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Aritoshi Iida

Showing results (51-60 of 106) with videos related to

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Nature Genetics|November 12, 2002
Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarctionKouichi Ozaki, Yozo Ohnishi, Aritoshi Iida, et al.
Journal of Human Genetics|November 11, 2016
Identification of a novel LRRK1 mutation in a family with osteosclerotic metaphyseal dysplasiaLong Guo, Katta M Girisha, Aritoshi Iida, et al.
Neuromuscular Disorders : NMD|May 8, 2022
Myoglobinopathy affecting facial and oropharyngeal musclesYuka Hama, Madoka Mori-Yoshimura, Kazutaka Aizawa, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|April 30, 2025
Two Brothers With ADSS1 Myopathy: A Report of Clinical, Radiological, and Autopsy FindingsYuka Hama, Terunori Sano, Yasushi Oya, et al.
Nature Communications|February 7, 2025
Retrotrans-genomics identifies aberrant THE1B endogenous retrovirus fusion transcripts in the pathogenesis of sarcoidosisShunsuke Funaguma, Aritoshi Iida, Yoshihiko Saito, et al.
Nature|May 7, 2004
Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-alpha secretion in vitroKouichi Ozaki, Katsumi Inoue, Hiroshi Sato, et al.
Journal of Human Genetics|January 27, 2017
Axial spondylometaphyseal dysplasia is also caused by NEK1 mutationsZheng Wang, Eva Horemuzova, Aritoshi Iida, et al.
Human Genome Variation|April 16, 2016
A novel FOXC2 mutation in spinal extradural arachnoid cystYoji Ogura, Shunsuke Fujibayashi, Aritoshi Iida, et al.
Nature Genetics|July 18, 2006
A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese populationKouichi Ozaki, Hiroshi Sato, Aritoshi Iida, et al.
Brain & Development|September 27, 2021
Successful treatment of congenital myasthenic syndrome caused by a novel compound heterozygous variant in RAPSNMaki Saito, Masashi Ogasawara, Yuji Inaba, et al.
Pageof 11

Showing results (51-60 of 106) with videos related to

Sort By:
Pageof 11
Nature Genetics|November 12, 2002
Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarctionKouichi Ozaki, Yozo Ohnishi, Aritoshi Iida, et al.
Journal of Human Genetics|November 11, 2016
Identification of a novel LRRK1 mutation in a family with osteosclerotic metaphyseal dysplasiaLong Guo, Katta M Girisha, Aritoshi Iida, et al.
Neuromuscular Disorders : NMD|May 8, 2022
Myoglobinopathy affecting facial and oropharyngeal musclesYuka Hama, Madoka Mori-Yoshimura, Kazutaka Aizawa, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|April 30, 2025
Two Brothers With ADSS1 Myopathy: A Report of Clinical, Radiological, and Autopsy FindingsYuka Hama, Terunori Sano, Yasushi Oya, et al.
Nature Communications|February 7, 2025
Retrotrans-genomics identifies aberrant THE1B endogenous retrovirus fusion transcripts in the pathogenesis of sarcoidosisShunsuke Funaguma, Aritoshi Iida, Yoshihiko Saito, et al.
Nature|May 7, 2004
Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-alpha secretion in vitroKouichi Ozaki, Katsumi Inoue, Hiroshi Sato, et al.
Journal of Human Genetics|January 27, 2017
Axial spondylometaphyseal dysplasia is also caused by NEK1 mutationsZheng Wang, Eva Horemuzova, Aritoshi Iida, et al.
Human Genome Variation|April 16, 2016
A novel FOXC2 mutation in spinal extradural arachnoid cystYoji Ogura, Shunsuke Fujibayashi, Aritoshi Iida, et al.
Nature Genetics|July 18, 2006
A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese populationKouichi Ozaki, Hiroshi Sato, Aritoshi Iida, et al.
Brain & Development|September 27, 2021
Successful treatment of congenital myasthenic syndrome caused by a novel compound heterozygous variant in RAPSNMaki Saito, Masashi Ogasawara, Yuji Inaba, et al.
Pageof 11