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Page 1
Mutations in dynein link motor neuron degeneration to defects in retrograde transport.
Hafezparast M, Klocke R, Ruhrberg C, Marquardt A, Ahmad-Annuar A, Bowen S, Lalli G, Witherden AS, Hummerich H, Nicholson S, Morgan PJ, Oozageer R, Priestley JV, Averill S, King VR, Ball S, Peters J, Toda T, Yamamoto A, Hiraoka Y, Augustin M, Korthaus D, Wattler S, Wabnitz P, Dickneite C, Lampel S, Boehme F, Peraus G, Popp A, Rudelius M, Schlegel J, Fuchs H, Hrabe de Angelis M, Schiavo G, Shima DT, Russ AP, Stumm G, Martin JE, Fisher EM. Hafezparast M, et al. Science. 2003 May 2;300(5620):808-12. doi: 10.1126/science.1083129. Science. 2003. PMID: 12730604
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: hafezparast m. Mamm Genome. 2000 Dec;11(12):1041-52. doi: 10.1007/s003350010205. Mamm Genome. 2000. PMID: 11130970 Review.
An integrated genetic, radiation hybrid, physical and transcription map of a region of distal mouse chromosome 12, including an imprinted locus and the 'Legs at odd angles' (Loa) mutation.
Witherden AS, Hafezparast M, Nicholson SJ, Ahmad-Annuar A, Bermingham N, Arac D, Rankin J, Iravani M, Ball S, Peters J, Martin JE, Huntley D, Hummerich H, Sergot M, Fisher EM. Witherden AS, et al. Among authors: hafezparast m. Gene. 2002 Jan 23;283(1-2):71-82. doi: 10.1016/s0378-1119(01)00853-8. Gene. 2002. PMID: 11867214
A new mouse mutant, skijumper.
Hafezparast M, Ball S, Nicholson SJ, Witherden A, Arac D, Broadway N, Saggerson D, Cooper E, Naase M, Gokhale S, Quant P, Lascelles C, Nickols C, Baker CS, Peters J, Martin JE, Fisher EM. Hafezparast M, et al. Mamm Genome. 2002 Jul;13(7):359-364. doi: 10.1007/pl00021068. Mamm Genome. 2002. PMID: 12152619
Mouse models for neurological disease.
Hafezparast M, Ahmad-Annuar A, Wood NW, Tabrizi SJ, Fisher EM. Hafezparast M, et al. Lancet Neurol. 2002 Aug;1(4):215-24. doi: 10.1016/s1474-4422(02)00100-x. Lancet Neurol. 2002. PMID: 12849454 Review.
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: hafezparast m. 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
Paradigms for the identification of new genes in motor neuron degeneration.
Hafezparast M, Ahmad-Annuar A, Hummerich H, Shah P, Ford M, Baker C, Bowen S, Martin JE, Fisher EM. Hafezparast M, et al. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003 Dec;4(4):249-57. doi: 10.1080/14660820310016084. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003. PMID: 14753659
56 results