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Amyotrophic Lateral Sclerosis Genes in Drosophila melanogaster

International journal of molecular sciences, 2021-01, Vol.22 (2), p.904

2021

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Prionoids in amyotrophic lateral sclerosis

Brain communications, 2022, Vol.4 (3), p.fcac145-fcac145

2022

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TNFα prevents FGF4-mediated rescue of astrocyte dysfunction and reactivity in human ALS models

Neurobiology of disease, 2024-10, Vol.201, p.106687, Article 106687

2024

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ROCK inhibition as a therapy for spinal muscular atrophy: understanding the repercussions on multiple cellular targets

Frontiers in neuroscience, 2014-08, Vol.8, p.271-271

2014

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Regulation of Brain Cholesterol: What Role Do Liver X Receptors Play in Neurodegenerative Diseases?

International journal of molecular sciences, 2019-08, Vol.20 (16), p.3858

2019

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Extrasynaptic α6 subunit-containing GABAA receptors modulate excitability in turtle spinal motoneurons

PloS one, 2014, Vol.9 (12), p.e115378-e115378

2014

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Age-Related Changes in Pre- and Postsynaptic Partners of the Cholinergic C-Boutons in Wild-Type and SOD1G93A Lumbar Motoneurons

PloS one, 2015-08, Vol.10 (8), p.e0135525-e0135525

2015

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Programmed Cell Death of Embryonic Motoneurons Triggered through the Fas Death Receptor

The Journal of cell biology, 1999-11, Vol.147 (5), p.1049-1061

1999

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Evaluation of Avulsion-Induced Neuropathology in Rat Spinal Cords with 18F-FDG Micro-PET/CT

PloS one, 2015, Vol.10 (5), p.e0127685-e0127685

2015

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A Novel De Novo Missense Mutation in KIF1A Associated with Young-Onset Upper-Limb Amyotrophic Lateral Sclerosis

International journal of molecular sciences, 2024-08, Vol.25 (15), p.8170

2024

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ALS-Associated KIF5A Mutation Causes Locomotor Deficits Associated with Cytoplasmic Inclusions, Alterations of Neuromuscular Junctions, and Motor Neuron Loss

The Journal of neuroscience, 2023-11, Vol.43 (47), p.8058-8072

2023

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Mitochondria-targeted catalase reverts the neurotoxicity of hSOD1G⁹³A astrocytes without extending the survival of ALS-linked mutant hSOD1 mice

PloS one, 2014-07, Vol.9 (7), p.e103438

2014

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Differential effect of Fas activation on spinal muscular atrophy motoneuron death and induction of axonal growth

Cellular and Molecular Biology, 2023-10, Vol.69 (10), p.1-8

2023

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Wildtype motoneurons, ALS‐Linked SOD1 mutation and glutamate profoundly modify astrocyte metabolism and lactate shuttling

Glia, 2017-04, Vol.65 (4), p.592-605

2017

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L1 syndrome mutations impair neuronal L1 function at different levels by divergent mechanisms

Neurobiology of disease, 2010-10, Vol.40 (1), p.222-237

2010

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Reduced calreticulin levels link endoplasmic reticulum stress and Fas-triggered cell death in motoneurons vulnerable to ALS

The Journal of neuroscience, 2012-04, Vol.32 (14), p.4901-4912

2012

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Spinal Motoneuron TMEM16F Acts at C-boutons to Modulate Motor Resistance and Contributes to ALS Pathogenesis

Cell reports (Cambridge), 2020-02, Vol.30 (8), p.2581-2593.e7

2020

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Vitamin D confers protection to motoneurons and is a prognostic factor of amyotrophic lateral sclerosis

Neurobiology of aging, 2014-05, Vol.35 (5), p.1198-1205

2014

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Liver X Receptor Genes Variants Modulate ALS Phenotype

Molecular neurobiology, 2018-03, Vol.55 (3), p.1959-1965

2018

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Calreticulin levels determine onset of early muscle denervation by fast motoneurons of ALS model mice

Neurobiology of disease, 2015-01, Vol.73, p.130-136

2015

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Progressive Cerebrocerebellar Uncoupling in Sporadic and Genetic Forms of Amyotrophic Lateral Sclerosis

Neurology, 2024-07, Vol.103 (2), p.e209623

2024

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Astrocyte‐targeting RNA interference against mutated superoxide dismutase 1 induces motoneuron plasticity and protects fast‐fatigable motor units in a mouse model of amyotrophic lateral sclerosis

Glia, 2022-05, Vol.70 (5), p.842-857

2022

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Lentiviral-mediated silencing of SOD1 through RNA interference retards disease onset and progression in a mouse model of ALS

Nature Medicine, 2005-04, Vol.11 (43), p.423-428

2005

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Cerebellar pathology in motor neuron disease: neuroplasticity and neurodegeneration

Neural regeneration research, 2022-11, Vol.17 (11), p.2335-2341

2022

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How Degeneration of Cells Surrounding Motoneurons Contributes to Amyotrophic Lateral Sclerosis

Cells (Basel, Switzerland), 2020-11, Vol.9 (12), p.2550

2020

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Amyotrophic Lateral Sclerosis Genes in Drosophila melanogaster

Prionoids in amyotrophic lateral sclerosis

TNFα prevents FGF4-mediated rescue of astrocyte dysfunction and reactivity in human ALS models

ROCK inhibition as a therapy for spinal muscular atrophy: understanding the repercussions on multiple cellular targets

Regulation of Brain Cholesterol: What Role Do Liver X Receptors Play in Neurodegenerative Diseases?

Extrasynaptic α6 subunit-containing GABAA receptors modulate excitability in turtle spinal motoneurons

Age-Related Changes in Pre- and Postsynaptic Partners of the Cholinergic C-Boutons in Wild-Type and SOD1G93A Lumbar Motoneurons

Programmed Cell Death of Embryonic Motoneurons Triggered through the Fas Death Receptor

Evaluation of Avulsion-Induced Neuropathology in Rat Spinal Cords with 18F-FDG Micro-PET/CT

A Novel De Novo Missense Mutation in KIF1A Associated with Young-Onset Upper-Limb Amyotrophic Lateral Sclerosis

ALS-Associated KIF5A Mutation Causes Locomotor Deficits Associated with Cytoplasmic Inclusions, Alterations of Neuromuscular Junctions, and Motor Neuron Loss

Mitochondria-targeted catalase reverts the neurotoxicity of hSOD1G⁹³A astrocytes without extending the survival of ALS-linked mutant hSOD1 mice

Differential effect of Fas activation on spinal muscular atrophy motoneuron death and induction of axonal growth

Wildtype motoneurons, ALS‐Linked SOD1 mutation and glutamate profoundly modify astrocyte metabolism and lactate shuttling

L1 syndrome mutations impair neuronal L1 function at different levels by divergent mechanisms

Reduced calreticulin levels link endoplasmic reticulum stress and Fas-triggered cell death in motoneurons vulnerable to ALS

Spinal Motoneuron TMEM16F Acts at C-boutons to Modulate Motor Resistance and Contributes to ALS Pathogenesis

Vitamin D confers protection to motoneurons and is a prognostic factor of amyotrophic lateral sclerosis

Liver X Receptor Genes Variants Modulate ALS Phenotype

Calreticulin levels determine onset of early muscle denervation by fast motoneurons of ALS model mice

Progressive Cerebrocerebellar Uncoupling in Sporadic and Genetic Forms of Amyotrophic Lateral Sclerosis

Astrocyte‐targeting RNA interference against mutated superoxide dismutase 1 induces motoneuron plasticity and protects fast‐fatigable motor units in a mouse model of amyotrophic lateral sclerosis

Lentiviral-mediated silencing of SOD1 through RNA interference retards disease onset and progression in a mouse model of ALS

Cerebellar pathology in motor neuron disease: neuroplasticity and neurodegeneration

How Degeneration of Cells Surrounding Motoneurons Contributes to Amyotrophic Lateral Sclerosis

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