|Peptide mapping by limited proteolysis in sodium dodecyl sulfate and analysis by gel electrophoresis.|
DW Cleveland, SG Fischer, MW Kirschner, UK Laemmli
Journal of Biological Chemistry 252 (3), 1102-1106, 1977
|Number and evolutionary conservation of α-and β-tubulin and cytoplasmic β-and γ-actin genes using specific cloned cDNA probes|
DW Cleveland, MA Lopata, RJ MacDonald, NJ Cowan, WJ Rutter, ...
Cell 20 (1), 95-105, 1980
|Onset and progression in inherited ALS determined by motor neurons and microglia|
S Boillée, K Yamanaka, CS Lobsiger, NG Copeland, NA Jenkins, ...
Science 312 (5778), 1389-1392, 2006
|An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria|
PC Wong, CA Pardo, DR Borchelt, MK Lee, NG Copeland, NA Jenkins, ...
Neuron 14 (6), 1105-1116, 1995
|ALS: a disease of motor neurons and their nonneuronal neighbors|
S Boillée, CV Velde, DW Cleveland
Neuron 52 (1), 39-59, 2006
|Unraveling the mechanisms involved in motor neuron degeneration in ALS|
LI Bruijn, TM Miller, DW Cleveland
Annu. Rev. Neurosci. 27, 723-749, 2004
|From Charcot to Lou Gehrig: deciphering selective motor neuron death in ALS|
DW Cleveland, JD Rothstein
Nature reviews neuroscience 2 (11), 806-819, 2001
|ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions|
LI Bruijn, MW Becher, MK Lee, KL Anderson, NA Jenkins, NG Copeland, ...
Neuron 18 (2), 327-338, 1997
|Aggregation and motor neuron toxicity of an ALS-linked SOD1 mutant independent from wild-type SOD1|
LI Bruijn, MK Houseweart, S Kato, KL Anderson, SD Anderson, E Ohama, ...
Science 281 (5384), 1851-1854, 1998
|On the road to cancer: aneuploidy and the mitotic checkpoint|
GJPL Kops, BAA Weaver, DW Cleveland
Nature Reviews Cancer 5 (10), 773-785, 2005
|Wild-type nonneuronal cells extend survival of SOD1 mutant motor neurons in ALS mice|
AM Clement, MD Nguyen, EA Roberts, ML Garcia, S Boillee, M Rule, ...
science 302 (5642), 113-117, 2003
|Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis|
SC Ling, M Polymenidou, DW Cleveland
Neuron 79 (3), 416-438, 2013
|A structural scaffolding of intermediate filaments in health and disease|
E Fuchs, DW Cleveland
Science 279 (5350), 514-519, 1998
|Decoding ALS: from genes to mechanism|
JP Taylor, RH Brown, DW Cleveland
Nature 539 (7628), 197-206, 2016
|Centromeres and kinetochores: from epigenetics to mitotic checkpoint signaling|
DW Cleveland, Y Mao, KF Sullivan
Cell 112 (4), 407-421, 2003
|Astrocytes as determinants of disease progression in inherited amyotrophic lateral sclerosis|
K Yamanaka, SJ Chun, S Boillee, N Fujimori-Tonou, H Yamashita, ...
Nature neuroscience 11 (3), 251-253, 2008
|Purification of tau, a microtubule-associated protein that induces assembly of microtubules from purified tubulin|
DW Cleveland, SY Hwo, MW Kirschner
Journal of molecular biology 116 (2), 207-225, 1977
|Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43|
M Polymenidou, C Lagier-Tourenne, KR Hutt, SC Huelga, J Moran, ...
Nature neuroscience 14 (4), 459, 2011
|Non–cell autonomous toxicity in neurodegenerative disorders: ALS and beyond|
H Ilieva, M Polymenidou, DW Cleveland
Journal of Cell Biology 187 (6), 761-772, 2009
|Focal loss of the glutamate transporter EAAT2 in a transgenic rat model of SOD1 mutant-mediated amyotrophic lateral sclerosis (ALS)|
DS Howland, J Liu, Y She, B Goad, NJ Maragakis, B Kim, J Erickson, ...
Proceedings of the National Academy of Sciences 99 (3), 1604-1609, 2002