Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Emilie Bricout-Neveu"'
Autor:
Marion Benazra, Marie-José Lecomte, Claire Colace, Andreas Müller, Cécile Machado, Severine Pechberty, Emilie Bricout-Neveu, Maud Grenier-Godard, Michele Solimena, Raphaël Scharfmann, Paul Czernichow, Philippe Ravassard
Publikováno v:
Molecular Metabolism, Vol 4, Iss 12, Pp 916-925 (2015)
Objectives: Access to immortalized human pancreatic beta cell lines that are phenotypically close to genuine adult beta cells, represent a major tool to better understand human beta cell physiology and develop new therapeutics for Diabetes. Here we d
Externí odkaz:
https://doaj.org/article/c99264b7f4324fab94afdcac5d1b45dc
Autor:
Philippe Ravassard, Emilie Bricout-Neveu, Yasmine Hazhouz, Severine Pechberty, Jacques Mallet, Paul Czernichow, Raphael Scharfmann
Publikováno v:
PLoS ONE, Vol 4, Iss 3, p e4731 (2009)
BACKGROUND: There is increasing interest in developing human cell lines to be used to better understand cell biology, but also for drug screening, toxicology analysis and future cell therapy. In the endocrine pancreatic field, functional human beta c
Externí odkaz:
https://doaj.org/article/b5c1bdb80444441f987b822cba4a6276
Autor:
Paul Czernichow, Karine Reynaud, Severine Pechberty, Marie José Lecomte, Cindy Maenhoudt, Philippe Ravassard, Emilie Bricout-Neveu
Publikováno v:
The Anatomical Record. 300:1429-1438
Our objectives were to describe, in Beagle dogs, the ontogenesis of beta (insulin-producing) and alpha (glucagon-producing) cells from fetal to early postnatal life and adulthood. In addition, to have some insight into interspecies comparison, Beagle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f72d6c6a721e17d2373875e38dee3a3
https://doi.org/10.1002/ar.23595
https://doi.org/10.1002/ar.23595
Autor:
Emilie Bricout-Neveu, Thomas Frogne, Raphael Scharfmann, Philippe Ravassard, Claude Rescan, Mads Grønborg, Ole D. Madsen, Marc Diedisheim, Olivier Albagli, Signe Ingvarsen, Jeannette S. Kirkegaard
Publikováno v:
Journal of Clinical Investigation
Journal of Clinical Investigation, 2016, 126 (3), pp.1109-1113. ⟨10.1172/JCI83573⟩
Journal of Clinical Investigation, American Society for Clinical Investigation, 2016, 126 (3), pp.1109-1113. ⟨10.1172/JCI83573⟩
Journal of Clinical Investigation, American Society for Clinical Investigation, 2016, 126 (3), pp.1109-1113. 〈10.1172/JCI83573〉
Journal of Clinical Investigation, 2016, 126 (3), pp.1109-1113. ⟨10.1172/JCI83573⟩
Journal of Clinical Investigation, American Society for Clinical Investigation, 2016, 126 (3), pp.1109-1113. ⟨10.1172/JCI83573⟩
Journal of Clinical Investigation, American Society for Clinical Investigation, 2016, 126 (3), pp.1109-1113. 〈10.1172/JCI83573〉
International audience; It has been reported that endogenous retroviruses can contaminate human cell lines that have been passaged as xenotransplants in immunocompromised mice. We previously developed and described 2 human pancreatic β cell lines (E
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa09b6f5794614b1960642c6501cb8eb
https://doi.org/10.1172/jci83573
https://doi.org/10.1172/jci83573
Autor:
Raphael Scharfmann, Manon von Bülow, Matthias Lohmann, Fanny Guez, Severine Pechberty, Yasmine Hazhouz, Paul Czernichow, Philippe Ravassard, Emilie Bricout-Neveu, Maud Grenier-Godard, Latif Rachdi
Publikováno v:
Journal of Clinical Investigation; Vol 124
Journal of Clinical Investigation
Journal of Clinical Investigation, American Society for Clinical Investigation, 2014, 124 (5), pp.2087-2098. 〈10.1172/JCI72674〉
Journal of Clinical Investigation, 2014, 124 (5), pp.2087-2098. ⟨10.1172/JCI72674⟩
Journal of Clinical Investigation, American Society for Clinical Investigation, 2014, 124 (5), pp.2087-2098. ⟨10.1172/JCI72674⟩
Journal of Clinical Investigation
Journal of Clinical Investigation, American Society for Clinical Investigation, 2014, 124 (5), pp.2087-2098. 〈10.1172/JCI72674〉
Journal of Clinical Investigation, 2014, 124 (5), pp.2087-2098. ⟨10.1172/JCI72674⟩
Journal of Clinical Investigation, American Society for Clinical Investigation, 2014, 124 (5), pp.2087-2098. ⟨10.1172/JCI72674⟩
International audience; Diabetic patients exhibit a reduction in β cells, which secrete insulin to help regulate glucose homeostasis; however, little is known about the factors that regulate proliferation of these cells in human pancreas. Access to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b71e8648c6872da3943ae47e021820ef
A genetically engineered human pancreatic β cell line exhibiting glucose-inducible insulin secretion
Autor:
Emilie Bricout-Neveu, Yasmine Hazhouz, Mathieu Armanet, Raphael Scharfmann, Severine Pechberty, Philippe Ravassard, Paul Czernichow
Publikováno v:
Journal of Clinical Investigation. 121:3589-3597
Despite intense efforts over the past 30 years, human pancreatic β cell lines have not been available. Here, we describe a robust technology for producing a functional human β cell line using targeted oncogenesis in human fetal tissue. Human fetal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0c11d696268eb0269c789d8260bc04e
https://doi.org/10.1172/jci58447
https://doi.org/10.1172/jci58447
Autor:
Ravassard P; Biotechnology & Biotherapy group Centre de Recherche Institut du Cerveau et de la Moelle CNRS UMR7225, INSERM UMRS795, Université Pierre et Marie Curie, Paris, France. mail: ravassar@chups.jussieu.fr, Emilie Bricout-Neveu, Hazhouz Y, Pechberty S, Mallet J, Czernichow P, Scharfmann R
Publikováno v:
PloS one [PLoS One] 2009; Vol. 4 (3), pp. e4731. Date of Electronic Publication: 2009 Mar 06.