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Brain & Development|July 29, 2019
Thermolabile polymorphism of carnitine palmitoyltransferase 2: A genetic risk factor of overall acute encephalopathyAkiko Shibata, Mariko Kasai, Ai Hoshino, et al.
Biochemical and Biophysical Research Communications|August 26, 2011
A novel splicing variant of CADM2 as a protective transcript of psoriasisAzusa Hiruma, Shigaku Ikeda, Tadashi Terui, et al.
Iscience|November 28, 2022
Urinary extracellular vesicles signature for diagnosis of kidney diseaseKeiichi Takizawa, Koji Ueda, Masahiro Sekiguchi, et al.
Clinical Epigenetics|June 18, 2020
Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patientsTakanobu Inoue, Akie Nakamura, Megumi Iwahashi-Odano, et al.
Cancer Research|March 29, 2014
Biallelic DICER1 mutations in sporadic pleuropulmonary blastomaMasafumi Seki, Kenichi Yoshida, Yuichi Shiraishi, et al.
Human Mutation|December 30, 2014
Recessive inheritance of population-specific intronic LINE-1 insertion causes a rotor syndrome phenotypeTatehiro Kagawa, Akira Oka, Yoshinao Kobayashi, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|October 29, 2019
Nonosmotic secretion of arginine vasopressin and salt loss in hyponatremia in Kawasaki diseaseKenichiro Miura, Yutaka Harita, Naoto Takahashi, et al.
Hypertension (Dallas, Tex. : 1979)|January 24, 2007
High-resolution mapping for essential hypertension using microsatellite markersKeisuke Yatsu, Nobuhisa Mizuki, Nobuhito Hirawa, et al.
The Journal of Investigative Dermatology|May 17, 2017
RXRB Is an MHC-Encoded Susceptibility Gene Associated with Anti-Topoisomerase I Antibody-Positive Systemic SclerosisAkira Oka, Yoshihide Asano, Minoru Hasegawa, et al.
Ebiomedicine|June 25, 2020
Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair lossAkira Oka, Atsushi Takagi, Etsuko Komiyama, et al.
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