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T lymphocytes potentiate endogenous neuroprotective inflammation in a mouse model of ALS

Proceedings of the National Academy of Sciences - PNAS, 2008-11, Vol.105 (46), p.17913-17918

2008

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Decoding ALS: from genes to mechanism

Nature (London), 2016-11, Vol.539 (7628), p.197-206

2016

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Extensive FUS-Immunoreactive Pathology in Juvenile Amyotrophic Lateral Sclerosis with Basophilic Inclusions

Brain pathology (Zurich, Switzerland), 2010-11, Vol.20 (6), p.1069-1076

2010

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Emerging mechanisms of molecular pathology in ALS

The Journal of clinical investigation, 2015-05, Vol.125 (5), p.1767-1779

2015

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Intrinsic membrane hyperexcitability of amyotrophic lateral sclerosis patient-derived motor neurons

Cell reports (Cambridge), 2014-04, Vol.7 (1), p.1-11

2014

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Wild-type and mutant SOD1 share an aberrant conformation and a common pathogenic pathway in ALS

Nature neuroscience, 2010-11, Vol.13 (11), p.1396-1403

2010

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EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humans

Nature medicine, 2012-09, Vol.18 (9), p.1418-1422

2012

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Axonal Transport Defects in Neurodegenerative Diseases

The Journal of neuroscience, 2009-10, Vol.29 (41), p.12776-12786

2009

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Hereditary Sensory Neuropathy Type 1 Is Caused by the Accumulation of Two Neurotoxic Sphingolipids

The Journal of biological chemistry, 2010-04, Vol.285 (15), p.11178-11187

2010

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Partial loss of TDP-43 function causes phenotypes of amyotrophic lateral sclerosis

Proceedings of the National Academy of Sciences - PNAS, 2014-03, Vol.111 (12), p.4362-4362

2014

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A yeast model of FUS/TLS-dependent cytotoxicity

PLoS biology, 2011-04, Vol.9 (4), p.e1001052-e1001052

2011

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Repeated mild traumatic brain injury triggers pathology in asymptomatic C9ORF72 transgenic mice

Brain (London, England : 1878), 2023-12, Vol.146 (12), p.5139-5152

2023

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Identification of Small Subunits of Mammalian Serine Palmitoyltransferase That Confer Distinct Acyl-CoA Substrate Specificities

Proceedings of the National Academy of Sciences - PNAS, 2009-05, Vol.106 (20), p.8186-8191

2009

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ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis

Nature genetics, 2006-04, Vol.38 (4), p.411-413

2006

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Two approaches to drug discovery in SOD1-mediated ALS

Journal of biomolecular screening, 2006-10, Vol.11 (7), p.729-735

2006

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Anti-SOD1 Nanobodies That Stabilize Misfolded SOD1 Proteins Also Promote Neurite Outgrowth in Mutant SOD1 Human Neurons

International journal of molecular sciences, 2022-12, Vol.23 (24), p.16013

2022

Volltextzugriff (PDF)

ATF3 expression improves motor function in the ALS mouse model by promoting motor neuron survival and retaining muscle innervation

Proceedings of the National Academy of Sciences - PNAS, 2014-01, Vol.111 (4), p.1622-1627

2014

Volltextzugriff (PDF)

The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder

European journal of human genetics : EJHG, 2013-01, Vol.21 (1), p.102-108

2013

Volltextzugriff (PDF)

Natural history and biomarkers in hereditary sensory neuropathy type 1

Muscle & nerve, 2015-04, Vol.51 (4), p.489-495

2015

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Genetic ablation of Sarm1 attenuates expression and mislocalization of phosphorylated TDP-43 after mouse repetitive traumatic brain injury

Acta neuropathologica communications, 2023-12, Vol.11 (1), p.206-16, Article 206

2023

Volltextzugriff (PDF)

Evaluating protein cross-linking as a therapeutic strategy to stabilize SOD1 variants in a mouse model of familial ALS

PLoS biology, 2024-01, Vol.22 (1), p.e3002462-e3002462, Article e3002462

2024

Volltextzugriff (PDF)

Dysferlin Interacts with Annexins A1 and A2 and Mediates Sarcolemmal Wound-healing

The Journal of biological chemistry, 2003-12, Vol.278 (50), p.50466-50473

2003

Volltextzugriff (PDF)

Rescue of GM3 synthase deficiency by spatially controlled, rAAV-mediated ST3GAL5 delivery

JCI insight, 2023-05, Vol.8 (9)

2023

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T lymphocytes potentiate endogenous neuroprotective inflammation in a mouse model of ALS

Decoding ALS: from genes to mechanism

Extensive FUS-Immunoreactive Pathology in Juvenile Amyotrophic Lateral Sclerosis with Basophilic Inclusions

Emerging mechanisms of molecular pathology in ALS

Intrinsic membrane hyperexcitability of amyotrophic lateral sclerosis patient-derived motor neurons

Wild-type and mutant SOD1 share an aberrant conformation and a common pathogenic pathway in ALS

EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humans

Axonal Transport Defects in Neurodegenerative Diseases

Hereditary Sensory Neuropathy Type 1 Is Caused by the Accumulation of Two Neurotoxic Sphingolipids

Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis

Partial loss of TDP-43 function causes phenotypes of amyotrophic lateral sclerosis

A yeast model of FUS/TLS-dependent cytotoxicity

Repeated mild traumatic brain injury triggers pathology in asymptomatic C9ORF72 transgenic mice

Debamestrocel multimodal effects on biomarker pathways in amyotrophic lateral sclerosis are linked to clinical outcomes

Identification of Small Subunits of Mammalian Serine Palmitoyltransferase That Confer Distinct Acyl-CoA Substrate Specificities

ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis

Two approaches to drug discovery in SOD1-mediated ALS

Anti-SOD1 Nanobodies That Stabilize Misfolded SOD1 Proteins Also Promote Neurite Outgrowth in Mutant SOD1 Human Neurons

ATF3 expression improves motor function in the ALS mouse model by promoting motor neuron survival and retaining muscle innervation

The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder

Natural history and biomarkers in hereditary sensory neuropathy type 1

Genetic ablation of Sarm1 attenuates expression and mislocalization of phosphorylated TDP-43 after mouse repetitive traumatic brain injury

Evaluating protein cross-linking as a therapeutic strategy to stabilize SOD1 variants in a mouse model of familial ALS

Dysferlin Interacts with Annexins A1 and A2 and Mediates Sarcolemmal Wound-healing

Rescue of GM3 synthase deficiency by spatially controlled, rAAV-mediated ST3GAL5 delivery

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