Cargando…
Nerve pathology is prevented by linker proteins in mouse models for LAMA2-related muscular dystrophy
LAMA2-related muscular dystrophy (LAMA2 MD or MDC1A) is a devastating congenital muscular dystrophy that is caused by mutations in the LAMA2 gene encoding laminin-α2, the long chain of several heterotrimeric laminins. Laminins are essential components of the extracellular matrix that interface with...
Autores principales: | Reinhard, Judith R, Porrello, Emanuela, Lin, Shuo, Pelczar, Pawel, Previtali, Stefano C, Rüegg, Markus A |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10082391/ https://www.ncbi.nlm.nih.gov/pubmed/37038437 http://dx.doi.org/10.1093/pnasnexus/pgad083 |
Ejemplares similares
-
Amelioration of Muscle and Nerve Pathology in LAMA2 Muscular Dystrophy by AAV9-Mini-Agrin
por: Qiao, Chunping, et al.
Publicado: (2018) -
Editorial: Current Insights Into LAMA2 Disease
por: Previtali, Stefano C., et al.
Publicado: (2021) -
Amelioration of muscle and nerve pathology of Lama2-related dystrophy by AAV9-laminin-αLN linker protein
por: McKee, Karen K., et al.
Publicado: (2022) -
Mesoangioblast delivery of miniagrin ameliorates murine model of merosin-deficient congenital muscular dystrophy type 1A
por: Domi, Teuta, et al.
Publicado: (2015) -
Linker molecules between laminins and dystroglycan ameliorate laminin-α2–deficient muscular dystrophy at all disease stages
por: Meinen, Sarina, et al.
Publicado: (2007)