Related references
Note: Only part of the references are listed.Astrocytes as determinants of disease progression in inherited amyotrophic lateral sclerosis
Koji Yamanaka et al.
NATURE NEUROSCIENCE (2008)
Proprioceptive sensory neuropathy in mice with a mutation in the cytoplasmic dynein heavy chain 1 gene
Xiang-Jun Chen et al.
JOURNAL OF NEUROSCIENCE (2007)
Wild-type microglia extend survival in PU.1 knockout mice with familial amyotrophic lateral sclerosis
David R. Beers et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Onset and progression in inherited ALS determined by motor neurons and microglia
Severine Boillee et al.
SCIENCE (2006)
A dynein mutation attenuates motor neuron degeneration in SOD1G93A mice
M Teuchert et al.
EXPERIMENTAL NEUROLOGY (2006)
No association of DYNC1H1 with sporadic ALS in a case-control study of a northern European derived population:: A tagging SNP approach
PR Shah et al.
AMYOTROPHIC LATERAL SCLEROSIS (2006)
Altered axonal architecture by removal of the heavily phosphorylated neurofilament tail domains strongly slows superoxide dismutase 1 mutant-mediated ALS
CS Lobsiger et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
The SOD1 transgene in the G93A mouse model of amyotrophic lateral sclerosis lies on distal mouse chromosome 12
F Achilli et al.
AMYOTROPHIC LATERAL SCLEROSIS (2005)
A mutation in dynein rescues axonal transport defects and extends the life span of ALS mice
D Kieran et al.
JOURNAL OF CELL BIOLOGY (2005)
Wild-type nonneuronal cells extend survival of SOD1 mutant motor neurons in ALS mice
AM Clement et al.
SCIENCE (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 disorders
A Ahmad-Annuar et al.
AMYOTROPHIC LATERAL SCLEROSIS (2003)
Mutations in dynein link motor neuron degeneration to defects in retrograde transport
M Hafezparast et al.
SCIENCE (2003)
Focal loss of the glutamate transporter EAAT2 in a transgenic rat model of SOD1 mutant-mediated amyotrophic lateral sclerosis (ALS)
DS Howland et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)