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New insights on schwann cell development

Glia, 2015-08, Vol.63 (8), p.1376-1393

2015

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The Adhesion GPCR GPR126 Has Distinct, Domain-Dependent Functions in Schwann Cell Development Mediated by Interaction with Laminin-211

Neuron (Cambridge, Mass.), 2015-02, Vol.85 (4), p.755-769

2015

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Brainstem development requires galactosylceramidase and is critical for pathogenesis in a model of Krabbe disease

Nature communications, 2020-10, Vol.11 (1), p.5356-5356, Article 5356

2020

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How Schwann Cells Sort Axons: New Concepts

The Neuroscientist, 2016-06, Vol.22 (3), p.252-265

2016

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Neuron-specific ablation of the Krabbe disease gene galactosylceramidase in mice results in neurodegeneration

PLoS biology, 2022-07, Vol.20 (7), p.e3001661-e3001661

2022

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Resetting translational homeostasis restores myelination in Charcot-Marie-Tooth disease type 1B mice

The Journal of experimental medicine, 2013-04, Vol.210 (4), p.821-838

2013

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Prohibitin 1 is essential to preserve mitochondria and myelin integrity in Schwann cells

Nature communications, 2021-06, Vol.12 (1), p.3285-3285, Article 3285

2021

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Activation of mTORC1 and c-Jun by Prohibitin1 loss in Schwann cells may link mitochondrial dysfunction to demyelination

eLife, 2021-09, Vol.10

2021

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Age-related neurodegeneration and cognitive impairments of NRMT1 knockout mice are preceded by misregulation of RB and abnormal neural stem cell development

Cell death & disease, 2021-10, Vol.12 (11), p.1014-1014, Article 1014

2021

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Tead1 regulates the expression of Peripheral Myelin Protein 22 during Schwann cell development

Human molecular genetics, 2016-07, Vol.25 (14), p.3055-3069

2016

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Curcumin derivatives promote Schwann cell differentiation and improve neuropathy in R98C CMT1B mice

Brain (London, England : 1878), 2012-12, Vol.135 (12), p.3551-3566

2012

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c-Jun is a negative regulator of myelination

The Journal of cell biology, 2008-05, Vol.181 (4), p.625-637

2008

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Rac1 and Rac3 have opposite functions in Schwann cells during developmental myelination

Neuroscience letters, 2021-05, Vol.753, p.135868-135868, Article 135868

2021

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Enhanced axonal neuregulin-1 type-III signaling ameliorates neurophysiology and hypomyelination in a Charcot–Marie–Tooth type 1B mouse model

Human molecular genetics, 2019-03, Vol.28 (6), p.992-1006

2019

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The Gdap1 knockout mouse mechanistically links redox control to Charcot-Marie-Tooth disease

Brain (London, England : 1878), 2014-03, Vol.137 (Pt 3), p.668-682

2014

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Macrophages Expressing GALC Improve Peripheral Krabbe Disease by a Mechanism Independent of Cross-Correction

Neuron (Cambridge, Mass.), 2020-07, Vol.107 (1), p.65-81.e9

2020

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A nonsense mutation in myelin protein zero causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal function

Human molecular genetics, 2019-01, Vol.28 (1), p.124-132

2019

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Impairment of protein degradation and proteasome function in hereditary neuropathies

Glia, 2018-02, Vol.66 (2), p.379-395

2018

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GPR56/ADGRG1 regulates development and maintenance of peripheral myelin

The Journal of experimental medicine, 2018-03, Vol.215 (3), p.941-961

2018

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Schwann cells ER-associated degradation contributes to myelin maintenance in adult nerves and limits demyelination in CMT1B mice

PLoS genetics, 2019-04, Vol.15 (4), p.e1008069-e1008069

2019

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Notch controls embryonic Schwann cell differentiation, postnatal myelination and adult plasticity

Nature neuroscience, 2009-07, Vol.12 (7), p.839-847

2009

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Ablation of Perk in Schwann Cells Improves Myelination in the S63del Charcot-Marie-Tooth 1B Mouse

The Journal of neuroscience, 2016-11, Vol.36 (44), p.11350-11361

2016

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Ablation of the UPR-Mediator CHOP Restores Motor Function and Reduces Demyelination in Charcot-Marie-Tooth 1B Mice

Neuron (Cambridge, Mass.), 2008-02, Vol.57 (3), p.393-405

2008

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Schwann cells expressing dismutase active mutant SOD1 unexpectedly slow disease progression in ALS mice

Proceedings of the National Academy of Sciences - PNAS, 2009-03, Vol.106 (11), p.4465-4470

2009

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YAP and TAZ Regulate Cc2d1b and Purβ in Schwann Cells

Frontiers in molecular neuroscience, 2019-07, Vol.12, p.177-177

2019

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New insights on schwann cell development

The Adhesion GPCR GPR126 Has Distinct, Domain-Dependent Functions in Schwann Cell Development Mediated by Interaction with Laminin-211

Brainstem development requires galactosylceramidase and is critical for pathogenesis in a model of Krabbe disease

How Schwann Cells Sort Axons: New Concepts

Neuron-specific ablation of the Krabbe disease gene galactosylceramidase in mice results in neurodegeneration

Resetting translational homeostasis restores myelination in Charcot-Marie-Tooth disease type 1B mice

Prohibitin 1 is essential to preserve mitochondria and myelin integrity in Schwann cells

Activation of mTORC1 and c-Jun by Prohibitin1 loss in Schwann cells may link mitochondrial dysfunction to demyelination

Age-related neurodegeneration and cognitive impairments of NRMT1 knockout mice are preceded by misregulation of RB and abnormal neural stem cell development

Tead1 regulates the expression of Peripheral Myelin Protein 22 during Schwann cell development

Curcumin derivatives promote Schwann cell differentiation and improve neuropathy in R98C CMT1B mice

c-Jun is a negative regulator of myelination

Rac1 and Rac3 have opposite functions in Schwann cells during developmental myelination

Enhanced axonal neuregulin-1 type-III signaling ameliorates neurophysiology and hypomyelination in a Charcot–Marie–Tooth type 1B mouse model

The Gdap1 knockout mouse mechanistically links redox control to Charcot-Marie-Tooth disease

Macrophages Expressing GALC Improve Peripheral Krabbe Disease by a Mechanism Independent of Cross-Correction

A nonsense mutation in myelin protein zero causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal function

Impairment of protein degradation and proteasome function in hereditary neuropathies

GPR56/ADGRG1 regulates development and maintenance of peripheral myelin

Schwann cells ER-associated degradation contributes to myelin maintenance in adult nerves and limits demyelination in CMT1B mice

Notch controls embryonic Schwann cell differentiation, postnatal myelination and adult plasticity

Ablation of Perk in Schwann Cells Improves Myelination in the S63del Charcot-Marie-Tooth 1B Mouse

Ablation of the UPR-Mediator CHOP Restores Motor Function and Reduces Demyelination in Charcot-Marie-Tooth 1B Mice

Schwann cells expressing dismutase active mutant SOD1 unexpectedly slow disease progression in ALS mice

YAP and TAZ Regulate Cc2d1b and Purβ in Schwann Cells

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