Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Julia Morere"'
Autor:
Lionel Perrier, Guillaume Grenet, Bruno Laviolle, Florence Gaillard-Bigot, Pascal Bilbault, Olivier Perche, Hélène Espérou, Jean-François Guérin, Julia Morere, Julien Thevenon, Caroline Guillot, Élodie Bégué, François Gueyffier, Damien Sanlaville, Pierre-Henry Longeray, Nathalie Varoqueaux
Publikováno v:
Thérapie
Thérapie, 2019, 74 (1), pp.1-8. ⟨10.1016/j.therap.2018.11.011⟩
Thérapie, EDP Sciences, 2019, 74 (1), pp.1-8. ⟨10.1016/j.therap.2018.11.011⟩
Thérapie, 2019, 74 (1), pp.1-8. ⟨10.1016/j.therap.2018.11.011⟩
Thérapie, EDP Sciences, 2019, 74 (1), pp.1-8. ⟨10.1016/j.therap.2018.11.011⟩
International audience; Le séquençage du génome est aujourd’hui accessible à la population mais il n’existe que peu de preuves de son utilité comme outil diagnostique, thérapeutique et pronostique. En France, le plan France médecine génom
Autor:
Camille Laberthonnière, Marie-Cécile Gaillard, Natacha Broucqsault, Cherif Badja, Stéphane Roche, Jérôme D. Robin, Julia Morere, Karine Nguyen, Frédérique Magdinier, Camille Dion
Publikováno v:
Scientific Reports
Scientific Reports, Nature Publishing Group, 2019, ⟨10.1038/s41598-019-46861-x⟩
Scientific Reports, 2019, 1, ⟨10.1038/s41598-019-46861-x⟩
Scientific Reports, Vol 9, Iss 1, Pp 1-15 (2019)
Scientific Reports, Nature Publishing Group, 2019, ⟨10.1038/s41598-019-46861-x⟩
Scientific Reports, 2019, 1, ⟨10.1038/s41598-019-46861-x⟩
Scientific Reports, Vol 9, Iss 1, Pp 1-15 (2019)
International audience; 1 Facio-Scapulo Humeral dystrophy (FSHD) is the third most common myopathy, affecting 1 amongst 10,000 individuals (FSHD1, OMIM #158900). This autosomal dominant pathology is associated in 95% of cases with genetic and epigene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bd636a86000d8f6d6952d1613d637c7
https://hal.archives-ouvertes.fr/hal-01951503v2/document
https://hal.archives-ouvertes.fr/hal-01951503v2/document
Autor:
Florence Gaillard-Bigot, Patrice Denèfle, Nathalie Varoqueaux, Damien Sanlaville, Jean-François Guérin, Lionel Perrier, Olivier Perche, Julia Morere, Caroline Guillot, Pascal Bilbault, François Gueyffier, Pierre-Henry Longeray, Guillaume Grenet, Élodie Bégué, Bruno Laviolle, Julien Thevenon, Hélène Espérou
Publikováno v:
Thérapie
Thérapie, 2019, 74 (1), pp.9-15. ⟨10.1016/j.therap.2018.11.012⟩
Thérapie, EDP Sciences, 2019, 74 (1), pp.9-15. ⟨10.1016/j.therap.2018.11.012⟩
Thérapie, 2019, 74 (1), pp.9-15. ⟨10.1016/j.therap.2018.11.012⟩
Thérapie, EDP Sciences, 2019, 74 (1), pp.9-15. ⟨10.1016/j.therap.2018.11.012⟩
International audience; Fifteen years after the completion of first human genome sequencing, the technique is almost a commodity but there is still little evidence of its usefulness as a diagnostic, prognostic or therapeutic tool. In France, the Fran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0d6ca4884b213831d9c3265da70e7da
https://shs.hal.science/halshs-02193717
https://shs.hal.science/halshs-02193717
Autor:
Annamaria Biroccio, Eric Gilson, Anaïs Poulet, Christelle Lenain, Anna Bizard, Delphine Benarroch, Arturo Londoño-Vallejo, Erica Salvati, Laure Sabatier, Els Verhoeyen, Julia Morere, Jing Ye, Sébastien Britton, Bernard Salles, Yunlin Wu, Angela Maria Rizzo, Marc Nadal, Patrick Calsou, Adelaïde Saint-Léger, Marie Josèphe Giraud-Panis, Frédérique Magdinier, Simon Amiard, Serge Bauwens
Publikováno v:
Cell
Cell, 2010, 142 (2), pp.230-242. ⟨10.1016/j.cell.2010.05.032⟩
Cell, Elsevier, 2010, 142 (2), pp.230-242. ⟨10.1016/j.cell.2010.05.032⟩
Cell, Elsevier, 2010, 142 (2), pp.230-42. ⟨10.1016/j.cell.2010.05.032⟩
Cell, 2010, 142 (2), pp.230-242. ⟨10.1016/j.cell.2010.05.032⟩
Cell, Elsevier, 2010, 142 (2), pp.230-242. ⟨10.1016/j.cell.2010.05.032⟩
Cell, Elsevier, 2010, 142 (2), pp.230-42. ⟨10.1016/j.cell.2010.05.032⟩
International audience; Human telomeres are protected from DNA damage by a nucleoprotein complex that includes the repeat-binding factor TRF2. Here, we report that TRF2 regulates the 5' exonuclease activity of its binding partner, Apollo, a member of
Autor:
Frédérique Magdinier, Rafaëlle Bernard, Stéphane Roche, Emmanuelle Salort-Campana, Natacha Broucqsault, Julia Morere, Marie-Cécile Gaillard, Karine Nguyen, Marc Bartoli, Camille Dion, Nicolas Lévy, Armand Tasmadjian, Francesca Puppo, Catherine Vovan, Gwenaëlle Bouget, Charlene Chaix, Shahram Attarian
Publikováno v:
Neurology
Neurology, 2014, 83 (8), pp.733-742. ⟨10.1212/WNL.0000000000000708⟩
ResearcherID
Neurology, American Academy of Neurology, 2014, 83 (8), pp.733-742. ⟨10.1212/WNL.0000000000000708⟩
Neurology, 2014, 83 (8), pp.733-742. ⟨10.1212/WNL.0000000000000708⟩
ResearcherID
Neurology, American Academy of Neurology, 2014, 83 (8), pp.733-742. ⟨10.1212/WNL.0000000000000708⟩
International audience; Objective: We investigated the link between DNA hypomethylation and clinical penetrance in facioscapulohumeral dystrophy (FSHD) because hypomethylation is moderate and heterogeneous in patients and could not thus far be correl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e4412972dca3cbbdd3552b7409a092f
https://hal.science/hal-01610019/document
https://hal.science/hal-01610019/document
Autor:
Paula Frizera, Vassallo, Stéphanie, Simoncini, Isabelle, Ligi, Anne-Line, Chateau, Richard, Bachelier, Stéphane, Robert, Julia, Morere, Samantha, Fernandez, Benjamin, Guillet, Maxime, Marcelli, Edwige, Tellier, Alain, Pascal, Umberto, Simeoni, Francine, Anfosso, Frédérique, Magdinier, Françoise, Dignat-George, Florence, Sabatier
Publikováno v:
Blood. 123(13)
Epidemiological and experimental studies indicate that early vascular dysfunction occurs in low-birth-weight subjects, especially preterm (PT) infants. We recently reported impaired angiogenic activity of endothelial colony-forming cells (ECFCs) in t
Autor:
André Maues De Paula, Stéphane Roche, Julia Torrents, Marie Cécile Gaillard, Frédérique Magdinier, Henry Dufour, Natacha Broucqsault, Claude Desnuelle, Laure Sarda, Marc Bartoli, Carla Fernandez, Emmanuelle Salort-Campana, Karine Nguyen, Julie Dumonceaux, Anne Laure Chesnais, Julia Morere, Maxime Ferreboeuf, Shahram Attarian, Nicolas Lévy
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, 2013, 22 (20), pp.4206-4214. ⟨10.1093/hmg/ddt272⟩
Human Molecular Genetics, Oxford University Press (OUP), 2013, 22 (20), pp.4206-4214. ⟨10.1093/hmg/ddt272⟩
Human Molecular Genetics, 2013, 22 (20), pp.4206-4214. ⟨10.1093/hmg/ddt272⟩
Human Molecular Genetics, Oxford University Press (OUP), 2013, 22 (20), pp.4206-4214. ⟨10.1093/hmg/ddt272⟩
International audience; Facio-scapulo-humeral dystrophy (FSHD) results from deletions in the subtelomeric macrosatellite D4Z4 array on the 4q35 region. Upregulation of the DUX4 retrogene from the last D4Z4 repeated unit is thought to underlie FSHD pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76aec7c466d50eeeb3833d86c47f95b8
https://amu.hal.science/hal-01662672/file/ddt272.pdf
https://amu.hal.science/hal-01662672/file/ddt272.pdf
Autor:
Sophie Collardeau, Julia Morere, Virginie Mariot, Stéphane Roche, Vincent Mouly, Julie Dumonceaux, Sandra Whalen, Frédérique Magdinier, Bettina Bessières, Philippe Rameau, Alexandre Vasiljevic, Tania Attié-Bitach, Claude Desnuelle, Jérôme Robin-Ducellier, Gillian Butler-Browne, Maxime Ferreboeuf, Sabrina Sacconi
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2013, 23 (1), epub ahead of print. ⟨10.1093/hmg/ddt409⟩
Human Molecular Genetics, 2013, 23 (1), epub ahead of print. ⟨10.1093/hmg/ddt409⟩
Human Molecular Genetics, Oxford University Press (OUP), 2013, 23 (1), epub ahead of print. ⟨10.1093/hmg/ddt409⟩
Human Molecular Genetics, 2013, 23 (1), epub ahead of print. ⟨10.1093/hmg/ddt409⟩
International audience; : Facioscapulohumeral muscular dystrophy (FSHD) is one of the most prevalent adult muscular dystrophies. The common clinical signs usually appear during the second decade of life but when the first molecular dysregulations occ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e5da617fc64ef54a946f6a602b0aa99
https://hal.archives-ouvertes.fr/hal-00868855/file/ddt409.pdf
https://hal.archives-ouvertes.fr/hal-00868855/file/ddt409.pdf
Autor:
Frédérique Magdinier, Serge Bauwens, Eric Gilson, Alexandre Ottaviani, Sophie Gazzo, Sylvie Rival-Gervier, Julia Morere, Evelyne Callet-Bauchu, Amina Boussouar, Delphine Rondier, Caroline Schluth-Bolard, Andrea M. Foerster
Publikováno v:
EMBO Journal
EMBO Journal, EMBO Press, 2009, 28, pp.2428-2436
EMBO Journal, EMBO Press, 2009, 28 (16), pp.2428-2436. ⟨10.1038/emboj.2009.201⟩
EMBO Journal, 2009, 28, pp.2428-2436. ⟨10.1038/emboj.2009.201⟩
EMBO Journal, EMBO Press, 2009, 28, pp.2428-2436
EMBO Journal, EMBO Press, 2009, 28 (16), pp.2428-2436. ⟨10.1038/emboj.2009.201⟩
EMBO Journal, 2009, 28, pp.2428-2436. ⟨10.1038/emboj.2009.201⟩
International audience; The localization of genes within the nuclear space is of paramount importance for proper genome functions. However, very little is known on the cis-acting elements determining subnuclear positioning of chromosome segments. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::013e5daf95de02c8535442ca12e4f487
https://hal-amu.archives-ouvertes.fr/hal-01663788/file/2428.full.pdf
https://hal-amu.archives-ouvertes.fr/hal-01663788/file/2428.full.pdf