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Annals of the New York Academy of Sciences|November 1, 2003
Mechanistic diversity underlying fast channel congenital myasthenic syndromesSteven M Sine, Hai-Long Wang, Kinji Ohno, et al.Rinsho Shinkeigaku = Clinical Neurology|December 1, 2012
[Anti-MuSK antibodies in myasthenia gravis block binding of collagen Q to MuSK]Kinji OhnoRinsho Shinkeigaku = Clinical Neurology|January 24, 2008
[RNA pathologies in neurological disorders]Kinji OhnoClinical Calcium|February 25, 2017
[Studies on therapeutic strategies for congenital myasthenic syndromes.]Kinji OhnoBrain and Nerve = Shinkei Kenkyu No Shinpo|July 13, 2011
[Genetic defects and disorders at the neuromuscular junction]Kinji OhnoBrain and Nerve = Shinkei Kenkyu No Shinpo|January 8, 2024
[Congenital Myasthenic Syndromes]Kinji OhnoThe Journal of Clinical Investigation|February 18, 2003
Mutation causing severe myasthenia reveals functional asymmetry of AChR signature cystine loops in agonist binding and gatingXin-Ming Shen, Kinji Ohno, Akira Tsujino, et al.Scientific Reports|October 15, 2013
HnRNP L and hnRNP LL antagonistically modulate PTB-mediated splicing suppression of CHRNA1 pre-mRNAMohammad Alinoor Rahman, Akio Masuda, Kenji Ohe, et al.American Journal of Human Genetics|January 16, 2002
Rapsyn mutations in humans cause endplate acetylcholine-receptor deficiency and myasthenic syndromeKinji Ohno, Andrew G Engel, Xin-Ming Shen, et al.Pageof 31