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Neurobiology of axonal transport defects in motor neuron diseases: Opportunities for translational research?

Neurobiology of disease, 2017-09, Vol.105, p.283-299

2017

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The role of mitochondria in amyotrophic lateral sclerosis

Neuroscience letters, 2019-09, Vol.710, p.132933-132933, Article 132933

2019

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ER-mitochondria associations are regulated by the VAPB-PTPIP51 interaction and are disrupted by ALS/FTD-associated TDP-43

Nature communications, 2014-06, Vol.5 (1), p.3996-3996, Article 3996

2014

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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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Increasing microtubule acetylation rescues axonal transport and locomotor deficits caused by LRRK2 Roc-COR domain mutations

Nature communications, 2014-10, Vol.5 (1), p.5245-5245, Article 5245

2014

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Amyotrophic lateral sclerosis-associated mutant SOD1 inhibits anterograde axonal transport of mitochondria by reducing Miro1 levels

Human molecular genetics, 2017-12, Vol.26 (23), p.4668-4679

2017

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C9orf72 expansion disrupts ATM-mediated chromosomal break repair

Nature neuroscience, 2017-09, Vol.20 (9), p.1225-1235

2017

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Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6

Science (American Association for the Advancement of Science), 2009-02, Vol.323 (5918), p.1208-1211

2009

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Protein Homeostasis in Amyotrophic Lateral Sclerosis: Therapeutic Opportunities?

Frontiers in molecular neuroscience, 2017-05, Vol.10, p.123-123

2017

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Reduced number of axonal mitochondria and tau hypophosphorylation in mouse P301L tau knockin neurons

Neurobiology of disease, 2016-01, Vol.85, p.1-10

2016

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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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Role of Axonal Transport in Neurodegenerative Diseases

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

2008

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C9ORF72 hexanucleotide repeat exerts toxicity in a stable, inducible motor neuronal cell model, which is rescued by partial depletion of Pten

Human molecular genetics, 2017-03, Vol.26 (6), p.1133-1145

2017

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Phosphorylation of kinesin light chain 1 at serine 460 modulates binding and trafficking of calsyntenin-1

Journal of cell science, 2011-04, Vol.124 (Pt 7), p.1032-1042

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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C9ORF72 -derived poly-GA DPRs undergo endocytic uptake in iAstrocytes and spread to motor neurons

Life science alliance, 2022-09, Vol.5 (9), p.e202101276

2022

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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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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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ALS/FTD-associated FUS activates GSK-3β to disrupt the VAPB-PTPIP51 interaction and ER-mitochondria associations

EMBO reports, 2016-09, Vol.17 (9), p.1326-1342

2016

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ALS/FTD-associated FUS activates GSK-3[beta] to disrupt the VAPB-PTPIP51 interaction and ER-mitochondria associations

EMBO reports, 2016-09, Vol.17 (9), p.1326

2016

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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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A comparison of in vitro properties of resting SOD1 transgenic microglia reveals evidence of reduced neuroprotective function

BMC neuroscience, 2011-09, Vol.12 (1), p.91-91, Article 91

2011

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Astrocyte adenosine deaminase loss increases motor neuron toxicity in amyotrophic lateral sclerosis

Brain (London, England : 1878), 2019-03, Vol.142 (3), p.586-605

2019

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Visualization and Quantification of Mitochondrial Dynamics in Living Animal Cells

Methods in Cell Biology, 2007, Vol.80, p.627-682

2007

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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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Neurobiology of axonal transport defects in motor neuron diseases: Opportunities for translational research?

The role of mitochondria in amyotrophic lateral sclerosis

ER-mitochondria associations are regulated by the VAPB-PTPIP51 interaction and are disrupted by ALS/FTD-associated TDP-43

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

Increasing microtubule acetylation rescues axonal transport and locomotor deficits caused by LRRK2 Roc-COR domain mutations

Amyotrophic lateral sclerosis-associated mutant SOD1 inhibits anterograde axonal transport of mitochondria by reducing Miro1 levels

C9orf72 expansion disrupts ATM-mediated chromosomal break repair

Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6

Protein Homeostasis in Amyotrophic Lateral Sclerosis: Therapeutic Opportunities?

Reduced number of axonal mitochondria and tau hypophosphorylation in mouse P301L tau knockin neurons

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

Role of Axonal Transport in Neurodegenerative Diseases

C9ORF72 hexanucleotide repeat exerts toxicity in a stable, inducible motor neuronal cell model, which is rescued by partial depletion of Pten

Phosphorylation of kinesin light chain 1 at serine 460 modulates binding and trafficking of calsyntenin-1

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

C9ORF72 -derived poly-GA DPRs undergo endocytic uptake in iAstrocytes and spread to motor neurons

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

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

ALS/FTD-associated FUS activates GSK-3β to disrupt the VAPB-PTPIP51 interaction and ER-mitochondria associations

ALS/FTD-associated FUS activates GSK-3[beta] to disrupt the VAPB-PTPIP51 interaction and ER-mitochondria associations

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

A comparison of in vitro properties of resting SOD1 transgenic microglia reveals evidence of reduced neuroprotective function

Astrocyte adenosine deaminase loss increases motor neuron toxicity in amyotrophic lateral sclerosis

Visualization and Quantification of Mitochondrial Dynamics in Living Animal Cells

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

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