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Yaeko Ichikawa

Showing results (31-40 of 38) with videos related to

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American Journal of Human Genetics|August 14, 2012
The TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvementHiroyuki Ishiura, Wataru Sako, Mari Yoshida, et al.
Rheumatology (Oxford, England)|April 3, 2025
Clinicopathological features of anti-HMGCR and anti-SRP myopathies that do not satisfy the EULAR/ACR criteria of inflammatory myopathiesShogo Komaki, Akatsuki Kubota, Asuka Kitamura, et al.
Brain : a Journal of Neurology|June 29, 2014
Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genesSophie Tezenas du Montcel, Alexandra Durr, Peter Bauer, et al.
American Journal of Human Genetics|October 15, 2013
ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19Yuji Takahashi, Yoko Fukuda, Jun Yoshimura, et al.
Nature Genetics|July 24, 2019
Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping diseaseHiroyuki Ishiura, Shota Shibata, Jun Yoshimura, et al.
Nature Genetics|March 7, 2018
Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsyHiroyuki Ishiura, Koichiro Doi, Jun Mitsui, et al.
Annals of Clinical and Translational Neurology|April 25, 2015
Variants associated with Gaucher disease in multiple system atrophyJun Mitsui, Takashi Matsukawa, Hidenao Sasaki, et al.
Medrxiv : the Preprint Server for Health Sciences|July 10, 2023
Genome-wide association study identifies a new susceptibility locus in <i>PLA2G4C</i> for Multiple System AtrophyYasuo Nakahara, Jun Mitsui, Hidetoshi Date, et al.
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Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
American Journal of Human Genetics|August 14, 2012
The TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvementHiroyuki Ishiura, Wataru Sako, Mari Yoshida, et al.
Rheumatology (Oxford, England)|April 3, 2025
Clinicopathological features of anti-HMGCR and anti-SRP myopathies that do not satisfy the EULAR/ACR criteria of inflammatory myopathiesShogo Komaki, Akatsuki Kubota, Asuka Kitamura, et al.
Brain : a Journal of Neurology|June 29, 2014
Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genesSophie Tezenas du Montcel, Alexandra Durr, Peter Bauer, et al.
American Journal of Human Genetics|October 15, 2013
ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19Yuji Takahashi, Yoko Fukuda, Jun Yoshimura, et al.
Nature Genetics|July 24, 2019
Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping diseaseHiroyuki Ishiura, Shota Shibata, Jun Yoshimura, et al.
Nature Genetics|March 7, 2018
Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsyHiroyuki Ishiura, Koichiro Doi, Jun Mitsui, et al.
Annals of Clinical and Translational Neurology|April 25, 2015
Variants associated with Gaucher disease in multiple system atrophyJun Mitsui, Takashi Matsukawa, Hidenao Sasaki, et al.
Medrxiv : the Preprint Server for Health Sciences|July 10, 2023
Genome-wide association study identifies a new susceptibility locus in <i>PLA2G4C</i> for Multiple System AtrophyYasuo Nakahara, Jun Mitsui, Hidetoshi Date, et al.
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