Improved retroviral transfer of genes into canine hematopoietic progenitor cells kept in long-term marrow culture.
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R. Storb | A. Miller | R. Nash | F. Schuening | S. Goehle | R. Stead | Richard B. Stead | R. Storb | Richard Nash | Miller
[1] B. Balint,et al. [Transplantation of bone marrow cells]. , 1988, Vojnosanitetski pregled.
[2] R. Storb,et al. Canine model for gene therapy: inefficient gene expression in dogs reconstituted with autologous marrow infected with retroviral vectors. , 1988, Blood.
[3] P. Kantoff,et al. Expression of human adenosine deaminase in nonhuman primates after retrovirus-mediated gene transfer , 1987, The Journal of experimental medicine.
[4] Lehn Pm. Gene therapy using bone marrow transplantation. , 1987 .
[5] P. Lehn. Gene therapy using bone marrow transplantation. , 1987, Bone marrow transplantation.
[6] A. Miller,et al. Redesign of retrovirus packaging cell lines to avoid recombination leading to helper virus production , 1986, Molecular and cellular biology.
[7] A. Miller,et al. Retroviral transfer of genes into canine hemopoietic progenitor cells in culture: a model for human gene therapy. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[8] A. Miller,et al. Retrovirus-mediated transfer and expression of drug resistance genes in human haematopoietic progenitor cells , 1986, Nature.
[9] A. Miller,et al. Factors involved in production of helper virus-free retrovirus vectors , 1986, Somatic cell and molecular genetics.
[10] D. Deakin,et al. RECONSTITUTION OF HAEMOPOIETIC SYSTEM WITH AUTOLOGOUS MARROW TAKEN DURING RELAPSE OF ACUTE MYELOBLASTIC LEUKAEMIA AND GROWN IN LONG-TERM CULTURE , 1986, The Lancet.
[11] G. Keller,et al. Expression of a foreign gene in myeloid and lymphoid cells derived from multipotent haematopoietic precursors , 1985, Nature.
[12] C. Eaves,et al. Regulated proliferation of primitive hematopoietic progenitor cells in long-term human marrow cultures. , 1985, Blood.
[13] J. Dick,et al. Introduction of a selectable gene into primitive stem cells capable of long-term reconstitution of the hemopoietic system of W/Wv mice , 1985, Cell.
[14] S. Ruscetti,et al. Malignant transformation of erythroid cells in vivo by introduction of a nonreplicating retrovirus vector. , 1985, Science.
[15] I. Verma,et al. Generation of helper-free amphotropic retroviruses that transduce a dominant-acting, methotrexate-resistant dihydrofolate reductase gene , 1985, Molecular and cellular biology.
[16] T. Dexter,et al. TRANSPLANTATION OF LONG‐TERM CULTURED BONE MARROW CELLS , 1983, Transplantation.
[17] D. Baltimore,et al. Construction of a retrovirus packaging mutant and its use to produce helper-free defective retrovirus , 1983, Cell.
[18] E. Scolnick,et al. Construction and isolation of a transmissible retrovirus containing the src gene of Harvey murine sarcoma virus and the thymidine kinase gene of herpes simplex virus type 1 , 1981, Journal of virology.
[19] H. Deeg,et al. Long-term survival and reversal of iron overload after marrow transplantation in dogs with congenital hemolytic anemia. , 1981, Blood.
[20] L. Lajtha,et al. The regulation of hemopoiesis in long-term bone marrow cultures. II. Stimulation and inhibition of stem cell proliferation. , 1980, Blood.
[21] L. Lajtha,et al. Conditions controlling the proliferation of haemopoietic stem cells in vitro , 1977, Journal of cellular physiology.
[22] R. Storb,et al. Severe Hereditary Haemolytic Anaemia in Dogs Treated by Marrow Transplantation , 1976, British journal of haematology.