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Shu-Hong Hu

Showing results (1-10 of 29) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|May 23, 2007
Structure of the Munc18c/Syntaxin4 N-peptide complex defines universal features of the N-peptide binding mode of Sec1/Munc18 proteinsShu-Hong Hu, Catherine F Latham, Christine L Gee, et al.
Current Opinion in Structural Biology|October 6, 2014
SNARE-ing the structures of Sec1/Munc18 proteinsJulia K Archbold, Andrew E Whitten, Shu-Hong Hu, et al.
Iucrj|December 9, 2014
Reconciling the regulatory role of Munc18 proteins in SNARE-complex assemblyAsma Rehman, Julia K Archbold, Shu-Hong Hu, et al.
Medicine|July 7, 2023
The efficacy of Fuke Qianjin tablets combined with clomiphene citrate on infertility patients with polycystic ovary syndrome: A retrospective analysisYu Zhang, Shan Cao, Jun-Xia Liang, et al.
Clinical Genetics|August 19, 2015
Sclerosteosis caused by a novel nonsense mutation of SOST in a consanguineous familyWen-Tao He, Chen Chen, Chu Pan, et al.
Journal of Molecular Biology|December 9, 2008
Structure of West Nile virus NS3 protease: ligand stabilization of the catalytic conformationGautier Robin, Keith Chappell, Martin J Stoermer, et al.
Medicine|August 2, 2024
Effects of Zishen Yutai pills combined with metformin on women with polycystic ovary syndrome undergoing in vitro fertilizationYu Zhang, Shan Cao, Jun-Xia Liang, et al.
Plos One|September 7, 2012
The weak complex between RhoGAP protein ARHGAP22 and signal regulatory protein 14-3-3 has 1:2 stoichiometry and a single peptide binding modeShu-Hong Hu, Andrew E Whitten, Gordon J King, et al.
Nature Communications|June 11, 2022
Structural basis of resistance to herbicides that target acetohydroxyacid synthaseThierry Lonhienne, Yan Cheng, Mario D Garcia, et al.
Frontiers in Genetics|June 22, 2023
Case report: Autosomal recessive type 3 Stickler syndrome caused by compound heterozygous mutations in <i>COL11A2</i>Ying Su, Chun-Qiong Ran, Zhe-Long Liu, et al.
Pageof 3

Showing results (1-10 of 29) with videos related to

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Pageof 3
Proceedings of the National Academy of Sciences of the United States of America|May 23, 2007
Structure of the Munc18c/Syntaxin4 N-peptide complex defines universal features of the N-peptide binding mode of Sec1/Munc18 proteinsShu-Hong Hu, Catherine F Latham, Christine L Gee, et al.
Current Opinion in Structural Biology|October 6, 2014
SNARE-ing the structures of Sec1/Munc18 proteinsJulia K Archbold, Andrew E Whitten, Shu-Hong Hu, et al.
Iucrj|December 9, 2014
Reconciling the regulatory role of Munc18 proteins in SNARE-complex assemblyAsma Rehman, Julia K Archbold, Shu-Hong Hu, et al.
Medicine|July 7, 2023
The efficacy of Fuke Qianjin tablets combined with clomiphene citrate on infertility patients with polycystic ovary syndrome: A retrospective analysisYu Zhang, Shan Cao, Jun-Xia Liang, et al.
Clinical Genetics|August 19, 2015
Sclerosteosis caused by a novel nonsense mutation of SOST in a consanguineous familyWen-Tao He, Chen Chen, Chu Pan, et al.
Journal of Molecular Biology|December 9, 2008
Structure of West Nile virus NS3 protease: ligand stabilization of the catalytic conformationGautier Robin, Keith Chappell, Martin J Stoermer, et al.
Medicine|August 2, 2024
Effects of Zishen Yutai pills combined with metformin on women with polycystic ovary syndrome undergoing in vitro fertilizationYu Zhang, Shan Cao, Jun-Xia Liang, et al.
Plos One|September 7, 2012
The weak complex between RhoGAP protein ARHGAP22 and signal regulatory protein 14-3-3 has 1:2 stoichiometry and a single peptide binding modeShu-Hong Hu, Andrew E Whitten, Gordon J King, et al.
Nature Communications|June 11, 2022
Structural basis of resistance to herbicides that target acetohydroxyacid synthaseThierry Lonhienne, Yan Cheng, Mario D Garcia, et al.
Frontiers in Genetics|June 22, 2023
Case report: Autosomal recessive type 3 Stickler syndrome caused by compound heterozygous mutations in <i>COL11A2</i>Ying Su, Chun-Qiong Ran, Zhe-Long Liu, et al.
Pageof 3