Zobrazeno 11 - 20
of 89
pro vyhledávání: '"Juliette Albuisson"'
Autor:
Soto Romuald Kiando, Nathan R Tucker, Luis-Jaime Castro-Vega, Alexander Katz, Valentina D'Escamard, Cyrielle Tréard, Daniel Fraher, Juliette Albuisson, Daniella Kadian-Dodov, Zi Ye, Erin Austin, Min-Lee Yang, Kristina Hunker, Cristina Barlassina, Daniele Cusi, Pilar Galan, Jean-Philippe Empana, Xavier Jouven, Anne-Paule Gimenez-Roqueplo, Patrick Bruneval, Esther Soo Hyun Kim, Jeffrey W Olin, Heather L Gornik, Michel Azizi, Pierre-François Plouin, Patrick T Ellinor, Iftikhar J Kullo, David J Milan, Santhi K Ganesh, Pierre Boutouyrie, Jason C Kovacic, Xavier Jeunemaitre, Nabila Bouatia-Naji
Publikováno v:
PLoS Genetics, Vol 12, Iss 10, p e1006367 (2016)
Fibromuscular dysplasia (FMD) is a nonatherosclerotic vascular disease leading to stenosis, dissection and aneurysm affecting mainly the renal and cerebrovascular arteries. FMD is often an underdiagnosed cause of hypertension and stroke, has higher p
Externí odkaz:
https://doaj.org/article/81b279ae7ed0458d82b4b6846aee7c7e
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:
Frank Johannes, Emmanuelle Porcher, Felipe K Teixeira, Vera Saliba-Colombani, Matthieu Simon, Nicolas Agier, Agnès Bulski, Juliette Albuisson, Fabiana Heredia, Pascal Audigier, David Bouchez, Christine Dillmann, Philippe Guerche, Frédéric Hospital, Vincent Colot
Publikováno v:
PLoS Genetics, Vol 5, Iss 6, p e1000530 (2009)
Loss or gain of DNA methylation can affect gene expression and is sometimes transmitted across generations. Such epigenetic alterations are thus a possible source of heritable phenotypic variation in the absence of DNA sequence change. However, attem
Externí odkaz:
https://doaj.org/article/bafad8a6e27b4b59b4d9ffd954dd9a25
Autor:
Martin Chevarin, Diana Alcantara, Juliette Albuisson, Marie-Agnès Collonge-Rame, Céline Populaire, Zohair Selmani, Amandine Baurand, Caroline Sawka, Geoffrey Bertolone, Patrick Callier, Yannis Duffourd, Philippe Jonveaux, Yves-Jean Bignon, Isabelle Coupier, François Cornelis, Christophe Cordier, Monique Mozelle-Nivoix, Jean-Baptiste Rivière, Paul Kuentz, Christel Thauvin, Romain Boidot, François Ghiringhelli, Marc O'Driscoll, Laurence Faivre, Sophie Nambot
Publikováno v:
Oncotarget. 14:111-125
Autor:
Simon Verdez, Juliette Albuisson, Yannis Duffourd, Romain Boidot, Manon Reda, Christel Thauvin-Robinet, Jean-David Fumet, Sylvain Ladoire, Sophie Nambot, Patrick Callier, Laurence Faivre, François Ghiringhelli, Nicolas Picard
Publikováno v:
Pharmacogenomics. 23:759-770
Background: Germline sequencing of individual genomes can detect alleles responsible for adverse drug reactions (ADRs) in relation to chemotherapy, targeted agents, antiemetics or pain treatment. Materials & methods: To evaluate the interest of such
Autor:
Shai Carmi, Guillaume Goudot, Idit Tessler, Juliette Albuisson, Dan Gilon, Emmanuel Messas, Shoshana Shpitzen, Ronen Durst
Publikováno v:
AORTA
AORTA, 2021, 09, pp.139-146. ⟨10.1055/s-0041-1730294⟩
AORTA Journal
AORTA, 2021, 09, pp.139-146. ⟨10.1055/s-0041-1730294⟩
AORTA Journal
Bicuspid aortic valve (BAV) is the most common valvular congenital heart disease, with a prevalence of 0.5 to 2% in the general population. Patients with BAV are at risk for developing cardiovascular complications, some of which are life-threatening.
Autor:
Yue Jiao, Thérèse Truong, Séverine Eon-Marchais, Noura Mebirouk, Sandrine M. Caputo, Marie-Gabrielle Dondon, Mojgan Karimi, Dorothée Le Gal, Juana Beauvallet, Édith Le Floch, Claire Dandine-Roulland, Delphine Bacq-Daian, Robert Olaso, Juliette Albuisson, Séverine Audebert-Bellanger, Pascaline Berthet, Valérie Bonadona, Bruno Buecher, Olivier Caron, Mathias Cavaillé, Jean Chiesa, Chrystelle Colas, Marie-Agnès Collonge-Rame, Isabelle Coupier, Capucine Delnatte, Antoine De Pauw, Hélène Dreyfus, Sandra Fert-Ferrer, Marion Gauthier-Villars, Paul Gesta, Sophie Giraud, Laurence Gladieff, Lisa Golmard, Christine Lasset, Sophie Lejeune-Dumoulin, Mélanie Léoné, Jean-Marc Limacher, Alain Lortholary, Élisabeth Luporsi, Véronique Mari, Christine M. Maugard, Isabelle Mortemousque, Emmanuelle Mouret-Fourme, Sophie Nambot, Catherine Noguès, Cornel Popovici, Fabienne Prieur, Pascal Pujol, Nicolas Sevenet, Hagay Sobol, Christine Toulas, Nancy Uhrhammer, Dominique Vaur, Laurence Venat, Anne Boland-Augé, Pascal Guénel, Jean-François Deleuze, Dominique Stoppa-Lyonnet, Nadine Andrieu, Fabienne Lesueur
Publikováno v:
European journal of cancer (Oxford, England : 1990). 179
Three partially overlapping breast cancer polygenic risk scores (PRS) comprising 77, 179 and 313 SNPs have been proposed for European-ancestry women by the Breast Cancer Association Consortium (BCAC) for improving risk prediction in the general popul
Autor:
Sandy, Chevrier, Astrid, Brasselet, Marion, Carnet, Angélique, Chevriaux, Anne, Gibeaud, Marine, Jourdain, Hugo, Mananet, Caroline, Truntzer, Françoise, Beltjens, Céline, Charon-Barra, Laurent, Arnould, Juliette, Albuisson, Anthony, Comte, Valentin, Derangère, Vincent, Goussot, Romain, Boidot
Publikováno v:
International Journal of Molecular Medicine. 49
Molecular testing is extremely important in cancer care, starting as early as at diagnosis. In order to address the challenge of providing reliable results within the timeframe adapted to patient management and suitable to guide clinical decisions, a
Autor:
Yonatan Levin, Shoshana Shpitzen, Noga Reshef, Guy Kelman, Dan Gilon, Juliette Albuisson, Jean-Michaël Mazzella, Donna R. Zwas, Idit Tessler, Galina Levin, Emmanuel Messas, Ronen Durst, Shai Carmi, Guillaume Goudot, Charles Cheng
Publikováno v:
American Journal of Cardiology
American Journal of Cardiology, 2022, 163, pp.85-90. ⟨10.1016/j.amjcard.2021.09.051⟩
American Journal of Cardiology, 2022, 163, pp.85-90. ⟨10.1016/j.amjcard.2021.09.051⟩
International audience; Bicuspid aortic valve (BAV) is a common congenital heart disease, with a 10-fold higher prevalence in first-degree relatives. BAV has different phenotypes based on the morphology of cusp fusion. These phenotypes are associated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78c3b449fb57fac722e28416b96da517
https://www.hal.inserm.fr/inserm-03880653/document
https://www.hal.inserm.fr/inserm-03880653/document
Autor:
François Ghiringhelli, Isabelle Ray Coquard, Hugo Mananet, Caroline Truntzer, Zoé Tharin, Jean-David Fumet, Julie Lecuelle, Juliette Albuisson, Valentin Derangère, Laurent Arnould, Vincent Goussot, Romain Boidot
Publikováno v:
Cancers
Volume 13
Issue 17
Cancers, Vol 13, Iss 4394, p 4394 (2021)
Volume 13
Issue 17
Cancers, Vol 13, Iss 4394, p 4394 (2021)
Simple Summary High-grade serous ovarian carcinoma (HGSC) could be analyzed with a molecular stratification defined by different genomic instability signatures associated with specific mutational process and prognostic biomarkers. Immune infiltrate i