Majid Hafezparast
Cited by
Cited by
Genealogies of mouse inbred strains
JA Beck, S Lloyd, M Hafezparast, M Lennon-Pierce, JT Eppig, ...
Nature genetics 24 (1), 23-25, 2000
Mutations in dynein link motor neuron degeneration to defects in retrograde transport
M Hafezparast, R Klocke, C Ruhrberg, A Marquardt, A Ahmad-Annuar, ...
Science 300 (5620), 808-812, 2003
A mutation in dynein rescues axonal transport defects and extends the life span of ALS mice
D Kieran, M Hafezparast, S Bohnert, JRT Dick, J Martin, G Schiavo, ...
The Journal of cell biology 169 (4), 561-567, 2005
SHIRPA, a protocol for behavioral assessment: validation for longitudinal study of neurological dysfunction in mice
DC Rogers, JO Peters, JE Martin, S Ball, SJ Nicholson, AS Witherden, ...
Neuroscience letters 306 (1-2), 89-92, 2001
Mutations in BICD2 cause dominant congenital spinal muscular atrophy and hereditary spastic paraplegia
EC Oates, AM Rossor, M Hafezparast, M Gonzalez, F Speziani, ...
The American Journal of Human Genetics 92 (6), 965-973, 2013
PARP-1 dependent recruitment of the amyotrophic lateral sclerosis-associated protein FUS/TLS to sites of oxidative DNA damage
SL Rulten, A Rotheray, RL Green, GJ Grundy, DAQ Moore, ...
Nucleic acids research 42 (1), 307-314, 2014
Neurobiology of axonal transport defects in motor neuron diseases: Opportunities for translational research?
KJ De Vos, M Hafezparast
Neurobiology of disease 105, 283-299, 2017
Cytoplasmic dynein heavy chain: the servant of many masters
G Schiavo, L Greensmith, M Hafezparast, EMC Fisher
Trends in neurosciences 36 (11), 641-651, 2013
A comprehensive assessment of the SOD1G93A low-copy transgenic mouse, which models human amyotrophic lateral sclerosis
A Acevedo-Arozena, B Kalmar, S Essa, T Ricketts, P Joyce, R Kent, ...
Disease models & mechanisms 4 (5), 686-700, 2011
Localization of a DNA repair gene (XRCC5) involved in double-strand-break rejoining to human chromosome 2
PA Jeggo, M Hafezparast, AF Thompson, BC Broughton, GP Kaur, ...
Proceedings of the National Academy of Sciences 89 (14), 6423-6427, 1992
Novel mutations expand the clinical spectrum of DYNC1H1-associated spinal muscular atrophy
M Scoto, AM Rossor, MB Harms, S Cirak, M Calissano, S Robb, ...
Neurology 84 (7), 668-679, 2015
Mouse cytoplasmic dynein intermediate chains: identification of new isoforms, alternative splicing and tissue distribution of transcripts
A Kuta, W Deng, AM El-Kadi, GT Banks, M Hafezparast, KK Pfister, ...
PloS one 5 (7), e11682, 2010
Subchromosomal localization of a gene (XRCC5) involved in double strand break repair to the region 2q34-36
M Hafezparast, GP Kaur, M Zdzienicka, RS Athwal, AR Lehmann, ...
Somatic cell and molecular genetics 19 (5), 413-421, 1993
Mouse models for neurological disease
M Hafezparast, A Ahmad-Annuar, NW Wood, SJ Tabrizi, EMC Fisher
The Lancet Neurology 1 (4), 215-224, 2002
Defective axonal transport in motor neuron disease
AM El‐Kadi, V Soura, M Hafezparast
Journal of neuroscience research 85 (12), 2557-2566, 2007
Intermediate chain subunit as a probe for cytoplasmic dynein function: biochemical analyses and live cell imaging in PC12 cells
KR Myers, KWH Lo, RJ Lye, JM Kogoy, V Soura, M Hafezparast, ...
Journal of neuroscience research 85 (12), 2640-2647, 2007
Mice, the motor system, and human motor neuron pathology
SJ Nicholson, AS Witherden, M Hafezparast, JE Martin, EMC Fisher
Mammalian Genome 11 (12), 1041-1052, 2000
The phagocytic capacity of neurones
S Bowen, DD Ateh, K Deinhardt, MM Bird, KM Price, CS Baker, ...
European Journal of Neuroscience 25 (10), 2947-2955, 2007
Neurodegenerative mutation in cytoplasmic dynein alters its organization and dynein-dynactin and dynein-kinesin interactions
W Deng, C Garrett, B Dombert, V Soura, G Banks, EMC Fisher, ...
Journal of Biological Chemistry 285 (51), 39922-39934, 2010
The SOD1 transgene in the G93A mouse model of amyotrophic lateral sclerosis lies on distal mouse chromosome 12
F Achilli, S Boyle, D Kieran, R Chia, M Hafezparast, JE Martin, G Schiavo, ...
Amyotrophic Lateral Sclerosis 6 (2), 111-114, 2005
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