Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Françoise Conte-Auriol"'
Autor:
Lisa Cole Burnett, Françoise Conte Auriol, Eric Bieth, Jean Pierre Salles, Juliette Salles, Maithé Tauber, Gwenaelle Diene, Catherine Molinas, Rudolph L. Leibel, Boris V. Skryabin, Isabelle Gennero, Timofey S. Rozhdestvensky, Sanaa Eddiry
Publikováno v:
Genetics in Medicine
Genetics in Medicine, 2021, 23 (9), pp.1664-1672. ⟨10.1038/s41436-021-01185-y⟩
Genetics in Medicine, 2021, 23 (9), pp.1664-1672. ⟨10.1038/s41436-021-01185-y⟩
International audience; Purpose: Prader-Willi syndrome (PWS) is a neurodevelopmental disorder with hypothalamic dysfunction due to deficiency of imprinted genes located on the 15q11-q13 chromosome. Among them, the SNORD116 gene appears critical for t
Autor:
Jérôme Sales de Gauzy, Nicolas Beton, Aurélie Batut, Frank Accabled, Isabelle Gennero, Jean Pierre Salles, Françoise Conte Auriol, Ronan Barre, Sara Laurencin, Maithé Tauber, Sanaa Eddiry
Publikováno v:
Biochemistry and Biophysics Reports
Biochemistry and Biophysics Reports, 2020, 24, pp.100782-. ⟨10.1016/j.bbrep.2020.100782⟩
Biochemistry and Biophysics Reports, Vol 24, Iss, Pp 100782-(2020)
Biochemistry and Biophysics Reports, 2020, 24, pp.100782-. ⟨10.1016/j.bbrep.2020.100782⟩
Biochemistry and Biophysics Reports, Vol 24, Iss, Pp 100782-(2020)
We have examined the Acylated Ghrelin (AG)/Gi pathway in different human osteoblastic cell lines. We have found that: 1) AG induces differentiation/mineralization only in mature osteoblasts; 2) the expression of GHS-R1a increases up to the mature cel
Autor:
Romain Favre, Marie-Pierre Lavocat, Bernard Boudailliez, Charlotte Lucas, Camille Fédou, Jean-Sebastien Saulnier Blache, Anne-Sophie Weingertner, Blandine Hougas, Joost P. Schanstra, Pascal Gaucherand, Sylvie Cloarec, Julie Batut, Catherine Noel, J. Gondry, Philippe Eckart, Norbert Winer, Benjamin Breuil, Gérard Champion, Jean-Baptiste Benevent, Franck Perrotin, Christophe Vayssière, Florence Biquard, Harald Mischak, Gwenaelle Le Bouar, Jérôme Massardier, Françoise Conte Auriol, Pedro Magalhães, Sophie Martin, Jean-Paul Bory, Sophie Collardeau-Frachon, Eve Mousty, Lucie Bessenay, Corinne Floch, Julie Klein, Amelie Ryckewaert, Elisabeth Simon, Alain Martin, Guylène Bourdat-Michel, Marie-Françoise Froute, Franz Schaefer, Pascale Marcorelles, Stéphane Decramer, Nabila Moussaoui, Franck Boizard, Marie-Christine Manca-Pellissier, Mariannick Maupin-Hyvonnet, Marion Groussolles, Jean-Marie Delbosc, Guylène Feuillet, Anke Raaijmakers, François Nobili, Sophie Taque, Petra Zürbig, Vincent Guigonis, Audrey Casemayou, Patrick Blader, An Hindryckx, Luc Decatte, Karel Allegaert, Ophélie Lescat, Eric Neau, Odile Basmaison, Emma Allain-Launay, Agnes Sartor, Jean-Loup Bascands, Claudine Le Vaillant, Hélène Laurichesse Delmas, Bénédicte Buffin-Meyer, Nadia Lounis, Anne-Hélène Saliou, Véronique Baudouin, Elena Levtchenko, Maryse Fiorenza, Christine Pietrement, Valérie Goua, Marina Merveille, Laurent Bidat, Yves Aubard, Alexandra Benachi, Sylvie Kessler, Loic De Parscau, Jean-François Oury, Fabienne Prieur
Publikováno v:
Kidney International
Kidney International, Nature Publishing Group, 2020, ⟨10.1016/j.kint.2020.06.043⟩
Kidney International, Nature Publishing Group, 2021, 99 (3), pp.737-749. ⟨10.1016/j.kint.2020.06.043⟩
Kidney International, Nature Publishing Group, 2020, 99 (3), pp.737-749. ⟨10.1016/j.kint.2020.06.043⟩
Kidney International, 2021, 99 (3), pp.737-749. ⟨10.1016/j.kint.2020.06.043⟩
Kidney International, Nature Publishing Group, 2020, ⟨10.1016/j.kint.2020.06.043⟩
Kidney International, Nature Publishing Group, 2021, 99 (3), pp.737-749. ⟨10.1016/j.kint.2020.06.043⟩
Kidney International, Nature Publishing Group, 2020, 99 (3), pp.737-749. ⟨10.1016/j.kint.2020.06.043⟩
Kidney International, 2021, 99 (3), pp.737-749. ⟨10.1016/j.kint.2020.06.043⟩
Although a rare disease, bilateral congenital anomalies of the kidney and urinary tract (CAKUT) are the leading cause of end stage kidney disease in children. Ultrasound-based prenatal prediction of postnatal kidney survival in CAKUT pregnancies is f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d5ca47946f8c92399914c953f494aee
https://hal.archives-ouvertes.fr/hal-03063759
https://hal.archives-ouvertes.fr/hal-03063759
Autor:
Eric Bieth, Dorothée Cailley, Catherine Molinas, Alexandre Buffet, V. Gaston, Maithé Tauber, Benoit Arveiler, Françoise Lorenzini, Françoise Conte Auriol, Caroline Rooryck, Jérôme Cavaillé, Jean Pierre Salles, Sanaa Eddiry
Publikováno v:
European Journal of Human Genetics. 23:252-255
The SNORD116 locus lies in the 15q11-13 region of paternally expressed genes implicated in Prader–Willi Syndrome (PWS), a complex disease accompanied by obesity and severe neurobehavioural disturbances. Cases of PWS patients with a deletion encompa
Autor:
Philippe Galinier, Olivier Abbo, Marion Taurand, Louis Casteilla, Sandra De Barros, Paul Monsarrat, Valérie Planat-Benard, Isabelle Raymond, Emmanuelle Arnaud, Françoise Conte Auriol
Publikováno v:
Cytotherapy. 19(3)
Background Adipose-derived mesenchymalstromal cells (ASC) are currently tested in regenerative medicine to promote tissue reconstruction after injury. Regardingautologous purpose, the possible loss of therapeutic function and cell properties during a
Autor:
Anita Hokken-Koelega, Linda Fryklund, Janina Caliebe, Timothy Nugent, Adrian J. L. Clark, Wietske A. Ester, J. Fauvel, M. Tauber, Michael B. Ranke, Catherine Molinas, L.B. Johnston, Françoise Conte Auriol, M.O. Savage
Publikováno v:
Clinical Endocrinology. 67:457-461
Summary Objective The polymorphic deletion of exon 3 of the GH receptor (d3-GHR) has recently been linked to the magnitude of growth response to recombinant human GH (rhGH) therapy in short children with or without GH deficiency. We investigated this
Autor:
Maithé Tauber, Isabelle Gennero, Elsa Haine, Jean-Pierre Salles, Yves Dulac, Thomas Edouard, Kien Philippe Khau Van, Françoise Conte Auriol, Sophie Julia
Publikováno v:
Bone Abstracts.
Autor:
Elsa, Haine, Jean-Pierre, Salles, Philippe, Khau Van Kien, Françoise, Conte-Auriol, Isabelle, Gennero, Aurélie, Plancke, Sophie, Julia, Yves, Dulac, Maithé, Tauber, Thomas, Edouard
Publikováno v:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 30(8)
Marfan syndrome (MFS) is a rare connective tissue disorder caused by mutation in the gene encoding the extracellular matrix protein fibrillin-1 (FBN1), leading to transforming growth factor-beta (TGF-β) signaling dysregulation. Although decreased ax
Autor:
Laurence Vico, Isabelle Gennero, Danielle Laurencin, Jerold Chun, Jackie Rue, Nicole Malet, Gérard Brunel, Marianne Mus, Fabienne Briand-Mésange, Philippe Bourin, Sara Laurencin-Dalicieux, Nicolas Beton, Françoise Conte-Auriol, Akira Tokumura, Jean Pierre Salles, Richard O.C. Oreffo
Publikováno v:
BONE
BONE, Elsevier, 2011, 49, pp.395-403. ⟨10.1016/j.bone.2011.04.018⟩
BONE, Elsevier, 2011, 49, pp.395-403. ⟨10.1016/j.bone.2011.04.018⟩
International audience; Lysophosphatidic acid (LPA) is a lipid mediator that acts in paracrine systems via interaction with a subset of G protein-coupled receptors (GPCRs). LPA promotes cell growth and differentiation, and has been shown to be implic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4618b3e2b85e59d7f21fe32422089a1f
https://hal.archives-ouvertes.fr/hal-00615224
https://hal.archives-ouvertes.fr/hal-00615224
Autor:
Jean-Pierre Salles, Gwenaelle Diene, Eva Feigerlova, Maithé Tauber, Isabelle Gennero, Catherine Arnaud, Françoise Conte-Auriol, Catherine Molinas
Publikováno v:
The Journal of clinical endocrinology and metabolism. 93(7)
Background: High plasma ghrelin levels have been reported in Prader-Willi syndrome (PWS). However, little is known about plasma ghrelin in these children during the first years of life characterized by a failure to thrive.Objective: The objective of