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Jun Yoshimura

Showing results (31-40 of 52) with videos related to

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Journal of Human Genetics|December 9, 2016
TBCD may be a causal gene in progressive neurodegenerative encephalopathy with atypical infantile spinal muscular atrophyToshio Ikeda, Akihiko Nakahara, Rie Nagano, et al.
Molecular Biology of the Cell|March 1, 2013
ATF6α/β-mediated adjustment of ER chaperone levels is essential for development of the notochord in medaka fishTokiro Ishikawa, Tetsuya Okada, Tomoko Ishikawa-Fujiwara, et al.
Development (Cambridge, England)|August 1, 2014
Analysis of a novel gene, Sdgc, reveals sex chromosome-dependent differences of medaka germ cells prior to gonad formationToshiya Nishimura, Amaury Herpin, Tetsuaki Kimura, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 6, 2012
CSF1R mutations identified in three families with autosomal dominantly inherited leukoencephalopathyJun Mitsui, Takashi Matsukawa, Hiroyuki Ishiura, et al.
Scientific Reports|July 21, 2020
Comprehensive investigation of RNF213 nonsynonymous variants associated with intracranial artery stenosisHiroki Hongo, Satoru Miyawaki, Hideaki Imai, et al.
Neurobiology of Aging|October 17, 2017
Molecular epidemiological study of familial amyotrophic lateral sclerosis in Japanese population by whole-exome sequencing and identification of novel HNRNPA1 mutationHiroya Naruse, Hiroyuki Ishiura, Jun Mitsui, et al.
Parkinsonism & Related Disorders|December 12, 2018
Neuroimaging, genetic, and enzymatic study in a Japanese family with a GBA gross deletionYuta Ichinose, Hiroyuki Ishiura, Masaki Tanaka, et al.
Nucleic Acids Research|February 16, 2021
Hamster PIWI proteins bind to piRNAs with stage-specific size variations during oocyte maturationKyoko Ishino, Hidetoshi Hasuwa, Jun Yoshimura, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 14, 2017
Identification of candidate genes involved in the etiology of sporadic Tourette syndrome by exome sequencingYosuke Eriguchi, Hitoshi Kuwabara, Aya Inai, et al.
Neurology. Genetics|April 12, 2016
Atypical parkinsonism caused by Pro105Leu mutation of prion protein: A broad clinical spectrumKagari Koshi Mano, Takashi Matsukawa, Jun Mitsui, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

Sort By:
Pageof 6
Journal of Human Genetics|December 9, 2016
TBCD may be a causal gene in progressive neurodegenerative encephalopathy with atypical infantile spinal muscular atrophyToshio Ikeda, Akihiko Nakahara, Rie Nagano, et al.
Molecular Biology of the Cell|March 1, 2013
ATF6α/β-mediated adjustment of ER chaperone levels is essential for development of the notochord in medaka fishTokiro Ishikawa, Tetsuya Okada, Tomoko Ishikawa-Fujiwara, et al.
Development (Cambridge, England)|August 1, 2014
Analysis of a novel gene, Sdgc, reveals sex chromosome-dependent differences of medaka germ cells prior to gonad formationToshiya Nishimura, Amaury Herpin, Tetsuaki Kimura, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 6, 2012
CSF1R mutations identified in three families with autosomal dominantly inherited leukoencephalopathyJun Mitsui, Takashi Matsukawa, Hiroyuki Ishiura, et al.
Scientific Reports|July 21, 2020
Comprehensive investigation of RNF213 nonsynonymous variants associated with intracranial artery stenosisHiroki Hongo, Satoru Miyawaki, Hideaki Imai, et al.
Neurobiology of Aging|October 17, 2017
Molecular epidemiological study of familial amyotrophic lateral sclerosis in Japanese population by whole-exome sequencing and identification of novel HNRNPA1 mutationHiroya Naruse, Hiroyuki Ishiura, Jun Mitsui, et al.
Parkinsonism & Related Disorders|December 12, 2018
Neuroimaging, genetic, and enzymatic study in a Japanese family with a GBA gross deletionYuta Ichinose, Hiroyuki Ishiura, Masaki Tanaka, et al.
Nucleic Acids Research|February 16, 2021
Hamster PIWI proteins bind to piRNAs with stage-specific size variations during oocyte maturationKyoko Ishino, Hidetoshi Hasuwa, Jun Yoshimura, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 14, 2017
Identification of candidate genes involved in the etiology of sporadic Tourette syndrome by exome sequencingYosuke Eriguchi, Hitoshi Kuwabara, Aya Inai, et al.
Neurology. Genetics|April 12, 2016
Atypical parkinsonism caused by Pro105Leu mutation of prion protein: A broad clinical spectrumKagari Koshi Mano, Takashi Matsukawa, Jun Mitsui, et al.
Pageof 6