et al.
Journal of Ethnopharmacology|December 22, 2020
Kellerin from Ferula sinkiangensis exerts neuroprotective effects after focal cerebral ischemia in rats by inhibiting microglia-mediated inflammatory responsesYan Mi, Kun Jiao, Ji-Kai Xu, et al.
The Journal of Investigative Dermatology|August 16, 2020
Germline Mutation of PLCD1 Contributes to Human Multiple Pilomatricomas through Protein Kinase D/Extracellular Signal-Regulated Kinase1/2 Cascade and TRPV6Kai Liu, Junyu Luo, Tingbin Ma, et al.
Genetic Testing and Molecular Biomarkers|October 23, 2019
A Novel <i>CDH1</i> Mutation Causing Reduced E-Cadherin Dimerization Is Associated with Nonsyndromic Cleft Lip With or Without Cleft PalateShiyue Du, Yujie Yang, Ping Yi, et al.
The Journal of Biological Chemistry|February 18, 2017
Pathogenic mutations in retinitis pigmentosa 2 predominantly result in loss of RP2 protein stability in humans and zebrafishFei Liu, Yayun Qin, Shanshan Yu, et al.
Epilepsia|July 17, 2018
A PRRT2 variant in a Chinese family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures results in loss of interaction with STX1BHongying Ma, Shenglei Feng, Xuejun Deng, et al.
Pageof 13