Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Laura, Julien"'
Autor:
Amédée Mollard, Cécile Peccate, Anne Forand, Julie Chassagne, Laura Julien, Pierre Meunier, Zoheir Guesmia, Thibaut Marais, Marc Bitoun, France Piétri-Rouxel, Sofia Benkhelifa-Ziyyat, Stéphanie Lorain
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-11 (2022)
Abstract Duchenne muscular dystrophy is a severe neuromuscular disease causing a progressive muscle wasting due to mutations in the DMD gene that lead to the absence of dystrophin protein. Adeno-associated virus (AAV)-based therapies aiming to restor
Externí odkaz:
https://doaj.org/article/5ed91629937e4299abe5d7e2bb11aa5c
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
Autor:
Katarzyna Piekarowicz, Anne T. Bertrand, Feriel Azibani, Maud Beuvin, Laura Julien, Magdalena Machowska, Gisèle Bonne, Ryszard Rzepecki
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 15, Iss , Pp 157-169 (2019)
Gene therapy is a promising strategy to cure rare diseases. The lack of regulatory sequences ensuring specific and robust expression in skeletal and cardiac muscle is a substantial limitation of gene therapy efficiency targeting the muscle tissue. He
Externí odkaz:
https://doaj.org/article/d0332b0722974fadb605a4b15c9ce05f
Autor:
Delphine Trochet, Bernard Prudhon, Maud Beuvin, Cécile Peccate, Stéphanie Lorain, Laura Julien, Sofia Benkhelifa‐Ziyyat, Aymen Rabai, Kamel Mamchaoui, Arnaud Ferry, Jocelyn Laporte, Pascale Guicheney, Stéphane Vassilopoulos, Marc Bitoun
Publikováno v:
EMBO Molecular Medicine, Vol 10, Iss 2, Pp 239-253 (2017)
Abstract Rapid advances in allele‐specific silencing by RNA interference established a strategy of choice to cure dominant inherited diseases by targeting mutant alleles. We used this strategy for autosomal‐dominant centronuclear myopathy (CNM),
Externí odkaz:
https://doaj.org/article/a4426586b535417d812fa75336f2413c
Publikováno v:
Journal International of Lingua and Technology. 1:79-98
Along with the development of the times, the world is currently entering the 5.0 era, which means that all must be prepared for technology in this era, including the Indonesian education system. And this research focuses on the role of technology in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77d252a19774c60aa6a364011ee0ddbf
https://doi.org/10.55849/jiltech.v1i2.85
https://doi.org/10.55849/jiltech.v1i2.85
Autor:
Elena Gargaun, Sestina Falcone, Guilhem Solé, Julien Durigneux, Andoni Urtizberea, Jean Marie Cuisset, Sofia Benkhelifa-Ziyyat, Laura Julien, Anne Boland, Florian Sandron, Vincent Meyer, Jean François Deleuze, David Salgado, Jean-Pierre Desvignes, Christophe Béroud, Anatole Chessel, Alexia Blesius, Martin Krahn, Nicolas Levy, France Leturcq, France Pietri-Rouxel
Publikováno v:
Biomedicines, Vol 9, Iss 2, p 219 (2021)
In skeletal muscle, long noncoding RNAs (lncRNAs) are involved in dystrophin protein stabilization but also in the regulation of myocytes proliferation and differentiation. Hence, they could represent promising therapeutic targets and/or biomarkers f
Externí odkaz:
https://doaj.org/article/968c00f1b0d148c5bfa7adb3b5474094
Autor:
Mariko Okubo, Astrid Brull, Isabelle Nelson, Maud Beuvin, Laura Julien, Valérie Paradis, Bertrand, Anne T., Gisèle Bonne
Publikováno v:
12th French-Japanese Workshop on Neuromuscular Diseases
12th French-Japanese Workshop on Neuromuscular Diseases, Gisèle Bonne; Ichizo Nishino, Sep 2022, Giverny, France
HAL
12th French-Japanese Workshop on Neuromuscular Diseases, Gisèle Bonne; Ichizo Nishino, Sep 2022, Giverny, France
HAL
International audience; LMNA-related Congenital Muscular Dystrophy (L-CMD) is the most severe form of striated muscle laminopathies caused by mutations in LMNA. Our purpose is to development gene therapy for L-CMD to correct LMNA mutations at mRNA le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::8589fc0248e88c8795dbc20569d7ec71
https://hal.science/hal-03989233
https://hal.science/hal-03989233
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::af821a1c0d12fd09c34ea9e1c5470721
https://pubmed.ncbi.nlm.nih.gov/35282416
https://pubmed.ncbi.nlm.nih.gov/35282416
Autor:
Stéphane Vassilopoulos, Christophe Leterrier, Masayuki Nakamori, Ichizo Nishino, Florent Dingli, Denis Furling, Mégane Lemaître, Jeanne Lainé, Ghislaine Caillol, Kamel Mamchaoui, Damarys Loew, Laura Julien, Marc Bitoun, Gilles Moulay
Publikováno v:
Journal of Cell Biology
Journal of Cell Biology, 2020, 219 (9), ⟨10.1083/jcb.201912061⟩
Journal of Cell Biology, Rockefeller University Press, 2020, 219 (9), ⟨10.1083/jcb.201912061⟩
The Journal of Cell Biology
Journal of Cell Biology, 2020, 219 (9), ⟨10.1083/jcb.201912061⟩
Journal of Cell Biology, Rockefeller University Press, 2020, 219 (9), ⟨10.1083/jcb.201912061⟩
The Journal of Cell Biology
A single alternatively spliced exon in the CLTC gene contributes to clathrin coat organization. This event participates in the plasticity from clathrin-coated pits to plaques, structures that are essential for muscle fiber function and maintenance.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86cd348107004a017c7a447877e768f7
https://hal.science/hal-03005118
https://hal.science/hal-03005118
Autor:
Emilie Christin, Marc Bitoun, Alexandre Guiraud, Alexandre Janin, David Arnould, Nathalie Couturier, Vincent Gache, Alireza Ghasemizadeh, Carole Kretz-Remy, Norma B. Romero, Thao Mai Bui, Anne-Cécile Durieux, Laura Julien, Vladimir L. Buchman
The building block of skeletal muscle is the multinucleated muscle fiber, formed by the fusion of hundreds of mononucleated precursor cells, myoblasts. In the normal course of muscle fiber development or regeneration, myonuclei are actively positione
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd5e4e2050f75dda960db36088c34d92
https://doi.org/10.1101/2020.05.04.076208
https://doi.org/10.1101/2020.05.04.076208