Center-Authored Papers
Filters: Author is Kiem, H P [Clear All Filters]
Semi-automated closed system manufacturing of lentivirus gene-modified haematopoietic stem cells for gene therapy.. Nature communications. 7:13173. Abstract
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2016.
Gene therapy enhances chemotherapy tolerance and efficacy in glioblastoma patients.. The Journal of clinical investigation. 124(9):4082-92. Abstract
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2014.
Cyclophosphamide promotes engraftment of gene-modified cells in a mouse model of Fanconi anemia without causing cytogenetic abnormalities.. Journal of molecular medicine (Berlin, Germany). 90(11):1283-1294. Abstract
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2012.
Extended Survival of Glioblastoma Patients After Chemoprotective HSC Gene Therapy.. Science translational medicine. 4(133):133ra57. Abstract
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2012.
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2018.
Differential engraftment of genetically modified CD34(+) and CD34(-) hematopoietic cell subsets in lethally irradiated baboons.. Experimental hematology. 28(5):508-18. Abstract
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2000.
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2009.
Efficient and stable MGMT-mediated selection of long-term repopulating stem cells in nonhuman primates.. The Journal of clinical investigation. 120(7):2345-54. Abstract
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2010.
Canine models of gene-modified hematopoiesis.. Methods in molecular biology (Clifton, N.J.). 506:341-61. Abstract
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2009.
High-throughput genomic mapping of vector integration sites in gene therapy studies.. Methods in molecular biology (Clifton, N.J.). 1185:321-44. Abstract
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2014.
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2010.
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2013.
Haploidentical Bone Marrow Transplantation with Post-Transplant Cyclophosphamide for Children and Adolescents with Fanconi Anemia.. Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation. Abstract
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2016.
Blockade of alpha6-integrin reveals diversity in homing patterns among human, baboon, and murine cells.. Stem cells and development. 18(6):839-44. Abstract
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2009.
Concurrent blockade of alpha4-integrin and CXCR4 in hematopoietic stem/progenitor cell mobilization.. Stem cells (Dayton, Ohio). 27(4):836-7. Abstract
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2009.
Intravenous injection of a foamy virus vector to correct canine SCID-X1.. Blood. 123(23):3578-84. Abstract
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2014.
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2015.
HIV eradication-from Berlin to Boston.. Nature biotechnology. 32(4):315-6.
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2014.
Longitudinal assessment of morbidity and acute graft-versus-host disease after allogeneic hematopoietic cell transplantation: retrospective analysis of a multicenter phase III study.. Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation. 15(6):749-56. Abstract
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2009.
Coupling endonucleases with DNA end-processing enzymes to drive gene disruption.. Nature methods. 9(10):973-5. Abstract
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2012.
Modeling promising nonmyeloablative conditioning regimens in nonhuman primates.. Human gene therapy. Abstract
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2014.
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2014.
Challenges in vector and trial design using retroviral vectors for long-term gene correction in hematopoietic stem cell gene therapy.. Molecular therapy : the journal of the American Society of Gene Therapy. 20(6):1084-94.
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2012.
T-cell immunotherapy: looking forward.. Molecular therapy : the journal of the American Society of Gene Therapy. 22(9):1564-74.
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2014.
Devouring the Hematopoietic Stem Cell: Setting the Table for Marrow Cell Transplantation.. Molecular therapy : the journal of the American Society of Gene Therapy. 24(11):1892-1894.
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2016. Doing Business with Arnold Library
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