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Loss of function of C9orf72 causes motor deficits in a zebrafish model of amyotrophic lateral sclerosis

Annals of neurology, 2013-08, Vol.74 (2), p.180-187

2013

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Functional characterization of a FUS mutant zebrafish line as a novel genetic model for ALS

Neurobiology of disease, 2020-08, Vol.142, p.104935-104935, Article 104935

2020

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FUS and TARDBP but not SOD1 interact in genetic models of amyotrophic lateral sclerosis

PLoS genetics, 2011-08, Vol.7 (8), p.e1002214

2011

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Overexpression of Toxic Poly(Glycine-Alanine) Aggregates in Primary Neuronal Cultures Induces Time-Dependent Autophagic and Synaptic Alterations but Subtle Activity Impairments

Cells (Basel, Switzerland), 2024-08, Vol.13 (15), p.1300

2024

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Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo

Human molecular genetics, 2010-02, Vol.19 (4), p.671-683

2010

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The most prevalent genetic cause of ALS-FTD, C9orf72 synergizes the toxicity of ATXN2 intermediate polyglutamine repeats through the autophagy pathway

Autophagy, 2016-08, Vol.12 (8), p.1406-1408

2016

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Transcriptomic Analysis of Zebrafish TDP-43 Transgenic Lines

Frontiers in molecular neuroscience, 2018-12, Vol.11, p.463-463

2018

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Pharmacological reduction of ER stress protects against TDP-43 neuronal toxicity in vivo

Neurobiology of disease, 2013-07, Vol.55, p.64-75

2013

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Deep phenotyping unstructured data mining in an extensive pediatric database to unravel a common KCNA2 variant in neurodevelopmental syndromes

Genetics in medicine, 2021-05, Vol.23 (5), p.968-971

2021

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Integrative genetic analysis illuminates ALS heritability and identifies risk genes

Nature communications, 2023-01, Vol.14 (1), p.342-342, Article 342

2023

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Diagnostic Challenge and Neuromuscular Junction Contribution to ALS Pathogenesis

Frontiers in neurology, 2019, Vol.10, p.68-68

2019

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Loss of Function of Glucocerebrosidase GBA2 Is Responsible for Motor Neuron Defects in Hereditary Spastic Paraplegia

American journal of human genetics, 2013-02, Vol.92 (2), p.238-244

2013

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Heterozygous knockout of Synaptotagmin13 phenocopies ALS features and TP53 activation in human motor neurons

Cell death & disease, 2024-08, Vol.15 (8), p.560-12, Article 560

2024

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In the swim of things: recent insights to neurogenetic disorders from zebrafish

Trends in genetics, 2010-08, Vol.26 (8), p.373-381

2010

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Methylene blue protects against TDP-43 and FUS neuronal toxicity in C. elegans and D. rerio

PloS one, 2012-07, Vol.7 (7), p.e42117

2012

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Oxidized/misfolded superoxide dismutase-1: the cause of all amyotrophic lateral sclerosis?

Annals of neurology, 2007-12, Vol.62 (6), p.553-559

2007

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Synaptic disruption and CREB‐regulated transcription are restored by K+ channel blockers in ALS

EMBO molecular medicine, 2021-07, Vol.13 (7), p.e13131-n/a

2021

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Author Correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes

Nature communications, 2023-12, Vol.14 (1), p.8026-8026, Article 8026

2023

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TDP-43 Regulation of AChE Expression Can Mediate ALS-Like Phenotype in Zebrafish

Cells (Basel, Switzerland), 2021-01, Vol.10 (2), p.221

2021

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Investigating the contribution of VAPB/ALS8 loss of function in amyotrophic lateral sclerosis

Human molecular genetics, 2013-06, Vol.22 (12), p.2350-2360

2013

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Microglia Mitigate Neuronal Activation in a Zebrafish Model of Dravet Syndrome

Cells (Basel, Switzerland), 2024-04, Vol.13 (8), p.684

2024

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Neuromuscular Junction Impairment in Amyotrophic Lateral Sclerosis: Reassessing the Role of Acetylcholinesterase

Frontiers in molecular neuroscience, 2016-12, Vol.9, p.160-160

2016

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Failure of protein quality control in amyotrophic lateral sclerosis

Biochimica et biophysica acta, 2006-11, Vol.1762 (11), p.1038-1050

2006

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Neuroleptics as therapeutic compounds stabilizing neuromuscular transmission in amyotrophic lateral sclerosis

JCI insight, 2017-11, Vol.2 (22)

2017

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Fishing for causes and cures of motor neuron disorders

Disease models & mechanisms, 2014-07, Vol.7 (7), p.799-809

2014

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Loss of function of C9orf72 causes motor deficits in a zebrafish model of amyotrophic lateral sclerosis

Functional characterization of a FUS mutant zebrafish line as a novel genetic model for ALS

FUS and TARDBP but not SOD1 interact in genetic models of amyotrophic lateral sclerosis

Overexpression of Toxic Poly(Glycine-Alanine) Aggregates in Primary Neuronal Cultures Induces Time-Dependent Autophagic and Synaptic Alterations but Subtle Activity Impairments

Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo

The most prevalent genetic cause of ALS-FTD, C9orf72 synergizes the toxicity of ATXN2 intermediate polyglutamine repeats through the autophagy pathway

Transcriptomic Analysis of Zebrafish TDP-43 Transgenic Lines

Pharmacological reduction of ER stress protects against TDP-43 neuronal toxicity in vivo

Deep phenotyping unstructured data mining in an extensive pediatric database to unravel a common KCNA2 variant in neurodevelopmental syndromes

Integrative genetic analysis illuminates ALS heritability and identifies risk genes

Diagnostic Challenge and Neuromuscular Junction Contribution to ALS Pathogenesis

Loss of Function of Glucocerebrosidase GBA2 Is Responsible for Motor Neuron Defects in Hereditary Spastic Paraplegia

Heterozygous knockout of Synaptotagmin13 phenocopies ALS features and TP53 activation in human motor neurons

In the swim of things: recent insights to neurogenetic disorders from zebrafish

Methylene blue protects against TDP-43 and FUS neuronal toxicity in C. elegans and D. rerio

Oxidized/misfolded superoxide dismutase-1: the cause of all amyotrophic lateral sclerosis?

Synaptic disruption and CREB‐regulated transcription are restored by K+ channel blockers in ALS

Author Correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes

TDP-43 Regulation of AChE Expression Can Mediate ALS-Like Phenotype in Zebrafish

Investigating the contribution of VAPB/ALS8 loss of function in amyotrophic lateral sclerosis

Microglia Mitigate Neuronal Activation in a Zebrafish Model of Dravet Syndrome

Neuromuscular Junction Impairment in Amyotrophic Lateral Sclerosis: Reassessing the Role of Acetylcholinesterase

Failure of protein quality control in amyotrophic lateral sclerosis

Neuroleptics as therapeutic compounds stabilizing neuromuscular transmission in amyotrophic lateral sclerosis

Fishing for causes and cures of motor neuron disorders

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