-
1
-
-
0027443191
-
Gene marking to determine whether autologous marrow infusion restores long-term haemopoiesis in cancer patients
-
Brenner MK, Rill DR. Gene marking to determine whether autologous marrow infusion restores long-term haemopoiesis in cancer patients. Lancet 1993; 342: 1134–7.
-
(1993)
Lancet
, vol.342
, pp. 1134-1137
-
-
Brenner, M.K.1
Rill, D.R.2
-
2
-
-
0024988334
-
Gene transfer into humans—immunotherapy of patients with advanced melanoma, using tumor-infiltrating lymphocytes modified by retroviral gene transduction
-
Rosenberg SA, Aebersold P., Cornetta K. et al. Gene transfer into humans—immunotherapy of patients with advanced melanoma, using tumor-infiltrating lymphocytes modified by retroviral gene transduction. N. Engl. J. Med. 1990; 323: 570–8.
-
(1990)
N. Engl. J. Med.
, vol.323
, pp. 570-578
-
-
Rosenberg, S.A.1
Aebersold, P.2
Cornetta, K.3
-
3
-
-
0019784105
-
Formation of infectious progeny virus after insertion of herpes simplex thymidine kinase gene into DNA of an avian retrovirus
-
Shimotohno K., Temin HM. Formation of infectious progeny virus after insertion of herpes simplex thymidine kinase gene into DNA of an avian retrovirus. Cell 1981; 26: 67–77.
-
(1981)
Cell
, vol.26
, pp. 67-77
-
-
Shimotohno, K.1
Temin, H.M.2
-
4
-
-
0025398116
-
Retrovirus packaging cells
-
Miller AD. Retrovirus packaging cells. Hum. Gene Ther. 1993; 1: 5–14.
-
(1993)
Hum. Gene Ther.
, vol.1
, pp. 5-14
-
-
Miller, A.D.1
-
5
-
-
0025312728
-
A genetic model for colorectal tumorigenesis
-
Fearon ER, Vogelstein B. A genetic model for colorectal tumorigenesis. Cell 1990; 61: 759–67.
-
(1990)
Cell
, vol.61
, pp. 759-767
-
-
Fearon, E.R.1
Vogelstein, B.2
-
6
-
-
0026641562
-
Helper virus induced T cell lymphoma in nonhuman primates after retroviral mediated gene transfer
-
Donahue RE, Kessler SW, Bodine D. et al. Helper virus induced T cell lymphoma in nonhuman primates after retroviral mediated gene transfer. J. Exp. Med. 1992; 176: 1125–35.
-
(1992)
J. Exp. Med.
, vol.176
, pp. 1125-1135
-
-
Donahue, R.E.1
Kessler, S.W.2
Bodine, D.3
-
7
-
-
0023871422
-
A safe packaging line for gene transfer: Separating viral genes on two different plasmids
-
Markowitz D., Goff S., Bank A. A safe packaging line for gene transfer: Separating viral genes on two different plasmids. J. Virol. 1988; 62: 1120–4.
-
(1988)
J. Virol.
, vol.62
, pp. 1120-1124
-
-
Markowitz, D.1
Goff, S.2
Bank, A.3
-
8
-
-
0025279872
-
Gene transfer by retrovirus vectors occurs only in cells that are actively replicating at the time of infection
-
Miller DG, Adam MA, Miller AD. Gene transfer by retrovirus vectors occurs only in cells that are actively replicating at the time of infection. Mol. Cell. Biol. 1990; 10: 4239–42.
-
(1990)
Mol. Cell. Biol.
, vol.10
, pp. 4239-4242
-
-
Miller, D.G.1
Adam, M.A.2
Miller, A.D.3
-
9
-
-
0026591331
-
Expression of heterologous sequences in adenoviral vectors
-
Berkner KL. Expression of heterologous sequences in adenoviral vectors. Curr. Top. Microbiol. Immunol. 1992; 158: 39–66.
-
(1992)
Curr. Top. Microbiol. Immunol.
, vol.158
, pp. 39-66
-
-
Berkner, K.L.1
-
10
-
-
0025848772
-
Adenovirus-mediated transfer of a recombinant alpha I-antitrypsin gene to the lung epithelium in vivo
-
Rosenfeld MA, Siegfried W., Yoshimura K. et al. Adenovirus-mediated transfer of a recombinant alpha I-antitrypsin gene to the lung epithelium in vivo. Science 1991; 252: 431–4.
-
(1991)
Science
, vol.252
, pp. 431-434
-
-
Rosenfeld, M.A.1
Siegfried, W.2
Yoshimura, K.3
-
11
-
-
0026558496
-
In vivo transfer of the human cystic fibrosis transmembrane conductance regulator gene to the airway epithelium
-
Rosenfeld MA, Yoshimura K., Trapnell BC et al. In vivo transfer of the human cystic fibrosis transmembrane conductance regulator gene to the airway epithelium. Cell 1992; 68: 143–55.
-
(1992)
Cell
, vol.68
, pp. 143-155
-
-
Rosenfeld, M.A.1
Yoshimura, K.2
Trapnell, B.C.3
-
12
-
-
0028934815
-
Cellular and humoral immune response to adenoviral vectors containing factor IX gene: Tolerization of factor IX and vector antigens allows for long-term expression
-
USA
-
Dai Y., Schwarz EM, Gu D., Zhang W., Sarvetnick N., Verma IM. Cellular and humoral immune response to adenoviral vectors containing factor IX gene: Tolerization of factor IX and vector antigens allows for long-term expression. Proc. Natl Acad. Sci. USA 1995; 92: 1401–5.
-
(1995)
Proc. Natl Acad. Sci.
, vol.92
, pp. 1401-1405
-
-
Dai, Y.1
Schwarz, E.M.2
Gu, D.3
Zhang, W.4
Sarvetnick, N.5
Verma, I.M.6
-
13
-
-
0028559601
-
Long-term behavioral recovery in Parkinsonian rats by an HSV vector expressing tyrosine hydroxylase
-
During MJ, Naegele JR, O'Malley KL, Geller AI. Long-term behavioral recovery in Parkinsonian rats by an HSV vector expressing tyrosine hydroxylase. Science 1994; 266: 1399–403.
-
(1994)
Science
, vol.266
, pp. 1399-1403
-
-
During, M.J.1
Naegele, J.R.2
O'Malley, K.L.3
Geller, A.I.4
-
14
-
-
0028170362
-
Prospects for the use of adno-associated virus as a vector for human gene therapy
-
Kotin RM. Prospects for the use of adno-associated virus as a vector for human gene therapy. Hum. Gene Ther. 1994; 5: 793–801.
-
(1994)
Hum. Gene Ther.
, vol.5
, pp. 793-801
-
-
Kotin, R.M.1
-
15
-
-
0025997434
-
Targeted and highly efficient gene transfer into CD4 + cells by a recombinant human immunodeficiency virus retroviral vector
-
Shimada T., Fujii H., Mitsuya H., Nienhuis AW. Targeted and highly efficient gene transfer into CD4 + cells by a recombinant human immunodeficiency virus retroviral vector. J. Clin. Invest. 1991; 88: 1043–7.
-
(1991)
J. Clin. Invest.
, vol.88
, pp. 1043-1047
-
-
Shimada, T.1
Fujii, H.2
Mitsuya, H.3
Nienhuis, A.W.4
-
16
-
-
0028807727
-
T lymphocyte-directed gene therapy for ADA-SCID: Initial trial results after 4 years
-
Blaese RM, Culver KW, Miller AD et al. T lymphocyte-directed gene therapy for ADA-SCID: Initial trial results after 4 years. Science 1995; 270: 475–80.
-
(1995)
Science
, vol.270
, pp. 475-480
-
-
Blaese, R.M.1
Culver, K.W.2
Miller, A.D.3
-
17
-
-
0028864561
-
Engraftment of gene-modified umbilical cord blood cells in neonates with adenosine deaminase deficiency
-
Kohn DB, Weinberg KI, Nolta JA et al. Engraftment of gene-modified umbilical cord blood cells in neonates with adenosine deaminase deficiency. Nature Med. 1995; 1: 1017–23.
-
(1995)
Nature Med.
, vol.1
, pp. 1017-1023
-
-
Kohn, D.B.1
Weinberg, K.I.2
Nolta, J.A.3
-
18
-
-
0028292602
-
Successful ex vivo gene therapy directed to liver in a patient with familial hypercholesterolaemia
-
Grossman M., Raper SE, Kozarsky K. et al. Successful ex vivo gene therapy directed to liver in a patient with familial hypercholesterolaemia. Nature Genet. 1994; 6: 335–41.
-
(1994)
Nature Genet.
, vol.6
, pp. 335-341
-
-
Grossman, M.1
Raper, S.E.2
Kozarsky, K.3
-
19
-
-
0028168641
-
Administration of an adenovirus containing the human CFTR cDNA to the respiratory tract of individuals with cystic fibrosis
-
Crystal RG, McElvaney NG, Rosenfeld MA et al. Administration of an adenovirus containing the human CFTR cDNA to the respiratory tract of individuals with cystic fibrosis. Nature Genet. 1994; 8: 42–51.
-
(1994)
Nature Genet.
, vol.8
, pp. 42-51
-
-
Crystal, R.G.1
McElvaney, N.G.2
Rosenfeld, M.A.3
-
20
-
-
0028362901
-
A functionally active retrovirus vector for gene therapy in Fanconi anemia group C
-
Walsh CE, Grompe M., Vanin E. et al. A functionally active retrovirus vector for gene therapy in Fanconi anemia group C. Blood 1994; 84: 453–9.
-
(1994)
Blood
, vol.84
, pp. 453-459
-
-
Walsh, C.E.1
Grompe, M.2
Vanin, E.3
-
21
-
-
0029152181
-
Transfer of the human glucocerebrosidase gene into hematopoietic stem cells of nonablated recipients: Successful engraftment and long-term expression of the transgene
-
Schiffmann R., Medin JA, Ward JM, Stahl S., Cottier-Fox M., Karlsson S. Transfer of the human glucocerebrosidase gene into hematopoietic stem cells of nonablated recipients: Successful engraftment and long-term expression of the transgene. Blood 1995; 86: 1218–27.
-
(1995)
Blood
, vol.86
, pp. 1218-1227
-
-
Schiffmann, R.1
Medin, J.A.2
Ward, J.M.3
Stahl, S.4
Cottier-Fox, M.5
Karlsson, S.6
-
22
-
-
0027538181
-
Vaccination with irradiated tumor cells engineered to secrete murine granulocyte-macrophage colony-stimulating factor stimulates potent, specific, and long-lasting anti-tumor immunity
-
USA
-
Dranoff G., Jaffee E., Lazenby A. et al. 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 1993; 90: 3539–43.
-
(1993)
Proc. Natl Acad. Sci.
, vol.90
, pp. 3539-3543
-
-
Dranoff, G.1
Jaffee, E.2
Lazenby, A.3
-
23
-
-
0026772206
-
In vivo transfer with retroviral vector-producer cells for treatment of experimental brain tumors
-
Culver KW, Ram Z., Wallbridge S., Ishii H., Oldfield EH, Blaese RM. In vivo transfer with retroviral vector-producer cells for treatment of experimental brain tumors. Science 1992; 256: 1550–2.
-
(1992)
Science
, vol.256
, pp. 1550-1552
-
-
Culver, K.W.1
Ram, Z.2
Wallbridge, S.3
Ishii, H.4
Oldfield, E.H.5
Blaese, R.M.6
-
24
-
-
0028589416
-
Experimental and clinical studies of cytokine gene modified tumor cells
-
Tepper RI, Mule JJ. Experimental and clinical studies of cytokine gene modified tumor cells. Hum. Gene Ther. 1994; 5: 153–64.
-
(1994)
Hum. Gene Ther.
, vol.5
, pp. 153-164
-
-
Tepper, R.I.1
Mule, J.J.2
-
25
-
-
0027280569
-
Immunotherapy of malignancy by in vivo gene transfer into tumors
-
USA
-
Plautz GE, Yang Z., Wu B., Gao X., Huang L., Nabel GJ. Immunotherapy of malignancy by in vivo gene transfer into tumors. Proc. Natl Acad. Sci. USA 1993; 90: 4645–9.
-
(1993)
Proc. Natl Acad. Sci.
, vol.90
, pp. 4645-4649
-
-
Plautz, G.E.1
Yang, Z.2
Wu, B.3
Gao, X.4
Huang, L.5
Nabel, G.J.6
-
26
-
-
0028567517
-
Tissue-specific targeting of retroviral vectors through ligand-receptor interactions
-
Kasahara N., Dozy AM, Kan YW. Tissue-specific targeting of retroviral vectors through ligand-receptor interactions. Science 1994; 266: 1373–6.
-
(1994)
Science
, vol.266
, pp. 1373-1376
-
-
Kasahara, N.1
Dozy, A.M.2
Kan, Y.W.3
-
27
-
-
0029145999
-
Generation of targeted retroviral vectors by using single-chain variable fragment: An approach to in vivo gene delivery
-
USA
-
Somia NV, Zoppe M., Verma IM. Generation of targeted retroviral vectors by using single-chain variable fragment: An approach to in vivo gene delivery. Proc. Natl Acad Sci. USA 1995; 92: 7570–4.
-
(1995)
Proc. Natl Acad Sci.
, vol.92
, pp. 7570-7574
-
-
Somia, N.V.1
Zoppe, M.2
Verma, I.M.3
|