-
1
-
-
0015492624
-
Gene therapy for human genetic disease
-
Friedmann T, Roblin R. Gene therapy for human genetic disease. Science 1972;175:949-55
-
(1972)
Science
, vol.175
, pp. 949-955
-
-
Friedmann, T.1
Roblin, R.2
-
2
-
-
0030062296
-
Gene therapy - An immature genie but certainly out of the bottle
-
Friedmann T. Gene therapy - an immature genie but certainly out of the bottle. Nature Med 1996;2:144-7
-
(1996)
Nature Med
, vol.2
, pp. 144-147
-
-
Friedmann, T.1
-
3
-
-
0028916806
-
Human somatic gene therapy: Progress and problems
-
Brenner MK. Human somatic gene therapy: Progress and problems. J Intern Med 1995;237:229-39
-
(1995)
J Intern Med
, vol.237
, pp. 229-239
-
-
Brenner, M.K.1
-
4
-
-
0028962573
-
Scope and limitations of gene therapy
-
Weatherall DJ. Scope and limitations of gene therapy. Br Med Bull 1995;51:1-11
-
(1995)
Br Med Bull
, vol.51
, pp. 1-11
-
-
Weatherall, D.J.1
-
5
-
-
0027595949
-
The basic science of gene therapy
-
Mulligan RC. The basic science of gene therapy. Science 1993; 260:926-32
-
(1993)
Science
, vol.260
, pp. 926-932
-
-
Mulligan, R.C.1
-
6
-
-
0020472381
-
Adaptation of a retrovirus as a eucaryotic vector transmitting the herpes simplex thymidine kinase gene
-
Tabin CJ, Hoffmann JW, Goff SP, Weinberg RA. Adaptation of a retrovirus as a eucaryotic vector transmitting the herpes simplex thymidine kinase gene. Molec Cell Biol 1982;2:426-36
-
(1982)
Molec Cell Biol
, vol.2
, pp. 426-436
-
-
Tabin, C.J.1
Hoffmann, J.W.2
Goff, S.P.3
Weinberg, R.A.4
-
7
-
-
0019447450
-
Construction and isolation of a transmissible retrovirus containing the src gene from Harvey Murine Sarcoma Virus and the thymidine kinase gene from herpes simplex virus type I
-
Wei C, Gibson M, Spear PG, Scolnick EM. Construction and isolation of a transmissible retrovirus containing the src gene from Harvey Murine Sarcoma Virus and the thymidine kinase gene from herpes simplex virus type I. J Virol 1981;39:935-44
-
(1981)
J Virol
, vol.39
, pp. 935-944
-
-
Wei, C.1
Gibson, M.2
Spear, P.G.3
Scolnick, E.M.4
-
8
-
-
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
-
9
-
-
0021238736
-
Partial phenotypic correction of human Lesch-Nyhan (hypoxanthine-guanine phosphoribosyltransferase-deficient) lymphoblasts with a transmissible retroviral vector
-
Willis RCW, Jolly DJ, Miller AD, et al. Partial phenotypic correction of human Lesch-Nyhan (hypoxanthine-guanine phosphoribosyltransferase-deficient) lymphoblasts with a transmissible retroviral vector. J Biol Chem 1984;259:7842-9
-
(1984)
J Biol Chem
, vol.259
, pp. 7842-7849
-
-
Willis, R.C.W.1
Jolly, D.J.2
Miller, A.D.3
-
10
-
-
0345940337
-
Correction of adenosine deaminase deficiency in cultured human T and B cells by retrovirus-mediated gene transfer
-
Kantoff PW, Kohn DB, Mitsuya H, et al. Correction of adenosine deaminase deficiency in cultured human T and B cells by retrovirus-mediated gene transfer. Proc Natl Acad Sci USA 1986; 83:6563-7
-
(1986)
Proc Natl Acad Sci USA
, vol.83
, pp. 6563-6567
-
-
Kantoff, P.W.1
Kohn, D.B.2
Mitsuya, H.3
-
11
-
-
0024411916
-
Progress toward human gene therapy
-
Friedmann T. Progress toward human gene therapy. Science 1989;244:1275-81
-
(1989)
Science
, vol.244
, pp. 1275-1281
-
-
Friedmann, T.1
-
12
-
-
0020970755
-
Research on gene therapy
-
Cline MJ. Research on gene therapy. Basic Life Sci 1983;25:77-92
-
(1983)
Basic Life Sci
, vol.25
, pp. 77-92
-
-
Cline, M.J.1
-
13
-
-
0020732182
-
Moral problems and ethical issues in prospective human gene therapy
-
Fletcher JC, Moral problems and ethical issues in prospective human gene therapy. Virginia Law Rev 1983;69:515-46
-
(1983)
Virginia Law Rev
, vol.69
, pp. 515-546
-
-
Fletcher, J.C.1
-
14
-
-
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
-
15
-
-
0027415225
-
Development of gene therapy for immunodeficiency: Adenosine deaminase deficiency
-
Blaese RM. Development of gene therapy for immunodeficiency: Adenosine deaminase deficiency. Pediatr Res 1993;33 Suppl: S49-S55
-
(1993)
Pediatr Res
, vol.33
, Issue.SUPPL.
-
-
Blaese, R.M.1
-
16
-
-
0029100239
-
A controlled study of adenoviral-mediated gene transfer in the nasal epithelium of patients with cystic fibrosis
-
Knowles MR, Hohneker KW, Zhou Z, et al. A controlled study of adenoviral-mediated gene transfer in the nasal epithelium of patients with cystic fibrosis. N Engl J Med 1995;333:823-31
-
(1995)
N Engl J Med
, vol.333
, pp. 823-831
-
-
Knowles, M.R.1
Hohneker, K.W.2
Zhou, Z.3
-
17
-
-
0028789792
-
Gene therapy in peripheral blood lymphocytes and bone marrow for ADA-immunodeficient patients
-
Bordignon C, Notarangelo LD, Nobili N, et al. Gene therapy in peripheral blood lymphocytes and bone marrow for ADA-immunodeficient patients. Science 1995;270:470-5
-
(1995)
Science
, vol.270
, pp. 470-475
-
-
Bordignon, C.1
Notarangelo, L.D.2
Nobili, N.3
-
18
-
-
0028807727
-
T lymphopcyte-directed gene therapy for ADA-SCID: Initial trial results after 4 years
-
Blaese RM, Culver KW, Miller AD, et al. T lymphopcyte-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
-
19
-
-
0029129834
-
Myoblast transfer in the treatment of Duchenne's Muscular Dystrophy
-
Mendell JR, Kissel JT, Amato AA, et al. Myoblast transfer in the treatment of Duchenne's Muscular Dystrophy. N Engl J Med 1995;333:832-8
-
(1995)
N Engl J Med
, vol.333
, pp. 832-838
-
-
Mendell, J.R.1
Kissel, J.T.2
Amato, A.A.3
-
20
-
-
0028960770
-
NIH review of gene therapy protocols
-
Varmus H. NIH review of gene therapy protocols. Science 1995;267:1889
-
(1995)
Science
, vol.267
, pp. 1889
-
-
Varmus, H.1
-
21
-
-
0028933986
-
Varmus orders up a review of the science of gene therapy
-
Marshall E. Varmus orders up a review of the science of gene therapy. Science 1995;267:1588
-
(1995)
Science
, vol.267
, pp. 1588
-
-
Marshall, E.1
-
22
-
-
0028962405
-
Pseudotyped retroviral vectors for studies of human gene therapy
-
Friedmann T. Pseudotyped retroviral vectors for studies of human gene therapy. Nature Med 1995;1:275-7
-
(1995)
Nature Med
, vol.1
, pp. 275-277
-
-
Friedmann, T.1
-
23
-
-
0028917047
-
Retroviral vector particles displaying the antigen-binding site of an antibody enable cell-type-specific gene transfer
-
Chu T-HT, Dornburg R. Retroviral vector particles displaying the antigen-binding site of an antibody enable cell-type-specific gene transfer. J Virol 1995;69:2659-63
-
(1995)
J Virol
, vol.69
, pp. 2659-2663
-
-
Chu, T.-H.T.1
Dornburg, R.2
-
24
-
-
0029155688
-
Targeting retroviral vectors to specific cells
-
Kasahara N, Dozy A, Kan YW. Targeting retroviral vectors to specific cells. Science 1995;269:417
-
(1995)
Science
, vol.269
, pp. 417
-
-
Kasahara, N.1
Dozy, A.2
Kan, Y.W.3
-
25
-
-
0029094549
-
Retroviral retargeting by envelopes expressing an N-terminal binding domain
-
Cosset F-L, Morling FJ, Takeuchi Y, Weiss RA, Collins MKL, Russell SJ. Retroviral retargeting by envelopes expressing an N-terminal binding domain. J Virol 1995;69:6314-22
-
(1995)
J Virol
, vol.69
, pp. 6314-6322
-
-
Cosset, F.-L.1
Morling, F.J.2
Takeuchi, Y.3
Weiss, R.A.4
Collins, M.K.L.5
Russell, S.J.6
-
26
-
-
0029074517
-
Mapping of receptor binding domains in the envelope protein of spleen necrosis virus
-
Martinez I, Dornburg R. Mapping of receptor binding domains in the envelope protein of spleen necrosis virus. J Virol 1995;69:4339-46
-
(1995)
J Virol
, vol.69
, pp. 4339-4346
-
-
Martinez, I.1
Dornburg, R.2
-
27
-
-
0029996147
-
In vivo gene delivery and stable transduction of non-dividing cells by a lentiviral vector
-
Naldini L, Blömer U, Gallay P, et al. In vivo gene delivery and stable transduction of non-dividing cells by a lentiviral vector. Science 1996;272:263-7
-
(1996)
Science
, vol.272
, pp. 263-267
-
-
Naldini, L.1
Blömer, U.2
Gallay, P.3
-
28
-
-
0028074881
-
Tethering human immunodeficiency virus 1 integrase to a DNA site directs integration to nearby sequences
-
Bushman FD. Tethering human immunodeficiency virus 1 integrase to a DNA site directs integration to nearby sequences. Proc Natl Acad Sci USA 1994;91:9233-7
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 9233-9237
-
-
Bushman, F.D.1
-
29
-
-
0028246338
-
ABlation of E2A in recombinant adenoviruses improves transgene persistence and decreases inflammatory response in mouse liver
-
Engelhardt JF, Ye X, Doranz B, Wilson JM. ABlation of E2A in recombinant adenoviruses improves transgene persistence and decreases inflammatory response in mouse liver. Proc Natl Acad Sci USA 1994;91:6196-200
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 6196-6200
-
-
Engelhardt, J.F.1
Ye, X.2
Doranz, B.3
Wilson, J.M.4
-
30
-
-
0028863880
-
Characterization of an adenovirus gene transfer vector containing an E4 deletion
-
Armentano D, Sookdeo CC, Hehir KM, et al. Characterization of an adenovirus gene transfer vector containing an E4 deletion. Hum Gene Ther 1995;6:1343-53
-
(1995)
Hum Gene Ther
, vol.6
, pp. 1343-1353
-
-
Armentano, D.1
Sookdeo, C.C.2
Hehir, K.M.3
-
32
-
-
0028839655
-
Targeted tumor killing via an intracellular antibody against erbB-2
-
Deshane J, Siegal GP, Alvarez RD, et al. Targeted tumor killing via an intracellular antibody against erbB-2. J Clin Invest 1995; 96:2980-9
-
(1995)
J Clin Invest
, vol.96
, pp. 2980-2989
-
-
Deshane, J.1
Siegal, G.P.2
Alvarez, R.D.3
-
33
-
-
0026687453
-
Coupling of adenovirus to transferrin-polylysine/DNA complexes greatly enhances receptor-mediated gene delivery and expression of transfected genes
-
Wagner E, Zatloukal K, Cotten M, et al. Coupling of adenovirus to transferrin-polylysine/DNA complexes greatly enhances receptor-mediated gene delivery and expression of transfected genes. Proc Natl Acad Sci USA 1992;89:6099-103
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 6099-6103
-
-
Wagner, E.1
Zatloukal, K.2
Cotten, M.3
-
34
-
-
0025949812
-
Adenovirus enhancement of transferrin-polylysine-mediated gene delivery
-
Curiel D, Agarwal S, Wagner E, Cotten M. Adenovirus enhancement of transferrin-polylysine-mediated gene delivery Proc Natl Acad Sci USA 1991;88:8850-4
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 8850-8854
-
-
Curiel, D.1
Agarwal, S.2
Wagner, E.3
Cotten, M.4
-
35
-
-
0029051936
-
Regulation of tyrosine hydroxylase gene expression in IMR-32 neuroblastoma cells by basic fibroblast growth factor and ciliary neurotrophic factor
-
Rabinovsky ED, Ramchatesingh J, McManaman JL. Regulation of tyrosine hydroxylase gene expression in IMR-32 neuroblastoma cells by basic fibroblast growth factor and ciliary neurotrophic factor. J Neurochem 1995;64:2404-12
-
(1995)
J Neurochem
, vol.64
, pp. 2404-2412
-
-
Rabinovsky, E.D.1
Ramchatesingh, J.2
McManaman, J.L.3
-
36
-
-
0028060149
-
Intradermal gene immunization: The possible role of DNA uptake on the induction of cellular immunity to viruses
-
Raz E, Carson DA, Parker SE, et al. Intradermal gene immunization: The possible role of DNA uptake on the induction of cellular immunity to viruses. Proc Natl Acad Sci USA 1994;91: 9519-23
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 9519-9523
-
-
Raz, E.1
Carson, D.A.2
Parker, S.E.3
-
37
-
-
0027280565
-
Systemic immunological effects of cytokine genes injected into skeletal muscle
-
Raz E, Watanabe A, Baird SM, et al. Systemic immunological effects of cytokine genes injected into skeletal muscle. Proc Natl Acad Sci USA 1993;90:4523-27
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 4523-4527
-
-
Raz, E.1
Watanabe, A.2
Baird, S.M.3
|