Cargando…
Identification of the genetic mechanism that associates L3MBTL3 to multiple sclerosis
Multiple sclerosis (MS) is a complex and demyelinating disease of the central nervous system. One of the challenges of the post-genome-wide association studies (GWAS) era is to understand the molecular basis of statistical associations to reveal gene networks and potential therapeutic targets. The L...
Autores principales: | Alcina, Antonio, Fedetz, Maria, Vidal-Cobo, Isabel, Andrés-León, Eduardo, García-Sánchez, Maria-Isabel, Barroso-del-Jesus, Alicia, Eichau, Sara, Gil-Varea, Elia, Luisa-Maria Villar, Saiz, Albert, Leyva, Laura, Vandenbroeck, Koen, Otaegui, David, Izquierdo, Guillermo, Comabella, Manuel, Urcelay, Elena, Matesanz, Fuencisla |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9262392/ https://www.ncbi.nlm.nih.gov/pubmed/35088080 http://dx.doi.org/10.1093/hmg/ddac009 |
Ejemplares similares
-
A New Risk Variant for Multiple Sclerosis at 11q23.3 Locus Is Associated with Expansion of CXCR5+ Circulating Regulatory T Cells
por: Gil-Varea, Elia, et al.
Publicado: (2020) -
Human Endogenous Retrovirus HERV-Fc1 Association with Multiple Sclerosis Susceptibility: A Meta-Analysis
por: de la Hera, Belén, et al.
Publicado: (2014) -
Identification of a functional variant in the KIF5A-CYP27B1-METTL1-FAM119B locus associated with multiple sclerosis
por: Alcina, Antonio, et al.
Publicado: (2013) -
Splice-site variant in ACSL5: a marker promoting opposing effect on cell viability and protein expression
por: Pérez-Núñez, Iván, et al.
Publicado: (2019) -
Fine Mapping and Functional Analysis of the Multiple Sclerosis Risk Gene CD6
por: Swaminathan, Bhairavi, et al.
Publicado: (2013)