Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Audrey de Rocca Serra"'
Autor:
Gaëtan Herinckx, Emeline Bollaert, Virginie Vandewalle, Audrey de Rocca Serra, Manuel Johanns, Mark H. Rider, Jean-Baptiste Demoulin, Didier Vertommen, Violaine Havelange
Publikováno v:
Cellular Signalling. 44:158-170
The HMG-box protein 1 (HBP1) is a transcriptional regulator and a potential tumor suppressor that controls cell proliferation, differentiation and oncogene-mediated senescence. In a previous study, we showed that AKT activation through the PI3K/AKT/F
Autor:
Maria Debiec-Rychter, Bénédicte Brichard, Ann Van Damme, Raf Sciot, Amélie I. Velghe, Miikka Vikkula, Florence A. Arts, Guillaume Dachy, Christine Galant, Hélène Poirel, Laura A. Noël, Raphaël Helaers, Nisha Limaye, Marleen Renard, Audrey de Rocca Serra, Jean-Baptiste Demoulin
Publikováno v:
Human Molecular Genetics. 26:1801-1810
Infantile myofibromatosis is one of the most prevalent soft tissue tumors of infancy and childhood. Multifocal nodules with visceral lesions are associated with a poor prognosis. A few familial cases have been linked to mutations in various genes inc
Publikováno v:
Cellular and Molecular Life Sciences, (2019)
HMG box protein 1 (HBP1) is a transcription factor and a potent cell cycle inhibitor in normal and cancer cells. HBP1 activates or represses the expression of different cell cycle genes (such as CDKN2A, CDKN1A, and CCND1) through direct DNA binding,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a984d832b9fdcdce69608660ac14420
https://hdl.handle.net/2078.1/211250
https://hdl.handle.net/2078.1/211250
Autor:
Pieter Evenepoel, Julie Rodriguez, Giulio G. Muccioli, Audrey de Rocca Serra, Martin Roumain, Martin Beaumont, Laure B. Bindels, Audrey M. Neyrinck, Nathalie M. Delzenne, Patrice D. Cani, Jean-Baptiste Demoulin, Marta Olivares
Publikováno v:
The FASEB Journal
FASEB Journal
FASEB Journal, Federation of American Society of Experimental Biology, 2018, 32 (12), pp.6681-6693. ⟨10.1096/fj.201800544⟩
The FASEB Journal, Vol. 32, no. 12, p. fj201800544 [1-13] (2018)
FASEB Journal
FASEB Journal, Federation of American Society of Experimental Biology, 2018, 32 (12), pp.6681-6693. ⟨10.1096/fj.201800544⟩
The FASEB Journal, Vol. 32, no. 12, p. fj201800544 [1-13] (2018)
The gut microbiota regulates key hepatic functions, notably through the production of bacterial metabolites that are transported via the portal circulation. We evaluated the effects of metabolites produced by the gut microbiota from aromatic amino ac
Autor:
Donatienne Tyteca, Nicolas Dif, Audrey de Rocca Serra, Amélie I. Velghe, Yvan Larondelle, Jean-Baptiste Demoulin, Chloé Bonnineau, Alexandra Coomans De Brachene
Publikováno v:
F E B S Open Bio, Vol. 7, no.3, p. 414-423 (march 2017)
F E B S Open Bio, Vol. 7, no. 3, p. 414-423 (2017)
FEBS Open Bio
F E B S Open Bio, Vol. 7, no. 3, p. 414-423 (2017)
FEBS Open Bio
Stearoyl-coenzyme A desaturase (SCD) catalyzes the Δ9-cis desaturation of saturated fatty acids (SFA) to generate monounsaturated fatty acids (MUFA). This enzyme is highly up-regulated by platelet-derived growth factor (PDGF) in human fibroblasts. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef8759e04ed4ba83ff2de6f4428c979a
https://hdl.handle.net/2078.1/183362
https://hdl.handle.net/2078.1/183362
Publikováno v:
European journal of medical genetics. 58(10)
Over the two past decades, mutations of the PTPN11 gene, encoding the ubiquitous protein tyrosine phosphatase SHP2 (SH2 domain-containing tyrosine phosphatase 2), have been identified as the causal factor of several developmental diseases (Noonan syn
Autor:
Patrick Raynal, Karine Tréguer, Maithé Tauber, Mylène Tajan, Philippe Valet, Aurélie Batut, Sophie Le Gonidec, Marie-Adeline Marques, Armelle Yart, Thomas Edouard, Céline Saint Laurent, Claire Vinel, Jean-Pierre Salles, Oksana Kunduzova, Thomas Cadoudal, Hélène Cavé, Joffrey Pozzo, Estelle Wanecq, Simon Deleruyelle, Maëlle Vomscheid, Audrey De Rocca Serra-Nédélec
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2014, 111 (42), pp.E4494-E4503. ⟨10.1073/pnas.1406107111⟩
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2014, 111 (42), pp.E4494-E4503. ⟨10.1073/pnas.1406107111⟩
LEOPARD syndrome (multiple Lentigines, Electrocardiographic conduction abnormalities, Ocular hypertelorism, Pulmonary stenosis, Abnormal genitalia, Retardation of growth, sensorineural Deafness; LS), also called Noonan syndrome with multiple lentigin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b451e6588d1aded123426097dd19344
https://europepmc.org/articles/PMC4210352/
https://europepmc.org/articles/PMC4210352/
Autor:
Mylène Tajan, Marianne Mus, Thomas Edouard, Karine Tréguer, Jean-Pierre Salles, Alexandra Montagner, Armelle Yart, Patrick Raynal, Toshiyuki Araki, M. Tauber, Philippe Valet, Audrey De Rocca Serra-Nédélec, Marie Dance, Benjamin G. Neel
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America 11 (109), 4257-4262. (2012)
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2012, 109 (11), pp.4257-62. ⟨10.1073/pnas.1119803109⟩
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2012, 109 (11), pp.4257-4262. ⟨10.1073/pnas.1119803109⟩
Proceedings of the National Academy of Sciences of the United States of America, 2012, 109 (11), pp.4257-4262. ⟨10.1073/pnas.1119803109⟩
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2012, 109 (11), pp.4257-62. ⟨10.1073/pnas.1119803109⟩
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2012, 109 (11), pp.4257-4262. ⟨10.1073/pnas.1119803109⟩
Proceedings of the National Academy of Sciences of the United States of America, 2012, 109 (11), pp.4257-4262. ⟨10.1073/pnas.1119803109⟩
Noonan syndrome (NS), a genetic disease caused in half of cases by activating mutations of the tyrosine phosphatase SHP2 ( PTPN11 ), is characterized by congenital cardiopathies, facial dysmorphic features, and short stature. How mutated SHP2 induces
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b331c42273a01c5f8af7d797ede56951
http://prodinra.inra.fr/record/387290
http://prodinra.inra.fr/record/387290