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Norio Sakai

Showing results (121-130 of 272) with videos related to

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Acta Histochemica Et Cytochemica|September 28, 2007
Fragmentation of protein kinase N (PKN) in the hydrocephalic rat brainNorifumi Okii, Taku Amano, Takahiro Seki, et al.
Molecular Genetics and Metabolism|August 15, 2020
Safety of intrathecal delivery of recombinant human arylsulfatase A in children with metachromatic leukodystrophy: Results from a phase 1/2 clinical trialChristine Í Dali, Caroline Sevin, Ingeborg Krägeloh-Mann, et al.
DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|September 22, 2024
Functional landscape of genome-wide postzygotic somatic mutations between monozygotic twinsKenichi Yamamoto, Yoko Lee, Tatsuo Masuda, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|September 16, 2016
Modifications of tau protein after cerebral ischemia and reperfusion in rats are similar to those occurring in Alzheimer's disease - Hyperphosphorylation and cleavage of 4- and 3-repeat tauHiroki Fujii, Tetsuya Takahashi, Tomoya Mukai, et al.
Journal of Pharmacological Sciences|March 13, 2021
Syntaxin 3 interacts with serotonin transporter and regulates its functionSerika Motoike, Kei Taguchi, Kana Harada, et al.
Journal of Pharmacological Sciences|April 28, 2018
Propofol induced diverse and subtype-specific translocation of PKC familiesTakeshi Miyahara, Naoko Adachi, Takahiro Seki, et al.
Experimental Cell Research|October 31, 2006
The luminal domain participates in the endosomal trafficking of the cation-independent mannose 6-phosphate receptorSatoshi Waguri, Yuji Tomiyama, Hiroko Ikeda, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|April 20, 2010
Mutant protein kinase C gamma that causes spinocerebellar ataxia type 14 (SCA14) is selectively degraded by autophagyKazuhiro Yamamoto, Takahiro Seki, Naoko Adachi, et al.
Biochemical and Biophysical Research Communications|September 12, 2013
Mutant γPKC that causes spinocerebellar ataxia type 14 upregulates Hsp70, which protects cells from the mutant's cytotoxicityKota Ogawa, Takahiro Seki, Tomoya Onji, et al.
Scientific Reports|June 10, 2026
Reduced sensitivity to tactile stimuli associated with physical and mental disorders: A monozygotic twin studySaito Sakaguchi, Yusuke Morito, Masashi Konyo, et al.
Pageof 28

Showing results (121-130 of 272) with videos related to

Sort By:
Pageof 28
Acta Histochemica Et Cytochemica|September 28, 2007
Fragmentation of protein kinase N (PKN) in the hydrocephalic rat brainNorifumi Okii, Taku Amano, Takahiro Seki, et al.
Molecular Genetics and Metabolism|August 15, 2020
Safety of intrathecal delivery of recombinant human arylsulfatase A in children with metachromatic leukodystrophy: Results from a phase 1/2 clinical trialChristine Í Dali, Caroline Sevin, Ingeborg Krägeloh-Mann, et al.
DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|September 22, 2024
Functional landscape of genome-wide postzygotic somatic mutations between monozygotic twinsKenichi Yamamoto, Yoko Lee, Tatsuo Masuda, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|September 16, 2016
Modifications of tau protein after cerebral ischemia and reperfusion in rats are similar to those occurring in Alzheimer's disease - Hyperphosphorylation and cleavage of 4- and 3-repeat tauHiroki Fujii, Tetsuya Takahashi, Tomoya Mukai, et al.
Journal of Pharmacological Sciences|March 13, 2021
Syntaxin 3 interacts with serotonin transporter and regulates its functionSerika Motoike, Kei Taguchi, Kana Harada, et al.
Journal of Pharmacological Sciences|April 28, 2018
Propofol induced diverse and subtype-specific translocation of PKC familiesTakeshi Miyahara, Naoko Adachi, Takahiro Seki, et al.
Experimental Cell Research|October 31, 2006
The luminal domain participates in the endosomal trafficking of the cation-independent mannose 6-phosphate receptorSatoshi Waguri, Yuji Tomiyama, Hiroko Ikeda, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|April 20, 2010
Mutant protein kinase C gamma that causes spinocerebellar ataxia type 14 (SCA14) is selectively degraded by autophagyKazuhiro Yamamoto, Takahiro Seki, Naoko Adachi, et al.
Biochemical and Biophysical Research Communications|September 12, 2013
Mutant γPKC that causes spinocerebellar ataxia type 14 upregulates Hsp70, which protects cells from the mutant's cytotoxicityKota Ogawa, Takahiro Seki, Tomoya Onji, et al.
Scientific Reports|June 10, 2026
Reduced sensitivity to tactile stimuli associated with physical and mental disorders: A monozygotic twin studySaito Sakaguchi, Yusuke Morito, Masashi Konyo, et al.
Pageof 28