-
1
-
-
0032925803
-
Retroviral vectors for liver-directed gene therapy
-
Kalpana GV. Retroviral vectors for liver-directed gene therapy. Semin Liver Dis 1999; 19 (1): 27-37
-
(1999)
Semin Liver Dis
, vol.19
, Issue.1
, pp. 27-37
-
-
Kalpana, G.V.1
-
2
-
-
0030716959
-
Sustained expression of genes delivered directly into liver and muscle by lentiviral vectors
-
Kafri T, Blomer U, Peterson DA, et al. Sustained expression of genes delivered directly into liver and muscle by lentiviral vectors. Nat Genet 1997; 17 (3): 314-7
-
(1997)
Nat Genet
, vol.17
, Issue.3
, pp. 314-317
-
-
Kafri, T.1
Blomer, U.2
Peterson, D.A.3
-
3
-
-
0026355641
-
Long term improvement of hypercholesterolemia after ex vivo gene therapy in LDLR-deficient rabbits
-
Chowdhury JR, Grossman M, Gupta S, et al. Long term improvement of hypercholesterolemia after ex vivo gene therapy in LDLR-deficient rabbits. Science 1991; 254: 1802-5
-
(1991)
Science
, vol.254
, pp. 1802-1805
-
-
Chowdhury, J.R.1
Grossman, M.2
Gupta, S.3
-
4
-
-
0028292602
-
Successful ex vivo gene therapy directed to liver in a patient with familial hypercholesterolemia
-
Grossman M, Raper SE, Kosarsky K, et al. Successful ex vivo gene therapy directed to liver in a patient with familial hypercholesterolemia. Nat Get 1994; 6: 335-41
-
(1994)
Nat Get
, vol.6
, pp. 335-341
-
-
Grossman, M.1
Raper, S.E.2
Kosarsky, K.3
-
5
-
-
0031973035
-
Long term reduction of serum bilirubin levels in Gunn rats by retroviral gene transfer in vivo
-
Tada K, Chowdhury NR, Neufeld D, et al. Long term reduction of serum bilirubin levels in Gunn rats by retroviral gene transfer in vivo. Liver Transplant Surg 1998; 4: 78-88
-
(1998)
Liver Transplant Surg
, vol.4
, pp. 78-88
-
-
Tada, K.1
Chowdhury, N.R.2
Neufeld, D.3
-
6
-
-
0031917801
-
Retroviral gene transfer to the liver in vivo during tri-iodothyronine induced hyperplasia
-
Apr
-
Forbes SJ, Themis M, Alison MR, et al. Retroviral gene transfer to the liver in vivo during tri-iodothyronine induced hyperplasia. Gene Ther 1998 Apr; 5 (4): 552-5
-
(1998)
Gene Ther
, vol.5
, Issue.4
, pp. 552-555
-
-
Forbes, S.J.1
Themis, M.2
Alison, M.R.3
-
7
-
-
0031722263
-
Hepatocyte growth factor induces hepatocyte proliferation in vivo and allows for efficient retroviral-mediated gene transfer in mice
-
Sep
-
Patijn GA, Lieber A, Schowalter DB, et al. Hepatocyte growth factor induces hepatocyte proliferation in vivo and allows for efficient retroviral-mediated gene transfer in mice. Hepatology 1998 Sep; 28 (3): 707-16
-
(1998)
Hepatology
, vol.28
, Issue.3
, pp. 707-716
-
-
Patijn, G.A.1
Lieber, A.2
Schowalter, D.B.3
-
8
-
-
0033541641
-
Intramuscular injection of an adenoviral vector expressing hepatocyte growth factor facilitates hepatic transduction with a retroviral vector in mice
-
Apr 10
-
Gao C, Jokerst R, Gondipalli P, et al. Intramuscular injection of an adenoviral vector expressing hepatocyte growth factor facilitates hepatic transduction with a retroviral vector in mice. Hum Gene Ther 1999 Apr 10; 10 (6): 911-22
-
(1999)
Hum Gene Ther
, vol.10
, Issue.6
, pp. 911-922
-
-
Gao, C.1
Jokerst, R.2
Gondipalli, P.3
-
9
-
-
0032126779
-
High-efficiency retrovirus mediated gene transfer into livers of mice
-
Jul 1
-
Patijn GA, Lieber A, Meuse L, et al. High-efficiency retrovirus mediated gene transfer into livers of mice. Hum Gene Ther 1998 Jul 1; 9 (10): 1449-56
-
(1998)
Hum Gene Ther
, vol.9
, Issue.10
, pp. 1449-1456
-
-
Patijn, G.A.1
Lieber, A.2
Meuse, L.3
-
10
-
-
0032496152
-
Simultaneous up-regulation of viral receptor expression and DNA synthesis is required for increasing efficiency of retroviral hepatic gene transfer
-
May 8
-
Ott M, Stockert RJ, Ma Q. et al. Simultaneous up-regulation of viral receptor expression and DNA synthesis is required for increasing efficiency of retroviral hepatic gene transfer. J Biol Chem 1998 May 8; 273 (19): 11954-61
-
(1998)
J Biol Chem
, vol.273
, Issue.19
, pp. 11954-11961
-
-
Ott, M.1
Stockert, R.J.2
Ma, Q.3
-
11
-
-
0032525902
-
Therapeutic levels of human protein C in rats after retroviral vector-mediated hepatic gene therapy
-
Jun 15
-
Cai SR, Kennedy SC, Bowling WM, et al. Therapeutic levels of human protein C in rats after retroviral vector-mediated hepatic gene therapy. J Clin Invest 1998 Jun 15; 101 (12): 2831-41
-
(1998)
J Clin Invest
, vol.101
, Issue.12
, pp. 2831-2841
-
-
Cai, S.R.1
Kennedy, S.C.2
Bowling, W.M.3
-
12
-
-
0032948552
-
Adenovirus-mediated gene therapy of liver diseases
-
Ilan Y, Saito H, Thummala NR, et al. Adenovirus-mediated gene therapy of liver diseases. Semin Liver Dis 1999; 19 (1): 49-59
-
(1999)
Semin Liver Dis
, vol.19
, Issue.1
, pp. 49-59
-
-
Ilan, Y.1
Saito, H.2
Thummala, N.R.3
-
13
-
-
0030865752
-
Transient immunosuppression with FK506 permits long-term expression of therapeutic genes introduced into the liver using rccombinant adenoviruses in the rat
-
Ilan Y, Jona VK, Sengupta K, et al. Transient immunosuppression with FK506 permits long-term expression of therapeutic genes introduced into the liver using rccombinant adenoviruses in the rat. Hepatology 1997; 26: 949-56
-
(1997)
Hepatology
, vol.26
, pp. 949-956
-
-
Ilan, Y.1
Jona, V.K.2
Sengupta, K.3
-
14
-
-
0030984335
-
Transient immunomodulation w ith anti-CD40 ligand antibody and CTLA4Ig enhances persistence and secondary adenovirus-mediated gene transfer into mouse liver
-
Apr
-
Kay MA, Meuse L, Gown AM, et al. Transient immunomodulation w ith anti-CD40 ligand antibody and CTLA4Ig enhances persistence and secondary adenovirus-mediated gene transfer into mouse liver. Proc Nail Acad Sci U S A 1997 Apr; 94: 4686-91
-
(1997)
Proc Natl Acad Sci U S A
, vol.94
, pp. 4686-4691
-
-
Kay, M.A.1
Meuse, L.2
Gown, A.M.3
-
15
-
-
17344370857
-
Oral tolerization to adenoviral proteins permits repeated adenovirus-mediated gene therapy in rats with preexisting immunity to adenoviruses
-
Ilan Y, Sauter B, Chowdhury NR, et al. Oral tolerization to adenoviral proteins permits repeated adenovirus-mediated gene therapy in rats with preexisting immunity to adenoviruses. Hepatology 1998; 27: 1368-76
-
(1998)
Hepatology
, vol.27
, pp. 1368-1376
-
-
Ilan, Y.1
Sauter, B.2
Chowdhury, N.R.3
-
16
-
-
13144283616
-
An adenoviral vector deleted for all viral coding sequences results in enhanced safety and extended expression of a leptin transgene
-
Jul
-
Morsy MA, Gu M, Motzel S, et al. An adenoviral vector deleted for all viral coding sequences results in enhanced safety and extended expression of a leptin transgene. Proc Natl Acad Sci U S A 1998 Jul; 95: 7866-71
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 7866-7871
-
-
Morsy, M.A.1
Gu, M.2
Motzel, S.3
-
17
-
-
0032530110
-
Cellular immune response to adenoviral vector infected cells does not require de novo viral gene expression: Implication for gene therapy
-
Sep
-
Kafri T, Morgan D, Krahl T, et al. Cellular immune response to adenoviral vector infected cells does not require de novo viral gene expression: implication for gene therapy. Proc Natl Acad Sci U S A 1998 Sep; 95: 11377-82
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 11377-11382
-
-
Kafri, T.1
Morgan, D.2
Krahl, T.3
-
18
-
-
0033582216
-
Adenovirus-mediated regulable target gene expression in vivo
-
Jan
-
Burcin MM, Schiedner G, Kochanek S, et al. Adenovirus-mediated regulable target gene expression in vivo. Proc Natl Acad Sci U S A 1999 Jan; 96 (2): 355-60
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, Issue.2
, pp. 355-360
-
-
Burcin, M.M.1
Schiedner, G.2
Kochanek, S.3
-
19
-
-
13044260220
-
Imaging adenoviral-directed reporter gene expression in living animals with positron emission tomography
-
Mar
-
Gambhir SS, Barrio JR, Phelps MB, et al. Imaging adenoviral-directed reporter gene expression in living animals with positron emission tomography. Proc Natl Acad Sci U S A 1999 Mar; 96 (5): 2333-8
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, Issue.5
, pp. 2333-2338
-
-
Gambhir, S.S.1
Barrio, J.R.2
Phelps, M.B.3
-
20
-
-
0030988482
-
Insertion of the adenoviral E3 region into a recombinant viral vector prevents antiviral humoral and cellular immune responses and permits long-term gene expression
-
Ilan Y, Draguett G, Chowdhury NR, et al. Insertion of the adenoviral E3 region into a recombinant viral vector prevents antiviral humoral and cellular immune responses and permits long-term gene expression. Proc Natl Acad Sci U S A 1997; 94: 2587-92
-
(1997)
Proc Natl Acad Sci U S A
, vol.94
, pp. 2587-2592
-
-
Ilan, Y.1
Draguett, G.2
Chowdhury, N.R.3
-
21
-
-
0029967430
-
Correction of ornithine transcarbamylase deficiency in adult spf(ash) mice and OTC-deficient human hepatocytes with recombinant adenoviruses bearing the CAG promoter
-
Kiwaki K, Kanegae Y, Saito I, et al. Correction of ornithine transcarbamylase deficiency in adult spf(ash) mice and OTC-deficient human hepatocytes with recombinant adenoviruses bearing the CAG promoter. Hum Gene Ther 1996; 7: 821-30
-
(1996)
Hum Gene Ther
, vol.7
, pp. 821-830
-
-
Kiwaki, K.1
Kanegae, Y.2
Saito, I.3
-
22
-
-
0031903608
-
Developing adenoviral-mediated in vivo gene therapy for ornithine transcarbamylase deficiency
-
Raper SE, Wilson JM, Yudkoff M, et al. Developing adenoviral-mediated in vivo gene therapy for ornithine transcarbamylase deficiency. J Inher Metab Dis 1998; 21 Suppl. 1: 119-37
-
(1998)
J Inher Metab Dis
, vol.21
, Issue.SUPPL. 1
, pp. 119-137
-
-
Raper, S.E.1
Wilson, J.M.2
Yudkoff, M.3
-
23
-
-
13044270984
-
Hepatocyte gene therapy in a large animal: A neonatal bovine model of citrullinemia
-
Mar
-
Lee B, Dennis JA, Healy PJ, et al. Hepatocyte gene therapy in a large animal: a neonatal bovine model of citrullinemia. Proc Natl Acad Sci U S A 1999 Mar; 96 (7): 3981-6
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, Issue.7
, pp. 3981-3986
-
-
Lee, B.1
Dennis, J.A.2
Healy, P.J.3
-
24
-
-
0031916435
-
Genomic DNA transfer with a high-capacity adenovirus vector results in improved in vivo gene expression and decreased toxicity
-
Feb
-
Schiedner G, Morral N, Parks RJ, et al. Genomic DNA transfer with a high-capacity adenovirus vector results in improved in vivo gene expression and decreased toxicity. Nat Genet 1998 Feb; 18 (2): 180-3
-
(1998)
Nat Genet
, vol.18
, Issue.2
, pp. 180-183
-
-
Schiedner, G.1
Morral, N.2
Parks, R.J.3
-
25
-
-
0032896334
-
Hepatic gene therapy using adeno-associated virus vectors
-
Patijn GA, Kay MA. Hepatic gene therapy using adeno-associated virus vectors. Semin Liver Dis 1999; 19 (1): 61-9
-
(1999)
Semin Liver Dis
, vol.19
, Issue.1
, pp. 61-69
-
-
Patijn, G.A.1
Kay, M.A.2
-
26
-
-
0031906147
-
Membrane-associated heparan sulphate proteoglycan is a receptor for adeno-associated virus type 2 virions
-
Summerford C, Samulski RJ. Membrane-associated heparan sulphate proteoglycan is a receptor for adeno-associated virus type 2 virions. J Virol 1998; 72: 1438-45
-
(1998)
J Virol
, vol.72
, pp. 1438-1445
-
-
Summerford, C.1
Samulski, R.J.2
-
27
-
-
0033010884
-
Human fibroblast growth factor receptor 1 is a co-receptor for infection by adeno-associated virus 2
-
Jan
-
Qing K, Mah C, Hansen J, et al. Human fibroblast growth factor receptor 1 is a co-receptor for infection by adeno-associated virus 2. Nat Med 1999 Jan; 5 (1): 71-7
-
(1999)
Nat Med
, vol.5
, Issue.1
, pp. 71-77
-
-
Qing, K.1
Mah, C.2
Hansen, J.3
-
28
-
-
0032589751
-
AlphaVbeta5 integrin: A co-receptor for adeno-associated virus type 2 infection
-
Jan
-
Summerford C, Bartlett JS, Samulski RJ, et al. AlphaVbeta5 integrin: a co-receptor for adeno-associated virus type 2 infection. Nat Med 1999 Jan; 5 (1): 78-82
-
(1999)
Nat Med
, vol.5
, Issue.1
, pp. 78-82
-
-
Summerford, C.1
Bartlett, J.S.2
Samulski, R.J.3
-
29
-
-
0031019819
-
Persistent expression of human clotting factor IX from mouse liver after intravenous injection of adeno-associated virus vectors
-
Feb
-
Koeberl DD, Alexander IE, Halbert CL, et al. Persistent expression of human clotting factor IX from mouse liver after intravenous injection of adeno-associated virus vectors. Proc Natl Acad Sci U S A 1997 Feb; 94: 1426-31
-
(1997)
Proc Natl Acad Sci U S A
, vol.94
, pp. 1426-1431
-
-
Koeberl, D.D.1
Alexander, I.E.2
Halbert, C.L.3
-
30
-
-
0030902985
-
Stable gene transfer and expression of human blood coagulation factor IX after intramuscular injection of recombinant adeno-associated virus
-
May
-
Herzog RW, Hagstrom JN, Kung SH, et al. Stable gene transfer and expression of human blood coagulation factor IX after intramuscular injection of recombinant adeno-associated virus. Proc Natl Acad Sci U S A 1997 May; 94: 5804-9
-
(1997)
Proc Natl Acad Sci U S A
, vol.94
, pp. 5804-5809
-
-
Herzog, R.W.1
Hagstrom, J.N.2
Kung, S.H.3
-
31
-
-
17444387438
-
Long-term correction of canine hemophilia B by gene transfer of blood coagulation factor IX mediated by adeno-associated viral vector
-
Jan
-
Herzog RW, Yang EY, Couto LB, et al. Long-term correction of canine hemophilia B by gene transfer of blood coagulation factor IX mediated by adeno-associated viral vector. Nat Med 1999 Jan; 5 (1): 56-63
-
(1999)
Nat Med
, vol.5
, Issue.1
, pp. 56-63
-
-
Herzog, R.W.1
Yang, E.Y.2
Couto, L.B.3
-
32
-
-
17444372024
-
Correction of hemophilia B in canine and murine models using recombinant adeno-associated viral vectors
-
Jan
-
Snyder RO, Miao C, Meuse L, et al. Correction of hemophilia B in canine and murine models using recombinant adeno-associated viral vectors. Nat Med 1999 Jan; 5 (1): 64-70
-
(1999)
Nat Med
, vol.5
, Issue.1
, pp. 64-70
-
-
Snyder, R.O.1
Miao, C.2
Meuse, L.3
-
33
-
-
0033616680
-
Sustained correction of bleeding disorder in hemophilia B mice by gene therapy
-
Mar
-
Wang L, Takabe K, Bidlingmaier SM, et al. Sustained correction of bleeding disorder in hemophilia B mice by gene therapy. Proc Natl Acad Sci U S A 1999 Mar; 96: 3906-10
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 3906-3910
-
-
Wang, L.1
Takabe, K.2
Bidlingmaier, S.M.3
-
34
-
-
13144305062
-
Sustained secretion of human alpha-1-antitrypsin from murine muscle transduced with adeno-associated virus vectors
-
Nov
-
Song S, Morgan M, Ellis T, et al. Sustained secretion of human alpha-1-antitrypsin from murine muscle transduced with adeno-associated virus vectors. Proc Natl Acad Sci U S A 1998 Nov; 95: 14384-8
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 14384-14388
-
-
Song, S.1
Morgan, M.2
Ellis, T.3
-
35
-
-
0032945030
-
Hepatocyte-directed gene delivery by receptor-mediated endocytosis
-
Smith RM, Wu GY. Hepatocyte-directed gene delivery by receptor-mediated endocytosis. Semin Liver Dis; 19 (1): 83-92
-
Semin Liver Dis
, vol.19
, Issue.1
, pp. 83-92
-
-
Smith, R.M.1
Wu, G.Y.2
-
36
-
-
13044263134
-
Structural characteristics of supramolecular assemblies formed by guanidinium-cholesterol reagents for gene transfection
-
Mar
-
Pitard B, Oudrhiri N, Vigneron JP, et al. Structural characteristics of supramolecular assemblies formed by guanidinium-cholesterol reagents for gene transfection. Proc Natl Acad Sci U S A 1999 Mar; 96: 2621-6
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 2621-2626
-
-
Pitard, B.1
Oudrhiri, N.2
Vigneron, J.P.3
-
37
-
-
0031891520
-
Increased liver uptake of liposomes and improved targeting efficacy by labeling with asialofetuin in rodents
-
Wu J, Liu P, Zhu JL, et al. Increased liver uptake of liposomes and improved targeting efficacy by labeling with asialofetuin in rodents. Hepatology 1998; 27: 772-8
-
(1998)
Hepatology
, vol.27
, pp. 772-778
-
-
Wu, J.1
Liu, P.2
Zhu, J.L.3
-
38
-
-
0031768405
-
Safety study and characterization of E1A-liposome complex gene-delivery protocol in an ovarian cancer model
-
Nov
-
Xing X, Zhang S, Chang JY, et al. Safety study and characterization of E1A-liposome complex gene-delivery protocol in an ovarian cancer model. Gene Ther 1998 Nov; 5 (11): 1538-44
-
(1998)
Gene Ther
, vol.5
, Issue.11
, pp. 1538-1544
-
-
Xing, X.1
Zhang, S.2
Chang, J.Y.3
-
39
-
-
17344365059
-
A double-blind, placebo controlled, dose ranging study to evaluate the safety and biological efficacy of the lipid-DNA complex GR213487B in the nasal epithelium of adult patients with cystic fibrosis
-
Jan
-
Knowles MR, Noone PG, Hohneker K, et al. A double-blind, placebo controlled, dose ranging study to evaluate the safety and biological efficacy of the lipid-DNA complex GR213487B in the nasal epithelium of adult patients with cystic fibrosis. Hum Gene Ther 1998 Jan; 9 (2): 249-69
-
(1998)
Hum Gene Ther
, vol.9
, Issue.2
, pp. 249-269
-
-
Knowles, M.R.1
Noone, P.G.2
Hohneker, K.3
-
40
-
-
0023811723
-
Receptor-mediated gene delivery and expression in vivo
-
Wu GY, Wu CH. Receptor-mediated gene delivery and expression in vivo. J Biol Chem 1988; 263: 14621-4
-
(1988)
J Biol Chem
, vol.263
, pp. 14621-14624
-
-
Wu, G.Y.1
Wu, C.H.2
-
41
-
-
0028309752
-
Incorporation of adenovirus into a ligand-based DNA carrier system results in retention of original receptor specificity and enhances target gene expression
-
Wu G, Zhan P, Sze LL, et al. Incorporation of adenovirus into a ligand-based DNA carrier system results in retention of original receptor specificity and enhances target gene expression. J Biol Chem 1994; 269: 11542-6
-
(1994)
J Biol Chem
, vol.269
, pp. 11542-11546
-
-
Wu, G.1
Zhan, P.2
Sze, L.L.3
-
42
-
-
0027447460
-
Hepatic gene therapy: Adenovirus enhancement of receptor-mediated gene delivery and expression in primary hepatocytes
-
Cristiano RJ, Smith LC, Woo SLC. Hepatic gene therapy: adenovirus enhancement of receptor-mediated gene delivery and expression in primary hepatocytes. Proc Natl Acad Sci USA 1993; 90: 2122-6
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 2122-2126
-
-
Cristiano, R.J.1
Smith, L.C.2
Woo, S.L.C.3
-
43
-
-
0032502668
-
A modular DNA carrier protein based on the structure of diphtheria toxin mediates target cell-specific gene delivery
-
Apr
-
Uherek C, Fominaya J, Wels W. A modular DNA carrier protein based on the structure of diphtheria toxin mediates target cell-specific gene delivery. J Biol Chem 1998 Apr; 273 (15): 8835-41
-
(1998)
J Biol Chem
, vol.273
, Issue.15
, pp. 8835-8841
-
-
Uherek, C.1
Fominaya, J.2
Wels, W.3
-
44
-
-
0030050983
-
Microtubular disruption prolongs the expression of human bilirubinuridinediphosphoglucuronate-glucurunosyltransferase-1 gene transferred into Gunn rat livers
-
Chowdhury NR, Hays RM, Bommineni VR, et al. Microtubular disruption prolongs the expression of human bilirubinuridinediphosphoglucuronate-glucurunosyltransferase-1 gene transferred into Gunn rat livers. J Biol Chem 1996; 271: 2341-6
-
(1996)
J Biol Chem
, vol.271
, pp. 2341-2346
-
-
Chowdhury, N.R.1
Hays, R.M.2
Bommineni, V.R.3
-
45
-
-
0031281282
-
In vitro gene delivery to hepatocytes with galactosylated polyethylenimine
-
Zanta MA, Boussif O, Adib A, et al. In vitro gene delivery to hepatocytes with galactosylated polyethylenimine. Bioconjug Chem 1997; 8: 839-44
-
(1997)
Bioconjug Chem
, vol.8
, pp. 839-844
-
-
Zanta, M.A.1
Boussif, O.2
Adib, A.3
-
46
-
-
0033167367
-
Size reduction of galactosylated PEI/DNA complexes improves lectin-mediated gene transfer into hepatocytes
-
Jul-Aug
-
Bettinger T, Remy JS, Erbacher P. Size reduction of galacto-sylated PEI/DNA complexes improves lectin-mediated gene transfer into hepatocytes. Bioconjug Chem 1999 Jul-Aug; 10 (4): 558-61
-
(1999)
Bioconjug Chem
, vol.10
, Issue.4
, pp. 558-561
-
-
Bettinger, T.1
Remy, J.S.2
Erbacher, P.3
-
47
-
-
0030896557
-
Biochemical and functional characterization of DNA complexes capable of targeting genes to hepatocytes via the asialoglycoprotein receptor
-
Mar
-
Perales JC, Grossman GA, Molas M, et al. Biochemical and functional characterization of DNA complexes capable of targeting genes to hepatocytes via the asialoglycoprotein receptor. J Biol Chem 1997 Mar; 272 (11): 7398-407
-
(1997)
J Biol Chem
, vol.272
, Issue.11
, pp. 7398-7407
-
-
Perales, J.C.1
Grossman, G.A.2
Molas, M.3
-
48
-
-
0030858180
-
Gene transfer into hepatoma cell lines via the serpin enzyme complex receptor
-
Aug
-
Ziady AC, Perales JC, Ferkol T, et al. Gene transfer into hepatoma cell lines via the serpin enzyme complex receptor. Am J Physiol 1997 Aug; 273 (2 Pt 1): G545-52
-
(1997)
Am J Physiol
, vol.273
, Issue.2 PART 1
-
-
Ziady, A.C.1
Perales, J.C.2
Ferkol, T.3
-
49
-
-
0029817766
-
Correction of the mutation responsible for sickle cell anemia by an RNA-DNA oligonucleotide
-
Cole-Strauss A, Yoon K, Xiang Y, et al. Correction of the mutation responsible for sickle cell anemia by an RNA-DNA oligonucleotide. Science 1996; 273: 1386-9
-
(1996)
Science
, vol.273
, pp. 1386-1389
-
-
Cole-Strauss, A.1
Yoon, K.2
Xiang, Y.3
-
50
-
-
0031953132
-
In vivo site-directed mutagenesis of the factor IX gene by chimeric RNA/DNA oligonucleotides
-
Mar
-
Kren BT, Bandyopadhyay P, Steer CJ. In vivo site-directed mutagenesis of the factor IX gene by chimeric RNA/DNA oligonucleotides. Nat Med 1998 Mar; 4 (3): 285-90
-
(1998)
Nat Med
, vol.4
, Issue.3
, pp. 285-290
-
-
Kren, B.T.1
Bandyopadhyay, P.2
Steer, C.J.3
-
51
-
-
0033537836
-
Nucleotide exchange in genomic DNA of rat hepatocytes using RNA/DNA oligonucleotides. Targeted delivery of liposomes and polyethylenemine to the asialoglycoprotein receptor
-
Apr 9
-
Bandyopadhyay P, Ma X, Linehan-Stieers C, et al. Nucleotide exchange in genomic DNA of rat hepatocytes using RNA/DNA oligonucleotides. Targeted delivery of liposomes and polyethylenemine to the asialoglycoprotein receptor. J Biol Chem 1999 Apr 9; 274 (15): 10163-72
-
(1999)
J Biol Chem
, vol.274
, Issue.15
, pp. 10163-10172
-
-
Bandyopadhyay, P.1
Ma, X.2
Linehan-Stieers, C.3
-
52
-
-
0033104162
-
Targeted gene repair directed by the chimeric RNA/DNA oligonucleotide in a mammalian cell-free extract
-
Mar 1
-
Cole-Strauss A, Gamper H, Holloman WK, et al. Targeted gene repair directed by the chimeric RNA/DNA oligonucleotide in a mammalian cell-free extract. Nucleic Acids Res 1999 Mar 1; 27 (5): 1323-30
-
(1999)
Nucleic Acids Res
, vol.27
, Issue.5
, pp. 1323-1330
-
-
Cole-Strauss, A.1
Gamper, H.2
Holloman, W.K.3
-
53
-
-
0033621041
-
Correction of the UDP-glucuronosyltransferase gene defect in the Gunn rat model of Crigler-Najjar syndrome type I with a chimeric oligonucleotide
-
Aug
-
Kren BT, Parashar B, Bandyopadhyay P, et al. Correction of the UDP-glucuronosyltransferase gene defect in the Gunn rat model of Crigler-Najjar syndrome type I with a chimeric oligonucleotide. Proc Natl Acad Sci U S A 1999 Aug; 96: 10349-54
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 10349-10354
-
-
Kren, B.T.1
Parashar, B.2
Bandyopadhyay, P.3
-
54
-
-
0030481468
-
Intracellular cleavage of hepatitis C virus RNA and inhibition of viral protein translation by Hammerhead ribozymes
-
Dec
-
Sakamoto N, Wu CH, Wu GY. Intracellular cleavage of hepatitis C virus RNA and inhibition of viral protein translation by Hammerhead ribozymes. J Clin Invest 1996 Dec; 98 (12): 2720-8
-
(1996)
J Clin Invest
, vol.98
, Issue.12
, pp. 2720-2728
-
-
Sakamoto, N.1
Wu, C.H.2
Wu, G.Y.3
-
55
-
-
0032922168
-
A novel SV40-based vector successfully transduces and express an alpha 1-antitrypsin ribozyme in a human hepatoma-derived cell line
-
Jan
-
Zern MA, Ozaki I, Duan L, et al. A novel SV40-based vector successfully transduces and express an alpha 1-antitrypsin ribozyme in a human hepatoma-derived cell line. Gene Ther 1999 Jan; 6 (1): 114-20
-
(1999)
Gene Ther
, vol.6
, Issue.1
, pp. 114-120
-
-
Zern, M.A.1
Ozaki, I.2
Duan, L.3
-
56
-
-
0032992064
-
Ribozyme-mediated specific gene replacement of the alpha 1-antitrypsin gene in human hepatoma cells
-
Jul
-
Ozaki I, Zern MA, Liu S, et al. Ribozyme-mediated specific gene replacement of the alpha 1-antitrypsin gene in human hepatoma cells. J Hepatol 1999 Jul; 31 (1): 53-60
-
(1999)
J Hepatol
, vol.31
, Issue.1
, pp. 53-60
-
-
Ozaki, I.1
Zern, M.A.2
Liu, S.3
-
57
-
-
0033588158
-
Hammerhead ribozyme cleavage of apolipoprotein B mRNA generates a truncated protein
-
Aug 20
-
Wang JP, Enjoji M, Tiebel M, et al. Hammerhead ribozyme cleavage of apolipoprotein B mRNA generates a truncated protein. J Biol Chem 1999 Aug 20; 274 (34): 24161-70
-
(1999)
J Biol Chem
, vol.274
, Issue.34
, pp. 24161-24170
-
-
Wang, J.P.1
Enjoji, M.2
Tiebel, M.3
-
58
-
-
0033536026
-
A small nucleolar RNA:ribozyme hybrid cleaves a nucleolar RNA target in vivo with near-perfect efficiency
-
Jun
-
Samarsky DA, Ferbeyre G, Bertrand E, et al. A small nucleolar RNA:ribozyme hybrid cleaves a nucleolar RNA target in vivo with near-perfect efficiency. Proc Natl Acad Sci U S A 1999 Jun; 96: 6609-14
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 6609-6614
-
-
Samarsky, D.A.1
Ferbeyre, G.2
Bertrand, E.3
-
59
-
-
0029898537
-
Inhibition of hepatitis B virus replication by targeted pretreatment of complexed antisense DNA in vitro
-
Nakazono K, Ito Y, Wu CH, et al. Inhibition of hepatitis B virus replication by targeted pretreatment of complexed antisense DNA in vitro. Hepatology 1996; 23: 1297-303
-
(1996)
Hepatology
, vol.23
, pp. 1297-1303
-
-
Nakazono, K.1
Ito, Y.2
Wu, C.H.3
-
60
-
-
0031802131
-
Targeted inhibition of hepatitis C virus-directed gene expression in human hepatoma cell lines
-
Wu CH, Wu GY. Targeted inhibition of hepatitis C virus-directed gene expression in human hepatoma cell lines. Gastroenterology 1998; 114: 1304-12
-
(1998)
Gastroenterology
, vol.114
, pp. 1304-1312
-
-
Wu, C.H.1
Wu, G.Y.2
-
61
-
-
0032570684
-
Effect of antisense oligonucleotides against cholesteryl ester transfer protein on the development of atherosclerosis in cholesterol-fed rabbits
-
Feb 27
-
Sugano M, Makino N, Sawada S, et al. Effect of antisense oligonucleotides against cholesteryl ester transfer protein on the development of atherosclerosis in cholesterol-fed rabbits. J Biol Chem 1998 Feb 27; 273 (9): 5033-6
-
(1998)
J Biol Chem
, vol.273
, Issue.9
, pp. 5033-5036
-
-
Sugano, M.1
Makino, N.2
Sawada, S.3
-
62
-
-
0033515099
-
Blockade of type beta transforming growth factor signaling prevents liver fibrosis and dysfunction in the rat
-
Mar
-
Qi Z, Atsuchi N, Ooshima A, et al. Blockade of type beta transforming growth factor signaling prevents liver fibrosis and dysfunction in the rat. Proc Natl Acad Sci U S A 1999 Mar; 96: 2345-9
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 2345-2349
-
-
Qi, Z.1
Atsuchi, N.2
Ooshima, A.3
|