Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sabine Berhouet"'
Autor:
Audrey Gros, Elodie Laharanne, Marie Vergier, Martina Prochazkova-Carlotti, Anne Pham-Ledard, Thomas Bandres, Sandrine Poglio, Sabine Berhouet, Béatrice Vergier, Jean-Philippe Vial, Edith Chevret, Marie Beylot-Barry, Jean-Philippe Merlio
Publikováno v:
PLoS ONE, Vol 12, Iss 3, p e0173171 (2017)
Recent massive parallel sequencing data have evidenced the genetic diversity and complexity of Sézary syndrome mutational landscape with TP53 alterations being the most prevalent genetic abnormality. We analyzed a cohort of 35 patients with SS and a
Externí odkaz:
https://doaj.org/article/b135f7b5173749eaaea80d17cfc7e022
Autor:
Sandrine Poglio, Marie Beylot-Barry, François Moreau-Gaudry, Edith Chevret, David Cappellen, Sabine Berhouet, Martina Prochazkova-Carlotti, Jean-Philippe Merlio, Cécile Boucher, Elodie Laharanne, B. Vergier, Laetitia Andrique, Véronique Guyonnet-Dupérat, Pierre Mélard, Andréa Carla De Souza Góes, Yamina Idrissi, Alice Bibeyran, Anne Pham-Ledard
Publikováno v:
Oncotarget
// Pierre Melard 1, 2, * , Yamina Idrissi 1, * Laetitia Andrique 1, 3 , Sandrine Poglio 1 , Martina Prochazkova-Carlotti 1 , Sabine Berhouet 3 , Cecile Boucher 3 , Elodie Laharanne 1, 3 , Edith Chevret 1 , Anne Pham-Ledard 1, 4 , Andrea Carla De Souz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4731fab39cbffc1a21f202135c63790
https://doi.org/10.18632/oncotarget.11930
https://doi.org/10.18632/oncotarget.11930
Autor:
Elodie Laharanne, Sandrine Poglio, Edith Chevret, Sabine Berhouet, Jean-Philippe Vial, Thomas Bandres, Audrey Gros, B. Vergier, Jean-Philippe Merlio, Marie Vergier, Anne Pham-Ledard, Marie Beylot-Barry, Martina Prochazkova-Carlotti
Publikováno v:
PLoS ONE, Vol 12, Iss 3, p e0173171 (2017)
PLoS ONE
PLoS ONE
Recent massive parallel sequencing data have evidenced the genetic diversity and complexity of Sézary syndrome mutational landscape with TP53 alterations being the most prevalent genetic abnormality. We analyzed a cohort of 35 patients with SS and a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0196c839a64269d86164d97dce5b4e27
http://europepmc.org/articles/PMC5354275?pdf=render
http://europepmc.org/articles/PMC5354275?pdf=render
Autor:
Thomas Bandres, Audrey Gros, Jean-Philippe Merlio, Béatrice Vergier, Anne Pham-Ledard, Marie Vergier, Marie Beylot-Barry, Jean-Philippe Vial, Sandrine Poglio, Martina Prochazkova-Carlotti, Sabine Berhouet, Elodie Laharanne, Edith Chevret
Publikováno v:
Morphologie. 101:248
De recentes analyses de sequencage massif [1] , [2] ont permis de mettre en evidence la diversite et la complexite du profil mutationnel du syndrome de Sezary (SS). Ces differentes etudes ont cependant definit l’alteration de TP53 comme anomalie la
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2c91233fdf8f51ce51d1b530831c8a8
https://doi.org/10.1016/j.morpho.2017.07.022
https://doi.org/10.1016/j.morpho.2017.07.022