Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Floriane Petit"'
Autor:
Anna Almeida, Marc Gabriel, Virginie Firlej, Lorena Martin‐Jaular, Matthieu Lejars, Rocco Cipolla, Floriane Petit, Nicolas Vogt, Mabel San‐Roman, Florent Dingli, Damarys Loew, Damien Destouches, Francis Vacherot, Alexandre de la Taille, Clotilde Théry, Antonin Morillon
Publikováno v:
Journal of Extracellular Vesicles, Vol 11, Iss 5, Pp n/a-n/a (2022)
Abstract Long noncoding (lnc)RNAs modulate gene expression alongside presenting unexpected source of neoantigens. Despite their immense interest, their ability to be transferred and control adjacent cells is unknown. Extracellular Vesicles (EVs) offe
Externí odkaz:
https://doaj.org/article/cbeaf8d7285c4ecbb9ccb698e6c6b1b7
Autor:
Olivier Hermine, Agnès Rötig, Anthony Drecourt, Michael Dussiot, Arnold Munnich, Floriane Petit, Coralie Zangarelli
Publikováno v:
Blood
Blood, American Society of Hematology, 2021, 137 (15), pp.2090-2102. ⟨10.1182/blood.2020006987⟩
Blood, American Society of Hematology, 2021, 137 (15), pp.2090-2102. ⟨10.1182/blood.2020006987⟩
Friedreich ataxia (FRDA) is a frequent autosomal recessive disease caused by a GAA repeat expansion in the FXN gene encoding frataxin, a mitochondrial protein involved in iron-sulfur cluster (ISC) biogenesis. Resulting frataxin deficiency affects ISC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bcf3e36d7f4697a651d39cb2ea3d80d
https://doi.org/10.1182/blood.2020006987
https://doi.org/10.1182/blood.2020006987
Autor:
Julien Vibert, Olivier Saulnier, Céline Collin, Floriane Petit, Kyra J.E. Borgman, Jérômine Vigneau, Maud Gautier, Sakina Zaidi, Gaëlle Pierron, Sarah Watson, Nadège Gruel, Clémence Hénon, Sophie Postel-Vinay, Marc Deloger, Virginie Raynal, Sylvain Baulande, Karine Laud-Duval, Véronique Hill, Sandrine Grossetête, Florent Dingli, Damarys Loew, Jacob Torrejon, Olivier Ayrault, Martin F. Orth, Thomas G.P. Grünewald, Didier Surdez, Antoine Coulon, Joshua J. Waterfall, Olivier Delattre
Publikováno v:
Molecular Cell. 82:2458-2471.e9
Many cancers are characterized by gene fusions encoding oncogenic chimeric transcription factors (TFs) such as EWS::FLI1 in Ewing sarcoma (EwS). Here, we find that EWS::FLI1 induces the robust expression of a specific set of novel spliced and polyade
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::985d065fa87a1cf3dab58e6e739e0914
https://doi.org/10.1016/j.molcel.2022.04.019
https://doi.org/10.1016/j.molcel.2022.04.019
Autor:
Olivier Hermine, Meriem Garfa-Traore, Christine Bole-Feysot, Arnold Munnich, Agnès Rötig, Floriane Petit, Anthony Drecourt, Metodi D. Metodiev, Nicolas Goudin, Isabelle Desguerre, Chris Ottolenghi, Joel Babdor, Michael Dussiot, Florence Habarou, Nathalie Boddaert, Valérie Serre, Patrick Nitschke
Publikováno v:
American journal of human genetics. 102(2)
Neurodegeneration with brain iron accumulation (NBIA) is a genetically heterogeneous condition characterized by progressive dystonia with iron accumulation in the basal ganglia. How NBIA-associated mutations trigger iron overload remains poorly under
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cac46326e3baa47fb7089fd834e1e0ad
https://pubmed.ncbi.nlm.nih.gov/29395073
https://pubmed.ncbi.nlm.nih.gov/29395073
Autor:
Floriane Petit, Agnès Delahodde, Cécile Masson, Christine Bole-Feysot, Anthony Drecourt, Fanny Mochel, Christelle Domange, Souad Gherbi, Josseline Kaplan, Sylvie Gerber, Delphine Dupin Deguine, Olivier Sterkers, Georges Challe, Crystel Bonnet, Myriam Oufadem, Laurence Jonard, Oriane Mercati, Laurence Mahieu, Agnès Rötig, Patrick Nitschke, Saber Masmoudi, Stanislas Lyonnet, Isabelle Mosnier, Didier Bouccara, Antoine Paul, Sandrine Marlin, Christelle Vasnier, Ines Ben Aissa
Publikováno v:
American Journal of Human Genetics
American Journal of Human Genetics, 2017, ⟨10.1016/j.ajhg.2017.09.007⟩
American Journal of Human Genetics, Elsevier (Cell Press), 2017, ⟨10.1016/j.ajhg.2017.09.007⟩
American Journal of Human Genetics, 2017, ⟨10.1016/j.ajhg.2017.09.007⟩
American Journal of Human Genetics, Elsevier (Cell Press), 2017, ⟨10.1016/j.ajhg.2017.09.007⟩
Hearing loss and visual impairment in childhood have mostly genetic origins, some of them being related to sensorial neuronal defects. Here, we report on eight subjects from four independent families affected by auditory neuropathy and optic atrophy.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ad29350039c98a833cc62040151c981
https://pubmed.ncbi.nlm.nih.gov/28965846
https://pubmed.ncbi.nlm.nih.gov/28965846