Related references
Note: Only part of the references are listed.Combined preconditioning and in vivo chemoselection with 6-thioguanine alone achieves highly efficient reconstitution of normal hematopoiesis with HPRT-deficient bone marrow
Katrin Hacke et al.
EXPERIMENTAL HEMATOLOGY (2012)
Extended Survival of Glioblastoma Patients After Chemoprotective HSC Gene Therapy
Jennifer E. Adair et al.
SCIENCE TRANSLATIONAL MEDICINE (2012)
Clonal Inventory Screens Uncover Monoclonality Following Serial Transplantation of MGMTP140K-Transduced Stem Cells and Dose-Intense Chemotherapy
Frank A. Giordano et al.
HUMAN GENE THERAPY (2011)
Efficient and stable MGMT-mediated selection of long-term repopulating stem cells in nonhuman primates
Brian C. Beard et al.
JOURNAL OF CLINICAL INVESTIGATION (2010)
Stem-Cell Gene Therapy for the Wiskott-Aldrich Syndrome
Kaan Boztug et al.
NEW ENGLAND JOURNAL OF MEDICINE (2010)
Gene Therapy for Immunodeficiency Due to Adenosine Deaminase Deficiency.
Alessandro Aiuti et al.
NEW ENGLAND JOURNAL OF MEDICINE (2009)
Hematopoietic Stem Cell Gene Therapy with a Lentiviral Vector in X-Linked Adrenoleukodystrophy
Nathalie Cartier et al.
SCIENCE (2009)
Interfering RNA-mediated purine analog resistance for in vitro and in vivo cell selection
Christopher C. Porter et al.
BLOOD (2008)
The MDS1-EVI1 gene complex as a retrovirus integration site: Impact on behavior of hematopoietic cells and implications for gene therapy
Jean-Yves Metais et al.
MOLECULAR THERAPY (2008)
Meta-analysis of risk of malignancy with immunosuppressive drugs in inflammatory bowel disease
Yukari Masunaga et al.
ANNALS OF PHARMACOTHERAPY (2007)
Gene transfer in humans using a conditionally replicating lentiviral vector
Bruce L. Levine et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Cell-culture assays reveal the importance of retroviral vector design for insertional genotoxicity
Ute Modlich et al.
BLOOD (2006)
Hematopoietic stem cell gene transfer in a tumor-prone mouse model uncovers low genotoxicity of lentiviral vector integration
Eugenio Montini et al.
NATURE BIOTECHNOLOGY (2006)
Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1
MG Ott et al.
NATURE MEDICINE (2006)
LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1
S Hacein-Bey-Abina et al.
SCIENCE (2003)
In vivo selection of MGMT(P140K) lentivirus-transduced human NOD/SCID repopulating cells without pretransplant irradiation conditioning
SP Zielske et al.
JOURNAL OF CLINICAL INVESTIGATION (2003)
Sustained correction of X-linked severe combined immunodeficiency by ex vivo gene therapy
S Hacein-Bey-Abina et al.
NEW ENGLAND JOURNAL OF MEDICINE (2002)
In vivo selection of antifolate-resistant transgenic hematopoietic stem cells in a murine bone marrow transplant model
CA Warlick et al.
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS (2002)
Efficient retrovirus-mediated transfer of the multidrug resistance 1 gene into autologous human long-term repopulating hematopoietic stem cells
R Abonour et al.
NATURE MEDICINE (2000)
Topoisomerase II inhibitor-related acute myeloid leukaemia
CH Pui et al.
BRITISH JOURNAL OF HAEMATOLOGY (2000)
Share Paper
