-
1
-
-
0025160084
-
Expression of human factor IX in rabbit hepatocytes by retrovirus-mediated gene transfer: Potential for gene therapy of hemophilia B
-
Armentano D, Thompson G, Darlington G, Woo SL. Expression of human factor IX in rabbit hepatocytes by retrovirus-mediated gene transfer: potential for gene therapy of hemophilia B. Proc Natl Acad Sci USA 1990; 87: 6141-5.
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 6141-6145
-
-
Armentano, D.1
Thompson, G.2
Darlington, G.3
Woo, S.L.4
-
2
-
-
0026722489
-
Gene transfer in the hemophilias: Retrospect and prospect
-
Brinkhous KM. Gene transfer in the hemophilias: retrospect and prospect. Thromb Res 1992; 67: 329-38.
-
(1992)
Thromb Res
, vol.67
, pp. 329-338
-
-
Brinkhous, K.M.1
-
3
-
-
0028904215
-
Prospects for gene therapy of haemophilia A and B
-
Brownlee GG. Prospects for gene therapy of haemophilia A and B. Br Med Bull 1995; 51: 91-105.
-
(1995)
Br Med Bull
, vol.51
, pp. 91-105
-
-
Brownlee, G.G.1
-
4
-
-
44049120479
-
High efficient transfer and expression of human clotting factor IX cDNA in cultured human primary skin fibroblasts from hemophilia B patient by retroviral vectors
-
Dai YF, Qiu XF, Xue JL, Liu ZD. High efficient transfer and expression of human clotting factor IX cDNA in cultured human primary skin fibroblasts from hemophilia B patient by retroviral vectors. Sci China B 1992; 35: 183-93.
-
(1992)
Sci China B
, vol.35
, pp. 183-193
-
-
Dai, Y.F.1
Qiu, X.F.2
Xue, J.L.3
Liu, Z.D.4
-
6
-
-
0026586140
-
Expression of human alpha 1-antitrypsin in dogs after autologous transplantation of retroviral transduced hepatocytes
-
Kay MA, Baley P, Rothenberg S, Leland F, Fleming L, Ponder KP et al. Expression of human alpha 1-antitrypsin in dogs after autologous transplantation of retroviral transduced hepatocytes. Proc Natl Acad Sci USA 1992; 89: 89-93.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 89-93
-
-
Kay, M.A.1
Baley, P.2
Rothenberg, S.3
Leland, F.4
Fleming, L.5
Ponder, K.P.6
-
7
-
-
0030817391
-
A coagulation factor IX-deficient mouse model for human hemophilia B
-
Lin HF, Maeda N, Smithies O, Straight DL, Stafford DW. A coagulation factor IX-deficient mouse model for human hemophilia B. Blood 1997; 90: 3962-6.
-
(1997)
Blood
, vol.90
, pp. 3962-3966
-
-
Lin, H.F.1
Maeda, N.2
Smithies, O.3
Straight, D.L.4
Stafford, D.W.5
-
8
-
-
0030758328
-
A factor IX-deficient mouse model for hemophilia B gene therapy
-
Wang L, Zoppe M, Hackeng TM, Griffin JH, Lee KF, Verma IM. A factor IX-deficient mouse model for hemophilia B gene therapy. Proc Natl Acad Sci USA 1997; 94: 11563-6.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 11563-11566
-
-
Wang, L.1
Zoppe, M.2
Hackeng, T.M.3
Griffin, J.H.4
Lee, K.F.5
Verma, I.M.6
-
9
-
-
0027033259
-
Hepatic gene therapy: Persistent expression of human alpha 1-antitrypsin in mice after direct gene delivery in vivo
-
Kay MA, Li Q, Liu TJ, Leland F, Toman C, Finegold M, Woo SL. Hepatic gene therapy: persistent expression of human alpha 1-antitrypsin in mice after direct gene delivery in vivo. Hum Gene Ther 1992; 3: 641-7.
-
(1992)
Hum Gene Ther
, vol.3
, pp. 641-647
-
-
Kay, M.A.1
Li, Q.2
Liu, T.J.3
Leland, F.4
Toman, C.5
Finegold, M.6
Woo, S.L.7
-
10
-
-
0027686238
-
In vivo gene therapy of hemophilia B: Sustained partial correction in factor IX-deficient dogs
-
Kay MA, Rothenberg S, Landen CN, Bellinger DA, Leland F, Toman C et al. In vivo gene therapy of hemophilia B: sustained partial correction in factor IX-deficient dogs [see comments]. Science 1993; 262: 117-9.
-
(1993)
Science
, vol.262
, pp. 117-119
-
-
Kay, M.A.1
Rothenberg, S.2
Landen, C.N.3
Bellinger, D.A.4
Leland, F.5
Toman, C.6
-
11
-
-
0024805130
-
-
Evans JPK, Brinkhous M, Brayer GD, Reisner HM, High KA. Proc Natl Acad Sci USA 1992; 86: 10095-9.
-
(1992)
Proc Natl Acad Sci USA
, vol.86
, pp. 10095-10099
-
-
Evans, J.P.K.1
Brinkhous, M.2
Brayer, G.D.3
Reisner, H.M.4
High, K.A.5
-
12
-
-
0029088057
-
A modified urokinase plasminogen activator induces liver regeneration without bleeding
-
Lieber A, Vrancken Peeters MJTFD, Gown A, Perkins J, Kay MA. A modified urokinase plasminogen activator induces liver regeneration without bleeding. Hum Gene Ther 1995; 6.
-
(1995)
Hum Gene Ther
, pp. 6
-
-
Lieber, A.1
Vrancken Peeters, M.J.T.F.D.2
Gown, A.3
Perkins, J.4
Kay, M.A.5
-
13
-
-
0029010354
-
Adenovirus-mediated urokinase gene transfer induces liver regeneration and allows for efficient retrovirus transduction of hepatocytes in vivo
-
Lieber A, Vrancken Peeters MJTFD, Meuse L, Fausto N, Perkins J, Kay MA. Adenovirus-mediated urokinase gene transfer induces liver regeneration and allows for efficient retrovirus transduction of hepatocytes in vivo. Proc Natl Acad Sci USA 1995; 92: 6210-4.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 6210-6214
-
-
Lieber, A.1
Vrancken Peeters, M.J.T.F.D.2
Meuse, L.3
Fausto, N.4
Perkins, J.5
Kay, M.A.6
-
14
-
-
0030452791
-
Proliferation induced by keratinocyte growth factor enhances in vivo retroviral-mediated gene transfer to mouse hepatocytes
-
Bosch A, McCray PB-J, Chang SM, Ulich TR, Simonet WS, Jolly DJ, Davidson BL. Proliferation induced by keratinocyte growth factor enhances in vivo retroviral-mediated gene transfer to mouse hepatocytes. J Clin Invest 1996; 98: 2683-7.
-
(1996)
J Clin Invest
, vol.98
, pp. 2683-2687
-
-
Bosch, A.1
McCray, P.B.-J.2
Chang, S.M.3
Ulich, T.R.4
Simonet, W.S.5
Jolly, D.J.6
Davidson, B.L.7
-
15
-
-
0030716959
-
Sustained expression of genes delivered directly into liver and muscle by lentiviral vectors
-
Kafri T, Blomer U, Peterson DA, Gage FH, Verma IM. Sustained expression of genes delivered directly into liver and muscle by lentiviral vectors. Nature Genetics 1997; 17: 314-7.
-
(1997)
Nature Genetics
, vol.17
, pp. 314-317
-
-
Kafri, T.1
Blomer, U.2
Peterson, D.A.3
Gage, F.H.4
Verma, I.M.5
-
16
-
-
0027758609
-
Assessment of recombinant adenoviral vectors for hepatic gene therapy
-
Li Q, Kay MA, Finegold M, Stratford Perricaudet LD, Woo SL. Assessment of recombinant adenoviral vectors for hepatic gene therapy. Hum Gene Ther 1993; 4: 403-9.
-
(1993)
Hum Gene Ther
, vol.4
, pp. 403-409
-
-
Li, Q.1
Kay, M.A.2
Finegold, M.3
Stratford Perricaudet, L.D.4
Woo, S.L.5
-
17
-
-
0028274169
-
In vivo hepatic gene therapy: Complete albeit transient correction of factor IX deficiency in hemophilia B dogs
-
Kay MA, Landen CN, Rothenberg SR, Taylor LA, Leland F, Wiehle S, et al. In vivo hepatic gene therapy: complete albeit transient correction of factor IX deficiency in hemophilia B dogs. Proc Natl Acad Sei USA 1994; 91: 2353-7.
-
(1994)
Proc Natl Acad Sei USA
, vol.91
, pp. 2353-2357
-
-
Kay, M.A.1
Landen, C.N.2
Rothenberg, S.R.3
Taylor, L.A.4
Leland, F.5
Wiehle, S.6
-
18
-
-
0029113869
-
Long-term hepatic adenovirus mediated gene expression in mice following CTLA4Ig administration
-
Kay MA, Holterman A-X, Meuse L, Gown A, Ochs H, Linsley PS, Wilson CB. Long-term hepatic adenovirus mediated gene expression in mice following CTLA4Ig administration. Nature Genetics 1995; 11: 191-7.
-
(1995)
Nature Genetics
, vol.11
, pp. 191-197
-
-
Kay, M.A.1
Holterman, A.-X.2
Meuse, L.3
Gown, A.4
Ochs, H.5
Linsley, P.S.6
Wilson, C.B.7
-
19
-
-
0030984335
-
Transient immunomodulation with anti-CD40 ligand antibody and CTLA4Ig enhances persistence and secondary adenovirus
-
Kay MA, Meuse L, Gown AM, Linsley P, Hollenbaugh D, Aruffo A, et al. Transient immunomodulation with anti-CD40 ligand antibody and CTLA4Ig enhances persistence and secondary adenovirus. Proc Natl Acad Sci USA 1996; 94: 4686-91.
-
(1996)
Proc Natl Acad Sci USA
, vol.94
, pp. 4686-4691
-
-
Kay, M.A.1
Meuse, L.2
Gown, A.M.3
Linsley, P.4
Hollenbaugh, D.5
Aruffo, A.6
-
20
-
-
0030997346
-
Persistent and therapeutic concentrations of human factor IX in mice after hepatic gene transfer of recombinant AAV vectors
-
Snyder RO, Miao CH, Patijn GA, Spratt SK, Danos O, Nagy D et al. Persistent and therapeutic concentrations of human factor IX in mice after hepatic gene transfer of recombinant AAV vectors. Nature Genetics 1996; 16: 270-6.
-
(1996)
Nature Genetics
, vol.16
, pp. 270-276
-
-
Snyder, R.O.1
Miao, C.H.2
Patijn, G.A.3
Spratt, S.K.4
Danos, O.5
Nagy, D.6
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