4.5 Article

Dismutase-competent SOD1 mutant accumulation in myelinating Schwann cells is not detrimental to normal or transgenic ALS model mice

Related references

Note: Only part of the references are listed.
Article Multidisciplinary Sciences

Schwann cells expressing dismutase active mutant SOD1 unexpectedly slow disease progression in ALS mice

Christian S. Lobsiger et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)

Article Cell Biology

Skeletal Muscle Is a Primary Target of SOD1G93A-Mediated Toxicity

Gabriella Dobrowolny et al.

CELL METABOLISM (2008)

Article Multidisciplinary Sciences

Mutant SOD1 in cell types other than motor neurons and oligodendrocytes accelerates onset of disease in ALS mice

Koji Yamanaka et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)

Review Neurosciences

Transgenics, toxicity and therapeutics in rodent models of mutant SOD1-mediated familial ALS

Bradley J. Turner et al.

PROGRESS IN NEUROBIOLOGY (2008)

Review Neurosciences

Glial cells as intrinsic components of non-cell-autonomous neurodegenerative disease

Christian S. Lobsiger et al.

NATURE NEUROSCIENCE (2007)

Review Neurosciences

Roles of glial p75NTR in axonal regeneration

Xin-Fu Zhou et al.

JOURNAL OF NEUROSCIENCE RESEARCH (2007)

Article Multidisciplinary Sciences

Gene transfer demonstrates that muscle is not a primary target for non-cell-autonomous toxicity in familial amyotrophic lateral sclerosis

Timothy M. Miller et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)

Article Multidisciplinary Sciences

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)

Article Biochemical Research Methods

Practical nerve morphometry

Fulvio Urso-Baiarda et al.

JOURNAL OF NEUROSCIENCE METHODS (2006)

Article Multidisciplinary Sciences

Onset and progression in inherited ALS determined by motor neurons and microglia

Severine Boillee et al.

SCIENCE (2006)

Review Neurosciences

The origin and development of glial cells in peripheral nerves

KR Jessen et al.

NATURE REVIEWS NEUROSCIENCE (2005)

Article Neurosciences

Amyotrophic lateral sclerosis is a distal axonopathy: evidence in mice and man

LR Fischer et al.

EXPERIMENTAL NEUROLOGY (2004)

Article Multidisciplinary Sciences

Wild-type nonneuronal cells extend survival of SOD1 mutant motor neurons in ALS mice

AM Clement et al.

SCIENCE (2003)

Review Neurosciences

Disease mechanisms in inherited neuropathies

U Suter et al.

NATURE REVIEWS NEUROSCIENCE (2003)

Article Clinical Neurology

A potential role for the p75 low-affinity neurotrophin receptor in spinal motor neuron degeneration in marine and human amyotrophic lateral sclerosis

KS Lowry et al.

AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS (2001)