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European Journal of Human Genetics : EJHG|February 23, 2025
Two distinct phenotypes in Snijders Blok-Campeau syndrome and characterization of the behavioral phenotype in a zebrafish modelYumi Enomoto, Takashi Shiromizu, Sakyo Yasojima, et al.
Cell Reports|November 24, 2016
HIV-1 Control by NK Cells via Reduced Interaction between KIR2DL2 and HLA-C∗12:02/C∗14:03Zhansong Lin, Kimiko Kuroki, Nozomi Kuse, et al.
Acta Biomaterialia|October 25, 2025
Development of a three-dimensional experimental vascular model with smooth muscle cell-derived cross-linked elastic fiber assemblyYuri Sawada, Shota Tanifuji, Takashi Nakamura, et al.
Journal of Virology|February 14, 2014
Host-specific adaptation of HIV-1 subtype B in the Japanese populationTakayuki Chikata, Jonathan M Carlson, Yoshiko Tamura, et al.
The Journal of Medical Investigation : JMI|November 5, 2020
Next-generation sequencing for the diagnosis of patients with congenital multiple anomalies and / or intellectual disabilitiesKenichi Suga, Issei Imoto, Hiromichi Ito, et al.
Lung Cancer (Amsterdam, Netherlands)|August 26, 2017
Frequent silencing of RASSF1A by DNA methylation in thymic neuroendocrine tumoursKoichiro Kajiura, Hiromitsu Takizawa, Yuki Morimoto, et al.
The Lancet Regional Health. Western Pacific|August 9, 2023
Safety, efficacy and pharmacokinetics of palivizumab in off-label neonates, infants, and young children at risk for serious respiratory syncytial virus infection: a multicenter phase II clinical trialMasaaki Mori, Kanako Yoshizaki, Shinichi Watabe, et al.
Clinical Immunology (Orlando, Fla.)|September 9, 2019
A deep intronic mutation of c.1166-285 T > G in SLC46A1 is shared by four unrelated Japanese patients with hereditary folate malabsorption (HFM)Yusuke Tozawa, Shimaa Said Mohamed Ali Abdrabou, Natsuko Nogawa-Chida, et al.
International Journal of Hematology|November 19, 2013
Influence of pre-hydration and pharmacogenetics on plasma methotrexate concentration and renal dysfunction following high-dose methotrexate therapyMasakatsu Yanagimachi, Hiroaki Goto, Tetsuji Kaneko, et al.
Clinical Genetics|December 27, 2021
Divergent variant patterns among 19 patients with Rubinstein-Taybi syndrome uncovered by comprehensive genetic analysis including whole genome sequencingYumi Enomoto, Takayuki Yokoi, Yoshinori Tsurusaki, et al.
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