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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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Comprehensive immune profiling reveals substantial immune system alterations in a subset of patients with amyotrophic lateral sclerosis

PloS one, 2017-07, Vol.12 (7), p.e0182002-e0182002

2017

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Early changes of neuromuscular transmission in the SOD1(G93A) mice model of ALS start long before motor symptoms onset

PloS one, 2013-09, Vol.8 (9), p.e73846-e73846

2013

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Whole blood transcriptome analysis in amyotrophic lateral sclerosis: A biomarker study

PloS one, 2018-06, Vol.13 (6), p.e0198874-e0198874

2018

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RNAseq Analyses Identify Tumor Necrosis Factor-Mediated Inflammation as a Major Abnormality in ALS Spinal Cord

PloS one, 2016-08, Vol.11 (8), p.e0160520-e0160520

2016

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Tryptophan residue 32 in human Cu-Zn superoxide dismutase modulates prion-like propagation and strain selection

PloS one, 2020-01, Vol.15 (1), p.e0227655

2020

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Multi-parametric spinal cord MRI as potential progression marker in amyotrophic lateral sclerosis

PloS one, 2014-04, Vol.9 (4), p.e95516-e95516

2014

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Prionoids in amyotrophic lateral sclerosis

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

2022

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Nerve injury and repair in a ketogenic milieu: A systematic review of traumatic injuries to the spinal cord and peripheral nervous tissue

PloS one, 2021-01, Vol.16 (1), p.e0244244-e0244244

2021

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Formation and spreading of TDP-43 aggregates in cultured neuronal and glial cells demonstrated by time-lapse imaging

PloS one, 2017-06, Vol.12 (6), p.e0179375-e0179375

2017

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Locus-specific analysis of Transposable Elements during the progression of ALS in the SOD1G93A mouse model

PloS one, 2021-10, Vol.16 (10), p.e0258291-e0258291

2021

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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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CX3CR1 is a modifying gene of survival and progression in amyotrophic lateral sclerosis

PloS one, 2014-05, Vol.9 (5), p.e96528-e96528

2014

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Targeted delivery of TrkB receptor to phrenic motoneurons enhances functional recovery of rhythmic phrenic activity after cervical spinal hemisection

PloS one, 2013-05, Vol.8 (5), p.e64755-e64755

2013

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A novel splice-site mutation in ALS2 establishes the diagnosis of juvenile amyotrophic lateral sclerosis in a family with early onset anarthria and generalized dystonias

PloS one, 2014-12, Vol.9 (12), p.e113258-e113258

2014

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Incidence and geographical variation of amyotrophic lateral sclerosis (ALS) in Southern Germany--completeness of the ALS registry Swabia

PloS one, 2014-04, Vol.9 (4), p.e93932-e93932

2014

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Down-regulation of KCC2 expression and phosphorylation in motoneurons, and increases the number of in primary afferent projections to motoneurons in mice with post-stroke spasticity

PloS one, 2014-12, Vol.9 (12), p.e114328-e114328

2014

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Blood Cell Palmitoleate-Palmitate Ratio Is an Independent Prognostic Factor for Amyotrophic Lateral Sclerosis

PloS one, 2015-07, Vol.10 (7), p.e0131512-e0131512

2015

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How do SMA-linked mutations of SMN1 lead to structural/functional deficiency of the SMA protein?

PloS one, 2017-06, Vol.12 (6), p.e0178519-e0178519

2017

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Motor cortex-periaqueductal gray-spinal cord neuronal circuitry may involve in modulation of nociception: a virally mediated transsynaptic tracing study in spinally transected transgenic mouse model

PloS one, 2014-02, Vol.9 (2), p.e89486-e89486

2014

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MicroNeurotrophins Improve Survival in Motor Neuron-Astrocyte Co-Cultures but Do Not Improve Disease Phenotypes in a Mutant SOD1 Mouse Model of Amyotrophic Lateral Sclerosis

PloS one, 2016-10, Vol.11 (10), p.e0164103-e0164103

2016

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Electrophysiologic biomarkers for assessing disease progression and the effect of riluzole in SOD1 G93A ALS mice

PloS one, 2013-06, Vol.8 (6), p.e65976

2013

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Cervical Spinal Cord Atrophy Profile in Adult SMN1-Linked SMA

PloS one, 2016-04, Vol.11 (4), p.e0152439-e0152439

2016

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Differential regulation of glutamate transporter subtypes by pro-inflammatory cytokine TNF-α in cortical astrocytes from a rat model of amyotrophic lateral sclerosis

PloS one, 2014-05, Vol.9 (5), p.e97649

2014

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Altered intracellular localization of SOD1 in leukocytes from patients with sporadic amyotrophic lateral sclerosis

PloS one, 2013-10, Vol.8 (10), p.e75916

2013

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Amyotrophic Lateral Sclerosis Genes in Drosophila melanogaster

Comprehensive immune profiling reveals substantial immune system alterations in a subset of patients with amyotrophic lateral sclerosis

Early changes of neuromuscular transmission in the SOD1(G93A) mice model of ALS start long before motor symptoms onset

Whole blood transcriptome analysis in amyotrophic lateral sclerosis: A biomarker study

RNAseq Analyses Identify Tumor Necrosis Factor-Mediated Inflammation as a Major Abnormality in ALS Spinal Cord

Tryptophan residue 32 in human Cu-Zn superoxide dismutase modulates prion-like propagation and strain selection

Multi-parametric spinal cord MRI as potential progression marker in amyotrophic lateral sclerosis

Prionoids in amyotrophic lateral sclerosis

Nerve injury and repair in a ketogenic milieu: A systematic review of traumatic injuries to the spinal cord and peripheral nervous tissue

Formation and spreading of TDP-43 aggregates in cultured neuronal and glial cells demonstrated by time-lapse imaging

Locus-specific analysis of Transposable Elements during the progression of ALS in the SOD1G93A mouse model

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

CX3CR1 is a modifying gene of survival and progression in amyotrophic lateral sclerosis

Targeted delivery of TrkB receptor to phrenic motoneurons enhances functional recovery of rhythmic phrenic activity after cervical spinal hemisection

A novel splice-site mutation in ALS2 establishes the diagnosis of juvenile amyotrophic lateral sclerosis in a family with early onset anarthria and generalized dystonias

Incidence and geographical variation of amyotrophic lateral sclerosis (ALS) in Southern Germany--completeness of the ALS registry Swabia

Down-regulation of KCC2 expression and phosphorylation in motoneurons, and increases the number of in primary afferent projections to motoneurons in mice with post-stroke spasticity

Blood Cell Palmitoleate-Palmitate Ratio Is an Independent Prognostic Factor for Amyotrophic Lateral Sclerosis

How do SMA-linked mutations of SMN1 lead to structural/functional deficiency of the SMA protein?

Motor cortex-periaqueductal gray-spinal cord neuronal circuitry may involve in modulation of nociception: a virally mediated transsynaptic tracing study in spinally transected transgenic mouse model

MicroNeurotrophins Improve Survival in Motor Neuron-Astrocyte Co-Cultures but Do Not Improve Disease Phenotypes in a Mutant SOD1 Mouse Model of Amyotrophic Lateral Sclerosis

Electrophysiologic biomarkers for assessing disease progression and the effect of riluzole in SOD1 G93A ALS mice

Cervical Spinal Cord Atrophy Profile in Adult SMN1-Linked SMA

Differential regulation of glutamate transporter subtypes by pro-inflammatory cytokine TNF-α in cortical astrocytes from a rat model of amyotrophic lateral sclerosis

Altered intracellular localization of SOD1 in leukocytes from patients with sporadic amyotrophic lateral sclerosis

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