Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Aritoshi Iida

Showing results (81-90 of 106) with videos related to

Pageof 11
Sort By:
Plos Genetics|February 26, 2013
Ectopic expression of Ptf1a induces spinal defects, urogenital defects, and anorectal malformations in Danforth's short tail miceKei Semba, Kimi Araki, Ken-ichirou Matsumoto, et al.
Acta Neuropathologica|December 13, 2022
Distinctive chaperonopathy in skeletal muscle associated with the dominant variant in DNAJB4Michio Inoue, Satoru Noguchi, Yukiko U Inoue, et al.
Human Genetics|August 3, 2007
Polymorphisms in the 3' UTR in the neurocalcin delta gene affect mRNA stability, and confer susceptibility to diabetic nephropathyMasumi Kamiyama, Masaaki Kobayashi, Shin-ichi Araki, et al.
Journal of Human Genetics|January 26, 2008
A functional SNP in the NKX2.5-binding site of ITPR3 promoter is associated with susceptibility to systemic lupus erythematosus in Japanese populationTetsuya Oishi, Aritoshi Iida, Shigeru Otsubo, et al.
Neuropathology and Applied Neurobiology|December 20, 2021
Intranuclear inclusions in skin biopsies are not limited to neuronal intranuclear inclusion disease but can also be seen in oculopharyngodistal myopathyMasashi Ogasawara, Nobuyuki Eura, Utako Nagaoka, et al.
Neurobiology of Aging|February 8, 2011
Replication analysis of SNPs on 9p21.2 and 19p13.3 with amyotrophic lateral sclerosis in East AsiansAritoshi Iida, Atsushi Takahashi, Min Deng, et al.
American Journal of Human Genetics|February 6, 2002
Association between single-nucleotide polymorphisms in selectin genes and immunoglobulin A nephropathyTakashi Takei, Aritoshi Iida, Kosaku Nitta, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 24, 2018
RNA sequencing solved the most common but unrecognized NEB pathogenic variant in Japanese nemaline myopathyKohei Hamanaka, Satoko Miyatake, Eriko Koshimizu, et al.
Nature Communications|April 7, 2021
Deficiency of TMEM53 causes a previously unknown sclerosing bone disorder by dysregulation of BMP-SMAD signalingLong Guo, Aritoshi Iida, Gandham SriLakshmi Bhavani, et al.
Human Mutation|November 18, 2014
Identification and in vivo functional characterization of novel compound heterozygous BMP1 variants in osteogenesis imperfectaSung Yoon Cho, P V Asharani, Ok-Hwa Kim, et al.
Pageof 11

Showing results (81-90 of 106) with videos related to

Sort By:
Pageof 11
Plos Genetics|February 26, 2013
Ectopic expression of Ptf1a induces spinal defects, urogenital defects, and anorectal malformations in Danforth's short tail miceKei Semba, Kimi Araki, Ken-ichirou Matsumoto, et al.
Acta Neuropathologica|December 13, 2022
Distinctive chaperonopathy in skeletal muscle associated with the dominant variant in DNAJB4Michio Inoue, Satoru Noguchi, Yukiko U Inoue, et al.
Human Genetics|August 3, 2007
Polymorphisms in the 3' UTR in the neurocalcin delta gene affect mRNA stability, and confer susceptibility to diabetic nephropathyMasumi Kamiyama, Masaaki Kobayashi, Shin-ichi Araki, et al.
Journal of Human Genetics|January 26, 2008
A functional SNP in the NKX2.5-binding site of ITPR3 promoter is associated with susceptibility to systemic lupus erythematosus in Japanese populationTetsuya Oishi, Aritoshi Iida, Shigeru Otsubo, et al.
Neuropathology and Applied Neurobiology|December 20, 2021
Intranuclear inclusions in skin biopsies are not limited to neuronal intranuclear inclusion disease but can also be seen in oculopharyngodistal myopathyMasashi Ogasawara, Nobuyuki Eura, Utako Nagaoka, et al.
Neurobiology of Aging|February 8, 2011
Replication analysis of SNPs on 9p21.2 and 19p13.3 with amyotrophic lateral sclerosis in East AsiansAritoshi Iida, Atsushi Takahashi, Min Deng, et al.
American Journal of Human Genetics|February 6, 2002
Association between single-nucleotide polymorphisms in selectin genes and immunoglobulin A nephropathyTakashi Takei, Aritoshi Iida, Kosaku Nitta, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 24, 2018
RNA sequencing solved the most common but unrecognized NEB pathogenic variant in Japanese nemaline myopathyKohei Hamanaka, Satoko Miyatake, Eriko Koshimizu, et al.
Nature Communications|April 7, 2021
Deficiency of TMEM53 causes a previously unknown sclerosing bone disorder by dysregulation of BMP-SMAD signalingLong Guo, Aritoshi Iida, Gandham SriLakshmi Bhavani, et al.
Human Mutation|November 18, 2014
Identification and in vivo functional characterization of novel compound heterozygous BMP1 variants in osteogenesis imperfectaSung Yoon Cho, P V Asharani, Ok-Hwa Kim, et al.
Pageof 11