Celine Buon
Overview
Explore the profile of Celine Buon 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
6
Citations
43
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Sapaly D, Cheguillaume F, Weill L, Clerc Z, Biondi O, Bendris S, et al.
Brain
. 2024 Aug;
148(3):788-802.
PMID: 39197036
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder affecting motor neurons, with a typical lifespan of 3-5 years. Altered metabolism is a key feature of ALS that strongly influences...
2.
Lavollay M, Buon C, Le Moigne V, Compain F, Guyonvarch A, Fonvielle M
Front Microbiol
. 2024 May;
15:1327723.
PMID: 38784795
Six genes encoding putative high molecular weight penicillin-binding proteins (Pbp) are present in the genome of the β-lactam-resistant strain K411. In this study, we show that , one of these...
3.
Masingue M, Cattaneo O, Wolff N, Buon C, Sternberg D, Euchparmakian M, et al.
Sci Rep
. 2023 Aug;
13(1):14054.
PMID: 37640745
Congenital myasthenic syndromes (CMS) are a clinically and genetically heterogeneous group of rare diseases due to mutations in neuromuscular junction (NMJ) protein-coding genes. Until now, many mutations encoding postsynaptic proteins...
4.
Boex M, Cottin S, Halliez M, Bauche S, Buon C, Sans N, et al.
Sci Signal
. 2022 May;
15(734):eabg4982.
PMID: 35580169
The development of the neuromuscular junction (NMJ) requires dynamic trans-synaptic coordination orchestrated by secreted factors, including Wnt family morphogens. To investigate how these synaptic cues in NMJ development are transduced,...
5.
Bauche S, Sureau A, Sternberg D, Rendu J, Buon C, Messeant J, et al.
Neurol Genet
. 2021 Mar;
6(6):e534.
PMID: 33659639
Objective: To report the identification of 2 new homozygous recessive mutations in the synaptotagmin 2 () gene as the genetic cause of severe and early presynaptic forms of congenital myasthenic...
6.
Bauche S, ORegan S, Azuma Y, Laffargue F, McMacken G, Sternberg D, et al.
Am J Hum Genet
. 2016 Aug;
99(3):753-761.
PMID: 27569547
The neuromuscular junction (NMJ) is one of the best-studied cholinergic synapses. Inherited defects of peripheral neurotransmission result in congenital myasthenic syndromes (CMSs), a clinically and genetically heterogeneous group of rare...