Related references
Note: Only part of the references are listed.Diagnostic and prognostic value of CSF neurofilaments in a cohort of patients with motor neuron disease: A cross-sectional study
Delia Gagliardi et al.
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE (2021)
Novel STMN2 Variant Linked to Amyotrophic Lateral Sclerosis Risk and Clinical Phenotype
Frances Theunissen et al.
FRONTIERS IN AGING NEUROSCIENCE (2021)
Anatomo-Functional Origins of the Cortical Silent Period: Spotlight on the Basal Ganglia
David Zeugin et al.
BRAIN SCIENCES (2021)
Synaptotagmin 13 is neuroprotective across motor neuron diseases
M. Nizzardo et al.
ACTA NEUROPATHOLOGICA (2020)
Truncated stathmin-2 is a marker of TDP-43 pathology in frontotemporal dementia
Mercedes Prudencio et al.
JOURNAL OF CLINICAL INVESTIGATION (2020)
Stathmin-2: adding another piece to the puzzle of TDP-43 proteinopathies and neurodegeneration
Jonathan D. Glass
JOURNAL OF CLINICAL INVESTIGATION (2020)
AAV9-Stathmin1 gene delivery improves disease phenotype in an intermediate mouse model of spinal muscular atrophy
E. Villalon et al.
HUMAN MOLECULAR GENETICS (2019)
The landscape of multiscale transcriptomic networks and key regulators in Parkinson's disease
Qian Wang et al.
NATURE COMMUNICATIONS (2019)
Key role of SMN/SYNCRIP and RNA-Motif 7 in spinal muscular atrophy: RNA-Seq and motif analysis of human motor neurons
Federica Rizzo et al.
BRAIN (2019)
ALS-implicated protein TDP-43 sustains levels of STMN2, a mediator of motor neuron growth and repair
Joseph R. Klim et al.
NATURE NEUROSCIENCE (2019)
Premature polyadenylation-mediated loss of stathmin-2 is a hallmark of TDP-43-dependent neurodegeneration
Ze'ev Melamed et al.
NATURE NEUROSCIENCE (2019)
Comparison of independent screens on differentially vulnerable motor neurons reveals alpha-synuclein as a common modifier in motor neuron diseases
Rachel A. Kline et al.
PLOS GENETICS (2017)
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)
Stathmin 1/2-triggered microtubule loss mediates Golgi fragmentation in mutant SOD1 motor neurons
Sarah Bellouze et al.
MOLECULAR NEURODEGENERATION (2016)
Differential neuronal vulnerability identifies IGF-2 as a protective factor in ALS
Ilary Allodi et al.
SCIENTIFIC REPORTS (2016)
Building the Neuronal Microtubule Cytoskeleton
Lukas C. Kapitein et al.
NEURON (2015)
MOTOR NEURONS WITH DIFFERENTIAL VULNERABILITY TO DEGENERATION SHOW DISTINCT PROTEIN SIGNATURES IN HEALTH AND ALS
L. Comley et al.
NEUROSCIENCE (2015)
Neuronal stathmins: A family of phosphoproteins cooperating for neuronal development, plasticity and regeneration
Stephanie Chauvin et al.
PROGRESS IN NEUROBIOLOGY (2015)
Dynamic regulation of SCG10 in regenerating axons after injury
Jung Eun Shin et al.
EXPERIMENTAL NEUROLOGY (2014)
Axonal Transport of TDP-43 mRNA Granules Is Impaired by ALS-Causing Mutations
Nael H. Alami et al.
NEURON (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)
Progressive amnestic dementia, hippocampal sclerosis, and mutation in C9ORF72
Melissa E. Murray et al.
ACTA NEUROPATHOLOGICA (2013)
The intriguing case of motor neuron disease: ALS and SMA come closer
Tilmann Achsel et al.
BIOCHEMICAL SOCIETY TRANSACTIONS (2013)
Decreased stathmin expression ameliorates neuromuscular defects but fails to prolong survival in a mouse model of spinal muscular atrophy
Hsin-Lan Wen et al.
NEUROBIOLOGY OF DISEASE (2013)
The Microtubule Regulatory Protein Stathmin Is Required to Maintain the Integrity of Axonal Microtubules in Drosophila
Jason E. Duncan et al.
PLOS ONE (2013)
Severe neuromuscular denervation of clinically relevant muscles in a mouse model of spinal muscular atrophy
Karen K. Y. Ling et al.
HUMAN MOLECULAR GENETICS (2012)
Gains or losses: molecular mechanisms of TDP43-mediated neurodegeneration
Edward B. Lee et al.
NATURE REVIEWS NEUROSCIENCE (2012)
Genetic Correction of Human Induced Pluripotent Stem Cells from Patients with Spinal Muscular Atrophy
Stefania Corti et al.
SCIENCE TRANSLATIONAL MEDICINE (2012)
The Dying-Back Phenomenon of Motor Neurons in ALS
Michal Dadon-Nachum et al.
JOURNAL OF MOLECULAR NEUROSCIENCE (2011)
Stathmin is Required for Stability of the Drosophila Neuromuscular Junction
Ethan R. Graf et al.
JOURNAL OF NEUROSCIENCE (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)
Stathmin, a microtubule-destabilizing protein, is dysregulated in spinal muscular atrophy(dagger)
Hsin-Lan Wen et al.
HUMAN MOLECULAR GENETICS (2010)
TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration
Clotilde Lagier-Tourenne et al.
HUMAN MOLECULAR GENETICS (2010)
The Microtubule Regulator Stathmin Is an Endogenous Protein Agonist for TLR3
Malika Bsibsi et al.
JOURNAL OF IMMUNOLOGY (2010)
Selective vulnerability of motor neurons and dissociation of pre- and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy
Lyndsay M. Murray et al.
HUMAN MOLECULAR GENETICS (2008)
Superior cervical ganglion-10 protein as a molecular effector of c-Jun N-terminal kinase 1: implications for the therapeutic targeting of Jun N-terminal kinase in nerve regeneration
Nina Westerlund et al.
EXPERT OPINION ON THERAPEUTIC TARGETS (2008)
Axonal degeneration in motor neuron disease
Lindsey R. Fischer et al.
NEURODEGENERATIVE DISEASES (2007)
JNK1 phosphorylation of SCG10 determines microtubule dynamics and axodendritic length
T Tararuk et al.
JOURNAL OF CELL BIOLOGY (2006)
The role of stathmin in the regulation of the cell cycle
CI Rubin et al.
JOURNAL OF CELLULAR BIOCHEMISTRY (2004)
Phosphorylation disrupts the central helix in Op18/stathmin and suppresses binding to tubulin
MO Steinmetz et al.
EMBO REPORTS (2001)
New ocular movement detector system as a communication tool in ventilator-assisted Werdnig-Hoffmann disease
M Kubota et al.
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2000)