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Jun Yoshimura

Showing results (11-20 of 52) with videos related to

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Journal of the Neurological Sciences|June 22, 2013
Exome analysis reveals a Japanese family with spinocerebellar ataxia, autosomal recessive 1Yaeko Ichikawa, Hiroyuki Ishiura, Jun Mitsui, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 26, 2018
Burden of rare variants in causative genes for amyotrophic lateral sclerosis (ALS) accelerates age at onset of ALSHiroya Naruse, Hiroyuki Ishiura, Jun Mitsui, et al.
Bioinformatics (Oxford, England)|November 12, 2013
Rapid detection of expanded short tandem repeats in personal genomics using hybrid sequencingKoichiro Doi, Taku Monjo, Pham H Hoang, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 3, 2013
A recurrent de novo FAM111A mutation causes Kenny-Caffey syndrome type 2Tsuyoshi Isojima, Koichiro Doi, Jun Mitsui, et al.
Plos One|February 15, 2013
Identification of ATP1A3 mutations by exome sequencing as the cause of alternating hemiplegia of childhood in Japanese patientsAtsushi Ishii, Yoshiaki Saito, Jun Mitsui, et al.
CJC Open|June 25, 2021
Stentless Interventional Procedure Using Rotational Atherectomy and Drug-Coated Balloon for Noncalcified De Novo LesionsJun Shiraishi, Fumiaki Ito, Jun Yoshimura, et al.
Minerva Cardiology and Angiology|July 15, 2022
Mid-term results of stent-less coronary intervention using rotational atherectomy and drug-coated balloon for de-novo lesions in hemodialysis patientsJun Shiraishi, Yuya Asano, Yusuke Kakei, et al.
Journal of Medical Genetics|October 17, 2020
Targeted deep sequencing of DNA from multiple tissue types improves the diagnostic rate and reveals a highly diverse phenotype of mosaic neurofibromatosis type 2Yu Teranishi, Satoru Miyawaki, Hiroki Hongo, et al.
BMC Genomics|November 21, 2015
Associations between nucleosome phasing, sequence asymmetry, and tissue-specific expression in a set of inbred Medaka speciesYoichiro Nakatani, Cecilia C Mello, Shin-Ichi Hashimoto, et al.
Circulation Reports|May 12, 2025
Angiogenesis Using Recombinant Basic Fibroblast Growth Factor With Atelocollagen in Normal and Hind Limb Ischemia ModelsAtsushi Kotani, Shin Watanabe, Takao Kato, et al.
Pageof 6

Showing results (11-20 of 52) with videos related to

Sort By:
Pageof 6
Journal of the Neurological Sciences|June 22, 2013
Exome analysis reveals a Japanese family with spinocerebellar ataxia, autosomal recessive 1Yaeko Ichikawa, Hiroyuki Ishiura, Jun Mitsui, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 26, 2018
Burden of rare variants in causative genes for amyotrophic lateral sclerosis (ALS) accelerates age at onset of ALSHiroya Naruse, Hiroyuki Ishiura, Jun Mitsui, et al.
Bioinformatics (Oxford, England)|November 12, 2013
Rapid detection of expanded short tandem repeats in personal genomics using hybrid sequencingKoichiro Doi, Taku Monjo, Pham H Hoang, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 3, 2013
A recurrent de novo FAM111A mutation causes Kenny-Caffey syndrome type 2Tsuyoshi Isojima, Koichiro Doi, Jun Mitsui, et al.
Plos One|February 15, 2013
Identification of ATP1A3 mutations by exome sequencing as the cause of alternating hemiplegia of childhood in Japanese patientsAtsushi Ishii, Yoshiaki Saito, Jun Mitsui, et al.
CJC Open|June 25, 2021
Stentless Interventional Procedure Using Rotational Atherectomy and Drug-Coated Balloon for Noncalcified De Novo LesionsJun Shiraishi, Fumiaki Ito, Jun Yoshimura, et al.
Minerva Cardiology and Angiology|July 15, 2022
Mid-term results of stent-less coronary intervention using rotational atherectomy and drug-coated balloon for de-novo lesions in hemodialysis patientsJun Shiraishi, Yuya Asano, Yusuke Kakei, et al.
Journal of Medical Genetics|October 17, 2020
Targeted deep sequencing of DNA from multiple tissue types improves the diagnostic rate and reveals a highly diverse phenotype of mosaic neurofibromatosis type 2Yu Teranishi, Satoru Miyawaki, Hiroki Hongo, et al.
BMC Genomics|November 21, 2015
Associations between nucleosome phasing, sequence asymmetry, and tissue-specific expression in a set of inbred Medaka speciesYoichiro Nakatani, Cecilia C Mello, Shin-Ichi Hashimoto, et al.
Circulation Reports|May 12, 2025
Angiogenesis Using Recombinant Basic Fibroblast Growth Factor With Atelocollagen in Normal and Hind Limb Ischemia ModelsAtsushi Kotani, Shin Watanabe, Takao Kato, et al.
Pageof 6