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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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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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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

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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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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

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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

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Identification of selective and non-selective C9ORF72 targeting in vivo active siRNAs

Molecular therapy. Nucleic acids, 2024-09, Vol.35 (3), p.102291, Article 102291

2024

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

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

2023

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Intralingual and Intrapleural AAV Gene Therapy Prolongs Survival in a SOD1 ALS Mouse Model

Molecular therapy. Methods & clinical development, 2020-06, Vol.17, p.246-257

2020

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Caspase-3 Cleaves and Inactivates the Glutamate Transporter EAAT2

The Journal of biological chemistry, 2006-05, Vol.281 (20), p.14076-14084

2006

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Mutations in neurofilament genes are not a significant primary cause of non-SOD1-mediated amyotrophic lateral sclerosis

Neurobiology of disease, 2006, Vol.21 (1), p.102-109

2006

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Decreased Metallation and Activity in Subsets of Mutant Superoxide Dismutases Associated with Familial Amyotrophic Lateral Sclerosis

The Journal of biological chemistry, 2002-05, Vol.277 (18), p.15923-15931

2002

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International engagement by United States academic neurology departments: A national survey

Annals of neurology, 2015-07, Vol.78 (1), p.150-152

2015

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A Caspase-3-cleaved Fragment of the Glial Glutamate Transporter EAAT2 Is Sumoylated and Targeted to Promyelocytic Leukemia Nuclear Bodies in Mutant SOD1-linked Amyotrophic Lateral Sclerosis

The Journal of biological chemistry, 2007-11, Vol.282 (44), p.32480-32490

2007

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Introduction to a special edition of Annals: Therapeutic prospects

Annals of neurology, 2013-09, Vol.74 (3), p.A15-A16

2013

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Serum ferritin and metal levels as risk factors for amyotrophic lateral sclerosis

The open neurology journal, 2008-09, Vol.2 (1), p.51-54

2008

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Genetics of Amyotrophic Lateral Sclerosis

Cold Spring Harbor perspectives in medicine, 2018-05, Vol.8 (5), p.a024125

2018

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Motor unit number estimation predicts disease onset and survival in a transgenic mouse model of amyotrophic lateral sclerosis

Muscle & nerve, 2006-11, Vol.34 (5), p.603-607

2006

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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

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

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

Natural history and biomarkers in hereditary sensory neuropathy type 1

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

Identification of selective and non-selective C9ORF72 targeting in vivo active siRNAs

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

Intralingual and Intrapleural AAV Gene Therapy Prolongs Survival in a SOD1 ALS Mouse Model

Caspase-3 Cleaves and Inactivates the Glutamate Transporter EAAT2

Mutations in neurofilament genes are not a significant primary cause of non-SOD1-mediated amyotrophic lateral sclerosis

Decreased Metallation and Activity in Subsets of Mutant Superoxide Dismutases Associated with Familial Amyotrophic Lateral Sclerosis

International engagement by United States academic neurology departments: A national survey

A Caspase-3-cleaved Fragment of the Glial Glutamate Transporter EAAT2 Is Sumoylated and Targeted to Promyelocytic Leukemia Nuclear Bodies in Mutant SOD1-linked Amyotrophic Lateral Sclerosis

Introduction to a special edition of Annals: Therapeutic prospects

No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis

Serum ferritin and metal levels as risk factors for amyotrophic lateral sclerosis

Genetics of Amyotrophic Lateral Sclerosis

Motor unit number estimation predicts disease onset and survival in a transgenic mouse model of amyotrophic lateral sclerosis

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