相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Cross-disease comparison of amyotrophic lateral sclerosis and spinal muscular atrophy reveals conservation of selective vulnerability but differential neuromuscular junction pathology
Laura H. Comley et al.
JOURNAL OF COMPARATIVE NEUROLOGY (2016)
A perspective on stem cell modeling of amyotrophic lateral sclerosis
A. Sophie de Boer et al.
CELL CYCLE (2015)
IGF-1R Reduction Triggers Neuroprotective Signaling Pathways in Spinal Muscular Atrophy Mice
Olivier Biondi et al.
JOURNAL OF NEUROSCIENCE (2015)
MOTOR NEURONS WITH DIFFERENTIAL VULNERABILITY TO DEGENERATION SHOW DISTINCT PROTEIN SIGNATURES IN HEALTH AND ALS
L. Comley et al.
NEUROSCIENCE (2015)
ALS-causative mutations in FUS/TLS confer gain and loss of function by altered association with SMN and U1-snRNP
Shuying Sun et al.
NATURE COMMUNICATIONS (2015)
Effect of Combined Systemic and Local Morpholino Treatment on the Spinal Muscular Atrophy Δ7 Mouse Model Phenotype
Monica Nizzardo et al.
CLINICAL THERAPEUTICS (2014)
Insulin and insulin-like growth factor receptors in the brain: Physiological and pathological aspects
Haim Werner et al.
EUROPEAN NEUROPSYCHOPHARMACOLOGY (2014)
State of play in amyotrophic lateral sclerosis genetics
Alan E. Renton et al.
NATURE NEUROSCIENCE (2014)
Neuronal Matrix Metalloproteinase-9 Is a Determinant of Selective Neurodegeneration
Artem Kaplan et al.
NEURON (2014)
iPSC-Derived Neural Stem Cells Act via Kinase Inhibition to Exert Neuroprotective Effects in Spinal Muscular Atrophy with Respiratory Distress Type 1
Chiara Simone et al.
STEM CELL REPORTS (2014)
Unravelling the enigma of selective vulnerability in neurodegeneration: motor neurons resistant to degeneration in ALS show distinct gene expression characteristics and decreased susceptibility to excitotoxicity
Alice Brockington et al.
ACTA NEUROPATHOLOGICA (2013)
A Small Molecule Screen in Stem-Cell-Derived Motor Neurons Identifies a Kinase Inhibitor as a Candidate Therapeutic for ALS
Yin M. Yang et al.
CELL STEM CELL (2013)
Spliceosome integrity is defective in the motor neuron diseases ALS and SMA
Hitomi Tsuiji et al.
EMBO MOLECULAR MEDICINE (2013)
Eye tracking communication devices in amyotrophic lateral sclerosis: Impact on disability and quality of life
Marco Caligari et al.
AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION (2013)
The genetics and neuropathology of amyotrophic lateral sclerosis
Ammar Al-Chalabi et al.
ACTA NEUROPATHOLOGICA (2012)
Mutant superoxide dismutase 1 (SOD1), a cause of amyotrophic lateral sclerosis, disrupts the recruitment of SMN, the spinal muscular atrophy protein to nuclear Cajal bodies
Shingo Kariya et al.
HUMAN MOLECULAR GENETICS (2012)
EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humans
Annelies Van Hoecke et al.
NATURE MEDICINE (2012)
IGF-1 delivery to CNS attenuates motor neuron cell death but does not improve motor function in type III SMA mice
Li-Kai Tsai et al.
NEUROBIOLOGY OF DISEASE (2012)
Shared Resistance to Aging and ALS in Neuromuscular Junctions of Specific Muscles
Gregorio Valdez et al.
PLOS ONE (2012)
Genetic Correction of Human Induced Pluripotent Stem Cells from Patients with Spinal Muscular Atrophy
Stefania Corti et al.
SCIENCE TRANSLATIONAL MEDICINE (2012)
Memory enhancement: consolidation, reconsolidation and insulin-like growth factor 2
Cristina M. Alberini et al.
TRENDS IN NEUROSCIENCES (2012)
FUS-SMN Protein Interactions Link the Motor Neuron Diseases ALS and SMA
Tomohiro Yamazaki et al.
CELL REPORTS (2012)
Increased IGF-1 in muscle modulates the phenotype of severe SMA mice
Marta Bosch-Marce et al.
HUMAN MOLECULAR GENETICS (2011)
Global gene expression profiling of somatic motor neuron populations with different vulnerability identify molecules and pathways of degeneration and protection
Eva Hedlund et al.
BRAIN (2010)
Induced pluripotent stem cells from a spinal muscular atrophy patient
Allison D. Ebert et al.
NATURE (2009)
Differentiation of spinal motor neurons from pluripotent human stem cells
Bao-Yang Hu et al.
NATURE PROTOCOLS (2009)
Decreased motoneuron survival in Igf2 null mice after sciatic nerve transection
Delia Silva et al.
NEUROREPORT (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)
Human Embryonic Stem Cell-Derived Motor Neurons Are Sensitive to the Toxic Effect of Glial Cells Carrying an ALS-Causing Mutation
Francesco Paolo Di Giorgio et al.
CELL STEM CELL (2008)
Signalling by neurotrophins and hepatocyte growth factor regulates axon morphogenesis by differential β-catenin phosphorylation
Monica D. David et al.
JOURNAL OF CELL SCIENCE (2008)
Neuron-specific expression of mutant superoxide dismutase is sufficient to induce amyotrophic lateral sclerosis in transgenic mice
Dick Jaarsma et al.
JOURNAL OF NEUROSCIENCE (2008)
Subcutaneous IGF-1 is not beneficial in 2-year ALS trial
E. J. Sorenson et al.
NEUROLOGY (2008)
Embryonic stem cell-derived Pitx3-enhanced green fluorescent protein midbrain dopamine neurons survive enrichment by fluorescence-activated cell sorting and function in an animal model of Parkinson's disease
Eva Hedlund et al.
STEM CELLS (2008)
Astrocytes expressing ALS-linked mutated SOD1 release factors selectively toxic to motor neurons
Makiko Nagai et al.
NATURE NEUROSCIENCE (2007)
Onset and progression in inherited ALS determined by motor neurons and microglia
Severine Boillee et al.
SCIENCE (2006)
Identification of a primitive brain-derived neural stem cell population based on aldehyde dehydrogenase activity
Stefania Corti et al.
STEM CELLS (2006)
A compensatory subpopulation of motor neurons in a mouse model of amyotrophic lateral sclerosis
AM Schaefer et al.
JOURNAL OF COMPARATIVE NEUROLOGY (2005)
Amyotrophic lateral sclerosis is a distal axonopathy: evidence in mice and man
LR Fischer et al.
EXPERIMENTAL NEUROLOGY (2004)
Retrograde viral delivery of IGF-1 prolongs survival in a mouse ALS model
BK Kaspar et al.
SCIENCE (2003)
Insulin-like growth factor-II/mannose-6-phosphate receptor: Widespread distribution in neurons of the central nervous system including those expressing cholinergic phenotype
C Hawkes et al.
JOURNAL OF COMPARATIVE NEUROLOGY (2003)
Differential vulnerability of cranial motoneurons in mouse models with motor neuron degeneration
C Haenggeli et al.
NEUROSCIENCE LETTERS (2002)
Protective effect of parvalbumin on excitotoxic motor neuron death
L Van den Bosch et al.
EXPERIMENTAL NEUROLOGY (2002)
Target-derived cardiotrophin-1 and insulin-like growth factor-I promote neurite growth and survival of developing oculomotor neurons
HB Rind et al.
MOLECULAR AND CELLULAR NEUROSCIENCE (2002)
Synaptic sprouting increases the uptake capacities of motoneurons in amyotrophic lateral sclerosis mice
S Millecamps et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2001)
Transcription-dependent and -independent control of neuronal survival by the PI3K-Akt signaling pathway
A Brunet et al.
CURRENT OPINION IN NEUROBIOLOGY (2001)