Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Laetitia, Barrault"'
Autor:
Delphine Laustriat, Jacqueline Gide, Laetitia Barrault, Emilie Chautard, Clara Benoit, Didier Auboeuf, Anne Boland, Christophe Battail, François Artiguenave, Jean-François Deleuze, Paule Bénit, Pierre Rustin, Sylvia Franc, Guillaume Charpentier, Denis Furling, Guillaume Bassez, Xavier Nissan, Cécile Martinat, Marc Peschanski, Sandrine Baghdoyan
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 4, Iss C (2015)
Major physiological changes are governed by alternative splicing of RNA, and its misregulation may lead to specific diseases. With the use of a genome-wide approach, we show here that this splicing step can be modified by medication and demonstrate t
Externí odkaz:
https://doaj.org/article/984842a497714948b5781bf1e6127059
Autor:
Laetitia, Barrault, Jacqueline, Gide, Tingting, Qing, Lea, Lesueur, Jorg, Tost, Jerome Alexandre, Denis, Michel, Cailleret, Laetitia, Aubry, Marc, Peschanski, Cécile, Martinat, Sandrine, Baghdoyan
Publikováno v:
Cells
Substantial variations in differentiation properties have been reported among human pluripotent cell lines (hPSC), which could affect their utility and clinical safety. We characterized the variable osteogenic capacity observed between different huma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ed33c0b738993db8a632cd615ca4c7cf
https://pubmed.ncbi.nlm.nih.gov/31779280
https://pubmed.ncbi.nlm.nih.gov/31779280
Autor:
Tingting Qing, Jacqueline Gide, Jérôme Alexandre Denis, Laetitia Barrault, Laetitia Aubry, Michel Cailleret, Léa Lesueur, Sandrine Baghdoyan, Cécile Martinat, Jörg Tost, Marc Peschanski
Publikováno v:
Cells
Volume 8
Issue 12
Volume 8
Issue 12
Substantial variations in differentiation properties have been reported among human pluripotent cell lines (hPSC), which could affect their utility and clinical safety. We characterized the variable osteogenic capacity observed between different huma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ef1c38f3bb5981488942c9a259c02a4
https://doi.org/10.3390/cells8121523
https://doi.org/10.3390/cells8121523
Autor:
Anne Boland, Jean-François Deleuze, Sandrine Baghdoyan, Cécile Martinat, Sylvia Franc, Emilie Chautard, Marc Peschanski, Christophe Battail, Xavier Nissan, François Artiguenave, Laetitia Barrault, Jacqueline Gide, Pierre Rustin, Guillaume Charpentier, Clara Benoit, Didier Auboeuf, Paule Bénit, Guillaume Bassez, Delphine Laustriat, Denis Furling
Publikováno v:
Molecular Therapy-Nucleic Acids
Molecular Therapy-Nucleic Acids, Nature Publishing Group, 2015, 4 (11), pp.e262. <10.1038/mtna.2015.35>
Molecular Therapy-Nucleic Acids, 2015, 4 (11), pp.e262. ⟨10.1038/mtna.2015.35⟩
Molecular Therapy-Nucleic Acids, Elsevier, 2015, 4 (11), pp.e262. ⟨10.1038/mtna.2015.35⟩
Molecular Therapy. Nucleic Acids
Molecular Therapy: Nucleic Acids, Vol 4, Iss C (2015)
Molecular Therapy-Nucleic Acids, Nature Publishing Group, 2015, 4 (11), pp.e262. <10.1038/mtna.2015.35>
Molecular Therapy-Nucleic Acids, 2015, 4 (11), pp.e262. ⟨10.1038/mtna.2015.35⟩
Molecular Therapy-Nucleic Acids, Elsevier, 2015, 4 (11), pp.e262. ⟨10.1038/mtna.2015.35⟩
Molecular Therapy. Nucleic Acids
Molecular Therapy: Nucleic Acids, Vol 4, Iss C (2015)
International audience; Major physiological changes are governed by alternative splicing of RNA, and its misregulation may lead to specific diseases. With the use of a genome-wide approach, we show here that this splicing step can be modified by medi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c729ae1c209379b63227c845bb35f033
http://hal.upmc.fr/hal-01277500
http://hal.upmc.fr/hal-01277500
Autor:
Marc Bartoli, Jean-Baptiste Boucheteil, Sylvie Marchand, Azeddine Bentaïb, Nathalie Daniele, Karine Charton, Gaëlle Blandin, Evelyne Gicquel, Laetitia Barrault, Daniel Stockholm, Isabelle Richard
Publikováno v:
Skeletal Muscle
Skeletal Muscle, BioMed Central, 2013, 3 (1), pp.3. ⟨10.1186/2044-5040-3-3⟩
Skeletal Muscle, 2013, 3 (1), pp.3. ⟨10.1186/2044-5040-3-3⟩
Skeletal Muscle, BioMed Central, 2013, 3 (1), pp.3. ⟨10.1186/2044-5040-3-3⟩
Skeletal Muscle, 2013, 3 (1), pp.3. ⟨10.1186/2044-5040-3-3⟩
Background The complexity of the skeletal muscle and the identification of numerous human disease-causing mutations in its constitutive proteins make it an interesting tissue for proteomic studies aimed at understanding functional relationships of in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3adb6f3a5dcca027109820b90354e007
https://doi.org/10.1186/2044-5040-3-3
https://doi.org/10.1186/2044-5040-3-3
Autor:
Bjarne Udd, Laetitia Barrault, Marie Malissen, Isabelle Richard, Tayebeh Soheili, Norma Perez, Marc Bartoli, Bernard Malissen, Evelyne Gicquel, Olivier Danos, Nathalie Vincent-Lacaze
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2008, 17 (9), pp.1214-21. ⟨10.1093/hmg/ddn029⟩
Human Molecular Genetics, 2008, 17 (9), pp.1214-21. ⟨10.1093/hmg/ddn029⟩
Human Molecular Genetics, Oxford University Press (OUP), 2008, 17 (9), pp.1214-21. ⟨10.1093/hmg/ddn029⟩
Human Molecular Genetics, 2008, 17 (9), pp.1214-21. ⟨10.1093/hmg/ddn029⟩
International audience; Limb girdle muscular dystrophy type 2D (LGMD2D, OMIM600119) is a genetic progressive myopathy that is caused by mutations in the human alpha-sarcoglycan gene (SGCA). Here, we have introduced in mice the most prevalent LGMD2D m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4e419feb3c8aef64535c6368e0fa9ed
https://hal.archives-ouvertes.fr/hal-00294192
https://hal.archives-ouvertes.fr/hal-00294192