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American Journal of Medical Genetics. Part A|April 23, 2015
Delineation of the KIAA2022 mutation phenotype: two patients with X-linked intellectual disability and distinctive featuresYukiko Kuroda, Ikuko Ohashi, Takuya Naruto, et al.Plos One|February 10, 2017
PADI4 and the HLA-DRB1 shared epitope in juvenile idiopathic arthritisKaori Hisa, Masakatsu D Yanagimachi, Takuya Naruto, et al.American Journal of Medical Genetics. Part A|March 27, 2014
De novo duplication of 17p13.1-p13.2 in a patient with intellectual disability and obesityYukiko Kuroda, Ikuko Ohashi, Makiko Tominaga, et al.Human Genome Variation|September 23, 2016
A novel missense mutation of COL5A2 in a patient with Ehlers-Danlos syndromeMiki Watanabe, Ryuji Nakagawa, Takuya Naruto, et al.Human Genome Variation|April 16, 2016
A novel frameshift mutation of CHD7 in a Japanese patient with CHARGE syndromeTomohiro Kohmoto, Miki Shono, Takuya Naruto, et al.Scientific Reports|December 6, 2016
Novel human mutation and CRISPR/Cas genome-edited mice reveal the importance of C-terminal domain of MSX1 in tooth and palate developmentSilvia Naomi Mitsui, Akihiro Yasue, Kiyoshi Masuda, et al.Oncotarget|January 20, 2018
Prevalence of pathogenic germline variants detected by multigene sequencing in unselected Japanese patients with ovarian cancerAkira Hirasawa, Issei Imoto, Takuya Naruto, et al.Human Genome Variation|October 25, 2019
A severe form of Ellis-van Creveld syndrome caused by novel mutations in EVC2Ikuko Ohashi, Yumi Enomoto, Takuya Naruto, et al.Oncotarget|December 8, 2016
Frequent silencing of the candidate tumor suppressor TRIM58 by promoter methylation in early-stage lung adenocarcinomaKoichiro Kajiura, Kiyoshi Masuda, Takuya Naruto, et al.Plos One|July 14, 2012
Unbiased analysis of TCRα/β chains at the single-cell level in human CD8+ T-cell subsetsXiaoming Sun, Masumichi Saito, Yoshinori Sato, et al.Pageof 11