-
1
-
-
0005384869
-
Gene therapy: Not ready for prime time
-
Touchette, N. (1996). Gene therapy: Not ready for prime time. Nature Med. 2, 7-8.
-
(1996)
Nature Med.
, vol.2
, pp. 7-8
-
-
Touchette, N.1
-
2
-
-
0030062296
-
Human gene therapy: An immature genie, but certainly out of a bottle
-
Frledmann, T. (1996). Human gene therapy: An immature genie, but certainly out of a bottle. Nature Med. 2, 144-147.
-
(1996)
Nature Med.
, vol.2
, pp. 144-147
-
-
Frledmann, T.1
-
3
-
-
0023646810
-
Site-directed mutagenesis by gene targeting in mouse embryo-derived stem cells
-
Thomas, K.R. and Capecchi, M.R. (1987). Site-directed mutagenesis by gene targeting in mouse embryo-derived stem cells. Cell 51, 503-12.
-
(1987)
Cell
, vol.51
, pp. 503-512
-
-
Thomas, K.R.1
Capecchi, M.R.2
-
4
-
-
0024328536
-
Altering the genome by homologous recombination
-
Capecchi, M.R. (1989). Altering the genome by homologous recombination Science 244, 1288-92.
-
(1989)
Science
, vol.244
, pp. 1288-1292
-
-
Capecchi, M.R.1
-
5
-
-
0029892249
-
Targeted gene correction of episomal DNA in mammalian cells mediated by a chimeric RNA-DNA oligonucleotide
-
Yoon, K., Cole-Strauss, A. and Kmiec, E.B. (1996). Targeted gene correction of episomal DNA in mammalian cells mediated by a chimeric RNA-DNA oligonucleotide. Proc. Natl Acad. Sci. 93, 2071-2076.
-
(1996)
Proc. Natl Acad. Sci.
, vol.93
, pp. 2071-2076
-
-
Yoon, K.1
Cole-Strauss, A.2
Kmiec, E.B.3
-
6
-
-
0025279402
-
Progress toward human gene therapy
-
Miller, A. (1990). Progress toward human gene therapy. Blood 76, 271-78.
-
(1990)
Blood
, vol.76
, pp. 271-278
-
-
Miller, A.1
-
7
-
-
0028834822
-
Viral vectors in gene therapy
-
Smith, A. (1995). Viral vectors in gene therapy. Annu. Rev. Microbiol. 49, 807-838.
-
(1995)
Annu. Rev. Microbiol.
, vol.49
, pp. 807-838
-
-
Smith, A.1
-
8
-
-
0028875936
-
Transfer of genes to humans: Early lessons and obstacles to success
-
Crystal, R.G. (1995). Transfer of genes to humans: early lessons and obstacles to success. Science 270, 404-10.
-
(1995)
Science
, vol.270
, pp. 404-410
-
-
Crystal, R.G.1
-
9
-
-
0028168641
-
Administration of an adenovirus containing the human CFTR cDNA to the respiratory tract of individuals with cystic fibrosis
-
Crystal, R.G. et al. (1994). Administration of an adenovirus containing the human CFTR cDNA to the respiratory tract of individuals with cystic fibrosis. Nature Genetics 8, 42-51.
-
(1994)
Nature Genetics
, vol.8
, pp. 42-51
-
-
Crystal, R.G.1
-
10
-
-
0030563195
-
Adenoviruses as gene-delivery vehicles
-
Wilson, J.M. (1996). Adenoviruses as gene-delivery vehicles. New Eng. J. Med. 334, 1185-89.
-
(1996)
New Eng. J. Med.
, vol.334
, pp. 1185-1189
-
-
Wilson, J.M.1
-
11
-
-
0024311525
-
Helper-free stocks of recombinant adeno-associated viruses: Normal integration does not require viral gene expression
-
Samulskl, R.J., Chang, L.S. and Shenk, T. (1989). Helper-free stocks of recombinant adeno-associated viruses: normal integration does not require viral gene expression. J. Virol. 63, 3822-8.
-
(1989)
J. Virol.
, vol.63
, pp. 3822-3828
-
-
Samulskl, R.J.1
Chang, L.S.2
Shenk, T.3
-
12
-
-
0026070440
-
Targeted integration of adeno-associated virus (AAV) into human chromosome 19
-
Published erratum appears in EMBO J. (1992) 11, 1228
-
Samulskl, R.J. et al. (1991). Targeted integration of adeno-associated virus (AAV) into human chromosome 19. [Published erratum appears in EMBO J. (1992) 11, 1228]. EMBO J. 10, 3941-50.
-
(1991)
EMBO J.
, vol.10
, pp. 3941-3950
-
-
Samulskl, R.J.1
-
13
-
-
0029242185
-
AAV as a viral vector for human gene therapy. Generation of recombinant virus
-
Rolling, F. and Samulskl, R.J. (1995). AAV as a viral vector for human gene therapy. Generation of recombinant virus. Mol. Biotechnol. 3, 9-15.
-
(1995)
Mol. Biotechnol.
, vol.3
, pp. 9-15
-
-
Rolling, F.1
Samulskl, R.J.2
-
14
-
-
12644273509
-
Retroviral gene transfer into hematopoietic stem cells: The human MDR gene as a model system
-
(ed. D. Levitt and R. Mertlesmann), Marcel Dekker, New York
-
Bank, A., Ward, M., Richardson, C., Podda, S., Smith, L. and Hesdorffer, C. (1995). Retroviral gene transfer into hematopoietic stem cells: The human MDR gene as a model system. In Hematopoietic Stem Cells (ed. D. Levitt and R. Mertlesmann), pp. 229-243. Marcel Dekker, New York.
-
(1995)
Hematopoietic Stem Cells
, pp. 229-243
-
-
Bank, A.1
Ward, M.2
Richardson, C.3
Podda, S.4
Smith, L.5
Hesdorffer, C.6
-
15
-
-
0020582124
-
Construction of a retrovirus packaging mutant and its use to produce helper-free defective retrovirus
-
Mann, R., Mulligan, R.C. and Baltimore, D. (1983). Construction of a retrovirus packaging mutant and its use to produce helper-free defective retrovirus. Cell 33, 153-9.
-
(1983)
Cell
, vol.33
, pp. 153-159
-
-
Mann, R.1
Mulligan, R.C.2
Baltimore, D.3
-
16
-
-
0023871422
-
A safe packaging line for gene transfer: Separating viral genes on two different plasmids
-
Markowitz, D., Goff, S. and Bank, A. (1988). A safe packaging line for gene transfer: Separating viral genes on two different plasmids. J. Virol. 62, 1120-25.
-
(1988)
J. Virol.
, vol.62
, pp. 1120-1125
-
-
Markowitz, D.1
Goff, S.2
Bank, A.3
-
17
-
-
0024239024
-
Construction and use of a safe and efficient amphotropic packaging cell line
-
Markowitz, D., Goff, S. and Bank, A. (1988). Construction and use of a safe and efficient amphotropic packaging cell line. Virology 167, 400-405.
-
(1988)
Virology
, vol.167
, pp. 400-405
-
-
Markowitz, D.1
Goff, S.2
Bank, A.3
-
18
-
-
0023767237
-
Design of retrovirus vectors for transfer and expression of the human beta globin gene
-
Miller, A.D., Bender, M.A., Harris, E.A.S. and et al (1988). Design of retrovirus vectors for transfer and expression of the human beta globin gene. J. Virol. 62, 4337-45.
-
(1988)
J. Virol.
, vol.62
, pp. 4337-4345
-
-
Miller, A.D.1
Bender, M.A.2
Harris, E.A.S.3
-
19
-
-
0029128628
-
Retrovirus receptors
-
Weiss, R. and Tailor, C. (1995). Retrovirus receptors. Cell 82, 531-533.
-
(1995)
Cell
, vol.82
, pp. 531-533
-
-
Weiss, R.1
Tailor, C.2
-
20
-
-
0026641562
-
Helper virus induced T cell lymphoma in nonhuman primates after retroviral mediated gene transfer
-
Donahue, R.E., et al. (1992). Helper virus induced T cell lymphoma in nonhuman primates after retroviral mediated gene transfer. J. Exp. Med. 176.
-
(1992)
J. Exp. Med.
, pp. 176
-
-
Donahue, R.E.1
-
21
-
-
0022767368
-
Redesign of retrovirus packaging cell lines to avoid recombination leading to helper virus production
-
Miller, A.D. and Buttimore, C. (1986). Redesign of retrovirus packaging cell lines to avoid recombination leading to helper virus production. Mol. Cell. Biol. 6, 2895-2902.
-
(1986)
Mol. Cell. Biol.
, vol.6
, pp. 2895-2902
-
-
Miller, A.D.1
Buttimore, C.2
-
22
-
-
0342463159
-
Safe and efficient generation of recombinant retroviruses with amphotropic and ecotropic host ranges
-
Danos, O. and Mulligan, R.C. (1988). Safe and efficient generation of recombinant retroviruses with amphotropic and ecotropic host ranges. Proc. Natl Acad. Sci. USA 85, 6460-4.
-
(1988)
Proc. Natl Acad. Sci. USA
, vol.85
, pp. 6460-6464
-
-
Danos, O.1
Mulligan, R.C.2
-
23
-
-
0028807727
-
T lymphocyte-directed gene therapy for ADA-SCID: Initial trial results after 4 years
-
Blaese, R.M. et al. (1995). T lymphocyte-directed gene therapy for ADA-SCID: initial trial results after 4 years. Science 270, 475-80.
-
(1995)
Science
, vol.270
, pp. 475-480
-
-
Blaese, R.M.1
-
24
-
-
0023805807
-
Correction of the genetic defect in hepatocytes from the Watanabe heritable hyperlipidemic rabbit
-
Wilson, J.M., Johnston, D.E., Jefferson, D.M. and Mulligan, R.C. (1988). Correction of the genetic defect in hepatocytes from the Watanabe heritable hyperlipidemic rabbit. Proc. Natl Acad. Sci. USA 85, 4421-5.
-
(1988)
Proc. Natl Acad. Sci. USA
, vol.85
, pp. 4421-4425
-
-
Wilson, J.M.1
Johnston, D.E.2
Jefferson, D.M.3
Mulligan, R.C.4
-
25
-
-
0028292602
-
Successful ex vivo gene therapy directed to liver in a patient with familial hypercholesterolaemia
-
Grossman, M. et al. (1994). Successful ex vivo gene therapy directed to liver in a patient with familial hypercholesterolaemia. [See comments]. Nature Genetics 6, 335-41.
-
(1994)
Nature Genetics
, vol.6
, pp. 335-341
-
-
Grossman, M.1
-
26
-
-
0025035148
-
Peripheral blood and positive selection of marrow as a source of stem cells for transplantation
-
Bensinger, W.I. and Berenson, R.J. (1990). Peripheral blood and positive selection of marrow as a source of stem cells for transplantation. Prog. Clin. Biol. Res. 337, 93-8.
-
(1990)
Prog. Clin. Biol. Res.
, vol.337
, pp. 93-98
-
-
Bensinger, W.I.1
Berenson, R.J.2
-
27
-
-
0028575792
-
Towards therapy of Gaucher's disease by gene transfer into hematopoietic cells
-
Correll, P.H. and Karlsson, S. (1994). Towards therapy of Gaucher's disease by gene transfer into hematopoietic cells. Eur. J. Haematol. 53, 253-64.
-
(1994)
Eur. J. Haematol.
, vol.53
, pp. 253-264
-
-
Correll, P.H.1
Karlsson, S.2
-
28
-
-
0028131245
-
Phenotypic correction of Fanconi anemia in human hematopoietic cells with a recombinant adeno-associated virus vector
-
Walsh, C.E. et al. (1994). Phenotypic correction of Fanconi anemia in human hematopoietic cells with a recombinant adeno-associated virus vector. J. Clin. Invest. 94, 1440-8.
-
(1994)
J. Clin. Invest.
, vol.94
, pp. 1440-1448
-
-
Walsh, C.E.1
-
29
-
-
9044223652
-
Long-term in vitro correction of α-L-iduronidase deficiency (Hurler syndrome) in human bone marrow
-
Fairbairn, L. et al. (1996). Long-term in vitro correction of α-L-iduronidase deficiency (Hurler syndrome) in human bone marrow. Proc. Natl Acad. Sci. USA 93, 2025-2030.
-
(1996)
Proc. Natl Acad. Sci. USA
, vol.93
, pp. 2025-2030
-
-
Fairbairn, L.1
-
30
-
-
0030045657
-
A bicistronic retrovirus vector containing a picornavirus internal ribosome entry site allows for correction of x-linked CGD by selection for MDR1 expression
-
Sokolic, R. et al. (1996). A bicistronic retrovirus vector containing a picornavirus internal ribosome entry site allows for correction of x-linked CGD by selection for MDR1 expression. Blood 87, 42-50.
-
(1996)
Blood
, vol.87
, pp. 42-50
-
-
Sokolic, R.1
-
31
-
-
0028303758
-
Mutagenesis of retroviral vectors transducing human beta-globin gene and beta-globin locus control region derivatives results in stable transmission of an active transcriptional structure
-
Leboulch, P. et al. (1994). Mutagenesis of retroviral vectors transducing human beta-globin gene and beta-globin locus control region derivatives results in stable transmission of an active transcriptional structure. EMBO J. 13, 3065-76.
-
(1994)
EMBO J.
, vol.13
, pp. 3065-3076
-
-
Leboulch, P.1
-
32
-
-
0029084785
-
Generation of a high-titer retroviral vector capable of expressing high levels of the human beta-globin gene
-
Sadelain, M., Wang, C.H., Antonlou, M., Grosveld, F. and Mulligan, R.C. (1995). Generation of a high-titer retroviral vector capable of expressing high levels of the human beta-globin gene. Proc. Natl Acad. Sci. USA 92, 6728-32.
-
(1995)
Proc. Natl Acad. Sci. USA
, vol.92
, pp. 6728-6732
-
-
Sadelain, M.1
Wang, C.H.2
Antonlou, M.3
Grosveld, F.4
Mulligan, R.C.5
-
33
-
-
0029984381
-
Production of genetically stable high-titer retroviral vectors that carry a human gamma globin gene under the control of the alpha globin locus control region
-
Ren, S., Wong, B.W., Li, J., Luo, X., Wong, P.M.C. and Atweh, G.F. (1996). Production of genetically stable high-titer retroviral vectors that carry a human gamma globin gene under the control of the alpha globin locus control region. Blood 87, 2518-24.
-
(1996)
Blood
, vol.87
, pp. 2518-2524
-
-
Ren, S.1
Wong, B.W.2
Li, J.3
Luo, X.4
Wong, P.M.C.5
Atweh, G.F.6
-
34
-
-
0028071271
-
The effect of thymidine kinase transduction and ganciclovir therapy on tumor vasculature and growth of 9L gliomas in rats
-
Ram, Z., Walbridge, S., Shawker, T., Culver, K.W., Blaese, R.M. and Oldfield, E.H. (1994). The effect of thymidine kinase transduction and ganciclovir therapy on tumor vasculature and growth of 9L gliomas in rats. J. Neurosurgery 81, 256-60.
-
(1994)
J. Neurosurgery
, vol.81
, pp. 256-260
-
-
Ram, Z.1
Walbridge, S.2
Shawker, T.3
Culver, K.W.4
Blaese, R.M.5
Oldfield, E.H.6
-
36
-
-
0027508374
-
The development of gene therapy for the treatment of cancer
-
Rosenberg, S.A. et al. (1993). The development of gene therapy for the treatment of cancer. Ann. Surgery 218, 455-464.
-
(1993)
Ann. Surgery
, vol.218
, pp. 455-464
-
-
Rosenberg, S.A.1
-
37
-
-
0029019902
-
Cloning of a new gene encoding an antigen recognized by melanoma-specific HLA-A24-restricted tumor-infiltrating lymphocytes
-
Robbins, P.F. et al. (1995). Cloning of a new gene encoding an antigen recognized by melanoma-specific HLA-A24-restricted tumor-infiltrating lymphocytes. J. Immunol. 154, 5944-50.
-
(1995)
J. Immunol.
, vol.154
, pp. 5944-5950
-
-
Robbins, P.F.1
-
38
-
-
0028245240
-
Generation of specific anti-melanoma reactivity by stimulation of human tumor-infiltrating lymphocytes with MAGE-1 synthetic peptide
-
Salgaller, M.L., Weber, J.S., Koenig, S., Yannelli, J.R. and Rosenberg, S.A. (1994). Generation of specific anti-melanoma reactivity by stimulation of human tumor-infiltrating lymphocytes with MAGE-1 synthetic peptide. Cancer Immunol. Immunotherapy 39, 105-16.
-
(1994)
Cancer Immunol. Immunotherapy
, vol.39
, pp. 105-116
-
-
Salgaller, M.L.1
Weber, J.S.2
Koenig, S.3
Yannelli, J.R.4
Rosenberg, S.A.5
-
39
-
-
0027237210
-
Genetically engineered tumor vaccines
-
Pardoll, D.M. (1993). Genetically engineered tumor vaccines. Ann. NY Acad. Sci. 690, 301-10.
-
(1993)
Ann. NY Acad. Sci.
, vol.690
, pp. 301-310
-
-
Pardoll, D.M.1
-
40
-
-
0026472495
-
Retroviral gene transfer induced constitutive expression of interleukin-2 or interferon-gamma in irradiated human melanoma cells
-
Gansbacher, H. et al. (1992). Retroviral gene transfer induced constitutive expression of interleukin-2 or interferon-gamma in irradiated human melanoma cells. Blood 80, 2817-25.
-
(1992)
Blood
, vol.80
, pp. 2817-2825
-
-
Gansbacher, H.1
-
41
-
-
0027538181
-
Vaccination with irradiated tumor cells engineered to secrete murine granulocyte-macrophage colony-stimulating factor stimulates potent, specific, and long-lasting anti-tumor immunity
-
Dranoff, G. et al. (1993). Vaccination with irradiated tumor cells engineered to secrete murine granulocyte-macrophage colony-stimulating factor stimulates potent, specific, and long-lasting anti-tumor immunity. Proc. Natl Acad. Sci. USA 90, 3539-43
-
(1993)
Proc. Natl Acad. Sci. USA
, vol.90
, pp. 3539-3543
-
-
Dranoff, G.1
-
42
-
-
0028298850
-
Tumour antigens. A new look for the 1990s
-
Pardoll, D.M. (1994). Tumour antigens. A new look for the 1990s. Nature 369, 357.
-
(1994)
Nature
, vol.369
, pp. 357
-
-
Pardoll, D.M.1
-
43
-
-
0028009982
-
In vivo expression of the B7 costimulatory molecule by subsets of antigen-presenting cells and the malignant cells of Hodgkin's disease
-
Munro, J.M. et al. (1994). In vivo expression of the B7 costimulatory molecule by subsets of antigen-presenting cells and the malignant cells of Hodgkin's disease. Blood 83, 793-8.
-
(1994)
Blood
, vol.83
, pp. 793-798
-
-
Munro, J.M.1
-
44
-
-
0028952046
-
Role of B7-1 in mediating an immune response to myeloid leukemia cells
-
Matulonis, U.A. et al. (1995). Role of B7-1 in mediating an immune response to myeloid leukemia cells. Blood 85, 2507-15.
-
(1995)
Blood
, vol.85
, pp. 2507-2515
-
-
Matulonis, U.A.1
-
45
-
-
0029583864
-
Engineering an intracellular pathway for major histocompatibility complex class II presentation of antigens
-
Wu, T.C. et al. (1995). Engineering an intracellular pathway for major histocompatibility complex class II presentation of antigens. Proc. Natl Acad. Sci. USA 92, 11671-5.
-
(1995)
Proc. Natl Acad. Sci. USA
, vol.92
, pp. 11671-11675
-
-
Wu, T.C.1
-
46
-
-
0027743426
-
Dose intensity. The neglected variable in clinical trials
-
Surbone, A. and DeVita, V.T., Jr. (1993). Dose intensity. The neglected variable in clinical trials. Ann. NY Acad. Sci. 698, 279-88.
-
(1993)
Ann. NY Acad. Sci.
, vol.698
, pp. 279-288
-
-
Surbone, A.1
DeVita Jr., V.T.2
-
48
-
-
0026705269
-
Transfer and expression of the human multiple drug resistance gene into live mice
-
Podda, S., et al. (1992). Transfer and expression of the human multiple drug resistance gene into live mice. Proc. Natl Acad. Sci. USA 89, 9676-80.
-
(1992)
Proc. Natl Acad. Sci. USA
, vol.89
, pp. 9676-9680
-
-
Podda, S.1
-
49
-
-
0026637623
-
Selection of drug-resistant bone marrow cells in vivo after retroviral transfer of human MDR1
-
Sorrentino, B.P. et al. (1992). Selection of drug-resistant bone marrow cells in vivo after retroviral transfer of human MDR1. Science 257, 99-103.
-
(1992)
Science
, vol.257
, pp. 99-103
-
-
Sorrentino, B.P.1
-
50
-
-
0028305628
-
Mouse letal liver cells lack functional amphotropic retroviral receptors
-
Richardson, C., Ward, M., Podda, S. and Bank, A. (1994). Mouse letal liver cells lack functional amphotropic retroviral receptors. Blood 84, 433-439.
-
(1994)
Blood
, vol.84
, pp. 433-439
-
-
Richardson, C.1
Ward, M.2
Podda, S.3
Bank, A.4
-
51
-
-
0028900346
-
MDR gene transfer into live mice
-
Richardson, C., Ward, M. and Bank, A. (1995). MDR gene transfer into live mice. J. Mol. Med. 73, 189-95.
-
(1995)
J. Mol. Med.
, vol.73
, pp. 189-195
-
-
Richardson, C.1
Ward, M.2
Bank, A.3
-
52
-
-
0021250078
-
Antigenic analysis of hematopoietic progenitor cell surface antigen defined by a monoclonal antibody raised against KG-1a cells
-
Civin, I.C., Strauss, L.C., Broval, C., Fackler, M.J., Schwartz, J.F. and Shaper, J.H. (1984). Antigenic analysis of hematopoietic progenitor cell surface antigen defined by a monoclonal antibody raised against KG-1a cells. J. Immunol. 133, 157-160.
-
(1984)
J. Immunol.
, vol.133
, pp. 157-160
-
-
Civin, I.C.1
Strauss, L.C.2
Broval, C.3
Fackler, M.J.4
Schwartz, J.F.5
Shaper, J.H.6
-
53
-
-
0024983839
-
Stem cell selection - Clinical experience
-
Berenson, R.J. et al. (1990). Stem cell selection - clinical experience. Prog. Clin. Biol. Res. 333, 403-10.
-
(1990)
Prog. Clin. Biol. Res.
, vol.333
, pp. 403-410
-
-
Berenson, R.J.1
-
54
-
-
0028027109
-
Transfer and expression of the human multiple drug resistance gene in human CD34+ cells
-
Ward, M., et al. (1994). Transfer and expression of the human multiple drug resistance gene in human CD34+ cells. Blood 84, 1408-1414.
-
(1994)
Blood
, vol.84
, pp. 1408-1414
-
-
Ward, M.1
-
55
-
-
0029950274
-
Transfer and expression of the human MDR gene in peripheral blood progenitor cells
-
Ward, M. et al. (1996). Transfer and expression of the human MDR gene in peripheral blood progenitor cells. Clin. Cancer Res. 2, 873-876.
-
(1996)
Clin. Cancer Res.
, vol.2
, pp. 873-876
-
-
Ward, M.1
-
56
-
-
0028608124
-
Clinical protocol: Human MDR gene transfer in patients with advanced cancer
-
Hesdorffer, C., Antman, K., Bank, A., Fetell, M. and Mears, G. (1994). Clinical protocol: Human MDR gene transfer in patients with advanced cancer. Human Gene Therapy 5, 1151-1160.
-
(1994)
Human Gene Therapy
, vol.5
, pp. 1151-1160
-
-
Hesdorffer, C.1
Antman, K.2
Bank, A.3
Fetell, M.4
Mears, G.5
-
57
-
-
0025599897
-
Efficient gene transfer in live mice using a unique retroviral packaging line
-
Hesdorffer, C., Ward, M., Markowitz, D. and Bank, A. (1990). Efficient gene transfer in live mice using a unique retroviral packaging line. DNA Cell Biol. 9, 717-23.
-
(1990)
DNA Cell Biol.
, vol.9
, pp. 717-723
-
-
Hesdorffer, C.1
Ward, M.2
Markowitz, D.3
Bank, A.4
-
58
-
-
0028340408
-
Development of a retroviral construct containing a human mutated dihydrofolate reductase cDNA for hematopoietic stem cell transduction
-
Li, M.X. et al. (1994). Development of a retroviral construct containing a human mutated dihydrofolate reductase cDNA for hematopoietic stem cell transduction. Blood 83, 3403-8.
-
(1994)
Blood
, vol.83
, pp. 3403-3408
-
-
Li, M.X.1
-
59
-
-
0029056481
-
Retroviral transduction and expression of the human alkyltransferase cDNA provides nitrosourea resistance to hematopoietic cells
-
Allay, J.A., Dumenco, L.L., Koc, O.N., Liu, L. and Gerson, S.L. (1995). Retroviral transduction and expression of the human alkyltransferase cDNA provides nitrosourea resistance to hematopoietic cells. Blood 85, 3342-51.
-
(1995)
Blood
, vol.85
, pp. 3342-3351
-
-
Allay, J.A.1
Dumenco, L.L.2
Koc, O.N.3
Liu, L.4
Gerson, S.L.5
-
60
-
-
0030024868
-
Induction of cyclophosphamide resistance by aldehydedehydrogenase gene transfer
-
Magni, M., Shamma, S., Sciro, R., Mellado, W., Dalla-Favera, R. and Gianni, A.M. (1996). Induction of cyclophosphamide resistance by aldehydedehydrogenase gene transfer. Blood 87, 1097-1103.
-
(1996)
Blood
, vol.87
, pp. 1097-1103
-
-
Magni, M.1
Shamma, S.2
Sciro, R.3
Mellado, W.4
Dalla-Favera, R.5
Gianni, A.M.6
-
61
-
-
0027095653
-
Overexpression of a transporter gene in a multidrug-resistant human lung cancer cell line
-
Cole, S.P. et al. (1992). Overexpression of a transporter gene in a multidrug-resistant human lung cancer cell line. Science 258, 1650-4.
-
(1992)
Science
, vol.258
, pp. 1650-1654
-
-
Cole, S.P.1
-
62
-
-
0028054888
-
Overexpression of multidrug resistance-associated protein (MRP) increases resistance to natural product drugs
-
Grant, C.E., Valdimarsson, G., Hlpfner, D.R., Almquist, K.C., Cole, S.P. and Deeley, R.G. (1994). Overexpression of multidrug resistance-associated protein (MRP) increases resistance to natural product drugs. Cancer Res. 54, 357-61.
-
(1994)
Cancer Res.
, vol.54
, pp. 357-361
-
-
Grant, C.E.1
Valdimarsson, G.2
Hlpfner, D.R.3
Almquist, K.C.4
Cole, S.P.5
Deeley, R.G.6
-
63
-
-
12644319466
-
Expression of the multidrug resistance protein (MRP) gene using retroviral vectors
-
D'Hondt, V., Caruso, M., Ward, M., Deeley, R. and Bank, A. (1995). Expression of the multidrug resistance protein (MRP) gene using retroviral vectors. Blood (suppl.) 86, 466a.
-
(1995)
Blood (Suppl.)
, vol.86
-
-
D'Hondt, V.1
Caruso, M.2
Ward, M.3
Deeley, R.4
Bank, A.5
-
64
-
-
0028148012
-
A molecular genetic intervention for AIDS - Effects of a transdominant negative form of Rev
-
Nabel, G.J., Fox, B.A., Post, L., Thompson, C.B. and Woffendin, C. (1994). A molecular genetic intervention for AIDS - effects of a transdominant negative form of Rev. Human Gene Therapy 5, 79-92.
-
(1994)
Human Gene Therapy
, vol.5
, pp. 79-92
-
-
Nabel, G.J.1
Fox, B.A.2
Post, L.3
Thompson, C.B.4
Woffendin, C.5
-
65
-
-
0030008254
-
Expression of a protective gene prolongs survival of T cells in human immunodeficiency virus-infected patients
-
Woffendin, C., Ranga, U., Yang, Z.-Y., Xu, L. and Nabel, G. (1996). Expression of a protective gene prolongs survival of T cells in human immunodeficiency virus-infected patients. Proc. Natl Acad. Sci. USA 93, 2889-2894.
-
(1996)
Proc. Natl Acad. Sci. USA
, vol.93
, pp. 2889-2894
-
-
Woffendin, C.1
Ranga, U.2
Yang, Z.-Y.3
Xu, L.4
Nabel, G.5
-
66
-
-
0029099331
-
Preselection of transduced murine hematopoietic stem cell populations leads to increased long-term stability and expression of the human multiple drug resistance gene
-
Richardson, C. and Bank, A. (1995). Preselection of transduced murine hematopoietic stem cell populations leads to increased long-term stability and expression of the human multiple drug resistance gene. Blood 86, 2579-89.
-
(1995)
Blood
, vol.86
, pp. 2579-2589
-
-
Richardson, C.1
Bank, A.2
-
67
-
-
0029016628
-
Murine marrow cells expanded in culture with IL-3, IL-6, IL-11, and SCF acquire an engraftment defect in normal hosts
-
Peters, S.O., Kittler, E.L., Ramshaw, H.S. and Quesenberry, P.J. (1995). Murine marrow cells expanded in culture with IL-3, IL-6, IL-11, and SCF acquire an engraftment defect in normal hosts. Exp. Hematol. 23, 461-9.
-
(1995)
Exp. Hematol.
, vol.23
, pp. 461-469
-
-
Peters, S.O.1
Kittler, E.L.2
Ramshaw, H.S.3
Quesenberry, P.J.4
-
68
-
-
0030051967
-
Ex vivo expansion of murine marrow cells with interleukin-3 (IL-3), IL-6, IL-11, and stem cell factor leads to impaired engraftment in irradiated hosts
-
Peters, S.O., Kittler, E.L., Ramshaw, H.S. and Quesenberry, P.J. (1996). Ex vivo expansion of murine marrow cells with interleukin-3 (IL-3), IL-6, IL-11, and stem cell factor leads to impaired engraftment in irradiated hosts. Blood 87, 30-7.
-
(1996)
Blood
, vol.87
, pp. 30-37
-
-
Peters, S.O.1
Kittler, E.L.2
Ramshaw, H.S.3
Quesenberry, P.J.4
-
69
-
-
0028158266
-
Gene transfer into hematopoietic stem cells: Long-term maintenance of in vitro activated progenitors without marrow ablation
-
Bienzle, D. et al. (1994). Gene transfer into hematopoietic stem cells: long-term maintenance of in vitro activated progenitors without marrow ablation. Proc. Natl Acad. Sci. USA 91, 350-4.
-
(1994)
Proc. Natl Acad. Sci. USA
, vol.91
, pp. 350-354
-
-
Bienzle, D.1
-
70
-
-
0029016086
-
A phase I study of autologous bone marrow transplantation with stem cell gene marking in multiple myeloma
-
Stewart, A.K., Dube, I.D., Kamel-Reid, S. and Keeting, A. (1995). A phase I study of autologous bone marrow transplantation with stem cell gene marking in multiple myeloma. Human Gene Therapy 6, 107-19.
-
(1995)
Human Gene Therapy
, vol.6
, pp. 107-119
-
-
Stewart, A.K.1
Dube, I.D.2
Kamel-Reid, S.3
Keeting, A.4
-
71
-
-
0029981525
-
Ex vivo expansion of hematopoietic precursors, progenitors, and stem cells: The next generation of cellular therapeutics
-
Emerson, S. (1996). Ex vivo expansion of hematopoietic precursors, progenitors, and stem cells: The next generation of cellular therapeutics. Blood 87, 3082-3088.
-
(1996)
Blood
, vol.87
, pp. 3082-3088
-
-
Emerson, S.1
-
72
-
-
0028095020
-
A general method for the generation of high-titer pantropic retroviral vectors: Highly efficient infection of primary hepatocytes
-
Yee, J.K., Miyanohara, A.A., Laporte, P., Boulc, K., Burns, J.C. and Friedmann, T. (1994). A general method for the generation of high-titer pantropic retroviral vectors: highly efficient infection of primary hepatocytes. Proc. Natl Acad. Sci. USA 91, 9564-68.
-
(1994)
Proc. Natl Acad. Sci. USA
, vol.91
, pp. 9564-9568
-
-
Yee, J.K.1
Miyanohara, A.A.2
Laporte, P.3
Boulc, K.4
Burns, J.C.5
Friedmann, T.6
-
73
-
-
0028982237
-
Inducible, high-level production of infectious murine leukemia retroviral vector particles pseudotyped with vesicular stomatitis virus G envelope protein
-
Yang, Y. et al. (1995). Inducible, high-level production of infectious murine leukemia retroviral vector particles pseudotyped with vesicular stomatitis virus G envelope protein. Human Gene Therapy 6, 1203-1213.
-
(1995)
Human Gene Therapy
, vol.6
, pp. 1203-1213
-
-
Yang, Y.1
-
74
-
-
0029996147
-
In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector
-
Naldini, L. et al. (1996). In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector. Science 272, 263-267.
-
(1996)
Science
, vol.272
, pp. 263-267
-
-
Naldini, L.1
-
75
-
-
0029880213
-
A novel human amphotropic packaging cell line: High titer, complement resistance, and improved safety
-
Rigg, R., Chen, J., Dando, J., Forestell, S., Plavec, I. and Bohnlein, E. (1996). A novel human amphotropic packaging cell line: High titer, complement resistance, and improved safety. Virotogy 218, 290-295.
-
(1996)
Virotogy
, vol.218
, pp. 290-295
-
-
Rigg, R.1
Chen, J.2
Dando, J.3
Forestell, S.4
Plavec, I.5
Bohnlein, E.6
-
76
-
-
0028567517
-
Tissue-specific targeting of retroviral vectors through ligand-receptor interactions. [See comments]
-
Kasahara, N., Dozy, A.M. and Kan, Y.W. (1994) Tissue-specific targeting of retroviral vectors through ligand-receptor interactions. [See comments]. Science 266, 1373-6.
-
(1994)
Science
, vol.266
, pp. 1373-1376
-
-
Kasahara, N.1
Dozy, A.M.2
Kan, Y.W.3
-
77
-
-
0029145999
-
Generation of targeted retroviral vectors by using single-chain variable fragment: An approach to in vivo gene delivery
-
Somla, N., Zoppe, M. and Verma, I. (1995). Generation of targeted retroviral vectors by using single-chain variable fragment: An approach to in vivo gene delivery. Proc. Natl Acad. Sci. USA 92, 7570-7574.
-
(1995)
Proc. Natl Acad. Sci. USA
, vol.92
, pp. 7570-7574
-
-
Somla, N.1
Zoppe, M.2
Verma, I.3
-
78
-
-
0029655273
-
Foamy virus vectors
-
Russell, D.W. and Miller, A.D. (1996). Foamy virus vectors. J. Virol. 70, 217-22.
-
(1996)
J. Virol.
, vol.70
, pp. 217-222
-
-
Russell, D.W.1
Miller, A.D.2
-
79
-
-
0028857849
-
Efficient gene transfer into human hepatocytes by baculovirus vectors
-
Hofmann, C., Sandig, V., Jennings, G., Rudolph, M., Schlag, P. and Strauss, M. (1995). Efficient gene transfer into human hepatocytes by baculovirus vectors. Proc. Natl Acad. Sci. USA 92, 10099-10103.
-
(1995)
Proc. Natl Acad. Sci. USA
, vol.92
, pp. 10099-10103
-
-
Hofmann, C.1
Sandig, V.2
Jennings, G.3
Rudolph, M.4
Schlag, P.5
Strauss, M.6
-
80
-
-
0343667514
-
Human umbilical cord blood transplantation: The immunology, expansion, and therapeutic applications of hematopoietic stem and progenitor cells
-
(ed. D. Levitt and R. Mertlesmann), Marcel Dekker, New York
-
Broxmeyer, H.E., Lu, L., Gaddy, J., Ruggieri, L., Srlvastava, A. and Risdon, G. (1995). Human umbilical cord blood transplantation: The immunology, expansion, and therapeutic applications of hematopoietic stem and progenitor cells. In Hematopoietic Stem Cells (ed. D. Levitt and R. Mertlesmann), pp. 297-319. Marcel Dekker, New York.
-
(1995)
Hematopoietic Stem Cells
, pp. 297-319
-
-
Broxmeyer, H.E.1
Lu, L.2
Gaddy, J.3
Ruggieri, L.4
Srlvastava, A.5
Risdon, G.6
-
81
-
-
0028785797
-
Processing and cyropreservation of placental/umbilical cord blood for unrelated bone marrow reconstitution
-
Rubinstein, P. et al. (1995). Processing and cyropreservation of placental/umbilical cord blood for unrelated bone marrow reconstitution. Proc. Natl Acad. Sci. USA 92, 10119-10122.
-
(1995)
Proc. Natl Acad. Sci. USA
, vol.92
, pp. 10119-10122
-
-
Rubinstein, P.1
-
82
-
-
0028221579
-
Long-term repopulating ability of xenogeneic transplanted human fetal liver hematopoietic stem cells in sheep
-
Zanjanl, E.D., Flake, A.W., Rice, H., Hedrick, M. and Tavassoli, M. (1994). Long-term repopulating ability of xenogeneic transplanted human fetal liver hematopoietic stem cells in sheep. [See comments]. J. Clin. Invest. 93, 1051-5.
-
(1994)
J. Clin. Invest.
, vol.93
, pp. 1051-1055
-
-
Zanjanl, E.D.1
Flake, A.W.2
Rice, H.3
Hedrick, M.4
Tavassoli, M.5
-
83
-
-
0029328408
-
Retention of long-term repopulating ability of xenogeneic transplanted purified adult human bone marrow hematopoietic stem cells in sheep
-
Zanjanl, E.D., Srour, E.F. and Hoffman, R. (1995). Retention of long-term repopulating ability of xenogeneic transplanted purified adult human bone marrow hematopoietic stem cells in sheep. J. Lab. Clin. Med. 126, 24-8.
-
(1995)
J. Lab. Clin. Med.
, vol.126
, pp. 24-28
-
-
Zanjanl, E.D.1
Srour, E.F.2
Hoffman, R.3
-
84
-
-
0028825086
-
In utero transfer of adult bone marrow cells into recipients with severe combined immunodeficiency disorder yields lymphoid progeny with T and B cell functional capabilities
-
Blazar, B., Taylor, P. and Vallera, D. (1995). In utero transfer of adult bone marrow cells into recipients with severe combined immunodeficiency disorder yields lymphoid progeny with T and B cell functional capabilities. Blood 86, 4353-4366.
-
(1995)
Blood
, vol.86
, pp. 4353-4366
-
-
Blazar, B.1
Taylor, P.2
Vallera, D.3
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