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Cancer Genetics and Cytogenetics|July 15, 2009
Translocation (1;10)(p34;p15) in infant acute myeloid leukemia with extramedullary infiltration in multiple sitesMichinori Funato, Toshiyuki Fukao, Hideo Sasai, et al.Journal of Clinical Immunology|June 8, 2014
A complement factor B mutation in a large kindred with atypical hemolytic uremic syndromeMichinori Funato, Osamu Uemura, Katsumi Ushijima, et al.Neuroreport|February 7, 2019
Impairment of oligodendrocyte lineages in spinal muscular atrophy model systemsKazuki Ohuchi, Michinori Funato, Shiori Ando, et al.Neurochemical Research|May 26, 2018
A Docosahexaenoic Acid-Derived Pro-resolving Agent, Maresin 1, Protects Motor Neuron Cells DeathKazuki Ohuchi, Yoko Ono, Mina Joho, et al.International Journal of Molecular Medicine|March 15, 2011
Genetic variations in MyD88 adaptor-like are associated with atopic dermatitisYang An, Hidenori Ohnishi, Eiko Matsui, et al.European Journal of Pharmacology|August 23, 2017
Edaravone is a candidate agent for spinal muscular atrophy: In vitro analysis using a human induced pluripotent stem cells-derived disease modelShiori Ando, Michinori Funato, Kazuki Ohuchi, et al.Head & Neck|August 22, 2012
Paclitaxel-based chemotherapy for aggressive kaposiform hemangioendothelioma of the temporomastoid region: Case report and review of the literatureMichinori Funato, Toshiyuki Fukao, Hideo Sasai, et al.Brain & Development|December 27, 2005
Aberrant peroxisome morphology in peroxisomal beta-oxidation enzyme deficienciesMichinori Funato, Nobuyuki Shimozawa, Tomoko Nagase, et al.Scientific Reports|November 8, 2018
VGF nerve growth factor inducible is involved in retinal ganglion cells death induced by optic nerve crushHiroto Takeuchi, Satoshi Inagaki, Wataru Morozumi, et al.Annals of Clinical and Translational Neurology|December 7, 2020
Viltolarsen in Japanese Duchenne muscular dystrophy patients: A phase 1/2 studyHirofumi Komaki, Yasuhiro Takeshima, Tsuyoshi Matsumura, et al.Pageof 6