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Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders Volume 4, 2003 - Issue 3
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Original Research

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

Azlina Ahmad‐Annuar Department of Neurodegenerative Disease, Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UKCorrespondence[email protected]
,
Paresh Shah Department of Neurology, The Medical School, University of Birmingham, Edgbaston B15 2TT, UK
,
Majid Hafezparast Academic Neurology Unit, The Medical School, University of Sheffield, Sheffield S10 2RX, UK
,
Holger Hummerich Department of Clinical Neurosciences, Royal Free and University College Medical School, Rowland Hill Street, London NW3 2PF, UK
,
Abi S Witherden Department of Medical Genetics, St George's Hospital Medical School, Cranmer Terrace, London SW17 0RE, UK
,
Karen E Morrison Department of Histopathology, Queen Mary and Westfield College, The Royal London Hospital, Whitechapel, London E1 1BB, UK
,
Pamela J Shaw Department of Neurodegenerative Disease, Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK
,
Janine Kirby Department of Neurology, The Medical School, University of Birmingham, Edgbaston B15 2TT, UK
,
Thomas T Warner Academic Neurology Unit, The Medical School, University of Sheffield, Sheffield S10 2RX, UK
,
Andrew Crosby Department of Clinical Neurosciences, Royal Free and University College Medical School, Rowland Hill Street, London NW3 2PF, UK
,
Christos Proukakis Department of Medical Genetics, St George's Hospital Medical School, Cranmer Terrace, London SW17 0RE, UK
,
Philip Wilkinson Department of Histopathology, Queen Mary and Westfield College, The Royal London Hospital, Whitechapel, London E1 1BB, UK
,
Richard W Orrell Department of Neurodegenerative Disease, Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK
,
Lloyd Bradley Department of Neurology, The Medical School, University of Birmingham, Edgbaston B15 2TT, UK
,
Joanne E Martin Academic Neurology Unit, The Medical School, University of Sheffield, Sheffield S10 2RX, UK
&
Elizabeth MC Fisher Department of Clinical Neurosciences, Royal Free and University College Medical School, Rowland Hill Street, London NW3 2PF, UK
 show all
Pages 150-157 | Received 25 Apr 2003, Accepted 12 May 2003, Published online: 10 Jul 2009

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Eleni Christoforidou, Fabio A. Simoes, David Gordon, Kevin Talbot & Majid Hafezparast. (2023) Aberrant dynein function promotes TDP-43 aggregation and upregulation of p62 in male mice harboring transgenic human TDP-43. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 24:7-8, pages 746-755.
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Afnan A Alsultan, Rachel Waller, Paul R Heath & Janine Kirby. (2016) The genetics of amyotrophic lateral sclerosis: current insights. Degenerative Neurological and Neuromuscular Disease 6, pages 49-64.
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Ana Beleza-Meireles & Ammar Al-Chalabi. (2009) Genetic studies of amyotrophic lateral sclerosis: Controversies and perspectives. Amyotrophic Lateral Sclerosis 10:1, pages 1-14.
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Paresh R. Shah, Azlina Ahmad‐Annuar, Kourosh R. Ahmadi, Carsten Russ, Peter C. Sapp, H. Robert Horvitz, Robert H. Brown$suffix/text()$suffix/text(), David B. Goldstein & Elizabeth M. C. Fisher. (2006) No association of DYNC1H1 with sporadic ALS in a case‐control study of a northern European derived population: A tagging SNP approach. Amyotrophic Lateral Sclerosis 7:1, pages 46-56.
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Yukio Kawahara & Shin Kwak. (2005) Excitotoxicity and ALS: What is unique about the AMPA receptors expressed on spinal motor neurons?. Amyotrophic Lateral Sclerosis 6:3, pages 131-144.
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C. Oliver Hanemann & Albert C. Ludolph. (2005) Motor protein diseases of the nervous system. Amyotrophic Lateral Sclerosis 6:4, pages 197-201.
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Articles from other publishers (16)

Yu-lian Fang, Na Li, Xiu-fang Zhi, Jie Zheng, Yang Liu, Lin-jie Pu, Chun-yu Gu, Jian-bo Shu & Chun-quan Cai. (2020) Discovery of specific mutations in spinal muscular atrophy patients by next-generation sequencing. Neurological Sciences 42:5, pages 1827-1833.
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M.B. HarmsK.M. Ori-McKenneyM. ScotoE.P. TuckS. BellD. MaS. MasiP. AllredM. Al-LoziM.M. ReillyL.J. MillerA. Jani-AcsadiA. PestronkM.E. ShyF. MuntoniR.B. ValleeR.H. Baloh. (2012) Mutations in the tail domain of DYNC1H1 cause dominant spinal muscular atrophy . Neurology 78:22, pages 1714-1720.
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Judith Eschbach & Luc Dupuis. (2011) Cytoplasmic dynein in neurodegeneration. Pharmacology & Therapeutics 130:3, pages 348-363.
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V. A. Young & G. F. Rall. 2009. Measles. Measles 3 30 .
Hristelina S. IlievaKoji Yamanaka, Shelle Malkmus, Osamu Kakinohana, Tony Yaksh, Martin Marsala & Don W. Cleveland. (2008) Mutant dynein (Loa) triggers proprioceptive axon loss that extends survival only in the SOD1 ALS model with highest motor neuron death. Proceedings of the National Academy of Sciences 105:34, pages 12599-12604.
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Mauro CozzolinoAlberto FerriMaria Teresa Carrì. (2008) Amyotrophic Lateral Sclerosis: From Current Developments in the Laboratory to Clinical Implications. Antioxidants & Redox Signaling 10:3, pages 405-444.
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Xiang-Jun Chen, Eleni N. Levedakou, Kathleen J. Millen, Robert L. Wollmann, Betty Soliven & Brian Popko. (2007) Proprioceptive Sensory Neuropathy in Mice with a Mutation in the Cytoplasmic Dynein Heavy Chain 1 Gene. The Journal of Neuroscience 27:52, pages 14515-14524.
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Jennifer Motil, Maya Dubey, Walter K.-H. Chan & Thomas B. Shea. (2007) Inhibition of dynein but not kinesin induces aberrant focal accumulation of neurofilaments within axonal neurites. Brain Research 1164, pages 125-131.
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Christopher E. Shaw, Virginia Arechavala-Gomeza & Ammar Al-Chalabi. 2007. Motor neuron disorders and related diseases. Motor neuron disorders and related diseases 279 300 .
Claire L. Simpson & Ammar Al-Chalabi. (2006) Amyotrophic lateral sclerosis as a complex genetic disease. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 1762:11-12, pages 973-985.
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Paul A. James & Kevin Talbot. (2006) The molecular genetics of non-ALS motor neuron diseases. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 1762:11-12, pages 986-1000.
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Peter M. Andersen. (2006) Amyotrophic lateral sclerosis associated with mutations in the CuZn superoxide dismutase gene. Current Neurology and Neuroscience Reports 6:1, pages 37-46.
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K. Kevin Pfister, Paresh R Shah, Holger Hummerich, Andreas Russ, James Cotton, Azlina Ahmad Annuar, Stephen M King & Elizabeth M. C Fisher. (2006) Genetic Analysis of the Cytoplasmic Dynein Subunit Families. PLoS Genetics 2:1, pages e1.
Crossref
M. Flint Beal, Anthony E. Lang & Albert C. LudolphAmmar Al-Chalabi & Robert H. Brown. 2010. Neurodegenerative Diseases. Neurodegenerative Diseases 758 771 .
AMMAR AL-CHALABI & P. NIGEL LEIGH. 2005. Peripheral Neuropathy. Peripheral Neuropathy 1533 1544 .
M. Dewil, P.M. Andersen, L. Van Den Bosch & W. Robberecht. 2004. Clinical Neurophysiology of Motor Neuron Diseases. Clinical Neurophysiology of Motor Neuron Diseases 169 186 .

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