Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ana Ortalli"'
Autor:
Fatou K. Ndiaye, Ana Ortalli, Mickaël Canouil, Marlène Huyvaert, Clara Salazar-Cardozo, Cécile Lecoeur, Marie Verbanck, Valérie Pawlowski, Raphaël Boutry, Emmanuelle Durand, Iandry Rabearivelo, Olivier Sand, Lorella Marselli, Julie Kerr-Conte, Vikash Chandra, Raphaël Scharfmann, Odile Poulain-Godefroy, Piero Marchetti, François Pattou, Amar Abderrahmani, Philippe Froguel, Amélie Bonnefond
Publikováno v:
Molecular Metabolism, Vol 6, Iss 6, Pp 459-470 (2017)
Objectives: Genome-wide association studies (GWAS) have identified >100 loci independently contributing to type 2 diabetes (T2D) risk. However, translational implications for precision medicine and for the development of novel treatments have been di
Externí odkaz:
https://doaj.org/article/34aced17f41e4cc38485bd3672620da0
Autor:
Ana Ortalli, Marlène Huyvaert, Amélie Bonnefond, Lorella Marselli, Piero Marchetti, Marie Verbanck, Fatou K. Ndiaye, Julie Kerr-Conte, Raphaël Scharfmann, Emmanuelle Durand, Philippe Froguel, Amar Abderrahmani, Mickaël Canouil, Olivier Sand, Vikash Chandra, François Pattou, Raphaël Boutry, Valérie Pawlowski, Odile Poulain-Godefroy, C. Lecoeur, Iandry Rabearivelo, Clara Salazar-Cardozo
Publikováno v:
Molecular Metabolism, Vol 6, Iss 6, Pp 459-470 (2017)
Molecular Metabolism
Molecular Metabolism
Objectives Genome-wide association studies (GWAS) have identified >100 loci independently contributing to type 2 diabetes (T2D) risk. However, translational implications for precision medicine and for the development of novel treatments have been dis
Autor:
Amna Khamis, Ana Ortalli, Marlène Huyvaert, Julie Kerr-Conte, Amélie Bonnefond, François Pattou, Beverley Balkau, Mickaël Canouil, Stéphane Lobbens, Cecile Lecoeur, Lorella Marselli, Marie Verbanck, Michel Marre, Ronan Roussel, Piero Marchetti, Fatou K. Ndiaye, Philippe Froguel
Publikováno v:
International journal of obesity (2005)
Genome-wide association studies (GWAS) have identified more than 250 loci associated with body mass index (BMI) and obesity. However, post-GWAS functional genomic investigations have been inadequate for understanding how these genetic loci physiologi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6df276038507fd1358d7d4e1a1fbc19
http://hdl.handle.net/11568/1017715
http://hdl.handle.net/11568/1017715
Autor:
Lorella Marselli, Philippe Froguel, Julie Kerr-Conte, Clara Salazar-Cardozo, Ana Ortalli, Marlène Huyvaert, Amélie Bonnefond, Raphael Scharfmann, François Pattou, Piero Marchetti, Fatou K. Ndiaye, Mickaël Canouil
Publikováno v:
Diabetes & Metabolism. 43:A15-A16
Autor:
Sandra Hübner, Anja Voigt, Jean-Pierre Montmayeur, Wolfgang Meyerhof, Ana Ortalli, Ulrich Boehm, Veit Flockerzi, Soumya Kusumakshi, Martina Pyrski, Frank Zufall, Janka Dörr, Irm Hermans-Borgmeyer
Publikováno v:
Chemical Senses
Chemical Senses, Oxford University Press (OUP), 2015, 40 (6), pp.413-425. ⟨10.1093/chemse/bjv023⟩
Chemical Senses, Oxford University Press (OUP), 2015, 40 (6), pp.413-425. ⟨10.1093/chemse/bjv023⟩
International audience; Transient receptor potential channel subfamily M member 5 (TRPM5) is an important downstream signaling component in a subset of taste receptor cells making it a potential target for taste modulation. Interestingly, TRPM5 has b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::153d2f98bc60bb9e960c14326674f381
https://hal.inrae.fr/hal-02639372
https://hal.inrae.fr/hal-02639372
Autor:
Piero Marchetti, Amélie Bonnefond, Fatou K. Ndiaye, Lorella Marselli, Ana Ortalli, Clara Salazar-Cardozo, Marie Verbanck, Marlène Huyvaert, Loic Yengo, Philippe Froguel
Publikováno v:
Diabetes & Metabolism. 42:A20-A21
Introduction Grâce aux etudes d'association pangenomique [GWAS], plusieurs variants genetiques frequents [SNPs] ont ete identifies associes au diabete de type 2 (DT2). Des les premiers GWAS, les geneticiens ont rapidement considere que les genes pro
Autor:
Ana Ortalli, Gianni Pasquetti, Martine Vaxillaire, Julie Kerr-Conte, A. Leloire, Amélie Bonnefond, Olivier Feraud, Bernadette Neve, Philippe Froguel, Annelise Bennaceur-Griscelli
Publikováno v:
Diabetes & Metabolism. 41:A84
Introduction Des mutations du gene KCNJ11 sont responsables de differentes formes de diabete precoce. La mutation KCNJ11-E227K est associee a la fois au MODY et au diabete neonatal dans differentes familles, suggerant que le fonds genetique familial