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Cancer Biology & Therapy|February 9, 2012
Lack of AKT activation in lung cancer cells with EGFR mutation is a novel marker of cetuximab sensitivityMiyako Takata, Hiroki Chikumi, Naomi Miyake, et al.Brain & Development|January 3, 2009
Intracerebral cell transplantation therapy for murine GM1 gangliosidosisTomo Sawada, Akemi Tanaka, Katsumi Higaki, et al.Human Genome Variation|May 17, 2022
Clinical course of a Japanese patient with developmental delay linked to a small 6q16.1 deletionTetsuya Okazaki, Tatsuya Kawaguchi, Yusuke Saiki, et al.Brain & Development|August 29, 2020
Gallbladder cancer with ascites in a child with metachromatic leukodystrophyKiri Koshu, Takahiro Ikeda, Daisuke Tamura, et al.Brain & Development|April 24, 2012
Quantitative computed tomography for enzyme replacement therapy in Pompe diseaseChihiro Yonee, Mitsuo Toyoshima, Sarah P Young, et al.American Journal of Medical Genetics. Part A|June 12, 2008
Novel beta-galactosidase gene mutation p.W273R in a woman with mucopolysaccharidosis type IVB (Morquio B) and lack of response to in vitro chaperone treatment of her skin fibroblastsZoran S Gucev, Velibor Tasic, Aleksandra Jancevska, et al.Biochemical and Biophysical Research Communications|September 20, 2005
Polyhistidine tract expansions in HOXA1 result in intranuclear aggregation and increased cell deathRubigilda C Paraguison, Katsumi Higaki, Yumiko Sakamoto, et al.European Journal of Pharmacology|May 15, 2007
Cyclohexenonic long-chain fatty alcohol has therapeutic effects on diabetes-induced angiopathy in the rat aortaChiko Shinbori, Motoaki Saito, Yukako Kinoshita, et al.Brain & Development|August 4, 2016
Epileptic phenotype of FGFR3-related bilateral medial temporal lobe dysgenesisTetsuya Okazaki, Yoshiaki Saito, Riyo Ueda, et al.Brain & Development|June 8, 2017
Miglustat therapy in a case of early-infantile Niemann-Pick type CMiho Usui, Akihiko Miyauchi, Yuko Nakano, et al.Pageof 15