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Adeno-associated virus-delivered artificial microRNA extends survival and delays paralysis in an amyotrophic lateral sclerosis mouse model

Annals of neurology, 2016-04, Vol.79 (4), p.687-700

2016

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Dysferlin overexpression in skeletal muscle produces a progressive myopathy

Annals of neurology, 2010-03, Vol.67 (3), p.384-393

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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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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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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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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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

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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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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

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Tetanus toxin C fragment-conjugated nanoparticles for targeted drug delivery to neurons

Biomaterials, 2007-12, Vol.28 (34), p.5176-5184

2007

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Overexpression of the Wild-Type SPT1 Subunit Lowers Desoxysphingolipid Levels and Rescues the Phenotype of HSAN1

The Journal of neuroscience, 2009-11, Vol.29 (46), p.14646-14651

2009

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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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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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Familial Amyotrophic Lateral Sclerosis-associated Mutations Decrease the Thermal Stability of Distinctly Metallated Species of Human Copper/Zinc Superoxide Dismutase

The Journal of biological chemistry, 2002-05, Vol.277 (18), p.15932-15937

2002

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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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Prophylactic Creatine Administration Mediates Neuroprotection in Cerebral Ischemia in Mice

The Journal of neuroscience, 2004-06, Vol.24 (26), p.5909-5912

2004

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Adeno-associated virus-delivered artificial microRNA extends survival and delays paralysis in an amyotrophic lateral sclerosis mouse model

Dysferlin overexpression in skeletal muscle produces a progressive myopathy

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

Axonal Transport Defects in Neurodegenerative Diseases

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

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

Two approaches to drug discovery in SOD1-mediated ALS

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

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

Tetanus toxin C fragment-conjugated nanoparticles for targeted drug delivery to neurons

Overexpression of the Wild-Type SPT1 Subunit Lowers Desoxysphingolipid Levels and Rescues the Phenotype of HSAN1

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

Caspase-3 Cleaves and Inactivates the Glutamate Transporter EAAT2

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

Familial Amyotrophic Lateral Sclerosis-associated Mutations Decrease the Thermal Stability of Distinctly Metallated Species of Human Copper/Zinc Superoxide Dismutase

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

Prophylactic Creatine Administration Mediates Neuroprotection in Cerebral Ischemia in Mice

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