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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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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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Association of UBQLN1 mutation with Brown–Vialetto–Van Laere syndrome but not typical ALS

Neurobiology of disease, 2012-12, Vol.48 (3), p.391-398

2012

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Identification of Two Novel Loci for Dominantly Inherited Familial Amyotrophic Lateral Sclerosis

American journal of human genetics, 2003-08, Vol.73 (2), p.397-403

2003

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Human C9ORF72 Hexanucleotide Expansion Reproduces RNA Foci and Dipeptide Repeat Proteins but Not Neurodegeneration in BAC Transgenic Mice

Neuron (Cambridge, Mass.), 2015-12, Vol.88 (5), p.902-909

2015

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A Novel Locus for Familial Amyotrophic Lateral Sclerosis, on Chromosome 18q

American journal of human genetics, 2002-01, Vol.70 (1), p.251-256

2002

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Increased affinity for copper mediated by cysteine 111 in forms of mutant superoxide dismutase 1 linked to amyotrophic lateral sclerosis

Free radical biology & medicine, 2007-05, Vol.42 (10), p.1534-1542

2007

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Silencing strategies for therapy of SOD1-mediated ALS

Neuroscience letters, 2017-01, Vol.636, p.32-39

2017

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Age-Dependent TDP-43-Mediated Motor Neuron Degeneration Requires GSK3, hat-trick, and xmas-2

Current biology, 2015-08, Vol.25 (16), p.2130-2136

2015

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AAV-Mediated Gene Therapy for Glycosphingolipid Biosynthesis Deficiencies

Trends in molecular medicine, 2021-06, Vol.27 (6), p.520-523

2021

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Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS

Neuron (Cambridge, Mass.), 2014-10, Vol.84 (2), p.324-331

2014

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Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

Neuron (Cambridge, Mass.), 2021-02, Vol.109 (3), p.448-460.e4

2021

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Mutations in Potassium Channel Kir2.6 Cause Susceptibility to Thyrotoxic Hypokalemic Periodic Paralysis

Cell, 2010-01, Vol.140 (1), p.88-98

2010

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Amyotrophic Lateral Sclerosis-Associated SOD1 Mutant Proteins Bind and Aggregate with Bcl-2 in Spinal Cord Mitochondria

Neuron (Cambridge, Mass.), 2004-07, Vol.43 (1), p.19-30

2004

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Novel mutations support a role for Profilin 1 in the pathogenesis of ALS

Neurobiology of aging, 2015-03, Vol.36 (3), p.1602.e17-1602.e27

2015

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Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study

Lancet neurology, 2010-10, Vol.9 (10), p.986-994

2010

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Mutations in the N-terminal Actin-Binding Domain of Filamin C Cause a Distal Myopathy

American journal of human genetics, 2011-06, Vol.88 (6), p.729-740

2011

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RNA metabolism and the pathogenesis of motor neuron diseases

Trends in neurosciences (Regular ed.), 2010-05, Vol.33 (5), p.249-258

2010

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Defective daily temperature regulation in a mouse model of amyotrophic lateral sclerosis

Experimental neurology, 2019-01, Vol.311, p.305-312

2019

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VEGF increases blood–brain barrier permeability to Evans blue dye and tetanus toxin fragment C but not adeno-associated virus in ALS mice

Brain research, 2008-10, Vol.1234, p.198-205

2008

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Mutational analysis of TARDBP in neurodegenerative diseases

Neurobiology of aging, 2011-11, Vol.32 (11), p.2096-2099

2011

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Genetic ablation of phospholipase C delta 1 increases survival in SOD1(G93A) mice

Neurobiology of disease, 2013-12, Vol.60, p.11-17

2013

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Dysferlinopathies

Handbook of Clinical Neurology, 2011, Vol.101, p.111-118

2011

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Genetic ablation of phospholipase C delta 1 increases survival in SOD1G93A mice

Neurobiology of disease, 2013-12, Vol.60, p.11-17

2013

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

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

Association of UBQLN1 mutation with Brown–Vialetto–Van Laere syndrome but not typical ALS

Identification of Two Novel Loci for Dominantly Inherited Familial Amyotrophic Lateral Sclerosis

Human C9ORF72 Hexanucleotide Expansion Reproduces RNA Foci and Dipeptide Repeat Proteins but Not Neurodegeneration in BAC Transgenic Mice

A Novel Locus for Familial Amyotrophic Lateral Sclerosis, on Chromosome 18q

Increased affinity for copper mediated by cysteine 111 in forms of mutant superoxide dismutase 1 linked to amyotrophic lateral sclerosis

Silencing strategies for therapy of SOD1-mediated ALS

Age-Dependent TDP-43-Mediated Motor Neuron Degeneration Requires GSK3, hat-trick, and xmas-2

AAV-Mediated Gene Therapy for Glycosphingolipid Biosynthesis Deficiencies

Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS

Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

Mutations in Potassium Channel Kir2.6 Cause Susceptibility to Thyrotoxic Hypokalemic Periodic Paralysis

ERBB4 Mutations that Disrupt the Neuregulin-ErbB4 Pathway Cause Amyotrophic Lateral Sclerosis Type 19

Amyotrophic Lateral Sclerosis-Associated SOD1 Mutant Proteins Bind and Aggregate with Bcl-2 in Spinal Cord Mitochondria

Novel mutations support a role for Profilin 1 in the pathogenesis of ALS

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study

Mutations in the N-terminal Actin-Binding Domain of Filamin C Cause a Distal Myopathy

RNA metabolism and the pathogenesis of motor neuron diseases

Defective daily temperature regulation in a mouse model of amyotrophic lateral sclerosis

VEGF increases blood–brain barrier permeability to Evans blue dye and tetanus toxin fragment C but not adeno-associated virus in ALS mice

Mutational analysis of TARDBP in neurodegenerative diseases

Genetic ablation of phospholipase C delta 1 increases survival in SOD1(G93A) mice

Dysferlinopathies

Genetic ablation of phospholipase C delta 1 increases survival in SOD1G93A mice

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