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Hiroyuki Tomimitsu

Showing results (31-40 of 35) with videos related to

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Journal of Human Genetics|March 8, 2003
Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in JapanMingshun Li, Kinya Ishikawa, Shuta Toru, et al.
Internal Medicine (Tokyo, Japan)|February 2, 2013
Evaluation of the efficacy of pramipexole for treating levodopa-induced dyskinesia in patients with Parkinson's diseaseHiroya Utsumi, Yasuyuki Okuma, Osamu Kano, et al.
The Journal of Biological Chemistry|August 15, 2009
Depletion of vitamin E increases amyloid beta accumulation by decreasing its clearances from brain and blood in a mouse model of Alzheimer diseaseYoichiro Nishida, Shingo Ito, Sumio Ohtsuki, et al.
Journal of the Neurological Sciences|April 18, 2012
Heterozygous UDP-GlcNAc 2-epimerase and N-acetylmannosamine kinase domain mutations in the GNE gene result in a less severe GNE myopathy phenotype compared to homozygous N-acetylmannosamine kinase domain mutationsMadoka Mori-Yoshimura, Kazunari Monma, Naoki Suzuki, et al.
American Journal of Human Genetics|July 8, 2005
An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domainsKinya Ishikawa, Shuta Toru, Taiji Tsunemi, et al.
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Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
Journal of Human Genetics|March 8, 2003
Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in JapanMingshun Li, Kinya Ishikawa, Shuta Toru, et al.
Internal Medicine (Tokyo, Japan)|February 2, 2013
Evaluation of the efficacy of pramipexole for treating levodopa-induced dyskinesia in patients with Parkinson's diseaseHiroya Utsumi, Yasuyuki Okuma, Osamu Kano, et al.
The Journal of Biological Chemistry|August 15, 2009
Depletion of vitamin E increases amyloid beta accumulation by decreasing its clearances from brain and blood in a mouse model of Alzheimer diseaseYoichiro Nishida, Shingo Ito, Sumio Ohtsuki, et al.
Journal of the Neurological Sciences|April 18, 2012
Heterozygous UDP-GlcNAc 2-epimerase and N-acetylmannosamine kinase domain mutations in the GNE gene result in a less severe GNE myopathy phenotype compared to homozygous N-acetylmannosamine kinase domain mutationsMadoka Mori-Yoshimura, Kazunari Monma, Naoki Suzuki, et al.
American Journal of Human Genetics|July 8, 2005
An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domainsKinya Ishikawa, Shuta Toru, Taiji Tsunemi, et al.
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