Baboon envelope LVs efficiently transduced human adult, fetal, and progenitor T cells and corrected SCID-X1 T-cell deficiency

Autor: Bernadin, Ornellie ^*, Amirache, Fouzia ^*, Girard-Gagnepain, Anais ^*, Moirangthem, Ranjita Devi ^*, Lévy, Camille, Ma, Kuiying, Costa, Caroline, Nègre, Didier, Reimann, Christian, Fenard, David, Cieslak, Agata, Asnafi, Vahid, Sadek, Hanem, Mhaidly, Rana, Cavazzana, Marina, Lagresle-Peyrou, Chantal, Cosset, François-Loïc, André, Isabelle, Verhoeyen, Els ^*

Publikováno v: In Blood Advances 12 February 2019 3(3):461-475

Gene transfer into hematopoietic stem cells reduces HLH manifestations in a murine model of Munc13-4 deficiency

Autor: Soheili, Tayebeh ^{1, 2}, Durand, Amandine ^{1, 2, *}, Sepulveda, Fernando E. ^{2, 3, *}, Rivière, Julie ¹, Lagresle-Peyrou, Chantal ^{1, 2}, Sadek, Hanem ^{1, 2}, de Saint Basile, Geneviève ^{2, 3}, Martin, Samia ⁴, Mavilio, Fulvio ⁴, Cavazzana, Marina ^{1, 2, 5}, André-Schmutz, Isabelle ^{1, 2, *}

Publikováno v: In Blood Advances 26 December 2017 1(27):2781-2789

The BLNK adaptor protein has a nonredundant role in human B-cell differentiation

Autor: Lagresle-Peyrou, Chantal, Millili, Michèle, Luce, Sonia, Boned, Annie, Sadek, Hanem, Rouiller, Julien, Frange, Pierre, Cros, Guilhem, Cavazzana, Marina, André-Schmutz, Isabelle, Schiff, Claudine

Publikováno v: In The Journal of Allergy and Clinical Immunology July 2014 134(1):145-154

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Plerixafor enables safe, rapid, efficient mobilization of hematopoietic stem cells in sickle cell disease patients after exchange transfusion

Autor: Lagresle-Peyrou, Chantal, Lefrère, François, Magrin, Elisa, Ribeil, Jean-Antoine, Romano, Oriana, Weber, Leslie, Magnani, Alessandra, Sadek, Hanem, Plantier, Clémence, Gabrion, Aurélie, Ternaux, Brigitte, Félix, Tristan, Couzin, Chloé, Stanislas, Aurélie, Tréluyer, Jean-Marc, Lamhaut, Lionel, Joseph, Laure, Delville, Marianne, Miccio, Annarita, André-Schmutz, Isabelle, Cavazzana, Marina

Publikováno v: Haematologica
HAEMATOLOGICA
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Universidad de las Islas Baleares

Sickle cell disease is characterized by chronic anemia and vaso-occlusive crises, which eventually lead to multi-organ damage and premature death. Hematopoietic stem cell transplantation is the only curative treatment but it is limited by toxicity an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::698aab5762199eceb3c55301268aeae6
https://pubmed.ncbi.nlm.nih.gov/29472357