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Jun Mitsui

Showing results (151-160 of 163) with videos related to

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Angiogenesis|July 28, 2022
Somatic GJA4 gain-of-function mutation in orbital cavernous venous malformationsHiroki Hongo, Satoru Miyawaki, Yu Teranishi, et al.
Journal of Atherosclerosis and Thrombosis|March 27, 2024
Genetic and Functional Analyses of Patients with Marked Hypo-High-Density Lipoprotein CholesterolemiaYasuhisa Furuta, Yoshinori Osaki, Yoshimi Nakagawa, et al.
Annals of Neurology|March 19, 2016
Mutations in MME cause an autosomal-recessive Charcot-Marie-Tooth disease type 2Yujiro Higuchi, Akihiro Hashiguchi, Junhui Yuan, et al.
Neurobiology of Aging|February 6, 2018
Frequency and characteristics of the TBK1 gene variants in Japanese patients with sporadic amyotrophic lateral sclerosisGenki Tohnai, Ryoichi Nakamura, Jun Sone, et al.
Eclinicalmedicine|May 31, 2023
High-dose ubiquinol supplementation in multiple-system atrophy: a multicentre, randomised, double-blinded, placebo-controlled phase 2 trialJun Mitsui, Takashi Matsukawa, Yukari Uemura, et al.
Neurobiology of Disease|June 24, 2019
Ataxic phenotype with altered Ca<sub>V</sub>3.1 channel property in a mouse model for spinocerebellar ataxia 42Shunta Hashiguchi, Hiroshi Doi, Misako Kunii, 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.
Brain Communications|September 21, 2020
Clinical efficacy of haematopoietic stem cell transplantation for adult adrenoleukodystrophyTakashi Matsukawa, Tomotaka Yamamoto, Akira Honda, 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.
Pageof 17

Showing results (151-160 of 163) with videos related to

Sort By:
Pageof 17
Angiogenesis|July 28, 2022
Somatic GJA4 gain-of-function mutation in orbital cavernous venous malformationsHiroki Hongo, Satoru Miyawaki, Yu Teranishi, et al.
Journal of Atherosclerosis and Thrombosis|March 27, 2024
Genetic and Functional Analyses of Patients with Marked Hypo-High-Density Lipoprotein CholesterolemiaYasuhisa Furuta, Yoshinori Osaki, Yoshimi Nakagawa, et al.
Annals of Neurology|March 19, 2016
Mutations in MME cause an autosomal-recessive Charcot-Marie-Tooth disease type 2Yujiro Higuchi, Akihiro Hashiguchi, Junhui Yuan, et al.
Neurobiology of Aging|February 6, 2018
Frequency and characteristics of the TBK1 gene variants in Japanese patients with sporadic amyotrophic lateral sclerosisGenki Tohnai, Ryoichi Nakamura, Jun Sone, et al.
Eclinicalmedicine|May 31, 2023
High-dose ubiquinol supplementation in multiple-system atrophy: a multicentre, randomised, double-blinded, placebo-controlled phase 2 trialJun Mitsui, Takashi Matsukawa, Yukari Uemura, et al.
Neurobiology of Disease|June 24, 2019
Ataxic phenotype with altered Ca<sub>V</sub>3.1 channel property in a mouse model for spinocerebellar ataxia 42Shunta Hashiguchi, Hiroshi Doi, Misako Kunii, 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.
Brain Communications|September 21, 2020
Clinical efficacy of haematopoietic stem cell transplantation for adult adrenoleukodystrophyTakashi Matsukawa, Tomotaka Yamamoto, Akira Honda, 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.
Pageof 17