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Neuromuscular Disorders : NMD|June 26, 1999
Congenital myasthenic syndrome caused by a mutation in the Ets-binding site of the promoter region of the acetylcholine receptor epsilon subunit geneK Ohno, B Anlar, A G EngelJournal of Physiology, Paris|October 23, 1998
Congenital myasthenic syndromes: experiments of natureA G Engel, K Ohno, S M SineArchives of Neurology|February 20, 1999
Congenital myasthenic syndromes: recent advancesA G Engel, K Ohno, S M SineProceedings of the National Academy of Sciences of the United States of America|August 5, 1998
Human endplate acetylcholinesterase deficiency caused by mutations in the collagen-like tail subunit (ColQ) of the asymmetric enzymeK Ohno, J Brengman, A Tsujino, et al.Neuroreport|July 17, 1998
Quinidine normalizes the open duration of slow-channel mutants of the acetylcholine receptorT Fukudome, K Ohno, J M Brengman, et al.Journal of Medical Genetics|August 3, 2005
Spectrum of splicing errors caused by CHRNE mutations affecting introns and intron/exon boundariesK Ohno, A Tsujino, X-M Shen, et al.Annals of Neurology|November 1, 1996
End-plate acetylcholine receptor deficiency due to nonsense mutations in the epsilon subunitA G Engel, K Ohno, C Bouzat, et al.American Journal of Human Genetics|August 12, 1999
Congenital end-plate acetylcholinesterase deficiency caused by a nonsense mutation and an A-->G splice-donor-site mutation at position +3 of the collagenlike-tail-subunit gene (COLQ): how does G at position +3 result in aberrant splicing?K Ohno, J M Brengman, K J Felice, et al.The Journal of General Physiology|June 1, 1997
Mutation in the M1 domain of the acetylcholine receptor alpha subunit decreases the rate of agonist dissociationH L Wang, A Auerbach, N Bren, et al.Annals of Neurology|August 26, 1998
Myasthenic syndromes in Turkish kinships due to mutations in the acetylcholine receptorK Ohno, B Anlar, E Ozdirim, et al.Pageof 88