Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Madeleine Erard-Garcia"'
Autor:
Madeleine Erard-Garcia, Sylvie Mavel, Ana Dudas, Michael J. Mihatsch, Julie Pailloux, Claire Mackowiak, Frédéric Foucher, Pauline Rontani, Nicolas Erard, Elodie Culerier, Bernhard Ryffel, Marc Le Bert, Valérie F. J. Quesniaux, Delphine Sedda, Antoine Lefevre, Patrick Emond
Publikováno v:
Kidney360
Kidney360, 2021, pp.10.34067/KID.0001732021. ⟨10.34067/kid.0001732021⟩
Kidney360, 2021, pp.10.34067/KID.0001732021. ⟨10.34067/kid.0001732021⟩
Background Xanthinuria type II is a rare autosomal purine disorder. This recessive defect of purine metabolism remains an under-recognized disorder. Methods Mice with targeted disruption of the molybdenum cofactor sulfurase (Mocos) gene were generate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a958596497f8a263cf84344fc6abc3b8
https://hal.archives-ouvertes.fr/hal-03429645
https://hal.archives-ouvertes.fr/hal-03429645
Autor:
Antoine Gruet, Jean-Jacques Remy, Yoanne M. Clovis, Francois Feron, Kévin Baranger, Diana Andrea Fernandes De Abreu, Madeleine Erard-Garcia, Marie-Pierre Blanchard
Imprinting is an early sensory life experience that induces adult behaviours, such as mother recognition or homing. In a previous study, we demonstrated a striking olfactory imprinting in C. elegans that can be inherited over generations. When expose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de4a3c13cf3afb07b512f00e871d0b8a
https://doi.org/10.1101/2021.06.30.449753
https://doi.org/10.1101/2021.06.30.449753
Autor:
Madeleine Erard-Garcia, Louise Greetham, Pauline Rontani, Francois Feron, Emmanuel Nivet, Nicolas Jullien, Bruno Gepner, Olivier Perche
Publikováno v:
Molecular Psychiatry
Molecular Psychiatry, Nature Publishing Group, 2020, ⟨10.1038/s41380-020-0728-2⟩
Molecular Psychiatry, 2020, 26, pp.1606-1618. ⟨10.1038/s41380-020-0728-2⟩
Molecular Psychiatry, 2020, ⟨10.1038/s41380-020-0728-2⟩
Molecular Psychiatry, Nature Publishing Group, 2020, ⟨10.1038/s41380-020-0728-2⟩
Molecular Psychiatry, 2020, 26, pp.1606-1618. ⟨10.1038/s41380-020-0728-2⟩
Molecular Psychiatry, 2020, ⟨10.1038/s41380-020-0728-2⟩
Autism spectrum disorders (ASD) are complex neurodevelopmental disorders with a very large number of risk loci detected in the genome. However, at best, each of them explains rare cases, the majority being idiopathic. Genomic data on ASD derive mostl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d2288477b977aba66bde5e363e271f7
https://pubmed.ncbi.nlm.nih.gov/32327736
https://pubmed.ncbi.nlm.nih.gov/32327736
