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Molecular pathways of motor neuron injury in amyotrophic lateral sclerosis

Nature reviews. Neurology, 2011-11, Vol.7 (11), p.616-630

2011

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Role of Axonal Transport in Neurodegenerative Diseases

Annual review of neuroscience, 2008-01, Vol.31 (1), p.151-173

2008

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Mutations in CHMP2B in lower motor neuron predominant amyotrophic lateral sclerosis (ALS)

PloS one, 2010-03, Vol.5 (3), p.e9872-e9872

2010

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Systemic delivery of scAAV9 expressing SMN prolongs survival in a model of spinal muscular atrophy

Science translational medicine, 2010-06, Vol.2 (35), p.35ra42

2010

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Axonal Transport Defects in a Mitofusin 2 Loss of Function Model of Charcot-Marie-Tooth Disease in Zebrafish

PloS one, 2013-06, Vol.8 (6), p.e67276-e67276

2013

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Superoxide dismutase 1 mutation in a cellular model of amyotrophic lateral sclerosis shifts energy generation from oxidative phosphorylation to glycolysis

Neurobiology of aging, 2014-06, Vol.35 (6), p.1499-1509

2014

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Familial amyotrophic lateral sclerosis-linked SOD1 mutants perturb fast axonal transport to reduce axonal mitochondria content

Human molecular genetics, 2007-11, Vol.16 (22), p.2720-2728

2007

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Mitochondrial Function and Actin Regulate Dynamin-Related Protein 1-Dependent Mitochondrial Fission

Current biology, 2005-04, Vol.15 (7), p.678-683

2005

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The effect of SOD1 mutation on cellular bioenergetic profile and viability in response to oxidative stress and influence of mutation-type

PloS one, 2013-06, Vol.8 (6), p.e68256

2013

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Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients

Journal of neurochemistry, 2009-07, Vol.110 (1), p.34-44

2009

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Tardbpl splicing rescues motor neuron and axonal development in a mutant tardbp zebrafish

Human molecular genetics, 2013-06, Vol.22 (12), p.2376-2386

2013

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Loss of TMEM106B exacerbates C9ALS/FTD DPR pathology by disrupting autophagosome maturation

Frontiers in cellular neuroscience, 2022-12, Vol.16, p.1061559

2022

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Impairment of the tRNA-splicing endonuclease subunit 54 (tsen54) gene causes neurological abnormalities and larval death in zebrafish models of pontocerebellar hypoplasia

Human molecular genetics, 2011-04, Vol.20 (8), p.1574-1584

2011

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The C9orf72 protein interacts with Rab1a and the ULK1 complex to regulate initiation of autophagy

The EMBO journal, 2016-08, Vol.35 (15), p.1656-1676

2016

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Discovery of Western European R1b1a2 Y chromosome variants in 1000 genomes project data: an online community approach

PloS one, 2012-07, Vol.7 (7), p.e41634-e41634

2012

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AAV9-mediated central nervous system-targeted gene delivery via cisterna magna route in mice

Molecular therapy. Methods & clinical development, 2016-01, Vol.3 (C), p.15055-15055, Article 15055

2016

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Neurofilament Heavy Chain Side Arm Phosphorylation Regulates Axonal Transport of Neurofilaments

The Journal of cell biology, 2003-05, Vol.161 (3), p.489-495

2003

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Loss of Deacetylation Enzymes Hdac6 and Sirt2 Promotes Acetylation of Cytoplasmic Tubulin, but Suppresses Axonemal Acetylation in Zebrafish Cilia

Frontiers in cell and developmental biology, 2021-06, Vol.9, p.676214-676214

2021

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Early detection of motor dysfunction in the SOD1G93A mouse model of Amyotrophic Lateral Sclerosis (ALS) using home cage running wheels

PloS one, 2014, Vol.9 (9), p.e107918-e107918

2014

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No evidence for cardiac dysfunction in Kif6 mutant mice

PloS one, 2013-01, Vol.8 (1), p.e54636-e54636

2013

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An interaction between synapsin and C9orf72 regulates excitatory synapses and is impaired in ALS/FTD

Acta neuropathologica, 2022-09, Vol.144 (3), p.437-464

2022

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Altered age-related changes in bioenergetic properties and mitochondrial morphology in fibroblasts from sporadic amyotrophic lateral sclerosis patients

Neurobiology of aging, 2015-10, Vol.36 (10), p.2893-2903

2015

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Neutrophils use selective autophagy receptor Sqstm1/p62 to target Staphylococcus aureus for degradation in vivo in zebrafish

Autophagy, 2021-06, Vol.17 (6), p.1448-1457

2021

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Lamb1a regulates atrial growth by limiting second heart field addition during zebrafish heart development

Development (Cambridge), 2021-10, Vol.148 (20)

2021

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The Cellular and Molecular Pathology of the Motor System in Hereditary Spastic Paraparesis due to Mutation of the Spastin Gene

Journal of neuropathology and experimental neurology, 2003-11, Vol.62 (11), p.1166-1177

2003

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Molecular pathways of motor neuron injury in amyotrophic lateral sclerosis

Role of Axonal Transport in Neurodegenerative Diseases

Mutations in CHMP2B in lower motor neuron predominant amyotrophic lateral sclerosis (ALS)

Systemic delivery of scAAV9 expressing SMN prolongs survival in a model of spinal muscular atrophy

Axonal Transport Defects in a Mitofusin 2 Loss of Function Model of Charcot-Marie-Tooth Disease in Zebrafish

Superoxide dismutase 1 mutation in a cellular model of amyotrophic lateral sclerosis shifts energy generation from oxidative phosphorylation to glycolysis

Familial amyotrophic lateral sclerosis-linked SOD1 mutants perturb fast axonal transport to reduce axonal mitochondria content

Mitochondrial Function and Actin Regulate Dynamin-Related Protein 1-Dependent Mitochondrial Fission

The effect of SOD1 mutation on cellular bioenergetic profile and viability in response to oxidative stress and influence of mutation-type

Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients

Tardbpl splicing rescues motor neuron and axonal development in a mutant tardbp zebrafish

Loss of TMEM106B exacerbates C9ALS/FTD DPR pathology by disrupting autophagosome maturation

Impairment of the tRNA-splicing endonuclease subunit 54 (tsen54) gene causes neurological abnormalities and larval death in zebrafish models of pontocerebellar hypoplasia

The C9orf72 protein interacts with Rab1a and the ULK1 complex to regulate initiation of autophagy

Discovery of Western European R1b1a2 Y chromosome variants in 1000 genomes project data: an online community approach

AAV9-mediated central nervous system-targeted gene delivery via cisterna magna route in mice

Neurofilament Heavy Chain Side Arm Phosphorylation Regulates Axonal Transport of Neurofilaments

Loss of Deacetylation Enzymes Hdac6 and Sirt2 Promotes Acetylation of Cytoplasmic Tubulin, but Suppresses Axonemal Acetylation in Zebrafish Cilia

Early detection of motor dysfunction in the SOD1G93A mouse model of Amyotrophic Lateral Sclerosis (ALS) using home cage running wheels

No evidence for cardiac dysfunction in Kif6 mutant mice

An interaction between synapsin and C9orf72 regulates excitatory synapses and is impaired in ALS/FTD

Altered age-related changes in bioenergetic properties and mitochondrial morphology in fibroblasts from sporadic amyotrophic lateral sclerosis patients

Neutrophils use selective autophagy receptor Sqstm1/p62 to target Staphylococcus aureus for degradation in vivo in zebrafish

Lamb1a regulates atrial growth by limiting second heart field addition during zebrafish heart development

The Cellular and Molecular Pathology of the Motor System in Hereditary Spastic Paraparesis due to Mutation of the Spastin Gene

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