Search Results - "Salsac, Céline"
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Cytotoxic CD8⁺ T lymphocytes expressing ALS-causing SOD1 mutant selectively trigger death of spinal motoneurons
Published in Proceedings of the National Academy of Sciences - PNAS (05-02-2019)“…Adaptive immune response is part of the dynamic changes that accompany motoneuron loss in amyotrophic lateral sclerosis (ALS). CD4+ T cells that regulate a…”
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2
Spinal Motoneuron TMEM16F Acts at C-boutons to Modulate Motor Resistance and Contributes to ALS Pathogenesis
Published in Cell reports (Cambridge) (25-02-2020)“…Neuronal Ca2+ entry elicited by electrical activity contributes to information coding via activation of K+ and Cl− channels. While Ca2+-dependent K+ channels…”
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3
Vitamin D confers protection to motoneurons and is a prognostic factor of amyotrophic lateral sclerosis
Published in Neurobiology of aging (01-05-2014)“…Abstract Amyotrophic lateral sclerosis (ALS) is an incurable paralytic disorder primarily typified by the selective and progressive degeneration of motoneurons…”
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Lack of confirmation of anti-inward rectifying potassium channel 4.1 antibodies as reliable markers of multiple sclerosis
Published in Multiple sclerosis (01-11-2014)“…Background: auto-antibodies against the potassium channel inward rectifying potassium channel 4.1 (Kir4.1) have previously been identified in 46% of patients…”
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5
Functional remission in Belgian forensic psychotic patients - story of a virtuous cycle?
Published in The journal of forensic psychiatry & psychology (04-07-2021)“…In this article, we examine the associations between functional remission, psychotic symptoms and protective risk factors, and we study the reliability and…”
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KCC3 loss-of-function contributes to Andermann syndrome by inducing activity-dependent neuromuscular junction defects
Published in Neurobiology of disease (01-10-2017)“…Abstract Loss-of-function mutations in the potassium-chloride cotransporter KCC3 lead to Andermann syndrome, a severe sensorimotor neuropathy characterized by…”
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Distribution of de novo Donor-Specific Antibody Subclasses Quantified by Mass Spectrometry: High IgG3 Proportion Is Associated With Antibody-Mediated Rejection Occurrence and Severity
Published in Frontiers in immunology (02-06-2020)“…Donor-specific antibodies (DSAs) are the main risk factor for antibody-mediated rejection (ABMR) and graft loss but could have variable pathogenicity according…”
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8
Myotube elasticity of an amyotrophic lateral sclerosis mouse model
Published in Scientific reports (12-04-2018)“…Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that affects the motor system leading to generalized paralysis and death of patients…”
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Tweak regulates astrogliosis, microgliosis and skeletal muscle atrophy in a mouse model of amyotrophic lateral sclerosis
Published in Human molecular genetics (15-06-2015)“…Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder that primarily affects motoneurons in the brain and spinal cord. Astrocyte and…”
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10
Somatic and axonal LIGHT signaling elicit degenerative and regenerative responses in motoneurons, respectively
Published in EMBO reports (01-05-2014)“…A receptor–ligand interaction can evoke a broad range of biological activities in different cell types depending on receptor identity and cell type‐specific…”
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Cytotoxic CD8^sup +^ T lymphocytes expressing ALS-causing SOD1 mutant selectively trigger death of spinal motoneurons
Published in Proceedings of the National Academy of Sciences - PNAS (05-02-2019)“…Adaptive immune response is part of the dynamic changes that accompany motoneuron loss in amyotrophic lateral sclerosis (ALS). CD4+ T cells that regulate a…”
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Journal Article -
12
Vitamin D Is A Prognostic Factor Of Amyotrophic Lateral Sclerosis And Confers Protection To Motoneurons In Vitro (P4.084)
Published in Neurology (08-04-2014)“…Abstract only…”
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13
Is KIR4.1 Antibody a Marker of Multiple Sclerosis? (P4.130)
Published in Neurology (08-04-2014)“…Abstract only…”
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