-
1
-
-
0024988334
-
Gene transfer into humans: Immonotherapy of patients with advanced melanoma using tumor infiltrating lymphocytes modified by retroviral gene transduction
-
Rosenberg SA, Aebersold P, Cornetta K, Kasid A, Morgan AA, Moen R, et al. Gene transfer into humans: immonotherapy 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
Kasid, A.4
Morgan, A.A.5
Moen, R.6
-
3
-
-
0028958358
-
Sustained delivery of erythropoietin in mice by genetically modified skin tibroblasts
-
Naffakh N, Henri A, Villeval JL, Rouyer-Fessard P, Moullier P, Blumenfeld N, et al. Sustained delivery of erythropoietin in mice by genetically modified skin tibroblasts. Proc Natl Acad Sci USA 1995;92:3194-8.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 3194-3198
-
-
Naffakh, N.1
Henri, A.2
Villeval, J.L.3
Rouyer-Fessard, P.4
Moullier, P.5
Blumenfeld, N.6
-
4
-
-
0027231473
-
Correction of lysosomal storage in the liver and spleen of MPS VII mice by implantation of genetically modified skin tibroblasts
-
Moullier P, Bohl D, Heard J-M, Danos O. Correction of lysosomal storage in the liver and spleen of MPS VII mice by implantation of genetically modified skin tibroblasts. Nat Genet 1993;4:154-9.
-
(1993)
Nat Genet
, vol.4
, pp. 154-159
-
-
Moullier, P.1
Bohl, D.2
Heard, J.-M.3
Danos, O.4
-
5
-
-
0031046584
-
Modulation of erythropoietin delivery from engineered muscles in mice
-
Bohl D, Heard J-M. Modulation of erythropoietin delivery from engineered muscles in mice. Hum Gene Ther 1997;8:195-204.
-
(1997)
Hum Gene Ther
, vol.8
, pp. 195-204
-
-
Bohl, D.1
Heard, J.-M.2
-
6
-
-
19144364120
-
Clinical trial to assess the safety, feasibility, and efficacy of transferring a potentially anti-arthritic cytokine gene to human joints with rheuniatoid arthritis
-
Evans CH, Mankin HJ, Fergason AB, Robbins PD, Ghivizzani SC, Herndon JH, et al. Clinical trial to assess the safety, feasibility, and efficacy of transferring a potentially anti-arthritic cytokine gene to human joints with rheuniatoid arthritis. Hum Gene Ther 1996;7:1261-80.
-
(1996)
Hum Gene Ther
, vol.7
, pp. 1261-1280
-
-
Evans, C.H.1
Mankin, H.J.2
Fergason, A.B.3
Robbins, P.D.4
Ghivizzani, S.C.5
Herndon, J.H.6
-
7
-
-
0029871453
-
In situ use of suicide genes for cancer therapy
-
Freeman SM, Whartenby KA, Freeman JL, Abboud CN, Marrogi AJ. In situ use of suicide genes for cancer therapy. Semin Oncol 1996;23:31-45.
-
(1996)
Semin Oncol
, vol.23
, pp. 31-45
-
-
Freeman, S.M.1
Whartenby, K.A.2
Freeman, J.L.3
Abboud, C.N.4
Marrogi, A.J.5
-
8
-
-
0029803727
-
Vectors for cancer gene therapy
-
Zhang J, Russell SJ. Vectors for cancer gene therapy, Semin Oncol 1996;15:385-401.
-
(1996)
Semin Oncol
, vol.15
, pp. 385-401
-
-
Zhang, J.1
Russell, S.J.2
-
9
-
-
0030984929
-
The TMC worldwide gene therapy enrollment report, end 1996
-
Marcel T, Grausz JD. The TMC worldwide gene therapy enrollment report, end 1996. Hum Gene Ther 1997;8:775-800.
-
(1997)
Hum Gene Ther
, vol.8
, pp. 775-800
-
-
Marcel, T.1
Grausz, J.D.2
-
10
-
-
8244238394
-
A placebo-controlled study of liposome-mediated gene transfer to the nasal epithelium of patients with cystic fibrosis
-
Gill DR, Southern KW, Mofford KA, Seddon T, Huang L, Sorgi F. et al. A placebo-controlled study of liposome-mediated gene transfer to the nasal epithelium of patients with cystic fibrosis. Gene Ther 1997;4:199-209.
-
(1997)
Gene Ther
, vol.4
, pp. 199-209
-
-
Gill, D.R.1
Southern, K.W.2
Mofford, K.A.3
Seddon, T.4
Huang, L.5
Sorgi, F.6
-
11
-
-
8244245761
-
Evidence for safety and efficacy of DOTAP cationic liposome mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosis
-
Porteous DJ, Dorin JR, McLachlan G, Davidson-Smith H, Sievenson BJ, et al. Evidence for safety and efficacy of DOTAP cationic liposome mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosis. Grue Ther 1997;4:210-18.
-
(1997)
Grue Ther
, vol.4
, pp. 210-218
-
-
Porteous, D.J.1
Dorin, J.R.2
McLachlan, G.3
Davidson-Smith, H.4
Sievenson, B.J.5
-
12
-
-
0028807727
-
I lymphocyte-directed gene therapy tnr ADA-SCID: Initial trial results after 4 years
-
Blaese RM, Culver KW, Miller D, Carter CS, Fleisher T, Clerici M, et al I lymphocyte-directed gene therapy tnr 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, D.3
Carter, C.S.4
Fleisher, T.5
Clerici, M.6
-
13
-
-
0030843493
-
HSV-TK gene transfer into donor lymphocytes for control of allogeneic graft-versus-leukemia
-
Bonini C, Ferrari G, Verzeletti S, Servida P, Zappone E, Ruggieri L, et al HSV-TK gene transfer into donor lymphocytes for control of allogeneic graft-versus-leukemia. Science 1907;276:1719-24.
-
(1907)
Science
, vol.276
, pp. 1719-1724
-
-
Bonini, C.1
Ferrari, G.2
Verzeletti, S.3
Servida, P.4
Zappone, E.5
Ruggieri, L.6
-
14
-
-
0002509433
-
Overcoming the obstacles to gene therapy
-
Friedmann T. Overcoming the obstacles to gene therapy. Sci Am 1997;276:80-5.
-
(1997)
Sci Am
, vol.276
, pp. 80-85
-
-
Friedmann, T.1
-
15
-
-
0002356428
-
Nonviral strategies for gene therapy
-
Felgner P. Nonviral strategies for gene therapy. Sci Am 1997;276:86-91.
-
(1997)
Sci Am
, vol.276
, pp. 86-91
-
-
Felgner, P.1
-
17
-
-
16944362067
-
A pilot study of idiotypic vaccination follicular B-cell lyniphoma using a genetic approach
-
Haukins RF, Russell SJ, Marrus R, Ashworth LJ, Brissinck J, Zhang J, et al A pilot study of idiotypic vaccination follicular B-cell lyniphoma using a genetic approach. Hum Gene Ther 1997;81287-99.
-
(1997)
Hum Gene Ther
, vol.8
, pp. 1287-1299
-
-
Haukins, R.F.1
Russell, S.J.2
Marrus, R.3
Ashworth, L.J.4
Brissinck, J.5
Zhang, J.6
|