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Proceedings of the National Academy of Sciences of the United States of America|August 8, 2012
Overexpression of the Hspa13 (Stch) gene reduces prion disease incubation time in miceJulia Grizenkova, Shaheen Akhtar, Holger Hummerich, et al.
The Lancet. Neurology|December 17, 2008
Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association studySimon Mead, Mark Poulter, James Uphill, et al.
Gene|February 28, 2002
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) mutationAbi S Witherden, Majid Hafezparast, Sharon J Nicholson, et al.
Neurology|June 8, 2012
Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseasesAnna Sailer, Sonja W Scholz, J Raphael Gibbs, et al.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|September 18, 2003
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 disordersAzlina Ahmad-Annuar, Paresh Shah, Majid Hafezparast, et al.
Human Molecular Genetics|January 3, 2012
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNPSimon Mead, James Uphill, John Beck, et al.
Somatic Cell and Molecular Genetics|January 1, 1994
Structure and expression of the Huntington's disease gene: evidence against simple inactivation due to an expanded CAG repeatChristine M Ambrose, Mabel P Duyao, Glenn Barnes, et al.
Brain : a Journal of Neurology|January 25, 2014
HTT-lowering reverses Huntington's disease immune dysfunction caused by NFκB pathway dysregulationUlrike Träger, Ralph Andre, Nayana Lahiri, et al.
Nature Genetics|July 26, 2005
Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementiaGaia Skibinski, Nicholas J Parkinson, Jeremy M Brown, et al.
Science (New York, N.Y.)|May 6, 2003
Mutations in dynein link motor neuron degeneration to defects in retrograde transportMajid Hafezparast, Rainer Klocke, Christiana Ruhrberg, et al.
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