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Nicotinamide-N-methyltransferase controls behavior, neurodegeneration and lifespan by regulating neuronal autophagy

PLoS genetics, 2018-09, Vol.14 (9), p.e1007561

2018

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Deletion of C9ORF72 results in motor neuron degeneration and stress sensitivity in C. elegans

PloS one, 2013-12, Vol.8 (12), p.e83450

2013

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Heritable transmission of stress resistance by high dietary glucose in Caenorhabditis elegans

PLoS genetics, 2014-05, Vol.10 (5), p.e1004346-e1004346

2014

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Pleiotropic Effects of mTOR and Autophagy During Development and Aging

Frontiers in cell and developmental biology, 2019-09, Vol.7, p.192-192

2019

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G3BP1 promotes stress-induced RNA granule interactions to preserve polyadenylated mRNA

The Journal of cell biology, 2015-04, Vol.209 (1), p.73-84

2015

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Phosphoglycolate phosphatase homologs act as glycerol-3-phosphate phosphatase to control stress and healthspan in C. elegans

Nature communications, 2022-01, Vol.13 (1), p.177-177, Article 177

2022

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Small Molecule Rescue of ATXN3 Toxicity in C. elegans via TFEB/HLH-30

Neurotherapeutics, 2021-04, Vol.18 (2), p.1151-1165

2021

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AMPK activation protects from neuronal dysfunction and vulnerability across nematode, cellular and mouse models of Huntington's disease

Human molecular genetics, 2016-03, Vol.25 (6), p.1043-1058

2016

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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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Worming forward: amyotrophic lateral sclerosis toxicity mechanisms and genetic interactions in Caenorhabditis elegans

Frontiers in genetics, 2014-04, Vol.5, p.85-85

2014

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Mutant TDP-43 and FUS cause age-dependent paralysis and neurodegeneration in C. elegans

PloS one, 2012-02, Vol.7 (2), p.e31321-e31321

2012

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The Novel Small Molecule TRVA242 Stabilizes Neuromuscular Junction Defects in Multiple Animal Models of Amyotrophic Lateral Sclerosis

Neurotherapeutics, 2019-10, Vol.16 (4), p.1149-1166

2019

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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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Fatty acids derived from the probiotic Lacticaseibacillus rhamnosus HA-114 suppress age-dependent neurodegeneration

Communications biology, 2022-12, Vol.5 (1), p.1340-1340, Article 1340

2022

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Maple Syrup Decreases TDP-43 Proteotoxicity in a Caenorhabditis elegans Model of Amyotrophic Lateral Sclerosis (ALS)

Journal of agricultural and food chemistry, 2016-05, Vol.64 (17), p.3338-3344

2016

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Modulating the endoplasmic reticulum stress response attenuates neurodegeneration in a Caenorhabditis elegans model of spinal muscular atrophy

Disease models & mechanisms, 2020-12, Vol.13 (12)

2020

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Rescue of ATXN3 neuronal toxicity in Caenorhabditis elegans by chemical modification of endoplasmic reticulum stress

Disease models & mechanisms, 2017-12, Vol.10 (12), p.1465-1480

2017

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The stress response factor daf-16/FOXO is required for multiple compound families to prolong the function of neurons with Huntington’s disease

Scientific reports, 2017-06, Vol.7 (1), p.4014-15, Article 4014

2017

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Stress-induced propagation of neurodegeneration by wild-type proteins in simple models of ALS

M.S. Médecine sciences, 2013-04, Vol.29 (4), p.343

2013

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Tau hyperphosphorylation and deregulation of calcineurin in mouse models of Huntington's disease

Human molecular genetics, 2015-01, Vol.24 (1), p.86-99

2015

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TDP-1/TDP-43 regulates stress signaling and age-dependent proteotoxicity in Caenorhabditis elegans

PLoS genetics, 2012-07, Vol.8 (7), p.e1002806

2012

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Restless legs syndrome-associated MEIS1 risk variant influences iron homeostasis

Annals of neurology, 2011-07, Vol.70 (1), p.170-175

2011

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Correction to: The Novel Small Molecule TRVA242 Stabilizes Neuromuscular Junction Defects in Multiple Animal Models of Amyotrophic Lateral Sclerosis

Neurotherapeutics, 2021-07, Vol.18 (3), p.2128-2128

2021

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Integration of β-catenin, sirtuin, and FOXO signaling protects from mutant huntingtin toxicity

The Journal of neuroscience, 2012-09, Vol.32 (36), p.12630-12640

2012

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Cystamine and cysteamine increase brain levels of BDNF in Huntington disease via HSJ1b and transglutaminase

The Journal of clinical investigation, 2006-05, Vol.116 (5), p.1410-1424

2006

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Nicotinamide-N-methyltransferase controls behavior, neurodegeneration and lifespan by regulating neuronal autophagy

Deletion of C9ORF72 results in motor neuron degeneration and stress sensitivity in C. elegans

Heritable transmission of stress resistance by high dietary glucose in Caenorhabditis elegans

Pleiotropic Effects of mTOR and Autophagy During Development and Aging

G3BP1 promotes stress-induced RNA granule interactions to preserve polyadenylated mRNA

Phosphoglycolate phosphatase homologs act as glycerol-3-phosphate phosphatase to control stress and healthspan in C. elegans

Small Molecule Rescue of ATXN3 Toxicity in C. elegans via TFEB/HLH-30

AMPK activation protects from neuronal dysfunction and vulnerability across nematode, cellular and mouse models of Huntington's disease

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

Worming forward: amyotrophic lateral sclerosis toxicity mechanisms and genetic interactions in Caenorhabditis elegans

Mutant TDP-43 and FUS cause age-dependent paralysis and neurodegeneration in C. elegans

The Novel Small Molecule TRVA242 Stabilizes Neuromuscular Junction Defects in Multiple Animal Models of Amyotrophic Lateral Sclerosis

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

Fatty acids derived from the probiotic Lacticaseibacillus rhamnosus HA-114 suppress age-dependent neurodegeneration

Maple Syrup Decreases TDP-43 Proteotoxicity in a Caenorhabditis elegans Model of Amyotrophic Lateral Sclerosis (ALS)

Modulating the endoplasmic reticulum stress response attenuates neurodegeneration in a Caenorhabditis elegans model of spinal muscular atrophy

Rescue of ATXN3 neuronal toxicity in Caenorhabditis elegans by chemical modification of endoplasmic reticulum stress

The stress response factor daf-16/FOXO is required for multiple compound families to prolong the function of neurons with Huntington’s disease

Stress-induced propagation of neurodegeneration by wild-type proteins in simple models of ALS

Tau hyperphosphorylation and deregulation of calcineurin in mouse models of Huntington's disease

TDP-1/TDP-43 regulates stress signaling and age-dependent proteotoxicity in Caenorhabditis elegans

Restless legs syndrome-associated MEIS1 risk variant influences iron homeostasis

Correction to: The Novel Small Molecule TRVA242 Stabilizes Neuromuscular Junction Defects in Multiple Animal Models of Amyotrophic Lateral Sclerosis

Integration of β-catenin, sirtuin, and FOXO signaling protects from mutant huntingtin toxicity

Cystamine and cysteamine increase brain levels of BDNF in Huntington disease via HSJ1b and transglutaminase

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