Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Justine Paoli"'
Autor:
Cyrielle Holuka, Chloé Morel, Sarah Roth, Yordenca Lamartinière, Sophie B. Mériaux, Justine Paoli, Pauline Guébels, Radu C. Duca, Lode Godderis, An van Nieuwenhuyse, Pascaline Kremarik-Bouillaud, Ronan Cariou, Claude Emond, Henri Schroeder, Jonathan D. Turner, Nathalie Grova
Publikováno v:
Environment International, Vol 178, Iss , Pp 108103- (2023)
There is a growing evidence that methylation at the N6 position of adenine (6-mA), whose modulation occurs primarily during development, would be a reliable epigenetic marker in eukaryotic organisms. The present study raises the question as to whethe
Externí odkaz:
https://doaj.org/article/88260a08dc3a4812a24e8431f63e90c9
Autor:
Katleen Pinchaud, Zeeshan Hafeez, Sandrine Auger, Jean-Marc Chatel, Sead Chadi, Philippe Langella, Justine Paoli, Annie Dary-Mourot, Katy Maguin-Gaté, Jean Luc Olivier
Publikováno v:
Nutrients, Vol 14, Iss 24, p 5338 (2022)
Although arachidonic acid (ARA) is the precursor of the majority of eicosanoids, its influence as a food component on health is not well known. Therefore, we investigated its impact on the gut microbiota and gut–brain axis. Groups of male BALB/c mi
Externí odkaz:
https://doaj.org/article/ce580f3232064aa3b68c480fb70f34e9
Autor:
Chloé Morel, Armelle Christophe, Katy Maguin-Gaté, Justine Paoli, Jonathan David Turner, Henri Schroeder, Nathalie Grova
Publikováno v:
Toxics, Vol 10, Iss 4, p 180 (2022)
Evidence is now growing that exposure to environmental pollutants during the critical early-life period of brain development may contribute to the emergence of Autism Spectrum Disorders (ASD). This study seeks to compare the developmental neurotoxici
Externí odkaz:
https://doaj.org/article/2a83c24025444d288fd31c7ecb83a44c
Autor:
Natacha Dreumont, David Coelho, Rose Ghemrawi, Mariam Ndiongue, Guillaume Gauchotte, Jean-Marc Alberto, Sébastien Hergalant, Shyue-Fang Battaglia-Hsu, Jean-Louis Guéant, Aurélie Robert, Rémy Umoret, Justine Paoli, Jeffrey M. Sequeira, Edward V. Quadros, Rémi Houlgatte, Martin Jung, Pauline Mosca
Publikováno v:
Nucleic Acids Research
Nucleic Acids Research, Oxford University Press, 2018, 46 (15), pp.7844-7857. ⟨10.1093/nar/gky634⟩
Nucleic Acids Research, Oxford University Press, 2018, ⟨10.1093/nar/gky634⟩
Nucleic Acids Research, Oxford University Press, 2018, 46 (15), pp.7844-7857. ⟨10.1093/nar/gky634⟩
Nucleic Acids Research, Oxford University Press, 2018, ⟨10.1093/nar/gky634⟩
The molecular mechanisms that underlie the neurological manifestations of patients with inherited diseases of vitamin B12 (cobalamin) metabolism remain to date obscure. We observed transcriptomic changes of genes involved in RNA metabolism and endopl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22e14ace2f84f7166664a42af5b2346d
https://doi.org/10.1093/nar/gky634
https://doi.org/10.1093/nar/gky634
Autor:
Brigitte Leininger-Muller, Jérèmy Willekens, Jean-Louis Guéant, Fabian Marin, Grégory Pourié, Lucie Georges, Justine Paoli, Jean-Luc Daval, Christophe Nemos, Natacha Dreumont, Jean-Marc Alberto, Sébastien Hergalant
Publikováno v:
Molecular Neurobiology
Molecular Neurobiology, Humana Press, 2019, 56 (2), pp.892-906. ⟨10.1007/s12035-018-1128-3⟩
Molecular Neurobiology, Humana Press, 2019, 56 (2), pp.892-906. ⟨10.1007/s12035-018-1128-3⟩
Gestational methyl donor (especially B9 and B12 vitamins) deficiency is involved in birth defects and brain development retardation. The underlying molecular mechanisms that are dysregulated still remain poorly understood, in particular in the cerebe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75e338174e1c9a49c79c00dd6bb06231
https://hal.univ-lorraine.fr/hal-01804097
https://hal.univ-lorraine.fr/hal-01804097
Autor:
Rosa Maria Guéant-Rodriguez, Paolo Bosco, Jean-Louis Guéant, Maurizzio Elia, Emile Amouzou, Nicodème W. Chabi, Cyril Besseau, Laurent Peyrin-Biroulet, Guido Anello, Elise Jeannesson, Céline Chéry, Justine Paoli, Ambaliou Sanni, Abderrahim Oussalah, Philippe Gérard, Jean-Pierre Bronowicki, Patrice Hodonou Avogbe, Antonino Romano
Publikováno v:
The American Journal of Clinical Nutrition. 95:514-521
Background: Genomewide association studies have shown a relation between plasma vitamin B-12 concentration and the 461G/A polymorphism of fucosyltransferase 2 (FUT2), a gene associated with susceptibility to Helicobacter pylori infection. Objective:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8b7d64a99593288906367bc775e989a
https://doi.org/10.3945/ajcn.111.016410
https://doi.org/10.3945/ajcn.111.016410
Autor:
Alain Le Faou, Mosaad A. Abdel-Wahhab, Bertrand H. Rihn, Jérôme Chevrier, Olivier Joubert, Justine Paoli, Roudayna Diab, Carole Ronzani, Ramia Safar
Publikováno v:
Cell Biology and Toxicology
Cell Biology and Toxicology, Springer Verlag, 2014, 30 (3), pp.137-46. ⟨10.1007/s10565-014-9275-4⟩
Cell Biology and Toxicology, Springer Verlag, 2014, 30 (3), pp.137-46. ⟨10.1007/s10565-014-9275-4⟩
International audience; Applications of polymeric nanoparticles (NP) in medical fields are rapidly expanding. However, the influence of polymeric NP on cell growth and functions is widely underestimated. Therefore, we have studied cell and polymeric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6656f6a854cbd21d285da8d86a6ccda1
https://hal.archives-ouvertes.fr/hal-01274268
https://hal.archives-ouvertes.fr/hal-01274268
Autor:
Mihaela Pupavac, Jean-Marc Alberto, François Feillet, David S. Rosenblatt, Brian Fowler, Natacha Dreumont, Jean-Louis Guéant, Nadir T. Mrabet, Jean-Michel Camadro, Justine Flayac, David Coelho, David Watkins, Céline Chéry, Justine Paoli, Ma'atem B. Fofou-Caillierez
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2013, 22 (22), pp.4591-601. ⟨10.1093/hmg/ddt308⟩
HUMAN MOLECULAR GENETICS
Human Molecular Genetics, Oxford University Press (OUP), 2013, 22 (22), pp.4591-601. ⟨10.1093/hmg/ddt308⟩
HUMAN MOLECULAR GENETICS
International audience; The cblG and cblC disorders of cobalamin (Cbl) metabolism are two inherited causes of megaloblastic anaemia. In cblG, mutations in methionine synthase (MTR) decrease conversion of hydroxocobalamin (HOCbl) to methylcobalamin, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa57be78e97c12504e27d92371d3e2da
https://hal.archives-ouvertes.fr/hal-00916700
https://hal.archives-ouvertes.fr/hal-00916700