Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Fatine Benjelloun"'
Autor:
Julien Rouiller, Alexandrine Garrigue, Isabelle André-Schmutz, Estelle Morillon, Kheira Beldjord, Salima Hacein-Bey-Abina, Marina Cavazzana-Calvo, Delphine Bonhomme, Laure Cacavelli, Fatine Benjelloun, Johanna Blondeau, Emmanuelle Six
Publikováno v:
Blood Cells, Molecules, and Diseases. 47:72-78
An important proof of principle has been achieved with the development of an in vitro T-cell differentiation assay based on the coculture of hematopoietic progenitors with the OP9-Delta1 stromal cell line. The original murine T cell differentiation a
Autor:
Naziha Bakouh, Philippe Hulin, Gabrielle Planelles, Baya Cherif-Zahar, Franck Brouillard, Aleksander Edelman, Fatine Benjelloun
Publikováno v:
Journal of Biological Chemistry. 279:15975-15983
Renal ammonium (NH3 + ) transport is a key process for body acid-base balance. It is well known that several ionic transport systems allow transmembrane translocation without high specificity , but it is still debated whether NH3, and more generally,
Autor:
Pierre Charneau, Julia Hauer, Julie Rivière, Marc Le Lorc'h, Jean-Pierre de Villartay, Pauline Soulas-Sprauel, Anne Galy, Michèle Malassis-Séris, Johanna Blondeau, Alexandrine Garrigue, Alain Fischer, Frederique Pâques, Nicole Brousse, Marina Cavazzana-Calvo, Serge Romana, Fatine Benjelloun, Daniel Stockholm, Annick Lim, Corinne Demerens-de Chappedelaine
Publikováno v:
Molecular Therapy
Molecular Therapy, Cell Press, 2008, 16 (8), pp.1490-9. ⟨10.1038/mt.2008.118⟩
Molecular Therapy, 2008, 16 (8), pp.1490-1499. ⟨10.1038/mt.2008.118⟩
Molecular Therapy, Nature Publishing Group, 2008, 16 (8), pp.1490-9. 〈10.1038/mt.2008.118〉
Molecular Therapy, 2008, 16 (8), pp.1490-9. ⟨10.1038/mt.2008.118⟩
Molecular Therapy, Nature Publishing Group, 2008, 16 (8), pp.1490-9. ⟨10.1038/mt.2008.118⟩
Molecular Therapy, Cell Press, 2008, 16 (8), pp.1490-9. ⟨10.1038/mt.2008.118⟩
Molecular Therapy, 2008, 16 (8), pp.1490-1499. ⟨10.1038/mt.2008.118⟩
Molecular Therapy, Nature Publishing Group, 2008, 16 (8), pp.1490-9. 〈10.1038/mt.2008.118〉
Molecular Therapy, 2008, 16 (8), pp.1490-9. ⟨10.1038/mt.2008.118⟩
Molecular Therapy, Nature Publishing Group, 2008, 16 (8), pp.1490-9. ⟨10.1038/mt.2008.118⟩
International audience; Patients with mutations in the Artemis gene display a complete absence of T- and B lymphocytes, together with increased cellular radiosensitivity; this leads to a radiosensitive severe combined immunodeficiency (RS-SCID). Allo
Autor:
Alain Fischer, Pierre Charneau, Chantal Lagresle-Peyrou, Monique Forveille, Kheira Beldjord, Christophe Hue, Fatine Benjelloun, Marina Cavazzana-Calvo, Isabelle André-Schmutz, Salima Hacein-Bey-Abina, Delphine Bonhomme, Jean-Pierre de Villartay, Anne Durandy
Publikováno v:
Molecular Therapy
Molecular Therapy, Cell Press, 2008, 16 (2), pp.396-403. ⟨10.1038/sj.mt.6300353⟩
Molecular Therapy, 2008, 16 (2), pp.396-403. ⟨10.1038/sj.mt.6300353⟩
Molecular Therapy, Nature Publishing Group, 2008, 16 (2), pp.396-403. ⟨10.1038/sj.mt.6300353⟩
Molecular Therapy, Nature Publishing Group, 2008, 16 (2), pp.396-403. 〈10.1038/sj.mt.6300353〉
Molecular Therapy, Cell Press, 2008, 16 (2), pp.396-403. ⟨10.1038/sj.mt.6300353⟩
Molecular Therapy, 2008, 16 (2), pp.396-403. ⟨10.1038/sj.mt.6300353⟩
Molecular Therapy, Nature Publishing Group, 2008, 16 (2), pp.396-403. ⟨10.1038/sj.mt.6300353⟩
Molecular Therapy, Nature Publishing Group, 2008, 16 (2), pp.396-403. 〈10.1038/sj.mt.6300353〉
International audience; Severe combined immunodeficiency (SCID) caused by mutation of the recombination-activating gene 1 (RAG1) or Artemis gene lead to the absence of B- and T-cell differentiation. The only curative treatment is allogeneic bone marr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c630eb39db78b9c98b129c1ba341e47c
https://hal-pasteur.archives-ouvertes.fr/pasteur-00457747
https://hal-pasteur.archives-ouvertes.fr/pasteur-00457747
Publikováno v:
Current genetics. 49(6)
Ammonium transport proteins belonging to the Mep/Amt/Rh family are spread throughout all domains of life. A conserved aspartate residue plays a key role in the function of Escherichia coli AmtB. Here, we show that the analogous aspartate residue is c
Autor:
Naziha, Bakouh, Fatine, Benjelloun, Philippe, Hulin, Franck, Brouillard, Aleksander, Edelman, Baya, Chérif-Zahar, Gabrielle, Planelles
Publikováno v:
The Journal of biological chemistry. 279(16)
Renal ammonium (NH3 + NH4+) transport is a key process for body acid-base balance. It is well known that several ionic transport systems allow NH4+ transmembrane translocation without high specificity NH4+, but it is still debated whether NH3, and mo
Autor:
Salima Hacein-Bey-Abina, Fatine Benjelloun, Gary P. Wang, Keshet Ronen, Jeremy Leipzig, Marina Cavazzana-Calvo, Chantal Lagresle-Peyrou, Alain Fischer, Charles C. Berry, Frederic D. Bushman, Angela Ciuffi, Alexandrine Garrigue
Publikováno v:
Nucleic Acids Research
Gene transfer has been used to correct inherited immunodeficiencies, but in several patients integration of therapeutic retroviral vectors activated proto-oncogenes and caused leukemia. Here, we describe improved methods for characterizing integratio
Autor:
Alain Fischer, Marina Cavazzana-Calvo, Serge Romana, Julia Hauer, M. Lelorc’h, Fatine Benjelloun, Jean-Pierre Villartay de
Publikováno v:
Blood. 110:5140-5140
Correction of Artemis deficiency, which causes a T−/−B−/− negative and radiosensitive type of SCID, is subject of murine gene therapy trials as an alternative treatment protocol for Hematopoietic Stem Cell Transplantation (HSCT). A conditioni