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Journal of the American Chemical Society|October 24, 2023
Validation of a New Methodology to Create Oral Drugs beyond the Rule of 5 for Intracellular Tough TargetsAtsushi Ohta, Mikimasa Tanada, Shojiro Shinohara, et al.Journal of Medical Genetics|July 5, 2022
Clinical, biochemical and genetic characteristics of MOGS-CDG: a rare congenital disorder of glycosylationShino Shimada, Bobby G Ng, Amy L White, et al.Allergology International : Official Journal of the Japanese Society of Allergology|October 19, 2024
Skin health survey on atopic dermatitis among Japanese children: The Tohoku Medical Megabank Project Birth and Three-Generation Cohort StudyChikana Kawaguchi, Maki Ozawa, Takanori Hidaka, et al.Nature Genetics|January 10, 2017
SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndromeNatalie D Shaw, Harrison Brand, Zachary A Kupchinsky, et al.Pageof 190