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Aritoshi Iida

Showing results (91-100 of 106) with videos related to

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Journal of Human Genetics|May 13, 2003
Association of single-nucleotide polymorphisms in the polymeric immunoglobulin receptor gene with immunoglobulin A nephropathy (IgAN) in Japanese patientsWataru Obara, Aritoshi Iida, Yasushi Suzuki, et al.
Nature Genetics|July 2, 2003
Functional haplotypes of PADI4, encoding citrullinating enzyme peptidylarginine deiminase 4, are associated with rheumatoid arthritisAkari Suzuki, Ryo Yamada, Xiaotian Chang, et al.
Journal of Human Genetics|December 16, 2004
Association of a single-nucleotide polymorphism in the immunoglobulin mu-binding protein 2 gene with immunoglobulin A nephropathyShigeru Ohtsubo, Aritoshi Iida, Kosaku Nitta, et al.
Plos One|March 15, 2016
Axial Spondylometaphyseal Dysplasia Is Caused by C21orf2 MutationsZheng Wang, Aritoshi Iida, Noriko Miyake, et al.
The Journal of Clinical Endocrinology and Metabolism|January 4, 2007
Functional single-nucleotide polymorphisms in the secretogranin III (SCG3) gene that form secretory granules with appetite-related neuropeptides are associated with obesityAtsushi Tanabe, Takahiro Yanagiya, Aritoshi Iida, et al.
American Journal of Medical Genetics. Part A|February 24, 2021
Whole genome sequencing of 45 Japanese patients with intellectual disabilityChihiro Abe-Hatano, Aritoshi Iida, Shunichi Kosugi, et al.
American Journal of Human Genetics|May 14, 2013
Mutations in B3GALT6, which encodes a glycosaminoglycan linker region enzyme, cause a spectrum of skeletal and connective tissue disordersMasahiro Nakajima, Shuji Mizumoto, Noriko Miyake, et al.
Human Molecular Genetics|September 15, 2007
Association of single-nucleotide polymorphisms in MTMR9 gene with obesityTakahiro Yanagiya, Atsushi Tanabe, Aritoshi Iida, et al.
Human Molecular Genetics|June 14, 2011
A functional variant in ZNF512B is associated with susceptibility to amyotrophic lateral sclerosis in JapaneseAritoshi Iida, Atsushi Takahashi, Michiaki Kubo, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 10, 2016
A rapid functional decline type of amyotrophic lateral sclerosis is linked to low expression of TTNHazuki Watanabe, Naoki Atsuta, Akihiro Hirakawa, et al.
Pageof 11

Showing results (91-100 of 106) with videos related to

Sort By:
Pageof 11
Journal of Human Genetics|May 13, 2003
Association of single-nucleotide polymorphisms in the polymeric immunoglobulin receptor gene with immunoglobulin A nephropathy (IgAN) in Japanese patientsWataru Obara, Aritoshi Iida, Yasushi Suzuki, et al.
Nature Genetics|July 2, 2003
Functional haplotypes of PADI4, encoding citrullinating enzyme peptidylarginine deiminase 4, are associated with rheumatoid arthritisAkari Suzuki, Ryo Yamada, Xiaotian Chang, et al.
Journal of Human Genetics|December 16, 2004
Association of a single-nucleotide polymorphism in the immunoglobulin mu-binding protein 2 gene with immunoglobulin A nephropathyShigeru Ohtsubo, Aritoshi Iida, Kosaku Nitta, et al.
Plos One|March 15, 2016
Axial Spondylometaphyseal Dysplasia Is Caused by C21orf2 MutationsZheng Wang, Aritoshi Iida, Noriko Miyake, et al.
The Journal of Clinical Endocrinology and Metabolism|January 4, 2007
Functional single-nucleotide polymorphisms in the secretogranin III (SCG3) gene that form secretory granules with appetite-related neuropeptides are associated with obesityAtsushi Tanabe, Takahiro Yanagiya, Aritoshi Iida, et al.
American Journal of Medical Genetics. Part A|February 24, 2021
Whole genome sequencing of 45 Japanese patients with intellectual disabilityChihiro Abe-Hatano, Aritoshi Iida, Shunichi Kosugi, et al.
American Journal of Human Genetics|May 14, 2013
Mutations in B3GALT6, which encodes a glycosaminoglycan linker region enzyme, cause a spectrum of skeletal and connective tissue disordersMasahiro Nakajima, Shuji Mizumoto, Noriko Miyake, et al.
Human Molecular Genetics|September 15, 2007
Association of single-nucleotide polymorphisms in MTMR9 gene with obesityTakahiro Yanagiya, Atsushi Tanabe, Aritoshi Iida, et al.
Human Molecular Genetics|June 14, 2011
A functional variant in ZNF512B is associated with susceptibility to amyotrophic lateral sclerosis in JapaneseAritoshi Iida, Atsushi Takahashi, Michiaki Kubo, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 10, 2016
A rapid functional decline type of amyotrophic lateral sclerosis is linked to low expression of TTNHazuki Watanabe, Naoki Atsuta, Akihiro Hirakawa, et al.
Pageof 11