Celine Salsac
Overview
Explore the profile of Celine Salsac including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
9
Citations
181
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Pernin V, Beyze A, Szwarc I, Bec N, Salsac C, Perez-Garcia E, et al.
Front Immunol
. 2020 Jul;
11:919.
PMID: 32670261
Donor-specific antibodies (DSAs) are the main risk factor for antibody-mediated rejection (ABMR) and graft loss but could have variable pathogenicity according to their IgG subclass composition. Luminex-based test might lack...
2.
Soulard C, Salsac C, Mouzat K, Hilaire C, Roussel J, Mezghrani A, et al.
Cell Rep
. 2020 Feb;
30(8):2581-2593.e7.
PMID: 32101737
Neuronal Ca entry elicited by electrical activity contributes to information coding via activation of K and Cl channels. While Ca-dependent K channels have been extensively studied, the molecular identity and...
3.
Coque E, Salsac C, Espinosa-Carrasco G, Varga B, Degauque N, Cadoux M, et al.
Proc Natl Acad Sci U S A
. 2019 Jan;
116(6):2312-2317.
PMID: 30674678
Adaptive immune response is part of the dynamic changes that accompany motoneuron loss in amyotrophic lateral sclerosis (ALS). CD4 T cells that regulate a protective immunity during the neurodegenerative process...
4.
Varga B, Martin-Fernandez M, Hilaire C, Sanchez-Vicente A, Areias J, Salsac C, et al.
Sci Rep
. 2018 Apr;
8(1):5917.
PMID: 29650983
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that affects the motor system leading to generalized paralysis and death of patients. The understanding of early pathogenic mechanisms will help...
5.
Bowerman M, Salsac C, Bernard V, Soulard C, Dionne A, Coque E, et al.
Neurobiol Dis
. 2017 Jun;
106:35-48.
PMID: 28647557
Loss-of-function mutations in the potassium-chloride cotransporter KCC3 lead to Andermann syndrome, a severe sensorimotor neuropathy characterized by areflexia, amyotrophy and locomotor abnormalities. The molecular events responsible for axonal loss remain...
6.
Bowerman M, Salsac C, Coque E, Eiselt E, Deschaumes R, Brodovitch A, et al.
Hum Mol Genet
. 2015 Mar;
24(12):3440-56.
PMID: 25765661
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder that primarily affects motoneurons in the brain and spinal cord. Astrocyte and microglia activation as well as skeletal muscle atrophy are...
7.
Nerrant E, Salsac C, Charif M, Ayrignac X, Carra-Dalliere C, Castelnovo G, et al.
Mult Scler
. 2014 Apr;
20(13):1699-703.
PMID: 24756568
Background: auto-antibodies against the potassium channel inward rectifying potassium channel 4.1 (Kir4.1) have previously been identified in 46% of patients with multiple sclerosis (MS). Objectives: to confirm these findings. Methods:...
8.
Otsmane B, Moumen A, Aebischer J, Coque E, Sar C, Sunyach C, et al.
EMBO Rep
. 2014 Mar;
15(5):540-7.
PMID: 24668263
A receptor-ligand interaction can evoke a broad range of biological activities in different cell types depending on receptor identity and cell type-specific post-receptor signaling intermediates. Here, we show that the...
9.
Camu W, Tremblier B, Plassot C, Alphandery S, Salsac C, Pageot N, et al.
Neurobiol Aging
. 2014 Jan;
35(5):1198-205.
PMID: 24378089
Amyotrophic lateral sclerosis (ALS) is an incurable paralytic disorder primarily typified by the selective and progressive degeneration of motoneurons in the brain and spinal cord. ALS causes muscle wasting and...