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Nature Immunology|February 19, 2002
Selective loss of gastrointestinal mast cells and impaired immunity in PI3K-deficient miceTaro Fukao, Taketo Yamada, Masanobu Tanabe, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 18, 2017
Prospective cohort study for identification of underlying genetic causes in neonatal encephalopathy using whole-exome sequencingTheodora U J Bruun, Caro-Lyne DesRoches, Diane Wilson, et al.
The Plant Journal : for Cell and Molecular Biology|April 6, 2017
Chloroplastic ATP synthase builds up a proton motive force preventing production of reactive oxygen species in photosystem IDaisuke Takagi, Katsumi Amako, Masaki Hashiguchi, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 15, 2001
Expression of MUC1 mucins in the subserosal layer correlates with postsurgical prognosis of pathological tumor stage 2 carcinoma of the gallbladderT Kawamoto, J Shoda, T Irimura, et al.
Investigational New Drugs|January 11, 2017
Safety, tolerability and pharmacokinetics of the fibroblast growth factor receptor inhibitor AZD4547 in Japanese patients with advanced solid tumours: a Phase I studyHideo Saka, Chiyoe Kitagawa, Yoshihito Kogure, et al.
Journal of Medical Virology|August 7, 2013
Serum prolactin levels and prolactin mRNA expression in peripheral blood mononuclear cells in hepatitis C virus infectionRika Ishii, Takafumi Saito, Li Shao, et al.
Human Genome Variation|August 23, 2018
Late-onset ornithine transcarbamylase deficiency caused by a somatic mosaic mutationTomoko Lee, Maiko Misaki, Hideki Shimomura, et al.
Journal of Infection and Chemotherapy : Official Journal of the Japan Society of Chemotherapy|June 14, 2019
Primary carnitine deficiency with severe acute hepatitis following rotavirus gastroenteritisMika Ishige, Tatsuo Fuchigami, Maki Furukawa, et al.
Pediatrics and Neonatology|April 28, 2023
Factors associated with the development of epilepsy in very low birth weight infantsToshimichi Fukao, Fumikazu Sano, Atsushi Nemoto, et al.
Human Mutation|September 23, 1998
Characterization of N93S, I312T, and A333P missense mutations in two Japanese families with mitochondrial acetoacetyl-CoA thiolase deficiencyT Fukao, H Nakamura, X Q Song, et al.
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