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of 4
pro vyhledávání: '"Lylia, Mekzine"'
Development of versatile allele-specific siRNAs able to silence all the dominant dynamin 2 mutations
Autor:
Swati Dudhal, Lylia Mekzine, Bernard Prudhon, Karishma Soocheta, Bruno Cadot, Kamel Mamchaoui, Delphine Trochet, Marc Bitoun
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 29, Iss , Pp 733-748 (2022)
Dominant centronuclear myopathy (CNM) is a rare form of congenital myopathy associated with a wide clinical spectrum, from severe neonatal to milder adult forms. There is no available treatment for this disease due to heterozygous mutations in the DN
Externí odkaz:
https://doaj.org/article/8e9a6b63ea2842319af2c41521d31680
Autor:
Delphine Trochet, Bernard Prudhon, Lylia Mekzine, Mégane Lemaitre, Maud Beuvin, Laura Julien, Sofia Benkhelifa-Ziyyat, Mai Thao Bui, Norma Romero, Marc Bitoun
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 27, Iss , Pp 1179-1190 (2022)
Dominant dynamin 2 (DNM2) mutations are responsible for the autosomal dominant centronuclear myopathy (AD-CNM), a rare progressive neuromuscular disorder ranging from severe neonatal to mild adult forms. We previously demonstrated that mutant-specifi
Externí odkaz:
https://doaj.org/article/3866d36cc9c9433796905ac149308456
Development of versatile allele-specific siRNAs able to silence all the dominant dynamin 2 mutations
Autor:
Delphine, Trochet, Swati, Dudhal, Lylia, Mekzine, Bernard, Prudhon, Bruno, Cadot, Kamel, Mamchaoui, Marc, Bitoun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______166::22504d18539a64fef04ceefbbdb1e08a
https://hal.science/hal-03875467
https://hal.science/hal-03875467
Autor:
Delphine, Trochet, Bernard, Prudhon, Lylia, Mekzine, Mégane, Lemaitre, Maud, Beuvin, Laura, Julien, Sofia, Benkhelifa-Ziyyat, Mai Thao, Bui, Norma, Romero, Marc, Bitoun
Publikováno v:
Molecular therapy. Nucleic acids. 27
Dominant dynamin 2 (DNM2) mutations are responsible for the autosomal dominant centronuclear myopathy (AD-CNM), a rare progressive neuromuscular disorder ranging from severe neonatal to mild adult forms. We previously demonstrated that mutant-specifi