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| Human endplate acetylcholinesterase deficiency caused by mutations in the collagen-like tail subunit (ColQ) of the asymmetric enzyme K Ohno, J Brengman, A Tsujino, AG Engel Proceedings of the National Academy of Sciences 95 (16), 9654-9659, 1998 | 276 | 1998 |
| Rapsyn mutations in humans cause endplate acetylcholine-receptor deficiency and myasthenic syndrome K Ohno, AG Engel, XM Shen, D Selcen, J Brengman, CM Harper, ... The American Journal of Human Genetics 70 (4), 875-885, 2002 | 272 | 2002 |
| Congenital myasthenic syndrome caused by decreased agonist binding affinity due to a mutation in the acetylcholine receptor ε subunit K Ohno, HL Wang, M Milone, N Bren, JM Brengman, S Nakano, P Quiram, ... Neuron 17 (1), 157-170, 1996 | 267 | 1996 |
| Molecular hydrogen is protective against 6-hydroxydopamine-induced nigrostriatal degeneration in a rat model of Parkinson's disease Y Fu, M Ito, Y Fujita, M Ito, M Ichihara, A Masuda, Y Suzuki, S Maesawa, ... Neuroscience letters 453 (2), 81-85, 2009 | 265 | 2009 |
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| Peroxisome targeting signal of rat liver acyl-coenzyme A oxidase resides at the carboxy terminus S Miyazawa, T Osumi, T Hashimoto, K Ohno, S Miura, Y Fujiki Molecular and cellular biology, 1989 | 245 | 1989 |
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