Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Juliette Albuisson"'
Autor:
Loïck Galland, Nicolas Roussot, Isabelle Desmoulins, Didier Mayeur, Courèche Kaderbhai, Silvia Ilie, Audrey Hennequin, Manon Reda, Juliette Albuisson, Laurent Arnould, Romain Boidot, Caroline Truntzer, François Ghiringhelli, Sylvain Ladoire
Publikováno v:
Cancers, Vol 15, Iss 4, p 1299 (2023)
Breast cancer is the most frequently occurring cancer worldwide. With its increasing incidence, it is a major public health problem, with many therapeutic challenges such as precision medicine for personalized treatment. Thanks to next-generation seq
Externí odkaz:
https://doaj.org/article/d71e691d1a4c414ea9df076c2af80ee1
Autor:
Julie Lecuelle, Romain Boidot, Hugo Mananet, Valentin Derangère, Juliette Albuisson, Vincent Goussot, Laurent Arnould, Zoé Tharin, Isabelle Ray Coquard, François Ghiringhelli, Caroline Truntzer, Jean-David Fumet
Publikováno v:
Cancers, Vol 13, Iss 17, p 4394 (2021)
Purpose: Immune infiltration is a prognostic factor in high-grade serous ovarian carcinoma (HGSC) but immunotherapy efficacy is disappointing. Genomic instability is now used to guide the therapeutic value of PARP inhibitors. We aimed to investigate
Externí odkaz:
https://doaj.org/article/3a66ce41f7a64d059f90bf4fdadd9296
Autor:
Hervé Crehalet, Gilles Millat, Juliette Albuisson, Véronique Bonnet, Isabelle Rouvet, Robert Rousson, Dominique Bozon
Publikováno v:
Cardiogenetics, Vol 2, Iss 1, Pp e6-e6 (2012)
The identification of molecular anomalies in patients with inherited arrhythmias or cardiomyopathies is a multi challenge due to: i) the number of genes involved; ii) the number of polymorphisms and the fact that most mutations are private; and iii)
Externí odkaz:
https://doaj.org/article/ce2807ab1b464ac8b8b76709dbdfc242
Autor:
Juliette Albuisson, Robert Rousson, Hervé Crehalet, Dominique Bozon, Gilles Millat, Véronique Bonnet, Isabelle Rouvet
Publikováno v:
Cardiogenetics, Vol 2, Iss 1, Pp e6-e6 (2012)
Cardiogenetics; Volume 2; Issue 1; Pages: e6
Cardiogenetics; Volume 2; Issue 1; Pages: e6
The identification of molecular anomalies in patients with inherited arrhythmias or cardiomyopathies is a multi challenge due to: i) the number of genes involved; ii) the number of polymorphisms and the fact that most mutations are private; and iii)