Ohno K - Search Results

1

HnRNP L and hnRNP LL antagonistically modulate PTB-mediated splicing suppression of CHRNA1 pre-mRNA.

Rahman MA, Masuda A, Ohe K, Ito M, Hutchinson DO, Mayeda A, Engel AG, Ohno K. Rahman MA, et al. Among authors: ohno k. Sci Rep. 2013 Oct 14;3:2931. doi: 10.1038/srep02931. Sci Rep. 2013. PMID: 24121633 Free PMC article.

2

Rapsyn mutations in humans cause endplate acetylcholine-receptor deficiency and myasthenic syndrome.

Ohno K, Engel AG, Shen XM, Selcen D, Brengman J, Harper CM, Tsujino A, Milone M. Ohno K, et al. Am J Hum Genet. 2002 Apr;70(4):875-85. doi: 10.1086/339465. Epub 2002 Jan 14. Am J Hum Genet. 2002. PMID: 11791205 Free PMC article.

3

Congenital myasthenic syndromes: genetic defects of the neuromuscular junction.

Ohno K, Engel AG. Ohno K, et al. Curr Neurol Neurosci Rep. 2002 Jan;2(1):78-88. doi: 10.1007/s11910-002-0057-7. Curr Neurol Neurosci Rep. 2002. PMID: 11898587 Review.

4

Congenital myasthenic syndromes.

Engel AG, Ohno K. Engel AG, et al. Among authors: ohno k. Adv Neurol. 2002;88:203-15. Adv Neurol. 2002. PMID: 11908226 Review. No abstract available.

5

Naturally occurring mutations at the acetylcholine receptor binding site independently alter ACh binding and channel gating.

Sine SM, Shen XM, Wang HL, Ohno K, Lee WY, Tsujino A, Brengmann J, Bren N, Vajsar J, Engel AG. Sine SM, et al. Among authors: ohno k. J Gen Physiol. 2002 Oct;120(4):483-96. doi: 10.1085/jgp.20028568. J Gen Physiol. 2002. PMID: 12356851 Free PMC article.

6

The spectrum of congenital myasthenic syndromes.

Engel AG, Ohno K, Sine SM. Engel AG, et al. Among authors: ohno k. Mol Neurobiol. 2002 Oct-Dec;26(2-3):347-67. doi: 10.1385/MN:26:2-3:347. Mol Neurobiol. 2002. PMID: 12428764 Review.

7

Congenital myasthenic syndromes: progress over the past decade.

Engel AG, Ohno K, Sine SM. Engel AG, et al. Among authors: ohno k. Muscle Nerve. 2003 Jan;27(1):4-25. doi: 10.1002/mus.10269. Muscle Nerve. 2003. PMID: 12508290 Review.

8

Mutation causing severe myasthenia reveals functional asymmetry of AChR signature cystine loops in agonist binding and gating.

Shen XM, Ohno K, Tsujino A, Brengman JM, Gingold M, Sine SM, Engel AG. Shen XM, et al. Among authors: ohno k. J Clin Invest. 2003 Feb;111(4):497-505. doi: 10.1172/JCI16997. J Clin Invest. 2003. PMID: 12588888 Free PMC article.

9

E-box mutations in the RAPSN promoter region in eight cases with congenital myasthenic syndrome.

Ohno K, Sadeh M, Blatt I, Brengman JM, Engel AG. Ohno K, et al. Hum Mol Genet. 2003 Apr 1;12(7):739-48. doi: 10.1093/hmg/ddg089. Hum Mol Genet. 2003. PMID: 12651869

10

Sleuthing molecular targets for neurological diseases at the neuromuscular junction.

Engel AG, Ohno K, Sine SM. Engel AG, et al. Among authors: ohno k. Nat Rev Neurosci. 2003 May;4(5):339-52. doi: 10.1038/nrn1101. Nat Rev Neurosci. 2003. PMID: 12728262 Review. No abstract available.

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