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of 434
pro vyhledávání: '"A. Pacault"'
Autor:
Margaux Geier, Jessica Nguyen, Estelle Dhamelincourt, Hélène Babey, Renaud Descourt, Gilles Quéré, Gilles Robinet, François Lucia, Mathilde Pacault
Publikováno v:
Heliyon, Vol 10, Iss 11, Pp e31944- (2024)
Background: MET exon 14 (METex14) skipping mutations are oncogenic drivers observed in approximately 3–4% of non-small cell lung cancers (NSCLC). Several distinct genetic alterations leading to METex14 have been reported but clinical significances
Externí odkaz:
https://doaj.org/article/a9c1e28597024255a1a7358d84bfa97a
Autor:
Verebi, Camille, Gravrand, Victor, Pacault, Mathilde, Audrezet, Marie-Pierre, Couque, Nathalie, Vincent, Marie-Claire, Leturcq, France, Tsatsaris, Vassilis, Bienvenu, Thierry, Nectoux, Juliette
Publikováno v:
In Gynécologie Obstétrique Fertilité & Sénologie October 2023 51(10):463-470
Autor:
Marine Delamare, Amandine Le Roy, Mathilde Pacault, Loïc Schmitt, Céline Garrec, Nada Maaziz, Matti Myllykoski, Antoine Rimbert, Valéna Karaghiannis, Bernard Aral, Mark Catherwood, Fabrice Airaud, Lamisse Mansour-Hendili, David Hoogewijs, Edoardo Peroni, Salam Idriss, Valentine Lesieur, Amandine Caillaud, Karim Si-Tayeb, Caroline Chariau, Anne Gaignerie, Minke Rab, Torsten Haferlach, Manja Meggendorfer, Stéphane Bézieau, Andrea Benetti, Nicole Casadevall, Pierre Hirsch, Christian Rose, Mathieu Wemeau, Frédéric Galacteros, Bruno Cassinat, Beatriz Bellosillo, Celeste Bento, Richard van Wijk, Petro E. Petrides, Maria Luigia Randi, Mary Frances McMullin, Peppi Koivunen, François Girodon, Betty Gardie, ECYT consortium
Publikováno v:
Haematologica, Vol 108, Iss 11 (2023)
Hereditary erythrocytosis is a rare hematologic disorder characterized by an excess of red blood cell production. Here we describe a European collaborative study involving a collection of 2,160 patients with erythrocytosis sequenced in ten different
Externí odkaz:
https://doaj.org/article/3f9446a9e07d45d496f7af7a30c39bce
Autor:
Mathilde Pacault, Camille Verebi, Magali Champion, Lucie Orhant, Alexandre Perrier, Emmanuelle Girodon, France Leturcq, Dominique Vidaud, Claude Férec, Thierry Bienvenu, Romain Daveau, Juliette Nectoux
Publikováno v:
PLoS ONE, Vol 18, Iss 4, p e0280976 (2023)
Non-invasive prenatal diagnosis of single-gene disorders (SGD-NIPD) has been widely accepted, but is mostly limited to the exclusion of either paternal or de novo mutations. Indeed, it is still difficult to infer the inheritance of the maternal allel
Externí odkaz:
https://doaj.org/article/924e81eb10694715866e532df5d26618
Akademický článek
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Autor:
Pietraccini, Matteo, Delon, Eloise, Santandrea, Audrey, Pacault, Stéphanie, Glaude, Pierre-Alexandre, Dufour, Anthony, Dufaud, Olivier
Publikováno v:
In Journal of Loss Prevention in the Process Industries November 2021 73
Autor:
Brakta, Charlyne, Tabet, Anne-Claude, Puel, Mathilde, Pacault, Mathilde, Stolzenberg, Marie-Claude, Goudet, Claire, Merger, Marguerite, Reumaux, Héloïse, Lambert, Nathalie, Alioua, Najiba, Malan, Valérie, Hanein, Sylvain, Dupin-Deguine, Delphine, Treiner, Emmanuel, Lefèvre, Guillaume, Farhat, Méryem-Maud, Luca, Luminita Elena, Hureaux, Marguerite, Li, Hailun, Chelloug, Nora
Publikováno v:
Journal of Clinical Immunology; 2025, Vol. 45 Issue 1, p1-10, 10p
Autor:
Santandrea, Audrey, Pacault, Stéphanie, Bau, Sébastien, Oudart, Yohan, Vignes, Alexis, Perrin, Laurent, Dufaud, Olivier
Publikováno v:
In Journal of Loss Prevention in the Process Industries March 2021 69
Autor:
Pacault, Mathilde1,2 (AUTHOR), Verebi, Camille2 (AUTHOR), Champion, Magali3 (AUTHOR), Orhant, Lucie2 (AUTHOR), Perrier, Alexandre2 (AUTHOR), Girodon, Emmanuelle2 (AUTHOR), Leturcq, France2 (AUTHOR), Vidaud, Dominique2 (AUTHOR), Férec, Claude1 (AUTHOR), Bienvenu, Thierry2 (AUTHOR), Daveau, Romain4 (AUTHOR), Nectoux, Juliette2 (AUTHOR) juliette.nectoux@aphp.fr
Publikováno v:
PLoS ONE. 4/24/2023, Vol. 17 Issue 4, p1-19. 19p.
Autor:
Hazotte, Claire, Laubie, Baptiste, Pacault, Stéphanie, Dufaud, Olivier, Simonnot, Marie-Odile
Publikováno v:
In Biomass and Bioenergy September 2020 140