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The FXG: A Presynaptic Fragile X Granule Expressed in a Subset of Developing Brain Circuits
Sean B. Christie et al.
JOURNAL OF NEUROSCIENCE (2009)
Axonal mRNA in Uninjured and Regenerating Cortical Mammalian Axons
Anne M. Taylor et al.
JOURNAL OF NEUROSCIENCE (2009)
A functional equivalent of endoplasmic reticulum and Golgi in axons for secretion of locally synthesized proteins
Tanuja T. Merianda et al.
MOLECULAR AND CELLULAR NEUROSCIENCE (2009)
Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6
Caroline Vance et al.
SCIENCE (2009)
Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis
T. J. Kwiatkowski et al.
SCIENCE (2009)
The Autistic Neuron: Troubled Translation?
Raymond J. Kelleher et al.
CELL (2008)
The endoplasmic reticulum-Golgi pathway is a target for translocation and aggregation of mutant superoxide dismutase linked to ALS
Makoto Urushitani et al.
FASEB JOURNAL (2008)
Effect of spastic paraplegia mutations in KIF5A kinesin on transport activity
Bettina Ebbing et al.
HUMAN MOLECULAR GENETICS (2008)
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
Edor Kabashi et al.
NATURE GENETICS (2008)
Astrocytes as determinants of disease progression in inherited amyotrophic lateral sclerosis
Koji Yamanaka et al.
NATURE NEUROSCIENCE (2008)
Fragile X Syndrome: Loss of Local mRNA Regulation Alters Synaptic Development and Function
Gary J. Bassell et al.
NEURON (2008)
Label-Free Biomedical Imaging with High Sensitivity by Stimulated Raman Scattering Microscopy
Christian W. Freudiger et al.
SCIENCE (2008)
Novel Mutations in TARDBP(TDP-43) in Patients with Familial Amyotrophic Lateral Sclerosis
Nicola J. Rutherford et al.
PLOS GENETICS (2008)
Deletion of the BH3-only protein puma protects motoneurons from ER stress-induced apoptosis and delays motoneuron loss in ALS mice
Dairin Kieran et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Familial amyotrophic lateral sclerosis-linked SOD1 mutants perturb fast axonal transport to reduce axonal mitochondria content
Kurt J. De Vos et al.
HUMAN MOLECULAR GENETICS (2007)
Extracellular stimuli specifically regulate localized levels of individual neuronal mRNAs
Dianna E. Willis et al.
JOURNAL OF CELL BIOLOGY (2007)
Microarray analysis of the cellular pathways involved in the adaptation to and progression of motor neuron injury in the SOD1 G93A mouse model of familial ALS
Laura Ferraiuolo et al.
JOURNAL OF NEUROSCIENCE (2007)
Muscle Nogo-A expression is a prognostic marker in lower motor neuron syndromes
Pierre-Francois Pradat et al.
ANNALS OF NEUROLOGY (2007)
Identification of a lectin causing the degeneration of neuronal processes using engineered embryonic stem cells
Nicolas Plachta et al.
NATURE NEUROSCIENCE (2007)
Astrocytes expressing ALS-linked mutated SOD1 release factors selectively toxic to motor neurons
Makiko Nagai et al.
NATURE NEUROSCIENCE (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)
Presynaptic Fmr1 genotype influences the degree of synaptic connectivity in a mosaic mouse model of fragile X syndrome
Jesse E. Hanson et al.
JOURNAL OF NEUROSCIENCE (2007)
Onset and progression in inherited ALS determined by motor neurons and microglia
Severine Boillee et al.
SCIENCE (2006)
Spinal cord endoplasmic reticulum stress associated with a microsomal accumulation of mutant superoxide dismutase-1 in an ALS model
H Kikuchi et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Altered axonal excitability properties in amyotrophic lateral sclerosis: impaired potassium channel function related to disease stage
K Kanai et al.
BRAIN (2006)
Axonal damage markers in cerebrospinal fluid are increased in ALS
J Brettschneider et al.
NEUROLOGY (2006)
Gene expression profile of spinal motor neurons in sporadic amyotrophic lateral sclerosis
YM Jiang et al.
ANNALS OF NEUROLOGY (2005)
Axonal transport defects: a common theme in neurodegenerative diseases
S Roy et al.
ACTA NEUROPATHOLOGICA (2005)
Amyotrophic lateral sclerosis is a distal axonopathy: evidence in mice and man
LR Fischer et al.
EXPERIMENTAL NEUROLOGY (2004)
Evidence of kinesin heavy chain (KIF5A) involvement in pure hereditary spastic paraplegia
M Fichera et al.
NEUROLOGY (2004)
Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS
C Münch et al.
NEUROLOGY (2004)
p38α stress-activated protein kinase phosphorylates neurofilaments and is associated with neurofilament pathology in amyotrophic lateral sclerosis
S Ackerley et al.
MOLECULAR AND CELLULAR NEUROSCIENCE (2004)
Knockdown of the survival motor neuron (Smn) protein in zebrafish causes defects in motor axon outgrowth and pathfinding
ML McWhorter et al.
JOURNAL OF CELL BIOLOGY (2003)
Mutant dynactin in motor neuron disease
I Puls et al.
NATURE GENETICS (2003)
Missense mutation in the tubulin-specific chaperone E (Tbce) gene in the mouse mutant progressive motor neuronopathy, a model of human motoneuron disease
H Bömmel et al.
JOURNAL OF CELL BIOLOGY (2002)
A missense mutation in Tbce causes progressive motor neuronopathy in mice
N Martin et al.
NATURE GENETICS (2002)
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)
A functional role for intra-axonal protein synthesis during axonal regeneration from adult sensory neurons
JQ Zheng et al.
JOURNAL OF NEUROSCIENCE (2001)