Related references
Note: Only part of the references are listed.Dismutase-competent SOD1 mutant accumulation in myelinating Schwann cells is not detrimental to normal or transgenic ALS model mice
Bradley J. Turner et al.
HUMAN MOLECULAR GENETICS (2010)
Live Imaging of Amyotrophic Lateral Sclerosis Pathogenesis: Disease Onset is Characterized by Marked Induction of GFAP in Schwann Cells
A. Florence Keller et al.
GLIA (2009)
Wild-type SOD1 overexpression accelerates disease onset of a G85R SOD1 mouse
Lijun Wang et al.
HUMAN MOLECULAR GENETICS (2009)
Non-cell autonomous toxicity in neurodegenerative disorders: ALS and beyond
Hristelina Ilieva et al.
JOURNAL OF CELL BIOLOGY (2009)
Intravascular AAV9 preferentially targets neonatal neurons and adult astrocytes
Kevin D. Foust et al.
NATURE BIOTECHNOLOGY (2009)
A role for motoneuron subtype-selective ER stress in disease manifestations of FALS mice
Smita Saxena et al.
NATURE NEUROSCIENCE (2009)
The effect of mutant SOD1 dismutase activity on non-cell autonomous degeneration in familial amyotrophic lateral sclerosis
Lijun Wang et al.
NEUROBIOLOGY OF DISEASE (2009)
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)
RNA Gain-of-Function in Spinocerebellar Ataxia Type 8
Randy S. Daughters et al.
PLOS GENETICS (2009)
Non-Cell-Autonomous Effect of Human SOD1G37R Astrocytes on Motor Neurons Derived from Human Embryonic Stem Cells
Maria C. N. Marchetto et al.
CELL STEM CELL (2008)
Astrocytes as determinants of disease progression in inherited amyotrophic lateral sclerosis
Koji Yamanaka et al.
NATURE NEUROSCIENCE (2008)
Common molecular signature in SOD1 for both sporadic and familial amyotrophic lateral sclerosis
Arie Gruzman et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Wild-type superoxide dismutase acquires binding and toxic properties of ALS-linked mutant forms through oxidation
Samer Abou Ezzi et al.
JOURNAL OF NEUROCHEMISTRY (2007)
Non-cell autonomous effect of glia on motor neurons in an embryonic stem cell-based ALS model
Francesco Paolo Di Giorgio et al.
NATURE NEUROSCIENCE (2007)
The presenilin hypothesis of Alzheimer's disease: Evidence for a loss-of-function pathogenic mechanism
Jie Shen et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
In vitro methods to prepare astrocyte and motoneuron cultures for the investigation of potential in vivo interactions
Anna R. Taylor et al.
NATURE PROTOCOLS (2007)
Loss of endogenous androgen receptor protein accelerates motor neuron degeneration and accentuates androgen insensitivity in a mouse model of X-linked spinal and bulbar muscular atrophy
Patrick S. Thomas et al.
HUMAN MOLECULAR GENETICS (2006)
Onset and progression in inherited ALS determined by motor neurons and microglia
Severine Boillee et al.
SCIENCE (2006)
Conversion to the amyotrophic lateral sclerosis phenotype is associated with intermolecular linked insoluble aggregates of SOD1 in mitochondria
HX Deng et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Disulphide-reduced superoxide dismutase-1 in CNS of transgenic amyotrophic lateral sclerosis models
PA Jonsson et al.
BRAIN (2006)
Truncated wild-type SOD1 and FALS-linked mutant SOD1 cause neural cell death in the chick embryo spinal cord
GD Ghadge et al.
NEUROBIOLOGY OF DISEASE (2006)
Cleavage pattern and emerging asymmetry of the mouse embryo
MZ Zernicka-Goetz
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2005)
Astrocyte-specific inactivation of the neurofibromatosis 1 gene (NF1) is insufficient for astrocytoma formation
ML Bajenaru et al.
MOLECULAR AND CELLULAR BIOLOGY (2002)