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Jing-Yu Liu

Showing results (81-90 of 130) with videos related to

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The Journal of Investigative Dermatology|December 15, 2007
Identification of a genetic locus for ichthyosis vulgaris on chromosome 10q22.3-q24.2Ping Liu, Qingyu Yang, Xu Wang, et al.
Biochemical and Biophysical Research Communications|January 8, 2008
Identification and functional characterization of a novel splicing mutation in RP gene PRPF31Jing Yu Liu, Xiaohua Dai, Jiqun Sheng, et al.
Molecular Genetics and Metabolism|October 19, 2010
Identification of compound heterozygous mutations in GNPTG in three siblings of a Chinese family with mucolipidosis type III gammaYong Gao, Kangjuan Yang, Shujiang Xu, et al.
Human Genetics|October 3, 2008
A novel genetic locus for familial febrile seizures and epilepsy on chromosome 3q26.2-q26.33Xiao-Hua Dai, Wen-Wu Chen, Xu Wang, et al.
DNA and Cell Biology|September 28, 2019
Identification and Analysis of Genes Involved in Auxin, Abscisic Acid, Gibberellin, and Brassinosteroid Metabolisms Under Drought Stress in Tender Shoots of Tea PlantsHui Li, Rui-Min Teng, Jie-Xia Liu, et al.
Frontiers in Cell and Developmental Biology|November 30, 2020
p.His16Arg of STXBP1 (MUNC18-1) Associated With Syntaxin 3B Causes Autosomal Dominant Congenital NystagmusYulei Li, Lei Jiang, Lejin Wang, et al.
Biomed Research International|May 3, 2021
Electroacupuncture Improves Pregnancy Outcomes in Rats with Thin Endometrium by Promoting the Expression of Pinopode-Related MoleculesJin Xi, Jie Cheng, Chun-Chun Jin, et al.
Yi Chuan Xue Bao = Acta Genetica Sinica|August 31, 2006
Mutation p.Arg954Trp of KIF21A causes congenital fibrosis of the extraocular muscles in a Chinese familyXian-Qin Zhang, Jian-Hong Peng, Zhao-Hui Tang, et al.
Pain|July 30, 2021
Protein arginine methyltransferase 7 modulates neuronal excitability by interacting with NaV1.9Tingbin Ma, Lulu Li, Rui Chen, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 10, 2019
Murine Placental-Fetal Phosphate Dyshomeostasis Caused by an Xpr1 Deficiency Accelerates Placental Calcification and Restricts Fetal Growth in Late GestationXuan Xu, Xiunan Li, Hao Sun, et al.
Pageof 13

Showing results (81-90 of 130) with videos related to

Sort By:
Pageof 13
The Journal of Investigative Dermatology|December 15, 2007
Identification of a genetic locus for ichthyosis vulgaris on chromosome 10q22.3-q24.2Ping Liu, Qingyu Yang, Xu Wang, et al.
Biochemical and Biophysical Research Communications|January 8, 2008
Identification and functional characterization of a novel splicing mutation in RP gene PRPF31Jing Yu Liu, Xiaohua Dai, Jiqun Sheng, et al.
Molecular Genetics and Metabolism|October 19, 2010
Identification of compound heterozygous mutations in GNPTG in three siblings of a Chinese family with mucolipidosis type III gammaYong Gao, Kangjuan Yang, Shujiang Xu, et al.
Human Genetics|October 3, 2008
A novel genetic locus for familial febrile seizures and epilepsy on chromosome 3q26.2-q26.33Xiao-Hua Dai, Wen-Wu Chen, Xu Wang, et al.
DNA and Cell Biology|September 28, 2019
Identification and Analysis of Genes Involved in Auxin, Abscisic Acid, Gibberellin, and Brassinosteroid Metabolisms Under Drought Stress in Tender Shoots of Tea PlantsHui Li, Rui-Min Teng, Jie-Xia Liu, et al.
Frontiers in Cell and Developmental Biology|November 30, 2020
p.His16Arg of STXBP1 (MUNC18-1) Associated With Syntaxin 3B Causes Autosomal Dominant Congenital NystagmusYulei Li, Lei Jiang, Lejin Wang, et al.
Biomed Research International|May 3, 2021
Electroacupuncture Improves Pregnancy Outcomes in Rats with Thin Endometrium by Promoting the Expression of Pinopode-Related MoleculesJin Xi, Jie Cheng, Chun-Chun Jin, et al.
Yi Chuan Xue Bao = Acta Genetica Sinica|August 31, 2006
Mutation p.Arg954Trp of KIF21A causes congenital fibrosis of the extraocular muscles in a Chinese familyXian-Qin Zhang, Jian-Hong Peng, Zhao-Hui Tang, et al.
Pain|July 30, 2021
Protein arginine methyltransferase 7 modulates neuronal excitability by interacting with NaV1.9Tingbin Ma, Lulu Li, Rui Chen, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 10, 2019
Murine Placental-Fetal Phosphate Dyshomeostasis Caused by an Xpr1 Deficiency Accelerates Placental Calcification and Restricts Fetal Growth in Late GestationXuan Xu, Xiunan Li, Hao Sun, et al.
Pageof 13