Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Sophie Ron"'
Autor:
Moran Rathaus, Loziana Azem, Rinat Livne, Sophie Ron, Idit Ron, Rotem Hadar, Gilat Efroni, Amnon Amir, Tzipi Braun, Yael Haberman, Amir Tirosh
Publikováno v:
Molecular Metabolism, Vol 88, Iss , Pp 101985- (2024)
Objective: Excessive consumption of added sugars has been linked to the rise in obesity and associated metabolic abnormalities. Non-nutritive sweeteners (NNSs) offer a potential solution to reduce sugar intake, yet their metabolic safety remains deba
Externí odkaz:
https://doaj.org/article/966702a3adb845ca832827acdbcbefa4
Autor:
Idit Ron, Reut Kassif Lerner, Moran Rathaus, Rinat Livne, Sophie Ron, Ehud Barhod, Rina Hemi, Amit Tirosh, Tzipora Strauss, Keren Ofir, Ido Goldstein, Itai M. Pessach, Amir Tirosh
Publikováno v:
JCI Insight, Vol 6, Iss 20 (2021)
During pregnancy, fetal glucose production is suppressed, with rapid activation immediately postpartum. Fatty acid–binding protein 4 (FABP4) was recently demonstrated as a regulator of hepatic glucose production and systemic metabolism in animal mo
Externí odkaz:
https://doaj.org/article/9128e759e9e1420eb809744ca1ac8e25
Publikováno v:
Diabetes. 71
Accumulating evidence link sugar-containing foods and beverages to adverse health outcomes. Non-Caloric Sweeteners (NCSs) are an alternative sugar source that lead to reduction in calories, and may mitigate body weight gain and hyperglycemia, especia
Publikováno v:
Diabetes. 71
Obesity is a leading global health concern and a major risk factor for type-2 diabetes. Thus, identifying mechanisms linking obesity to insulin resistance is of great importance. Chronic low-grade inflammation of the adipose tissue (AT) observed in o
Autor:
Abdulmonem Hamid, Alexandre Vallée, Sophie Rong, Olivier Boche, Sandra De Miranda, Laurence Beaumont-Azuar, Sylvie Colin de Verdière, Dominique Grenet, Marc Stern, Benjamin Zuber, Jerôme Devaquet, Julien Fessler, Julien De Wolf, Ciprian Pricopi, Matthieu Glorion, Edouard Sage, Jonathan Messika, Antoine Magnan, François Parquin, Clément Picard, Antoine Roux, Olivier Brugière
Publikováno v:
JHLT Open, Vol 6, Iss , Pp 100145- (2024)
Background: Gastroesophageal reflux disease (GERD) is highly prevalent after lung transplantation (LTx) and is suspected to favor the development of chronic lung allograft dysfunction (CLAD), almost of bronchiolitis obliterans syndrome (BOS) phenotyp
Externí odkaz:
https://doaj.org/article/b0d2a276db6d4a39b43489899653423f
Autor:
Tzipora Strauss, Sophie Ron, Rinat Livne, Keren Ofir, Idit Ron, Moran Rathaus, Ido Goldstein, Amir Tirosh, Reut Kassif Lerner, Amit Tirosh, Itai M. Pessach, Ehud Barhod, Rina Hemi
Publikováno v:
JCI Insight
During pregnancy, fetal glucose production is suppressed, with rapid activation immediately postpartum. Fatty acid-binding protein 4 (FABP4) was recently demonstrated as a regulator of hepatic glucose production and systemic metabolism in animal mode
Autor:
Idit Ron, Ediz S. Calay, Amir Tirosh, Rinat Livne, Amit Tirosh, Sophie Ron, Moran Rathaus, Abdullah Yalcin, Yankun G. Lee, Gurol Tuncman, Gökhan S. Hotamisligil, Ana Paula Arruda, Neri Minsky
Publikováno v:
Cell Metab
Endoplasmic reticulum stress (ERS) has a pathophysiological role in obesity-associated insulin resistance. Yet, the coordinated tissue response to ERS remains unclear. Increased connexin 43 (Cx43)-mediated intercellular communication has been implica
Autor:
David Dawei Yang, Marlene Rio, Caroline Michot, Nathalie Boddaert, Wael Yacoub, Nicolas Garcelon, Briac Thierry, Damien Bonnet, Sophie Rondeau, Dominique Herve, Stephanie Guey, Francois Angoulvant, Valerie Cormier-Daire
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-12 (2022)
Abstract Background Myhre syndrome (MS) is a rare genetic disease characterized by skeletal disorders, facial features and joint limitation, caused by a gain of function mutation in SMAD4 gene. The natural history of MS remains incompletely understoo
Externí odkaz:
https://doaj.org/article/aa57b9a4fd8f45b48190bef9b77eba66
Autor:
Margot Charlotte Riou, Muriel de La Dure-Molla, Stéphane Kerner, Sophie Rondeau, Adrien Legendre, Valerie Cormier-Daire, Benjamin P. J. Fournier
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: Singleton–Merten syndrome type 1 (SGMRT1) is a rare autosomal dominant disorder caused by IFIH1 variations with blood vessel calcifications, teeth anomalies, and bone defects.Aim: We aimed to summarize the oral findings in SGMRT1 throug
Externí odkaz:
https://doaj.org/article/41e8a73ba13a4718821b4f8562325c78
Autor:
Virginia Pannabecker, Cori Biddle, Julia Feerrar, Barbara Ferrara, Paige Flanagan, Susan La Paro, Sophie Rondeau, Lynda Wright
Publikováno v:
Virginia Libraries, Vol 63, Iss 1 (2020)
The Virginia Libraries Editorial Board is pleased to present volume 63 (Vol. 63), and with it, a transition to a new publishing platform, Ubiquity, provided by our publisher, VT Publishing of University Libraries, Virginia Tech. While Virginia Librar
Externí odkaz:
https://doaj.org/article/5b52e6765921467381d36758df41937d