Showing results (21-30 of 109) with videos related to

Sort By:
Pageof 11
Journal of Human Genetics|April 11, 2024
Role of TOE1 variants at the nuclear localization motif in pontocerebellar hypoplasia 7Yukiko Kuroda, Takuya Naruto, Yu Tsuyusaki, et al.
Cytokine|June 19, 2009
Interleukin-6 inhibits early differentiation of ATDC5 chondrogenic progenitor cellsShoko Nakajima, Takuya Naruto, Takako Miyamae, et al.
Modern Rheumatology|March 4, 2009
The role of heme oxygenase-1 in systemic-onset juvenile idiopathic arthritisAkitaka Takahashi, Masaaki Mori, Takuya Naruto, et al.
Journal of Virology|July 20, 2012
HLA class I-mediated control of HIV-1 in the Japanese population, in which the protective HLA-B*57 and HLA-B*27 alleles are absentTakuya Naruto, Hiroyuki Gatanaga, George Nelson, et al.
Human Genome Variation|April 16, 2016
A FRMD7 variant in a Japanese family causes congenital nystagmusTomohiro Kohmoto, Nana Okamoto, Shigeko Satomura, et al.
Scientific Reports|June 11, 2015
Deep intronic GPR143 mutation in a Japanese family with ocular albinismTakuya Naruto, Nobuhiko Okamoto, Kiyoshi Masuda, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|January 22, 2005
Dynamic movement of cytochrome c from mitochondria into cytosol and peripheral circulation in massive hepatic cell injuryYoshinori Kobayashi, Masaaki Mori, Takuya Naruto, et al.
Human Genome Variation|June 15, 2017
A novel UBE2A mutation causes X-linked intellectual disability type NascimentoYoshinori Tsurusaki, Ikuko Ohashi, Yumi Enomoto, et al.
American Journal of Medical Genetics. Part A|December 10, 2014
Microdeletion of 19p13.3 in a girl with Peutz-Jeghers syndrome, intellectual disability, hypotonia, and distinctive featuresYukiko Kuroda, Toshiyuki Saito, Jun-Ichi Nagai, et al.
Pageof 11