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Aritoshi Iida

Showing results (101-110 of 106) with videos related to

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Plos Genetics|December 7, 2023
Exploring the genetic diversity of the Japanese population: Insights from a large-scale whole genome sequencing analysisYosuke Kawai, Yusuke Watanabe, Yosuke Omae, et al.
American Journal of Human Genetics|May 16, 2020
Expansion of GGC Repeat in GIPC1 Is Associated with Oculopharyngodistal MyopathyJianwen Deng, Jiaxi Yu, Pidong Li, et al.
American Journal of Human Genetics|July 28, 2015
A Functional SNP in BNC2 Is Associated with Adolescent Idiopathic ScoliosisYoji Ogura, Ikuyo Kou, Shigenori Miura, et al.
American Journal of Human Genetics|November 20, 2020
Pathogenic Variants in the Myosin Chaperone UNC-45B Cause Progressive Myopathy with Eccentric CoresSandra Donkervoort, Carl E Kutzner, Ying Hu, et al.
Nature Communications|April 28, 2022
Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophyHong Joo Kim, Payam Mohassel, Sandra Donkervoort, et al.
JAMA Neurology|May 28, 2021
Clinicopathologic Features of Oculopharyngodistal Myopathy With LRP12 CGG Repeat Expansions Compared With Other Oculopharyngodistal Myopathy SubtypesTheerawat Kumutpongpanich, Masashi Ogasawara, Ayami Ozaki, et al.
Pageof 11

Showing results (101-110 of 106) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 106 results.
Plos Genetics|December 7, 2023
Exploring the genetic diversity of the Japanese population: Insights from a large-scale whole genome sequencing analysisYosuke Kawai, Yusuke Watanabe, Yosuke Omae, et al.
American Journal of Human Genetics|May 16, 2020
Expansion of GGC Repeat in GIPC1 Is Associated with Oculopharyngodistal MyopathyJianwen Deng, Jiaxi Yu, Pidong Li, et al.
American Journal of Human Genetics|July 28, 2015
A Functional SNP in BNC2 Is Associated with Adolescent Idiopathic ScoliosisYoji Ogura, Ikuyo Kou, Shigenori Miura, et al.
American Journal of Human Genetics|November 20, 2020
Pathogenic Variants in the Myosin Chaperone UNC-45B Cause Progressive Myopathy with Eccentric CoresSandra Donkervoort, Carl E Kutzner, Ying Hu, et al.
Nature Communications|April 28, 2022
Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophyHong Joo Kim, Payam Mohassel, Sandra Donkervoort, et al.
JAMA Neurology|May 28, 2021
Clinicopathologic Features of Oculopharyngodistal Myopathy With LRP12 CGG Repeat Expansions Compared With Other Oculopharyngodistal Myopathy SubtypesTheerawat Kumutpongpanich, Masashi Ogasawara, Ayami Ozaki, et al.
Pageof 11