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Page 1
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: hummerich h. Gene. 2002 Jan 23;283(1-2):71-82. doi: 10.1016/s0378-1119(01)00853-8. Gene. 2002. PMID: 11867214
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: hummerich h. 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. Among authors: hummerich h. 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
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. Among authors: hummerich h. Science. 2003 May 2;300(5620):808-12. doi: 10.1126/science.1083129. Science. 2003. PMID: 12730604
GANESH: software for customized annotation of genome regions.
Huntley D, Hummerich H, Smedley D, Kittivoravitkul S, McCarthy M, Little P, Sergot M. Huntley D, et al. Among authors: hummerich h. Genome Res. 2003 Sep;13(9):2195-202. doi: 10.1101/gr.698103. Genome Res. 2003. PMID: 12952886 Free PMC article.
Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia.
Skibinski G, Parkinson NJ, Brown JM, Chakrabarti L, Lloyd SL, Hummerich H, Nielsen JE, Hodges JR, Spillantini MG, Thusgaard T, Brandner S, Brun A, Rossor MN, Gade A, Johannsen P, Sørensen SA, Gydesen S, Fisher EM, Collinge J. Skibinski G, et al. Among authors: hummerich h. Nat Genet. 2005 Aug;37(8):806-8. doi: 10.1038/ng1609. Epub 2005 Jul 24. Nat Genet. 2005. PMID: 16041373
Genetic analysis of the cytoplasmic dynein subunit families.
Pfister KK, Shah PR, Hummerich H, Russ A, Cotton J, Annuar AA, King SM, Fisher EM. Pfister KK, et al. Among authors: hummerich h. PLoS Genet. 2006 Jan;2(1):e1. doi: 10.1371/journal.pgen.0020001. PLoS Genet. 2006. PMID: 16440056 Free PMC article.
Overexpression of the Hspa13 (Stch) gene reduces prion disease incubation time in mice.
Grizenkova J, Akhtar S, Hummerich H, Tomlinson A, Asante EA, Wenborn A, Fizet J, Poulter M, Wiseman FK, Fisher EM, Tybulewicz VL, Brandner S, Collinge J, Lloyd SE. Grizenkova J, et al. Among authors: hummerich h. Proc Natl Acad Sci U S A. 2012 Aug 21;109(34):13722-7. doi: 10.1073/pnas.1208917109. Epub 2012 Aug 6. Proc Natl Acad Sci U S A. 2012. PMID: 22869728 Free PMC article.
55 results