-
1
-
-
0029557063
-
Liver-directed gene therapy: Molecular tools and current preclinical and clinical studies
-
ALT, M., and CASELMANN, W.H. (1995). Liver-directed gene therapy: molecular tools and current preclinical and clinical studies. J. Hepatol. 23, 746-758.
-
(1995)
J. Hepatol.
, vol.23
, pp. 746-758
-
-
Alt, M.1
Caselmann, W.H.2
-
2
-
-
0003747871
-
-
J.E. Coligan, A.M. Kruisbeek, E.M. Marguiles, E.M. Shevach, and W. Strober, eds. (John Wiley & Sons, New York)
-
ANONYMOUS. (1994). Current Protocols in Immunology. J.E. Coligan, A.M. Kruisbeek, E.M. Marguiles, E.M. Shevach, and W. Strober, eds. (John Wiley & Sons, New York).
-
(1994)
Current Protocols in Immunology
-
-
-
3
-
-
0024743528
-
In vivo transfection of murine lungs with a functioning prokaryotic gene using a liposome vehicle
-
BRIGHAM, K.L., MEYRICK, B., CHRISTMAN, B., MAGNUSON, M., KING, G., and BERRY, L.C. (1989). In vivo transfection of murine lungs with a functioning prokaryotic gene using a liposome vehicle. Am. J. Med. Sci. 298, 278-281.
-
(1989)
Am. J. Med. Sci.
, vol.298
, pp. 278-281
-
-
Brigham, K.L.1
Meyrick, B.2
Christman, B.3
Magnuson, M.4
King, G.5
Berry, L.C.6
-
4
-
-
0028237365
-
Adenovirus-mediated in vivo gene transfer
-
BRODY, S.L., and CRYSTAL, R.G. (1994). Adenovirus-mediated in vivo gene transfer. Ann. N.Y. Acad. Sci. 716, 90-101.
-
(1994)
Ann. N.Y. Acad. Sci.
, vol.716
, pp. 90-101
-
-
Brody, S.L.1
Crystal, R.G.2
-
5
-
-
0029685022
-
Gene therapy approaches for inherited and acquired lung diseases
-
CURIEL, D.T., PILEWSKI, J.M., and ALBELDA, S.M. (1996). Gene therapy approaches for inherited and acquired lung diseases. Am. J. Respir. Cell Mol. Biol. 14, 1-18.
-
(1996)
Am. J. Respir. Cell Mol. Biol.
, vol.14
, pp. 1-18
-
-
Curiel, D.T.1
Pilewski, J.M.2
Albelda, S.M.3
-
6
-
-
0028934815
-
Cellular and humoral immune responses to adenoviral vectors containing factor IX gene: Tolerization of factor IX and vector antigens allows for long-term expression
-
DAI, Y., SCHWARZ, E.M., GU, D., ZHANG, W-W., SARVETNICK, N., and VERMA, I.M. (1995). Cellular and humoral immune responses to adenoviral vectors containing factor IX gene: Tolerization of factor IX and vector antigens allows for long-term expression. Proc. Natl. Acad. Sci. USA 92, 1401-1405.
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 1401-1405
-
-
Dai, Y.1
Schwarz, E.M.2
Gu, D.3
Zhang, W.-W.4
Sarvetnick, N.5
Verma, I.M.6
-
7
-
-
0028618419
-
Prolonged transgene expression in cotton rat lung with recombinant adenoviruses defective in E2a
-
ENGLEHARDT, J.F., LITZKY, L., and WILSON, J.M. (1994a). Prolonged transgene expression in cotton rat lung with recombinant adenoviruses defective in E2a. Hum. Gene Ther. 5, 1217-1229.
-
(1994)
Hum. Gene Ther.
, vol.5
, pp. 1217-1229
-
-
Englehardt, J.F.1
Litzky, L.2
Wilson, J.M.3
-
8
-
-
0028246338
-
Ablation of E2A in recombinant adenoviruses improves transgene persistence and decreases inflammatory responses in mouse liver
-
ENGLEHARDT, J.F., YE, X., DORANZ, B., and WILSON, J.M. (1994b). Ablation of E2A in recombinant adenoviruses improves transgene persistence and decreases inflammatory responses in mouse liver. Proc. Natl. Acad. Sci. USA 91, 6196-6200.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 6196-6200
-
-
Englehardt, J.F.1
Ye, X.2
Doranz, B.3
Wilson, J.M.4
-
9
-
-
0029154012
-
Gene therapy for hemophilia B: Host immunosuppression prolongs that therapeutic effect of adenovirus-mediated factor IX expression
-
FANG, B., EISENSMITH, R.C., WANG, H., KAY, M.A., CROSS, R.E., LANDEN, C.N., GORDON, G., BELLINGER, D.A., READ, M.S., HU, P.C., BRINKHOUS, K.M., and WOO, S.L.C. (1995). Gene therapy for hemophilia B: Host immunosuppression prolongs that therapeutic effect of adenovirus-mediated factor IX expression. Hum. Gene Ther. 6, 1039-1044.
-
(1995)
Hum. Gene Ther.
, vol.6
, pp. 1039-1044
-
-
Fang, B.1
Eisensmith, R.C.2
Wang, H.3
Kay, M.A.4
Cross, R.E.5
Landen, C.N.6
Gordon, G.7
Bellinger, D.A.8
Read, M.S.9
Hu, P.C.10
Brinkhous, K.M.11
Woo, S.L.C.12
-
10
-
-
0029553015
-
Improved cationic lipid formulations for in vivo gene therapy
-
FELGNER, P.L., TSAI, Y.J., SUKHU, L., WHEELER, C.J., MANTHORPE, M., MARSHALL, J., and CHENG, S.H. (1995). Improved cationic lipid formulations for in vivo gene therapy. Ann. N.Y. Acad. Sci. 772, 126-139.
-
(1995)
Ann. N.Y. Acad. Sci.
, vol.772
, pp. 126-139
-
-
Felgner, P.L.1
Tsai, Y.J.2
Sukhu, L.3
Wheeler, C.J.4
Manthorpe, M.5
Marshall, J.6
Cheng, S.H.7
-
11
-
-
0029091783
-
Transfer of the CFTR gene to the lung of nonhuman primates with E1-deleted, E2a-defective recombinant adenoviruses: A preclinical toxicology study
-
GOLDMAN, M.J., LITZKY, L.A., ENGLEHARDT, J.F., and WILSON, J.M. (1995). Transfer of the CFTR gene to the lung of nonhuman primates with E1-deleted, E2a-defective recombinant adenoviruses: A preclinical toxicology study. Hum. Gene Ther. 6, 839-851.
-
(1995)
Hum. Gene Ther.
, vol.6
, pp. 839-851
-
-
Goldman, M.J.1
Litzky, L.A.2
Englehardt, J.F.3
Wilson, J.M.4
-
12
-
-
0028292602
-
Successful ex vivo gene therapy directed to liver in a patient with familial hypercholesterolemia
-
GROSSMAN, M., RAPER, S.E., KOZARSKY, K., STEIN, E.A., ENGELHARDT, J.F., MULLER, D., LUPIEN, P.J., and WILSON, J.M. (1994). Successful ex vivo gene therapy directed to liver in a patient with familial hypercholesterolemia. Nature Genet. 6, 335-341.
-
(1994)
Nature Genet.
, vol.6
, pp. 335-341
-
-
Grossman, M.1
Raper, S.E.2
Kozarsky, K.3
Stein, E.A.4
Engelhardt, J.F.5
Muller, D.6
Lupien, P.J.7
Wilson, J.M.8
-
13
-
-
0027409026
-
Adenovirus-mediated transfer of low density lipoprotein receptor gene acutely accelerates cholesterol clearance in normal mice
-
HERZ, J., and GERARD, R.D. (1993). Adenovirus-mediated transfer of low density lipoprotein receptor gene acutely accelerates cholesterol clearance in normal mice. Proc. Natl. Acad. Sci. USA 90, 2812-2816.
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 2812-2816
-
-
Herz, J.1
Gerard, R.D.2
-
14
-
-
0028982479
-
Trans-complementation of E1-deleted adenovirus: A new vector to reduce the possibility of codissemination of wild-type and recombinant adenoviruses
-
IMLER, J.-L., BOUT, A., DREYER, A., DIETERLE, A., SCHULTZ, H., VALERIO, D., MEHTALI, M., and PAVIRANI, A. (1995). Trans-complementation of E1-deleted adenovirus: A new vector to reduce the possibility of codissemination of wild-type and recombinant adenoviruses. Hum. Gene Ther. 6, 711-721.
-
(1995)
Hum. Gene Ther.
, vol.6
, pp. 711-721
-
-
Imler, J.-L.1
Bout, A.2
Dreyer, A.3
Dieterle, A.4
Schultz, H.5
Valerio, D.6
Mehtali, M.7
Pavirani, A.8
-
15
-
-
0026906987
-
Adenovirus-mediated in vivo gene transfer and expression in normal rat liver
-
JAFFE, H.A., DANIER, D., LONGENECKER, M., METZGER, M., SETOGUCHI, Y., ROSENFELD, M.A., GANT, T.W., THORGEIRSSON, S.S., STRATFORD-PERRICAUDET, L.D., PERRICAUDET, M., PAVIRANI, A., LECOCQ, J.P., and CRYSTAL, R.G. (1992). Adenovirus-mediated in vivo gene transfer and expression in normal rat liver. Nature Genet. 1, 372-378.
-
(1992)
Nature Genet.
, vol.1
, pp. 372-378
-
-
Jaffe, H.A.1
Danier, D.2
Longenecker, M.3
Metzger, M.4
Setoguchi, Y.5
Rosenfeld, M.A.6
Gant, T.W.7
Thorgeirsson, S.S.8
Stratford-Perricaudet, L.D.9
Perricaudet, M.10
Pavirani, A.11
Lecocq, J.P.12
Crystal, R.G.13
-
16
-
-
0028117228
-
Prolonged and effective blockade of tumor necrosis factor activity through adenovirus-mediated gene transfer
-
KOLLS, J., PEPPER, K., SILVA, M., and BEUTLER, B. (1994). Prolonged and effective blockade of tumor necrosis factor activity through adenovirus-mediated gene transfer. Proc. Natl. Acad. Sci. USA 91, 215-219.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 215-219
-
-
Kolls, J.1
Pepper, K.2
Silva, M.3
Beutler, B.4
-
17
-
-
0029875608
-
Use of transient CD4-lymphocyte depletion to prolong transgene expression of E1-deleted adenoviral vectors
-
KOLLS, J.K., LEI, D., ODOM, G., NELSON, S., SUMMER, W.R., GERBER, M.A., and SHELLITO, J.E. (1996). Use of transient CD4-lymphocyte depletion to prolong transgene expression of E1-deleted adenoviral vectors. Hum. Gene Ther. 7, 489-497.
-
(1996)
Hum. Gene Ther.
, vol.7
, pp. 489-497
-
-
Kolls, J.K.1
Lei, D.2
Odom, G.3
Nelson, S.4
Summer, W.R.5
Gerber, M.A.6
Shellito, J.E.7
-
18
-
-
0028234357
-
In vivo correction of low density lipoprotein receptor deficiency in the Wantanabe heritable hyperlipidemic rabbit with recombinant adenoviruses
-
KOZARSKY, K.F., MCKINLEY, D.R., AUSTIN, L.L., RAPER, S.E., STRATFORD-PERRICAUDET, L.D., and WILSON, J.M. (1994). In vivo correction of low density lipoprotein receptor deficiency in the Wantanabe heritable hyperlipidemic rabbit with recombinant adenoviruses. J. Biol. Chem. 269, 13695-13702.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 13695-13702
-
-
Kozarsky, K.F.1
Mckinley, D.R.2
Austin, L.L.3
Raper, S.E.4
Stratford-Perricaudet, L.D.5
Wilson, J.M.6
-
19
-
-
0028955770
-
Detection of hepatitis B virus sequences in liver tissues of seronegative organ donors
-
LEI, D., WU, J., SULLIVAN, D.E., DASH, S., and GERBER, M.A. (1995). Detection of hepatitis B virus sequences in liver tissues of seronegative organ donors. Int. Hepatol. Commun. 3, 154-160.
-
(1995)
Int. Hepatol. Commun.
, vol.3
, pp. 154-160
-
-
Lei, D.1
Wu, J.2
Sullivan, D.E.3
Dash, S.4
Gerber, M.A.5
-
20
-
-
0027758609
-
Assessment of recombinant adenoviral vectors for hepatic gene therapy
-
LI, Q., KAY, M.A., FIENGOLD, M., STRATFORD-PERRICAUDET, L.D., and WOO, S.L.C. (1993). Assessment of recombinant adenoviral vectors for hepatic gene therapy. Hum. Gene Ther. 4, 403-409.
-
(1993)
Hum. Gene Ther.
, vol.4
, pp. 403-409
-
-
Li, Q.1
Kay, M.A.2
Fiengold, M.3
Stratford-Perricaudet, L.D.4
Woo, S.L.C.5
-
21
-
-
0029861452
-
Recombinant adenoviruses with large deletions generated by cre-mediated excision exhibit different biological properties compared with first-generation vectors in vitro and in vivo
-
LIEBER, A., HE, C-Y., KIRILLOVA, I., and KAY, M.A. (1996). Recombinant adenoviruses with large deletions generated by cre-mediated excision exhibit different biological properties compared with first-generation vectors in vitro and in vivo. J. Virol. 70, 8944-8960.
-
(1996)
J. Virol.
, vol.70
, pp. 8944-8960
-
-
Lieber, A.1
He, C.-Y.2
Kirillova, I.3
Kay, M.A.4
-
22
-
-
0028303206
-
Adenoviral-mediated gene transfer to bladder in vivo
-
MORRIS, B.D. JR., DRAZAN, K.E., CSETE, M.E., WERTHMAN, P.E., VAN BREE, M.P., ROSENTHAL, J.T., and SHARED, A. (1994). Adenoviral-mediated gene transfer to bladder in vivo. J. Urol. 152, 506-509.
-
(1994)
J. Urol.
, vol.152
, pp. 506-509
-
-
Morris Jr., B.D.1
Drazan, K.E.2
Csete, M.E.3
Werthman, P.E.4
Van Bree, M.P.5
Rosenthal, J.T.6
Shared, A.7
-
23
-
-
0028030487
-
Adenoviral-mediated gene transfer to renal tubular cells in vivo
-
MOULLIER, P., FRIEDLANDER, G., CALISE, D., RONCO, P., PERRICAUDET, M. and FERRY, N. (1994). Adenoviral-mediated gene transfer to renal tubular cells in vivo. Kidney Int. 45, 1220-1225.
-
(1994)
Kidney Int.
, vol.45
, pp. 1220-1225
-
-
Moullier, P.1
Friedlander, G.2
Calise, D.3
Ronco, P.4
Perricaudet, M.5
Ferry, N.6
-
24
-
-
0027595949
-
The basic science of gene therapy
-
MULLIGAN, R.C. (1993). The basic science of gene therapy. Science 260, 926-932.
-
(1993)
Science
, vol.260
, pp. 926-932
-
-
Mulligan, R.C.1
-
25
-
-
85036488558
-
Gene transfer to primate liver using second generation recombinant adenovirus
-
NUNES, F.A., RAPER, S.E., and WILSON, J.M. (1995). Gene transfer to primate liver using second generation recombinant adenovirus. Gastroenterology 108, A1135.
-
(1995)
Gastroenterology
, vol.108
-
-
Nunes, F.A.1
Raper, S.E.2
Wilson, J.M.3
-
26
-
-
0027735897
-
Adenovirus-mediated transfer of the CFTR gene to lung of nonhuman primates: Toxicity study
-
SIMON, R.H., ENGELHARDT, J.F., YANG, Y., ZEPEDA, M., WEBER-PENDLETON, S., GROSSMAN, M., and WILSON, J.M. (1993). Adenovirus-mediated transfer of the CFTR gene to lung of nonhuman primates: Toxicity study. Hum. Gene Ther. 4, 771-780.
-
(1993)
Hum. Gene Ther.
, vol.4
, pp. 771-780
-
-
Simon, R.H.1
Engelhardt, J.F.2
Yang, Y.3
Zepeda, M.4
Weber-Pendleton, S.5
Grossman, M.6
Wilson, J.M.7
-
27
-
-
0028967275
-
Expression of the hepatitis C virus genome in rat liver after cationic liposome-mediated in vivo gene transfer
-
TAKEHARA, T., HAYASHI, N., MIYAMOTO, Y., YAMAMOTO, M., MITA, E., FUSAMOTO, H., and KAMADA, T. (1995). Expression of the hepatitis C virus genome in rat liver after cationic liposome-mediated in vivo gene transfer. Hepatology 21, 746-51.
-
(1995)
Hepatology
, vol.21
, pp. 746-751
-
-
Takehara, T.1
Hayashi, N.2
Miyamoto, Y.3
Yamamoto, M.4
Mita, E.5
Fusamoto, H.6
Kamada, T.7
-
28
-
-
0021208016
-
Complementation of an adenovirus 5 immediate early mutant by human cytomegalovirus
-
TEVETHIA, M.J., and SPECTOR, D.J. (1987). Complementation of an adenovirus 5 immediate early mutant by human cytomegalovirus. Virology 137, 428-431.
-
(1987)
Virology
, vol.137
, pp. 428-431
-
-
Tevethia, M.J.1
Spector, D.J.2
-
29
-
-
0030563195
-
Molecular medicine: Adenoviruses as gene-delivery vehicles
-
WILSON, J.M. (1996). Molecular medicine: adenoviruses as gene-delivery vehicles. Mol. Med. 334, 1185-1187.
-
(1996)
Mol. Med.
, vol.334
, pp. 1185-1187
-
-
Wilson, J.M.1
-
30
-
-
0026842933
-
Clinical protocol: Ex vivo gene therapy of familial hypercholesterolemia
-
WILSON, J.M., GROSSMAN, M., RAPER, S.E., BAKER, J.R., NEWMAN, R.S., and THOEN, J. (1992). Clinical protocol: Ex vivo gene therapy of familial hypercholesterolemia. Hum. Gene Ther. 3, 179-187.
-
(1992)
Hum. Gene Ther.
, vol.3
, pp. 179-187
-
-
Wilson, J.M.1
Grossman, M.2
Raper, S.E.3
Baker, J.R.4
Newman, R.S.5
Thoen, J.6
-
31
-
-
0027196615
-
An approach for treating the hepatobiliary disease of cystic fibrosis by somatic gene transfer
-
YANG, Y., RAPER, S.E., COHN, J.A., ENGELHARDT, J.F., and WILSON, J.M. (1993). An approach for treating the hepatobiliary disease of cystic fibrosis by somatic gene transfer. Proc. Natl. Acad. Sci. USA 90, 4601-1605.
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 4601-11605
-
-
Yang, Y.1
Raper, S.E.2
Cohn, J.A.3
Engelhardt, J.F.4
Wilson, J.M.5
-
32
-
-
0028328261
-
Cellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapy
-
YANG, Y., NUNES, F.A., BERENCSI, K., FURTH, E.E., GONCZOL, E., and WILSON, J.M. (1994). Cellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapy. Proc. Natl. Acad. Sci. USA 91, 4407-4411.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 4407-4411
-
-
Yang, Y.1
Nunes, F.A.2
Berencsi, K.3
Furth, E.E.4
Gonczol, E.5
Wilson, J.M.6
-
33
-
-
0028937785
-
Cellular and humoral immune responses to viral antigens create barriers to lung-directed gene therapy with recombinant adenoviruses
-
YANG, Y., LI, Q., ERTL, H.C.J., and WILSON, J.M. (1995). Cellular and humoral immune responses to viral antigens create barriers to lung-directed gene therapy with recombinant adenoviruses. J. Virol. 69, 2004-2015.
-
(1995)
J. Virol.
, vol.69
, pp. 2004-2015
-
-
Yang, Y.1
Li, Q.2
Ertl, H.C.J.3
Wilson, J.M.4
-
34
-
-
0030042794
-
Prolonged metabolic correction in adult ornithine transcarbamylase-deficient mice with adenoviral vectors
-
YE, X.H., ROBINSON, M.B., BATSHAW, M.L., FURTH, E.E., SMITH, I., and WILSON, J.M. (1996). Prolonged metabolic correction in adult ornithine transcarbamylase-deficient mice with adenoviral vectors. J. Biol. Chem. 271, 3639-3646.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 3639-3646
-
-
Ye, X.H.1
Robinson, M.B.2
Batshaw, M.L.3
Furth, E.E.4
Smith, I.5
Wilson, J.M.6
-
35
-
-
0028800687
-
Detection of wild-type contamination in a recombinant adenoviral preparation by PCR
-
ZHANG, W-W., KOCH, P.E., and ROTH, J.A. (1995). Detection of wild-type contamination in a recombinant adenoviral preparation by PCR. Biotechniques 18, 444-447.
-
(1995)
Biotechniques
, vol.18
, pp. 444-447
-
-
Zhang, W.-W.1
Koch, P.E.2
Roth, J.A.3
-
36
-
-
0027313072
-
Systemic gene expression after intravenous DNA delivery into adult mice
-
ZHU, N., LIGGITT, D., LIU, Y., and DEBS, R. (1993). Systemic gene expression after intravenous DNA delivery into adult mice. Science 261, 209-211.
-
(1993)
Science
, vol.261
, pp. 209-211
-
-
Zhu, N.1
Liggitt, D.2
Liu, Y.3
Debs, R.4
|