Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Stéphanie Giraudet"'
Autor:
Régis Josien, Jerome Martin, Karine Amouriaux, Marie Rimbert, Audrey Besançon, Stéphanie Giraudet, Mohamed Hamidou, Marine Aliaga, Caroline Hémont, Cécile Braudeau, Nina Salabert-Le Guen, Caroline Terrien, Antoine Néel
Publikováno v:
Frontiers in Immunology
Frontiers in Immunology, 2017, 8, ⟨10.3389/fimmu.2017.00102⟩
Frontiers in Immunology, Frontiers, 2017, 8, ⟨10.3389/fimmu.2017.00102⟩
Frontiers in Immunology, 2017, 8, ⟨10.3389/fimmu.2017.00102⟩
Frontiers in Immunology, Frontiers, 2017, 8, ⟨10.3389/fimmu.2017.00102⟩
International audience; Objective: Dendritic cells (DCs) are critical effectors of innate and adaptive immunity playing crucial roles in autoimmune responses. We previously showed that blood DC numbers were reduced in autoimmune antineutrophil cytopl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d0d18ab1fe3b383ed22b7c16ed82bbb
https://www.hal.inserm.fr/inserm-02156159
https://www.hal.inserm.fr/inserm-02156159
Autor:
Julie Graveleau, Stéphanie Giraudet, Antoine Néel, Mohamed Hamidou, Agathe Masseau, Caroline Terrien, Régis Josien, Bernard Grosbois, Cécile Braudeau, Marie Rimbert, Audrey Besançon
Publikováno v:
Blood Cells, Molecules and Diseases
Blood Cells, Molecules and Diseases, 2013, 50 (4), pp.281-288. ⟨10.1016/j.bcmd.2013.01.001⟩
Blood Cells, Molecules and Diseases, Elsevier, 2013, 50 (4), pp.281-288. ⟨10.1016/j.bcmd.2013.01.001⟩
Blood Cells, Molecules and Diseases, 2013, 50 (4), pp.281-288. ⟨10.1016/j.bcmd.2013.01.001⟩
Blood Cells, Molecules and Diseases, Elsevier, 2013, 50 (4), pp.281-288. ⟨10.1016/j.bcmd.2013.01.001⟩
Background Gaucher disease (GD) is caused by an autosomal-recessive deficiency of β-glucocerebrosidase leading to an accumulation of glucosylceramide in monocytes/macrophage lineage. We analyzed immune cells and especially the function of dendritic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65d214f426c1dadade87c0e6026d1289
https://www.hal.inserm.fr/inserm-02164593/document
https://www.hal.inserm.fr/inserm-02164593/document
Autor:
Sébastien Küry, Stéphane Bézieau, Jean-Paul Moisan, Brigitte Dréno, Monia Kharfi, Stéphanie Giraudet, Ridha Kamoun
Publikováno v:
Nature genetics. 31(3)
We have characterized the human gene SLC39A4, which encodes a protein with features characteristic of a ZIP zinc transporter. The chromosomal location and expression of SLC39A4, together with mutational analysis of eight families affected with acrode
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d684817a01301a2446053520fa8e4ad1
https://pubmed.ncbi.nlm.nih.gov/12068297
https://pubmed.ncbi.nlm.nih.gov/12068297
Autor:
Andre Chaventre, O. Herbert, Alban Jauffrit, Stéphanie Giraudet, Jean-Paul Moisan, Christel Richard, Fabrice Airaud, Marie-Therese Andre, Hamid El Amri, Gaëlle Landeau-Trottier
Publikováno v:
Journal of Forensic Sciences. 48:2002264
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e97131ac0a427fa4709ffd25716abcc
https://doi.org/10.1520/jfs2002264
https://doi.org/10.1520/jfs2002264