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Ying-Hui Fu

Showing results (91-100 of 101) with videos related to

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Circulation|May 25, 2005
Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotypeLi Zhang, D Woodrow Benson, Martin Tristani-Firouzi, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 24, 2016
A PERIOD3 variant causes a circadian phenotype and is associated with a seasonal mood traitLuoying Zhang, Arisa Hirano, Pei-Ken Hsu, et al.
Neurology|October 19, 2012
PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraineRobin Cloarec, Nadine Bruneau, Gabrielle Rudolf, et al.
Cell|May 29, 2026
Physiological brain clearance architecture revealed by neuronal protein tracingYuichi Chayama, Nalini R Rao, Daniela Perla, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 22, 2002
Polyglutamine-expanded ataxin-7 promotes non-cell-autonomous purkinje cell degeneration and displays proteolytic cleavage in ataxic transgenic miceGwenn A Garden, Randell T Libby, Ying-Hui Fu, et al.
Human Molecular Genetics|October 22, 2004
The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathwayHsien-Yang Lee, Ying Xu, Yong Huang, et al.
Annals of Neurology|August 29, 2012
Familial cortical myoclonus with a mutation in NOL3Jonathan F Russell, Jamie L Steckley, Giovanni Coppola, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2024
The ZFHX3 GGC Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral FounderZhongbo Chen, Pilar Alvarez Jerez, Claire Anderson, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 10, 2024
Adaptive Long-Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar Ataxia Type 4Zhongbo Chen, Emil K Gustavsson, Hannah Macpherson, et al.
Cell Reports|July 27, 2012
Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsionsHsien-Yang Lee, Yong Huang, Nadine Bruneau, et al.
Pageof 11

Showing results (91-100 of 101) with videos related to

Sort By:
Pageof 11
Circulation|May 25, 2005
Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotypeLi Zhang, D Woodrow Benson, Martin Tristani-Firouzi, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 24, 2016
A PERIOD3 variant causes a circadian phenotype and is associated with a seasonal mood traitLuoying Zhang, Arisa Hirano, Pei-Ken Hsu, et al.
Neurology|October 19, 2012
PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraineRobin Cloarec, Nadine Bruneau, Gabrielle Rudolf, et al.
Cell|May 29, 2026
Physiological brain clearance architecture revealed by neuronal protein tracingYuichi Chayama, Nalini R Rao, Daniela Perla, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 22, 2002
Polyglutamine-expanded ataxin-7 promotes non-cell-autonomous purkinje cell degeneration and displays proteolytic cleavage in ataxic transgenic miceGwenn A Garden, Randell T Libby, Ying-Hui Fu, et al.
Human Molecular Genetics|October 22, 2004
The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathwayHsien-Yang Lee, Ying Xu, Yong Huang, et al.
Annals of Neurology|August 29, 2012
Familial cortical myoclonus with a mutation in NOL3Jonathan F Russell, Jamie L Steckley, Giovanni Coppola, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2024
The ZFHX3 GGC Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral FounderZhongbo Chen, Pilar Alvarez Jerez, Claire Anderson, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 10, 2024
Adaptive Long-Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar Ataxia Type 4Zhongbo Chen, Emil K Gustavsson, Hannah Macpherson, et al.
Cell Reports|July 27, 2012
Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsionsHsien-Yang Lee, Yong Huang, Nadine Bruneau, et al.
Pageof 11