Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Esma Ziat"'
Autor:
Feriel Azibani, Astrid Brull, Ludovic Arandel, Maud Beuvin, Isabelle Nelson, Arnaud Jollet, Esma Ziat, Bernard Prudhon, Sofia Benkhelifa-Ziyyat, Marc Bitoun, Stéphanie Lorain, Gisèle Bonne, Anne T. Bertrand
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 10, Iss , Pp 376-386 (2018)
We assessed the potential of Lmna-mRNA repair by spliceosome-mediated RNA trans-splicing as a therapeutic approach for LMNA-related congenital muscular dystrophy. This gene therapy strategy leads to reduction of mutated transcript expression for the
Externí odkaz:
https://doaj.org/article/2bc39faefe1040038e4222aaa680707a
Autor:
Maud Beuvin, Kamel Mamchaoui, Isabelle Nelson, Anne Bertrand, Feriel Azibani, Simone Spuler, Esma Ziat, Gisèle Bonne
Publikováno v:
Journal of neuromuscular diseases. 3(4)
BACKGROUND: Emery-Dreifuss muscular dystrophy (EDMD) is associated with mutations in EMD and LMNA genes, encoding for the nuclear envelope proteins emerin and lamin A/C, indicating that EDMD is a nuclear envelope disease. We recently reported mutatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1be8e72daaf3316332e7afffc6fa9a59
https://pubmed.ncbi.nlm.nih.gov/27911330
https://pubmed.ncbi.nlm.nih.gov/27911330
Autor:
Anne Bertrand, Esma Ziat
Publikováno v:
Orphanet Journal of Rare Diseases
Emery-Dreifuss muscular dystrophy (EDMD) is a hereditary muscular disorder characterized by early joint contractures, progressive muscular wasting and weakness of scapuloperoneal distribution, and at adult age, patients develop cardiac abnormalities
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f339c9240dc78f8ab92267efb7780d3a
https://doi.org/10.1186/1750-1172-10-s2-o18
https://doi.org/10.1186/1750-1172-10-s2-o18