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Kei Watase

Showing results (11-20 of 22) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|January 25, 2008
The insulin-like growth factor pathway is altered in spinocerebellar ataxia type 1 and type 7Jennifer R Gatchel, Kei Watase, Christina Thaller, et al.
Plos Medicine|May 31, 2007
Lithium therapy improves neurological function and hippocampal dendritic arborization in a spinocerebellar ataxia type 1 mouse modelKei Watase, Jennifer R Gatchel, Yaling Sun, et al.
Nature Communications|December 2, 2017
Developmental YAPdeltaC determines adult pathology in a model of spinocerebellar ataxia type 1Kyota Fujita, Ying Mao, Shigenori Uchida, et al.
Human Molecular Genetics|May 17, 2017
Alternative splicing in the C-terminal tail of Cav2.1 is essential for preventing a neurological disease in miceTomonori Aikawa, Takaki Watanabe, Taisuke Miyazaki, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 24, 2005
Differential roles of glial and neuronal glutamate transporters in Purkinje cell synapsesYukihiro Takayasu, Masae Iino, Wataru Kakegawa, et al.
Human Molecular Genetics|February 8, 2017
RpA1 ameliorates symptoms of mutant ataxin-1 knock-in mice and enhances DNA damage repairJuliana Bosso Taniguchi, Kanoh Kondo, Kyota Fujita, et al.
Nature Cell Biology|March 27, 2007
Proteome analysis of soluble nuclear proteins reveals that HMGB1/2 suppress genotoxic stress in polyglutamine diseasesMei-Ling Qi, Kazuhiko Tagawa, Yasushi Enokido, et al.
Genome Research|June 12, 2023
Genome-wide identification of tandem repeats associated with splicing variation across 49 tissues in humansKohei Hamanaka, Daisuke Yamauchi, Eriko Koshimizu, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 9, 2008
Spinocerebellar ataxia type 6 knockin mice develop a progressive neuronal dysfunction with age-dependent accumulation of mutant CaV2.1 channelsKei Watase, Curtis F Barrett, Taisuke Miyazaki, et al.
Neuron|June 28, 2002
A long CAG repeat in the mouse Sca1 locus replicates SCA1 features and reveals the impact of protein solubility on selective neurodegenerationKei Watase, Edwin J Weeber, Bisong Xu, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Proceedings of the National Academy of Sciences of the United States of America|January 25, 2008
The insulin-like growth factor pathway is altered in spinocerebellar ataxia type 1 and type 7Jennifer R Gatchel, Kei Watase, Christina Thaller, et al.
Plos Medicine|May 31, 2007
Lithium therapy improves neurological function and hippocampal dendritic arborization in a spinocerebellar ataxia type 1 mouse modelKei Watase, Jennifer R Gatchel, Yaling Sun, et al.
Nature Communications|December 2, 2017
Developmental YAPdeltaC determines adult pathology in a model of spinocerebellar ataxia type 1Kyota Fujita, Ying Mao, Shigenori Uchida, et al.
Human Molecular Genetics|May 17, 2017
Alternative splicing in the C-terminal tail of Cav2.1 is essential for preventing a neurological disease in miceTomonori Aikawa, Takaki Watanabe, Taisuke Miyazaki, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 24, 2005
Differential roles of glial and neuronal glutamate transporters in Purkinje cell synapsesYukihiro Takayasu, Masae Iino, Wataru Kakegawa, et al.
Human Molecular Genetics|February 8, 2017
RpA1 ameliorates symptoms of mutant ataxin-1 knock-in mice and enhances DNA damage repairJuliana Bosso Taniguchi, Kanoh Kondo, Kyota Fujita, et al.
Nature Cell Biology|March 27, 2007
Proteome analysis of soluble nuclear proteins reveals that HMGB1/2 suppress genotoxic stress in polyglutamine diseasesMei-Ling Qi, Kazuhiko Tagawa, Yasushi Enokido, et al.
Genome Research|June 12, 2023
Genome-wide identification of tandem repeats associated with splicing variation across 49 tissues in humansKohei Hamanaka, Daisuke Yamauchi, Eriko Koshimizu, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 9, 2008
Spinocerebellar ataxia type 6 knockin mice develop a progressive neuronal dysfunction with age-dependent accumulation of mutant CaV2.1 channelsKei Watase, Curtis F Barrett, Taisuke Miyazaki, et al.
Neuron|June 28, 2002
A long CAG repeat in the mouse Sca1 locus replicates SCA1 features and reveals the impact of protein solubility on selective neurodegenerationKei Watase, Edwin J Weeber, Bisong Xu, et al.
Pageof 3