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Causative Genes in Amyotrophic Lateral Sclerosis and Protein Degradation Pathways: a Link to Neurodegeneration

Molecular neurobiology, 2018-08, Vol.55 (8), p.6480-6499

2018

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Ptchd1 deficiency induces excitatory synaptic and cognitive dysfunctions in mouse

Molecular psychiatry, 2018-05, Vol.23 (5), p.1356-1367

2018

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GABA/Glutamate synaptic pathways targeted by integrative genomic and electrophysiological explorations distinguish autism from intellectual disability

Molecular psychiatry, 2016-03, Vol.21 (3), p.411-418

2016

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Typical bulbar ALS can be linked to GARS mutation

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2019-04, Vol.20 (3-4), p.275-277

2019

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Association study of the NF1 gene and autistic disorder

American journal of medical genetics, 1999-12, Vol.88 (6), p.729-732

1999

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Comparative impact of cephaloridine on glutathione and related enzymes in LLC-PK1, LLC-RK1, and primary cultures of rat and rabbit proximal tubule cells

Cell Biology and Toxicology, 1996-12, Vol.12 (4-6), p.275-282

1996

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Some milestones in in vitro organ Toxicity Assessment. The Kidney as a Case Study

Toxicology In Vitro, 1995-12, Vol.9 (6), p.795-814

1995

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Molecular analysis of the oligodendrocyte myelin glycoprotein gene in autistic disorder

Neuroscience letters, 2003-02, Vol.338 (2), p.115-118

2003

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Cell lines with extended in vitro growth potential from human renal proximal tubule: Characterization, response to inducers, and comparison with established cell lines

The Journal of laboratory and clinical medicine, 1997-03, Vol.129 (3), p.318-329

1997

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Impact of cephaloridine on glutathione and related enzymes : comparison of in vivo and in vitro rat models

Archives of toxicology, 1995, Vol.70 (2), p.104-111

1995

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Mutation screening and association study of the UBE2H gene on chromosome 7q32 in autistic disorder

Psychiatric genetics, 2003-12, Vol.13 (4), p.221-225

2003

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Effects of the medium HCO3-/CO2 buffer system on differentiation and intermediary metabolism properties of rabbit proximal tubule cells in primary culture

Epithelial cell biology, 1995, Vol.4 (3), p.131

1995

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Oligodendrocyte myelin glycoprotein growth inhibition function requires its conserved leucine‐rich repeat domain, not its glycosylphosphatidyl‐inositol anchor

Journal of neurochemistry, 2003-05, Vol.85 (4), p.889-897

2003

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Typical bulbar ALS can be linked to GARS mutation

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 2019, Vol.20 (3-4), p.275-277

2019

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The oligodendrocyte-myelin glycoprotein gene is highly expressed during the late stages of myelination in the rat central nervous system

Brain research. Developmental brain research, 2003-09, Vol.144 (2), p.159-168

2003

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22 Characterization of highly differentiated rat renal kidney proximal tubule cells in primary cultures: the use of hormonally defined culture media without growth factors

Cell biology and toxicology, 1996-12, Vol.12 (4-6), p.377-377

1996

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23 Phenotypic characterization of the rabbit kidney cell line LLC-RK1. implication for pharmacotoxicological studies

Cell biology and toxicology, 1996-12, Vol.12 (4-6), p.378-378

1996

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Post-Translational Variants of Major Proteins in Amyotrophic Lateral Sclerosis Provide New Insights into the Pathophysiology of the Disease

International journal of molecular sciences, 2024-08, Vol.25 (16), p.8664

2024

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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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The Roles of NEDD4 Subfamily of HECT E3 Ubiquitin Ligases in Neurodevelopment and Neurodegeneration

International journal of molecular sciences, 2022-03, Vol.23 (7), p.3882

2022

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A role for SUMOylation in the Formation and Cellular Localization of TDP-43 Aggregates in Amyotrophic Lateral Sclerosis

Molecular neurobiology, 2020-03, Vol.57 (3), p.1361-1373

2020

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Study of Ubiquitin Pathway Genes in a French Population with Amyotrophic Lateral Sclerosis: Focus on HECW1 Encoding the E3 Ligase NEDL1

International journal of molecular sciences, 2023-01, Vol.24 (2), p.1268

2023

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Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth

Human genetics, 2021-06, Vol.140 (6), p.885-896

2021

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Dysregulations of Expression of Genes of the Ubiquitin/SUMO Pathways in an In Vitro Model of Amyotrophic Lateral Sclerosis Combining Oxidative Stress and SOD1 Gene Mutation

International journal of molecular sciences, 2021-02, Vol.22 (4), p.1796

2021

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The effect of pH alterations on TDP-43 in a cellular model of amyotrophic lateral sclerosis

Biochemistry and biophysics reports, 2024-07, Vol.38, p.101664, Article 101664

2024

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Causative Genes in Amyotrophic Lateral Sclerosis and Protein Degradation Pathways: a Link to Neurodegeneration

Ptchd1 deficiency induces excitatory synaptic and cognitive dysfunctions in mouse

GABA/Glutamate synaptic pathways targeted by integrative genomic and electrophysiological explorations distinguish autism from intellectual disability

Typical bulbar ALS can be linked to GARS mutation

Association study of the NF1 gene and autistic disorder

Comparative impact of cephaloridine on glutathione and related enzymes in LLC-PK1, LLC-RK1, and primary cultures of rat and rabbit proximal tubule cells

Some milestones in in vitro organ Toxicity Assessment. The Kidney as a Case Study

Molecular analysis of the oligodendrocyte myelin glycoprotein gene in autistic disorder

Cell lines with extended in vitro growth potential from human renal proximal tubule: Characterization, response to inducers, and comparison with established cell lines

Impact of cephaloridine on glutathione and related enzymes : comparison of in vivo and in vitro rat models

Mutation screening and association study of the UBE2H gene on chromosome 7q32 in autistic disorder

Effects of the medium HCO3-/CO2 buffer system on differentiation and intermediary metabolism properties of rabbit proximal tubule cells in primary culture

Oligodendrocyte myelin glycoprotein growth inhibition function requires its conserved leucine‐rich repeat domain, not its glycosylphosphatidyl‐inositol anchor

Typical bulbar ALS can be linked to GARS mutation

The oligodendrocyte-myelin glycoprotein gene is highly expressed during the late stages of myelination in the rat central nervous system

22 Characterization of highly differentiated rat renal kidney proximal tubule cells in primary cultures: the use of hormonally defined culture media without growth factors

23 Phenotypic characterization of the rabbit kidney cell line LLC-RK1. implication for pharmacotoxicological studies

Post-Translational Variants of Major Proteins in Amyotrophic Lateral Sclerosis Provide New Insights into the Pathophysiology of the Disease

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

The Roles of NEDD4 Subfamily of HECT E3 Ubiquitin Ligases in Neurodevelopment and Neurodegeneration

A role for SUMOylation in the Formation and Cellular Localization of TDP-43 Aggregates in Amyotrophic Lateral Sclerosis

Study of Ubiquitin Pathway Genes in a French Population with Amyotrophic Lateral Sclerosis: Focus on HECW1 Encoding the E3 Ligase NEDL1

Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth

Dysregulations of Expression of Genes of the Ubiquitin/SUMO Pathways in an In Vitro Model of Amyotrophic Lateral Sclerosis Combining Oxidative Stress and SOD1 Gene Mutation

The effect of pH alterations on TDP-43 in a cellular model of amyotrophic lateral sclerosis

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