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No association with common Caucasian genotypes in exons 8, 13 and 14 of the human cytoplasmic dynein heavy chain gene (DNCHC1) and familial motor neuron disorders.
Ahmad-Annuar A, Shah P, Hafezparast M, Hummerich H, Witherden AS, Morrison KE, Shaw PJ, Kirby J, Warner TT, Crosby A, Proukakis C, Wilkinson P, Orrell RW, Bradley L, Martin JE, Fisher EM. Ahmad-Annuar A, et al. Among authors: fisher em. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003 Sep;4(3):150-7. doi: 10.1080/14660820310011737. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003. PMID: 13129801
Phenotypic analysis--making the most of your mouse.
Martin JE, Fisher EM. Martin JE, et al. Among authors: fisher em. Trends Genet. 1997 Jul;13(7):254-6. doi: 10.1016/s0168-9525(97)01193-1. Trends Genet. 1997. PMID: 9242043 No abstract available.
Wasted by an elongation factor.
Hafezparast M, Fisher E. Hafezparast M, et al. Trends Genet. 1998 Jun;14(6):215-7. doi: 10.1016/s0168-9525(98)01478-4. Trends Genet. 1998. PMID: 9635401 No abstract available.
Mice, the motor system, and human motor neuron pathology.
Nicholson SJ, Witherden AS, Hafezparast M, Martin JE, Fisher EM. Nicholson SJ, et al. Among authors: fisher em. Mamm Genome. 2000 Dec;11(12):1041-52. doi: 10.1007/s003350010205. Mamm Genome. 2000. PMID: 11130970 Review.
323 results