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Genomics|August 22, 2000
Phemx, a novel mouse gene expressed in hematopoietic cells maps to the imprinted cluster on distal chromosome 7R H Nicholson, S Pantano, J F Eliason, et al.
Blood|October 15, 1994
Engraftment of human hematopoietic precursor cells with secondary transfer potential in SCID-hu miceB P Chen, A Galy, S Kyoizumi, et al.
Leukemia|October 1, 1995
Cytokine-mobilized peripheral blood CD34+Thy-1+Lin- human hematopoietic stem cells as target cells for transplantation-based gene therapyB P Chen, C Fraser, C Reading, et al.
Gene Therapy|March 6, 2009
Validation of a mutated PRE sequence allowing high and sustained transgene expression while abrogating WHV-X protein synthesis: application to the gene therapy of WASM A Zanta-Boussif, S Charrier, A Brice-Ouzet, et al.
Gene Therapy|December 17, 2010
Quantification of lentiviral vector copy numbers in individual hematopoietic colony-forming cells shows vector dose-dependent effects on the frequency and level of transductionS Charrier, M Ferrand, M Zerbato, et al.
Gene Therapy|September 12, 2015
Lymphopoiesis in transgenic mice over-expressing ArtemisP Rivera-Munoz, V Abramowski, S Jacquot, et al.
Gene Therapy|December 24, 2004
A lentiviral vector encoding the human Wiskott-Aldrich syndrome protein corrects immune and cytoskeletal defects in WASP knockout miceS Charrier, D Stockholm, K Seye, et al.
Gene Therapy|October 20, 2006
Lentiviral vectors targeting WASp expression to hematopoietic cells, efficiently transduce and correct cells from WAS patientsS Charrier, L Dupré, S Scaramuzza, et al.
Nature Medicine|January 25, 2022
Long-term safety and efficacy of lentiviral hematopoietic stem/progenitor cell gene therapy for Wiskott-Aldrich syndromeA Magnani, M Semeraro, F Adam, et al.
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