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Kinji Ohno

Showing results (241-250 of 245) with videos related to

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The Lancet. Neurology|February 10, 2015
CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing studyManabu Funayama, Kenji Ohe, Taku Amo, et al.
BMC Genomics|April 17, 2013
Exome sequencing of senescence-accelerated mice (SAM) reveals deleterious mutations in degenerative disease-causing genesKumpei Tanisawa, Eri Mikami, Noriyuki Fuku, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 13, 2018
Randomized, double-blind, multicenter trial of hydrogen water for Parkinson's diseaseAsako Yoritaka, Chigumi Ohtsuka, Tetsuya Maeda, et al.
Cell|March 7, 2020
Ubiquitination of DNA Damage-Stalled RNAPII Promotes Transcription-Coupled RepairYuka Nakazawa, Yuichiro Hara, Yasuyoshi Oka, et al.
Translational Psychiatry|January 11, 2018
Rare loss of function mutations in N-methyl-D-aspartate glutamate receptors and their contributions to schizophrenia susceptibilityYanjie Yu, Yingni Lin, Yuto Takasaki, et al.
Pageof 25

Showing results (241-250 of 245) with videos related to

Sort By:
Pageof 25
You have reached the last page of results.This site can display upto 245 results.
The Lancet. Neurology|February 10, 2015
CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing studyManabu Funayama, Kenji Ohe, Taku Amo, et al.
BMC Genomics|April 17, 2013
Exome sequencing of senescence-accelerated mice (SAM) reveals deleterious mutations in degenerative disease-causing genesKumpei Tanisawa, Eri Mikami, Noriyuki Fuku, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 13, 2018
Randomized, double-blind, multicenter trial of hydrogen water for Parkinson's diseaseAsako Yoritaka, Chigumi Ohtsuka, Tetsuya Maeda, et al.
Cell|March 7, 2020
Ubiquitination of DNA Damage-Stalled RNAPII Promotes Transcription-Coupled RepairYuka Nakazawa, Yuichiro Hara, Yasuyoshi Oka, et al.
Translational Psychiatry|January 11, 2018
Rare loss of function mutations in N-methyl-D-aspartate glutamate receptors and their contributions to schizophrenia susceptibilityYanjie Yu, Yingni Lin, Yuto Takasaki, et al.
Pageof 25