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Wallerian degeneration: an emerging axon death pathway linking injury and disease

Nature reviews. Neuroscience, 2014-06, Vol.15 (6), p.394-409

2014

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NMN Deamidase Delays Wallerian Degeneration and Rescues Axonal Defects Caused by NMNAT2 Deficiency In Vivo

Current biology, 2017-03, Vol.27 (6), p.784-794

2017

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Wallerian degeneration, wld(s), and nmnat

Annual review of neuroscience, 2010, Vol.33, p.245-267

2010

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A caspase cascade regulating developmental axon degeneration

The Journal of neuroscience, 2012-12, Vol.32 (49), p.17540-17553

2012

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Homozygous NMNAT2 mutation in sisters with polyneuropathy and erythromelalgia

Experimental neurology, 2019-10, Vol.320, p.112958-112958, Article 112958

2019

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A role for motoneuron subtype-selective ER stress in disease manifestations of FALS mice

Nature neuroscience, 2009-05, Vol.12 (5), p.627-636

2009

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Transcription factor Pebbled/RREB1 regulates injury-induced axon degeneration

Proceedings of the National Academy of Sciences - PNAS, 2018-02, Vol.115 (6), p.1358-1363

2018

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Autophagic myelin destruction by schwann cells during wallerian degeneration and segmental demyelination

Glia, 2016-05, Vol.64 (5), p.730-742

2016

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Diagnosis, natural history, and management of Charcot–Marie–Tooth disease

Lancet neurology, 2009-07, Vol.8 (7), p.654-667

2009

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The Ubiquitin Proteasome System in Synaptic and Axonal Degeneration: A New Twist to an Old Cycle

The Journal of cell biology, 2004-04, Vol.165 (1), p.27-30

2004

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Axon degeneration mechanisms: commonality amid diversity

Nature reviews. Neuroscience, 2005-11, Vol.6 (11), p.889-898

Coleman, Michael

2005

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Severe biallelic loss-of-function mutations in nicotinamide mononucleotide adenylyltransferase 2 (NMNAT2) in two fetuses with fetal akinesia deformation sequence

Experimental neurology, 2019-10, Vol.320, p.112961-112961, Article 112961

2019

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Cisplatin induced neurotoxicity is mediated by Sarm1 and calpain activation

Scientific reports, 2020-12, Vol.10 (1), p.21889-12, Article 21889

2020

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Axon Death Pathways Converge on Axundead to Promote Functional and Structural Axon Disassembly

Neuron (Cambridge, Mass.), 2017-07, Vol.95 (1), p.78-91.e5

2017

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Death Receptor 6 Promotes Wallerian Degeneration in Peripheral Axons

Current biology, 2017-03, Vol.27 (6), p.890-896

2017

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Complementation between Mouse Mfn1 and Mfn2 Protects Mitochondrial Fusion Defects Caused by CMT2A Disease Mutations

The Journal of cell biology, 2007-02, Vol.176 (4), p.405-414

2007

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Expression of beta-amyloid induced age-dependent presynaptic and axonal changes in Drosophila

The Journal of neuroscience, 2010-01, Vol.30 (4), p.1512-1522

2010

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Mislocalization of neuronal mitochondria reveals regulation of Wallerian degeneration and NMNAT/WLD(S)-mediated axon protection independent of axonal mitochondria

Human molecular genetics, 2013-04, Vol.22 (8), p.1601-1614

2013

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Signaling mechanisms regulating Wallerian degeneration

Current opinion in neurobiology, 2014-08, Vol.27, p.224-231

Freeman, Marc R

2014

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A Local Mechanism Mediates NAD-Dependent Protection of Axon Degeneration

The Journal of cell biology, 2005-08, Vol.170 (3), p.349-355

2005

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A dual leucine kinase-dependent axon self-destruction program promotes Wallerian degeneration

Nature neuroscience, 2009-04, Vol.12 (4), p.387-389

2009

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Mutations in a P-type ATPase gene cause axonal degeneration

PLoS genetics, 2012-08, Vol.8 (8), p.e1002853-e1002853

2012

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Axon retraction and degeneration in development and disease

Annual review of neuroscience, 2005-01, Vol.28 (1), p.127-156

2005

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Toll-Like Receptor Signaling Is Critical for Wallerian Degeneration and Functional Recovery after Peripheral Nerve Injury

The Journal of neuroscience, 2007-11, Vol.27 (46), p.12565-12576

2007

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Spatiotemporal ablation of myelinating glia-specific neurofascin (NfascNF155) in mice reveals gradual loss of paranodal axoglial junctions and concomitant disorganization of axonal domains

Journal of neuroscience research, 2009-06, Vol.87 (8), p.1773-1793

2009

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Wallerian degeneration: an emerging axon death pathway linking injury and disease

NMN Deamidase Delays Wallerian Degeneration and Rescues Axonal Defects Caused by NMNAT2 Deficiency In Vivo

Wallerian degeneration, wld(s), and nmnat

A caspase cascade regulating developmental axon degeneration

Homozygous NMNAT2 mutation in sisters with polyneuropathy and erythromelalgia

A role for motoneuron subtype-selective ER stress in disease manifestations of FALS mice

Transcription factor Pebbled/RREB1 regulates injury-induced axon degeneration

Autophagic myelin destruction by schwann cells during wallerian degeneration and segmental demyelination

Diagnosis, natural history, and management of Charcot–Marie–Tooth disease

The Ubiquitin Proteasome System in Synaptic and Axonal Degeneration: A New Twist to an Old Cycle

Axon degeneration mechanisms: commonality amid diversity

Severe biallelic loss-of-function mutations in nicotinamide mononucleotide adenylyltransferase 2 (NMNAT2) in two fetuses with fetal akinesia deformation sequence

Cisplatin induced neurotoxicity is mediated by Sarm1 and calpain activation

Axon Death Pathways Converge on Axundead to Promote Functional and Structural Axon Disassembly

Death Receptor 6 Promotes Wallerian Degeneration in Peripheral Axons

Complementation between Mouse Mfn1 and Mfn2 Protects Mitochondrial Fusion Defects Caused by CMT2A Disease Mutations

Expression of beta-amyloid induced age-dependent presynaptic and axonal changes in Drosophila

Mislocalization of neuronal mitochondria reveals regulation of Wallerian degeneration and NMNAT/WLD(S)-mediated axon protection independent of axonal mitochondria

Signaling mechanisms regulating Wallerian degeneration

A Local Mechanism Mediates NAD-Dependent Protection of Axon Degeneration

A dual leucine kinase-dependent axon self-destruction program promotes Wallerian degeneration

Mutations in a P-type ATPase gene cause axonal degeneration

Axon retraction and degeneration in development and disease

Toll-Like Receptor Signaling Is Critical for Wallerian Degeneration and Functional Recovery after Peripheral Nerve Injury

Spatiotemporal ablation of myelinating glia-specific neurofascin (NfascNF155) in mice reveals gradual loss of paranodal axoglial junctions and concomitant disorganization of axonal domains

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