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Amyotrophic Lateral Sclerosis Volume 7, 2006 - Issue 1
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Original

No association of DYNC1H1 with sporadic ALS in a case‐control study of a northern European derived population: A tagging SNP approach

Paresh R. Shah Department of Neurodegenerative Disease; MRC Prion Unit, Institute of Neurology, Queen Square, London, UK
,
Azlina Ahmad‐Annuar Department of Neurodegenerative Disease
,
Kourosh R. Ahmadi Department of Biology, University College London, UK
,
Carsten Russ Day Laboratory for Neuromuscular Research, Massachusetts General Hospital, MA
,
Peter C. Sapp Howard Hughes Medical Institute, Department of Biology, Massachusetts Institute of Technology, MA, USA
,
H. Robert Horvitz Howard Hughes Medical Institute, Department of Biology, Massachusetts Institute of Technology, MA, USA
,
Robert H. Brown JR Day Laboratory for Neuromuscular Research, Massachusetts General Hospital, MA
,
David B. Goldstein Department of Biology, University College London, UK
&
Elizabeth M. C. Fisher Department of Neurodegenerative DiseaseCorrespondence[email protected]
 show all
Pages 46-56 | Received 08 Jun 2005, Accepted 29 Sep 2005, 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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Articles from other publishers (7)

Yu-Ju Liu, Hung-Chih Kuo & Yijuang Chern. (2021) A system-wide mislocalization of RNA-binding proteins in motor neurons is a new feature of ALS. Neurobiology of Disease 160, pages 105531.
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Wenhui Huang & Liqing Zhang. (2010) Towards Constructing Disease Relationship Networks Using Genome-Wide Association Studies. Towards Constructing Disease Relationship Networks Using Genome-Wide Association Studies.
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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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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Dalia Kasperavičiūtė, Mike E. Weale, Kevin V. Shianna, Gareth T. Banks, Claire L. Simpson, Valerie K. Hansen, Martin R. Turner, Christopher E. Shaw, Ammar Al-Chalabi, Hardev S. Pall, Emily F. Goodall, Karen E. Morrison, Richard W. Orrell, Marcus Beck, Sibylle Jablonka, Michael Sendtner, Alice Brockington, Paul G. Ince, Judith Hartley, Hannah Nixon, Pamela J. Shaw, Giampietro Schiavo, Nicholas W. Wood, David B. Goldstein & Elizabeth M.C. Fisher. (2007) Large-scale pathways-based association study in amyotrophic lateral sclerosis. Brain 130:9, pages 2292-2301.
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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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David B. Goldstein, Anna C. Need, Rinki Singh & Sanjay M. Sisodiya. (2007) Potential Genetic Causes of Heterogeneity of Treatment Effects. The American Journal of Medicine 120:4, pages S21-S25.
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