-
1
-
-
0030809684
-
Complementation of helper-dependent adenoviral vectors: Size effects and titer fluctuations
-
Alemany R, Dai Y, Lou YC, et al. 1997. Complementation of helper-dependent adenoviral vectors: size effects and titer fluctuations. J Virol Methods 68:147-159.
-
(1997)
J Virol Methods
, vol.68
, pp. 147-159
-
-
Alemany, R.1
Dai, Y.2
Lou, Y.C.3
-
2
-
-
0031041586
-
Effect of the E4 region on the persistence of transgene expression from adenovirus vectors
-
Armentano D, ZabnerJ, Sacks C, et al. 1997. Effect of the E4 region on the persistence of transgene expression from adenovirus vectors. J Virol 71:2408-2416.
-
(1997)
J Virol
, vol.71
, pp. 2408-2416
-
-
Armentano, D.1
Zabner, J.2
Sacks, C.3
-
3
-
-
0027477148
-
Direct in vivo gene transfer to ependymal cells in the central nervous system using recombinant adenovirus vectors
-
Bajocchi G, Feldman SH, Crystal RG, et al. 1993. Direct in vivo gene transfer to ependymal cells in the central nervous system using recombinant adenovirus vectors Nat Genet 3:229-234.
-
(1993)
Nat Genet
, vol.3
, pp. 229-234
-
-
Bajocchi, G.1
Feldman, S.H.2
Crystal, R.G.3
-
4
-
-
0028914687
-
Strain-related variations in adenovirally mediated transgene expression from mouse hepatocytes in vivo: Comparisons between immunocompetent and immunodeficient inbred strains
-
Barr D, Tubb T, Ferguson D, et al. 1995. Strain-related variations in adenovirally mediated transgene expression from mouse hepatocytes in vivo: Comparisons between immunocompetent and immunodeficient inbred strains. Gene Ther 2:151-155.
-
(1995)
Gene Ther
, vol.2
, pp. 151-155
-
-
Barr, D.1
Tubb, T.2
Ferguson, D.3
-
5
-
-
0026056827
-
Disturbed myelination in patients with treated hyperphenylalaninemia: Evaluation with magnetic resonance imaging
-
Bick U, Fahrendorf G, Ludolph AC, et al. 1991. Disturbed myelination in patients with treated hyperphenylalaninemia: evaluation with magnetic resonance imaging. Eur J Pediatr 150: 185-189.
-
(1991)
Eur J Pediatr
, vol.150
, pp. 185-189
-
-
Bick, U.1
Fahrendorf, G.2
Ludolph, A.C.3
-
6
-
-
0003042138
-
The influence of phenylalanine intake on the chemistry and behavior of a phenylketonuria child
-
Bickel H, Gerrard J, Hickmans EM. 1954. The influence of phenylalanine intake on the chemistry and behavior of a phenylketonuria child. Acta Paediatr Scand 43:64-77.
-
(1954)
Acta Paediatr Scand
, vol.43
, pp. 64-77
-
-
Bickel, H.1
Gerrard, J.2
Hickmans, E.M.3
-
7
-
-
0029146012
-
Nuclear organization of replication and gene expression in adenovirus-infected cells
-
Bridge E, Pettersson U. 1995. Nuclear organization of replication and gene expression in adenovirus-infected cells. Curr. Top. Microbiol. Immunol. 199:99-117.
-
(1995)
Curr. Top. Microbiol. Immunol.
, vol.199
, pp. 99-117
-
-
Bridge, E.1
Pettersson, U.2
-
8
-
-
0030728433
-
Activation of transgene expression by early region 4 is responsible for a high level of persistent transgene expression from adenovirus vectors in vivo
-
Brough DE, Hsu C, Kulesa VA, et al. 1997. Activation of transgene expression by early region 4 is responsible for a high level of persistent transgene expression from adenovirus vectors in vivo. J Virol 71:9206-9213.
-
(1997)
J Virol
, vol.71
, pp. 9206-9213
-
-
Brough, D.E.1
Hsu, C.2
Kulesa, V.A.3
-
9
-
-
0031049699
-
Persistence in muscle of an adenoviral vector that lacks all viral genes
-
Chen HH, Mack LM, Kelly R, et al. 1997. Persistence in muscle of an adenoviral vector that lacks all viral genes. Proc Natl Acad Sci USA 94:1645-1650.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 1645-1650
-
-
Chen, H.H.1
Mack, L.M.2
Kelly, R.3
-
10
-
-
0031778879
-
Role of E4 in eliciting T-cell and B-cell responses to adenovirus vectors delivered to murine and nonhuman primate lungs
-
1998
-
Chirmule N, Hughes JV, Gao GP, et al. 1998. Role of E4 in eliciting T-cell and B-cell responses to adenovirus vectors delivered to murine and nonhuman primate lungs. J Virol 1998;72: 6138-6145.
-
(1998)
J Virol
, vol.72
, pp. 6138-6145
-
-
Chirmule, N.1
Hughes, J.V.2
Gao, G.P.3
-
11
-
-
0030477690
-
Efficient gene transfer by a human immunodeficiency virus 1 [HIV-2]-derived vector utilizing a stable HIV packaging cell line
-
Corbeau P, Kraus G, Wong-Staal F. 1996. Efficient gene transfer by a human immunodeficiency virus 1 [HIV-2]-derived vector utilizing a stable HIV packaging cell line. Proc Natl Acad Sci USA 93:14070-14075.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 14070-14075
-
-
Corbeau, P.1
Kraus, G.2
Wong-Staal, F.3
-
12
-
-
0019802723
-
Studies on human phenylalanine monooxygenase. I. Restricted expression
-
Crawfurd MD, Gibbs DA, Sheppard DM. 1981. Studies on human phenylalanine monooxygenase. I. restricted expression. J Inherited Metab Dis 4:191-195.
-
(1981)
J Inherited Metab Dis
, vol.4
, pp. 191-195
-
-
Crawfurd, M.D.1
Gibbs, D.A.2
Sheppard, D.M.3
-
13
-
-
0029655435
-
Use of the E2F transcription factor by DNA tumor virus regulatory proteins
-
Cress WD, Nevins JR. 1996. Use of the E2F transcription factor by DNA tumor virus regulatory proteins. Curr. Top. Microbiol. Immunol. 208:63-78.
-
(1996)
Curr. Top. Microbiol. Immunol.
, vol.208
, pp. 63-78
-
-
Cress, W.D.1
Nevins, J.R.2
-
14
-
-
0030923808
-
Long-term gene delivery into the livers of immunocompetent mice with E1/E4-defective adenoviruses
-
Dedieu JF, Vigne E, Torrent C, et al. 1997. Long-term gene delivery into the livers of immunocompetent mice with E1/E4-defective adenoviruses. J Virol 71:4626-4637.
-
(1997)
J Virol
, vol.71
, pp. 4626-4637
-
-
Dedieu, J.F.1
Vigne, E.2
Torrent, C.3
-
15
-
-
0031691257
-
Circular intermediates of recombinant adeno-associated virus have defined structural characteristics responsible for long-term episomal persistence in muscle tissue
-
Duan D, Sharma P, Yang J, et al. 1998. Circular intermediates of recombinant adeno-associated virus have defined structural characteristics responsible for long-term episomal persistence in muscle tissue. J Virol 72:8568-8577.
-
(1998)
J Virol
, vol.72
, pp. 8568-8577
-
-
Duan, D.1
Sharma, P.2
Yang, J.3
-
16
-
-
0028888322
-
Molecular genetics of phenylketonuria: From molecular anthropology to gene therapy
-
Hall JC, Dunlap JC, Friedmann T, Gianelli F, editors. San Diego: Academic Press
-
Eisensmith RC, Woo SLC. 1995. Molecular genetics of phenylketonuria: From molecular anthropology to gene therapy. In: Hall JC, Dunlap JC, Friedmann T, Gianelli F, editors. Advances in genetics, Volume 32. San Diego: Academic Press. p 199-272.
-
(1995)
Advances in Genetics
, vol.32
, pp. 199-272
-
-
Eisensmith, R.C.1
Woo, S.L.C.2
-
17
-
-
12644314130
-
Tumor necrosis factor alpha plays a central role in immune-mediated clearance of adenoviral vectors
-
Elkon KB, Liu CC, Gall JG, et al. 1997. Tumor necrosis factor alpha plays a central role in immune-mediated clearance of adenoviral vectors. Proc Natl Acad Sci USA 94:9814-9819.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 9814-9819
-
-
Elkon, K.B.1
Liu, C.C.2
Gall, J.G.3
-
18
-
-
0028246338
-
Ablation of E2A in recombinant adenoviruses improves transgene persistence and decreases inflammatory response in mouse liver
-
Engelhardt JF, Ye X, Doranz B, et al. 1994a. Ablation of E2A in recombinant adenoviruses improves transgene persistence and decreases inflammatory response in mouse liver. Proc Natl Acad Sci USA 91:6196-6200.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 6196-6200
-
-
Engelhardt, J.F.1
Ye, X.2
Doranz, B.3
-
19
-
-
0028246338
-
Ablation of E2A in recombinant adenoviruses improves transgene persistence and decreases inflammatory response in mouse liver
-
Engelhardt JF, Ye X, Doranz B, et al. 1994b. Ablation of E2A in recombinant adenoviruses improves transgene persistence and decreases inflammatory response in mouse liver. Proc Natl Acad Sci USA 91:6196-6200.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 6196-6200
-
-
Engelhardt, J.F.1
Ye, X.2
Doranz, B.3
-
20
-
-
0028464358
-
Gene therapy for phenylketonuria: Phenotypic correction in a genetically deficient mouse model by adenovirus-mediated hepatic gene transfer
-
Fang B, Eisensmith RC, Li XHC, et al. 1994. Gene therapy for phenylketonuria: phenotypic correction in a genetically deficient mouse model by adenovirus-mediated hepatic gene transfer. Gene Ther 1:247-254.
-
(1994)
Gene Ther
, vol.1
, pp. 247-254
-
-
Fang, B.1
Eisensmith, R.C.2
Li, X.H.C.3
-
21
-
-
0029154012
-
Gene therapy for hemophilia B: Host immunosuppression prolongs the therapeutic effect of adenovirus-mediated factor IX expression
-
Fang B, Eisensmith RC, Wang H, et al. 1995. Gene therapy for hemophilia B: host immunosuppression prolongs the 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
-
22
-
-
0029670374
-
Lack of persistence of E1-recombinant adenoviral vectors containing a temperature-sensitive E2A mutation in immunocompetent mice and dogs
-
Fang B, Wang H, Gordon G, et al. 1996. Lack of persistence of E1-recombinant adenoviral vectors containing a temperature-sensitive E2A mutation in immunocompetent mice and dogs. Gene Ther 3:217-222.
-
(1996)
Gene Ther
, vol.3
, pp. 217-222
-
-
Fang, B.1
Wang, H.2
Gordon, G.3
-
23
-
-
0030775646
-
Stable in vivo gene transduction via a novel adenoviral/retroviral chimeric vector
-
Feng M, Jackson WH Jr, Goldman CK, et al. 1997. Stable in vivo gene transduction via a novel adenoviral/retroviral chimeric vector. Nat Biotechnol 15:866-870.
-
(1997)
Nat Biotechnol
, vol.15
, pp. 866-870
-
-
Feng, M.1
Jackson W.H., Jr.2
Goldman, C.K.3
-
24
-
-
0029923638
-
Second-strand synthesis is a rate-limiting step for efficient transduction by recombinant adeno-associated virus vectors
-
Ferrari FK, Samulski T, Shenk T, et al. 1996. Second-strand synthesis is a rate-limiting step for efficient transduction by recombinant adeno-associated virus vectors. J Virol 70: 3227-3234.
-
(1996)
J Virol
, vol.70
, pp. 3227-3234
-
-
Ferrari, F.K.1
Samulski, T.2
Shenk, T.3
-
25
-
-
0025949806
-
Retroviral-mediated gene transfer into hepatocytes in vivo
-
Ferry N, Duplessis O, Houssin D, et al. 1991. Retroviral-mediated gene transfer into hepatocytes in vivo. Proc Natl Acad Sci USA 88:8377-8381.
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 8377-8381
-
-
Ferry, N.1
Duplessis, O.2
Houssin, D.3
-
26
-
-
0029966514
-
Recombinant adenovirus deleted of all viral genes for gene therapy of cystic fibrosis
-
Fisher KJ, Choi H, Burda J, et al. 1996a. Recombinant adenovirus deleted of all viral genes for gene therapy of cystic fibrosis. Virology 217:11-22.
-
(1996)
Virology
, vol.217
, pp. 11-22
-
-
Fisher, K.J.1
Choi, H.2
Burda, J.3
-
27
-
-
0029655894
-
Transduction with recombinant adeno-associated virus for gene therapy is limited by leading-strand synthesis
-
Fisher KJ, Gao GP, Weitzman MD, et al. 1996b. Transduction with recombinant adeno-associated virus for gene therapy is limited by leading-strand synthesis. J Virol 70:520-532.
-
(1996)
J Virol
, vol.70
, pp. 520-532
-
-
Fisher, K.J.1
Gao, G.P.2
Weitzman, M.D.3
-
28
-
-
0031058024
-
Recombinant adeno-associated virus for muscle directed gene therapy
-
Fisher KJ, Jooss K, Alston J, et al. 1997. Recombinant adeno-associated virus for muscle directed gene therapy. Nat Med 3:306-312.
-
(1997)
Nat Med
, vol.3
, pp. 306-312
-
-
Fisher, K.J.1
Jooss, K.2
Alston, J.3
-
29
-
-
0029823797
-
A novel adenovirus-adeno-associated virus hybrid vector that displays efficient rescue and delivery of the AAV genome
-
Fisher KJ, Kelley WM, Burda JF, et al. 1996. A novel adenovirus-adeno-associated virus hybrid vector that displays efficient rescue and delivery of the AAV genome. Hum Gene Ther 7:2079-2087.
-
(1996)
Hum Gene Ther
, vol.7
, pp. 2079-2087
-
-
Fisher, K.J.1
Kelley, W.M.2
Burda, J.F.3
-
30
-
-
6844257545
-
Ex vivo gene transfer using adenovirus-mediated full-length dystrophin delivery to dystrophic muscles
-
Floyd SS Jr, Clemens PK, Ontell MR, et al. 1998. Ex vivo gene transfer using adenovirus-mediated full-length dystrophin delivery to dystrophic muscles. Gene Ther 5:19-30.
-
(1998)
Gene Ther
, vol.5
, pp. 19-30
-
-
Floyd S.S., Jr.1
Clemens, P.K.2
Ontell, M.R.3
-
31
-
-
0025940476
-
Reduced plasma C-20 and C-22 polyunsaturated fatty acids in children with phenylketonuria during dietary intervention
-
Galli C, Agostini C, Mosconi C, et al. 1991. Reduced plasma C-20 and C-22 polyunsaturated fatty acids in children with phenylketonuria during dietary intervention. J Pediatr 119:562-567.
-
(1991)
J Pediatr
, vol.119
, pp. 562-567
-
-
Galli, C.1
Agostini, C.2
Mosconi, C.3
-
32
-
-
0029959867
-
Biology of adenovirus vectors with E1 and E4 deletions for liver-directed gene therapy
-
Gao GP, Yang Y, Wilson JM. 1996. Biology of adenovirus vectors with E1 and E4 deletions for liver-directed gene therapy. J Virol 70:8934-8943.
-
(1996)
J Virol
, vol.70
, pp. 8934-8943
-
-
Gao, G.P.1
Yang, Y.2
Wilson, J.M.3
-
33
-
-
0029091783
-
Transfer of the CFTR gene to the lung of nonhuman primates with E1-deleted, E2a-defective recombinant adenoviruses: A preclinical toxicology study
-
Goldman MJ, Litzky LA, Engelhardt JF, et al. 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
Engelhardt, J.F.3
-
34
-
-
0029664338
-
Elimination of both E1 and E2 from adenovirus vectors further improves prospects for in vivo human gene therapy
-
Gorziglia MI, Kadan MJ, Yei S, et al. 1996. Elimination of both E1 and E2 from adenovirus vectors further improves prospects for in vivo human gene therapy. J Virol 70:4173-4178.
-
(1996)
J Virol
, vol.70
, pp. 4173-4178
-
-
Gorziglia, M.I.1
Kadan, M.J.2
Yei, S.3
-
35
-
-
0023920456
-
Trace element status of children with PKU and normal children
-
Gropper SS, Acosta PB, Clarke-Sheehan N, et al. 1988. Trace element status of children with PKU and normal children. J Am Diet Assoc 88:459-465.
-
(1988)
J Am Diet Assoc
, vol.88
, pp. 459-465
-
-
Gropper, S.S.1
Acosta, P.B.2
Clarke-Sheehan, N.3
-
36
-
-
0025912865
-
Permanent engraftment and function of hepatocytes delivered to the liver: Implications for gene therapy and liver repopulation
-
Gupta S, Aragona E, Vemuru RP, et al. 1991. Permanent engraftment and function of hepatocytes delivered to the liver: Implications for gene therapy and liver repopulation. Hepatology 14:144-149.
-
(1991)
Hepatology
, vol.14
, pp. 144-149
-
-
Gupta, S.1
Aragona, E.2
Vemuru, R.P.3
-
37
-
-
0029962474
-
In vivo expression of full-length human dystrophin from adenoviral vectors deleted of all viral genes
-
Haecker SE, Stedman HH, Bailee-Gordon RJ, et al. 1996. In vivo expression of full-length human dystrophin from adenoviral vectors deleted of all viral genes. Hum Gene Ther 7:1907-1914.
-
(1996)
Hum Gene Ther
, vol.7
, pp. 1907-1914
-
-
Haecker, S.E.1
Stedman, H.H.2
Bailee-Gordon, R.J.3
-
38
-
-
0030763563
-
Improved adenoviral vectors for gene therapy of Duchenne muscular dystrophy
-
Hauser MA, Amalfitano A, Kumar-Singh R, et al. 1997. Improved adenoviral vectors for gene therapy of Duchenne muscular dystrophy. Neuromuscul Disord 7:277-283.
-
(1997)
Neuromuscul Disord
, vol.7
, pp. 277-283
-
-
Hauser, M.A.1
Amalfitano, A.2
Kumar-Singh, R.3
-
39
-
-
0027409026
-
Adenovirus-mediated transfer of low density lipoprotein receptor gene acutely accelerates cholesterol clearance in normal mice
-
Herz J, Gerard RD. 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
-
40
-
-
0030902985
-
Stable gene transfer and expression of human blood coagulation factor IX after intramuscular injection of recombinant adeno-associated virus
-
Herzog RW, Hagstrom JN, Kung SH, et al. 1997. Stable gene transfer and expression of human blood coagulation factor IX after intramuscular injection of recombinant adeno-associated virus. Proc Natl Acad Sci USA 94:5804-5809.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 5804-5809
-
-
Herzog, R.W.1
Hagstrom, J.N.2
Kung, S.H.3
-
41
-
-
0025061601
-
Tumor necrosis factors-alpha and -beta bind to the same two types of tumor necrosis factor receptors and maximally activate the transcription factor NK-kappa B at low receptor occupancy and within minutes after receptor binding
-
Hohmann HP, Remy R, Poschl B, et al. 1990. Tumor necrosis factors-alpha and -beta bind to the same two types of tumor necrosis factor receptors and maximally activate the transcription factor NK-kappa B at low receptor occupancy and within minutes after receptor binding. J Biol Chem 265:15183-15188.
-
(1990)
J Biol Chem
, vol.265
, pp. 15183-15188
-
-
Hohmann, H.P.1
Remy, R.2
Poschl, B.3
-
43
-
-
0026906987
-
Adenovirus-mediated in vivo gene transfer and expression in normal rat liver
-
Jaffe HA, Danel C, Longenecker G, et al. 1992. Adenovirus-mediated in vivo gene transfer and expression in normal rat liver. Nat Genet 1:372-378.
-
(1992)
Nat Genet
, vol.1
, pp. 372-378
-
-
Jaffe, H.A.1
Danel, C.2
Longenecker, G.3
-
44
-
-
0026131053
-
Persistent gene expression after retroviral gene transfer into liver cells in vivo
-
Kaleko M, Garcia JV, Miller AD. 1991. Persistent gene expression after retroviral gene transfer into liver cells in vivo. Hum Gene Ther 2:27-32.
-
(1991)
Hum Gene Ther
, vol.2
, pp. 27-32
-
-
Kaleko, M.1
Garcia, J.V.2
Miller, A.D.3
-
45
-
-
0028169741
-
Long-term gene expression and phenotypic correction using adeno-associated virus vectors in the mammalian brain
-
Kaplitt MG, Leone P, Samulski RJ, et al. 1994. Long-term gene expression and phenotypic correction using adeno-associated virus vectors in the mammalian brain. Nat Genet 8:148-154.
-
(1994)
Nat Genet
, vol.8
, pp. 148-154
-
-
Kaplitt, M.G.1
Leone, P.2
Samulski, R.J.3
-
46
-
-
0024524977
-
An evaluation of the possible neurotoxicity of metabolites of phenylalanine
-
Kaufman S. 1989. An evaluation of the possible neurotoxicity of metabolites of phenylalanine. J Pediatr 114:895-900.
-
(1989)
J Pediatr
, vol.114
, pp. 895-900
-
-
Kaufman, S.1
-
47
-
-
0029113869
-
Selective immune inhibition of recombinant adenovirus vectors using soluble CTLA4Ig results in persistent gene expression from hepatocytes in vivo
-
Kay MA, Holterman AX, Meuse L. 1995. Selective immune inhibition of recombinant adenovirus vectors using soluble CTLA4Ig results in persistent gene expression from hepatocytes in vivo. Nat Genet 11:191-197.
-
(1995)
Nat Genet
, vol.11
, pp. 191-197
-
-
Kay, M.A.1
Holterman, A.X.2
Meuse, L.3
-
48
-
-
0028274169
-
In vivo hepatic gene therapy: Complete albeit transient correction of factor IX deficiency in hemophilia B dogs
-
Kay MA, Landen CN, Rothenberg SR, et al. 1994. In vivo hepatic gene therapy: Complete albeit transient correction of factor IX deficiency in hemophilia B dogs. Proc Natl Acad Sci USA 91:2353-2357.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 2353-2357
-
-
Kay, M.A.1
Landen, C.N.2
Rothenberg, S.R.3
-
49
-
-
0027033259
-
1-antitrypsin in mice after direct gene delivery in vivo
-
1-antitrypsin in mice after direct gene delivery in vivo. Hum Gene Ther 3:641-647.
-
(1992)
Hum Gene Ther
, vol.3
, pp. 641-647
-
-
Kay, M.A.1
Li, Q.2
Liu, T.J.3
-
50
-
-
0030984335
-
Transient immunomodulation with anti-CD40 ligand antibody and CTLA4Ig enhances persistence and secondary adenovirus-mediated gene transfer into mouse liver
-
Kay MA, Meuse L, Gown AM, et al. 1997. Transient immunomodulation with anti-CD40 ligand antibody and CTLA4Ig enhances persistence and secondary adenovirus-mediated gene transfer into mouse liver. Proc Natl Acad Sci USA 94:4686-4691.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 4686-4691
-
-
Kay, M.A.1
Meuse, L.2
Gown, A.M.3
-
51
-
-
0027686238
-
In vivo gene therapy of hemophilia B: Sustained partial correction in factor IX deficient dogs
-
Kay MA, Rothenberg S, Landen C, et al. 1993. In vivo gene therapy of hemophilia B: Sustained partial correction in factor IX deficient dogs. Science 262:117-119.
-
(1993)
Science
, vol.262
, pp. 117-119
-
-
Kay, M.A.1
Rothenberg, S.2
Landen, C.3
-
52
-
-
0031019819
-
Persistent expression of human clotting factor IX from mouse liver after intravenous injection of adeno-associated virus vectors
-
Koeberl DD, Alexander IE, Halbert CL, et al. 1997. Persistent expression of human clotting factor IX from mouse liver after intravenous injection of adeno-associated virus vectors. Proc Natl Acad Sci USA 94:1426-1431.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 1426-1431
-
-
Koeberl, D.D.1
Alexander, I.E.2
Halbert, C.L.3
-
53
-
-
0029875608
-
Use of CD4 lymphocyte depletion to prolong transgene expression of E1-deleted adenoviral vectors
-
Kolls JK, Lei D, Odom G, et al. 1996. Use of CD4 lymphocyte depletion to prolong transgene expression of E1-deleted adenoviral vectors. Human Gene Ther 7:489-497.
-
(1996)
Human Gene Ther
, vol.7
, pp. 489-497
-
-
Kolls, J.K.1
Lei, D.2
Odom, G.3
-
54
-
-
0032503632
-
Retrovirus-mediated in vivo gene transfer in replicating liver using recombinant hepatocyte growth factor without liver injury or partial hepatectomy
-
Kosai KI, Finegold MJ, Thi Huynh BT, et al. 1998. Retrovirus-mediated in vivo gene transfer in replicating liver using recombinant hepatocyte growth factor without liver injury or partial hepatectomy. Hum Gene Ther 9:1293-1301.
-
(1998)
Hum Gene Ther
, vol.9
, pp. 1293-1301
-
-
Kosai, K.I.1
Finegold, M.J.2
Thi Huynh, B.T.3
-
55
-
-
0030943732
-
Macrophage depletion increases the safety, efficacy and persistence of adenovirus-mediated gene transfer in vivo
-
Kuzmin AI, Finegold MJ, Eisensmith RC. 1997. Macrophage depletion increases the safety, efficacy and persistence of adenovirus-mediated gene transfer in vivo. Gene Ther 4:309-316.
-
(1997)
Gene Ther
, vol.4
, pp. 309-316
-
-
Kuzmin, A.I.1
Finegold, M.J.2
Eisensmith, R.C.3
-
56
-
-
0021918515
-
Nucleotide sequence of a full-length complementary DNA clone and amino acid sequence of human phenylalanine hydroxylase
-
Kwok SCM, Ledley FD, DiLella AG, et al. 1985. Nucleotide sequence of a full-length complementary DNA clone and amino acid sequence of human phenylalanine hydroxylase. Biochemistry 24:556-561.
-
(1985)
Biochemistry
, vol.24
, pp. 556-561
-
-
Kwok, S.C.M.1
Ledley, F.D.2
DiLella, A.G.3
-
57
-
-
0021954909
-
Gene transfer and expression of human phenylalanine hydroxylase
-
Ledley FD, Grenett HE, DiLella AG, et al. 1985. Gene transfer and expression of human phenylalanine hydroxylase. Science 228:77-79.
-
(1985)
Science
, vol.228
, pp. 77-79
-
-
Ledley, F.D.1
Grenett, H.E.2
DiLella, A.G.3
-
58
-
-
0022536780
-
Retroviral-mediated gene transfer of human phenylalanine hydroxylase into NIH 3T3 and hepatoma cells
-
Ledley FD, Grenett H, McGinnis-Shelnutt M, et al. 1986. Retroviral-mediated gene transfer of human phenylalanine hydroxylase into NIH 3T3 and hepatoma cells. Proc Natl Acad Sci USA 83:409-413.
-
(1986)
Proc Natl Acad Sci USA
, vol.83
, pp. 409-413
-
-
Ledley, F.D.1
Grenett, H.2
McGinnis-Shelnutt, M.3
-
59
-
-
0019156116
-
Maternal phenylketonuria and hyperphenylalaninemia: An international survey of the outcome of untreated and treated pregnancies
-
Lenke RR, Levy HL. 1980. Maternal phenylketonuria and hyperphenylalaninemia: An international survey of the outcome of untreated and treated pregnancies. N Engl J Med 303:1202-1208.
-
(1980)
N Engl J Med
, vol.303
, pp. 1202-1208
-
-
Lenke, R.R.1
Levy, H.L.2
-
60
-
-
0030955245
-
E4 gene function in adenovirus, adenovirus vector and adeno-associated virus infections
-
Leppard KN. 1997. E4 gene function in adenovirus, adenovirus vector and adeno-associated virus infections. J Gen Virol 78:2131-2138.
-
(1997)
J Gen Virol
, vol.78
, pp. 2131-2138
-
-
Leppard, K.N.1
-
61
-
-
0028831356
-
In vivo gene therapy for hyperlipidemia: Phenotypic correction in Watanabe rabbits by hepatic delivery of the LDL receptor gene
-
Li J, Fang B, Eisensmith RC, et al. 1995. In vivo gene therapy for hyperlipidemia: Phenotypic correction in Watanabe rabbits by hepatic delivery of the LDL receptor gene. J Clin Invest 95:768-773.
-
(1995)
J Clin Invest
, vol.95
, pp. 768-773
-
-
Li, J.1
Fang, B.2
Eisensmith, R.C.3
-
62
-
-
0027758609
-
Assessment of recombinant adenoviral vectors for hepatic gene therapy
-
Li QT, Kay M, Finegold M, et al. 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.T.1
Kay, M.2
Finegold, M.3
-
63
-
-
0031452056
-
Adenoviral preterminal protein stabilizes mini-adenoviral genomes in vitro and in vivo
-
Lieber A, He CY, Kay MA. 1997. Adenoviral preterminal protein stabilizes mini-adenoviral genomes in vitro and in vivo. Nat Biotechnol 15:1383-1387.
-
(1997)
Nat Biotechnol
, vol.15
, pp. 1383-1387
-
-
Lieber, A.1
He, C.Y.2
Kay, M.A.3
-
64
-
-
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 CY, Kirillova I. 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
-
65
-
-
0030756389
-
The role of Kupffer cell activation and viral gene expression in early liver toxicity after infusion of recombinant adenovirus vectors
-
Lieber A, He CY, Meuse L, et al. 1997. The role of Kupffer cell activation and viral gene expression in early liver toxicity after infusion of recombinant adenovirus vectors. J Virol 71: 8798-8807.
-
(1997)
J Virol
, vol.71
, pp. 8798-8807
-
-
Lieber, A.1
He, C.Y.2
Meuse, L.3
-
66
-
-
0031596240
-
Inhibition ot NF-kappaB activation in combination with bcl-2 expression allows for persistence of first-generation adenovirus vectors in the mouse liver
-
Lieber A, He CY, Meuse L, et al. 1998. Inhibition ot NF-kappaB activation in combination with bcl-2 expression allows for persistence of first-generation adenovirus vectors in the mouse liver. J Virol 72:9267-9277.
-
(1998)
J Virol
, vol.72
, pp. 9267-9277
-
-
Lieber, A.1
He, C.Y.2
Meuse, L.3
-
67
-
-
0026519919
-
Reconstitution of enzymatic activity in hepatocytes of phenylalanine hydroxylase-deficient mice
-
Liu TJ, Kay MA, Darlington GJ, et al. 1992. Reconstitution of enzymatic activity in hepatocytes of phenylalanine hydroxylase-deficient mice. Som Cell and Molec Genet 18:89-96.
-
(1992)
Som Cell and Molec Genet
, vol.18
, pp. 89-96
-
-
Liu, T.J.1
Kay, M.A.2
Darlington, G.J.3
-
68
-
-
0032064006
-
The kinetics of rAAV integration in the liver
-
Miao CH, Snyder RO, Schowalter DB. 1998. The kinetics of rAAV integration in the liver [letter]. Nat Genet 19:13-15.
-
(1998)
Nat Genet
, vol.19
, pp. 13-15
-
-
Miao, C.H.1
Snyder, R.O.2
Schowalter, D.B.3
-
70
-
-
0029054932
-
Rescue, propagation, and partial purification of a helper virus-dependent adenovirus vector
-
Mitani K, Graham FL, Caskey CT, et al. 1995. Rescue, propagation, and partial purification of a helper virus-dependent adenovirus vector. Proc Natl Acad Sci USA 92:3854-3858.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 3854-3858
-
-
Mitani, K.1
Graham, F.L.2
Caskey, C.T.3
-
71
-
-
0031983639
-
Direct intramuscular injection with recombinant AAV vectors results in sustained expression in a dog model of hemophilia
-
Monahan PE, Samulski RJ, Tazelaar J, et al. 1998. Direct intramuscular injection with recombinant AAV vectors results in sustained expression in a dog model of hemophilia. Gene Ther 5:40-49.
-
(1998)
Gene Ther
, vol.5
, pp. 40-49
-
-
Monahan, P.E.1
Samulski, R.J.2
Tazelaar, J.3
-
72
-
-
0030824640
-
Immune responses to reporter proteins and high viral dose limit duration of expression with adenoviral vectors: Comparison of E2a wild type and E2a deleted vectors
-
Morral N, O'Neal W, Zhou H, et al. 1997. Immune responses to reporter proteins and high viral dose limit duration of expression with adenoviral vectors: Comparison of E2a wild type and E2a deleted vectors. Hum Gene Ther 8:1275-1286.
-
(1997)
Hum Gene Ther
, vol.8
, pp. 1275-1286
-
-
Morral, N.1
O'Neal, W.2
Zhou, H.3
-
73
-
-
13144283616
-
An adenoviral vector deleted for all viral coding sequences results in enhanced safety and extended expression of a leptin transgene
-
Morsy MA, Gu M, Motzel S, et al. 1998. An adenoviral vector deleted for all viral coding sequences results in enhanced safety and extended expression of a leptin transgene. Proc Natl Acad Sci USA 95:7866-7871.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 7866-7871
-
-
Morsy, M.A.1
Gu, M.2
Motzel, S.3
-
74
-
-
0031838721
-
Adeno-associated viral vector-mediated gene transfer of human blood coagulation factor IX into mouse liver
-
Nakai H, Herzog RW, Hagstrom JN, et al. 1998. Adeno-associated viral vector-mediated gene transfer of human blood coagulation factor IX into mouse liver. Blood 91:4600-4607.
-
(1998)
Blood
, vol.91
, pp. 4600-4607
-
-
Nakai, H.1
Herzog, R.W.2
Hagstrom, J.N.3
-
75
-
-
0029996147
-
In vivo gene delivery and stable transduction of nondividing fells by a lentiviral vector
-
Naldini L, Blomer U, Gallay P, et al. 1996. In vivo gene delivery and stable transduction of nondividing fells by a lentiviral vector. Science 272:263-267.
-
(1996)
Science
, vol.272
, pp. 263-267
-
-
Naldini, L.1
Blomer, U.2
Gallay, P.3
-
76
-
-
0030462599
-
A helper-dependent adenovirus vector system: Removal of helper virus by Crc-mediated excision of the viral packaging signal
-
Parks RJ, Chen L, Anton M, et al. 1996. A helper-dependent adenovirus vector system: Removal of helper virus by Crc-mediated excision of the viral packaging signal. Proc Natl Acad Sci USA 93:13565-13570.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 13565-13570
-
-
Parks, R.J.1
Chen, L.2
Anton, M.3
-
77
-
-
0032126779
-
High-efficiency retrovirus-mediated gene transfer into the livers of mice
-
Patijn GA, Lieber A, Meuse L, et al. 1998. High-efficiency retrovirus-mediated gene transfer into the livers of mice. Hum Gene Ther 9:1449-1456.
-
(1998)
Hum Gene Ther
, vol.9
, pp. 1449-1456
-
-
Patijn, G.A.1
Lieber, A.2
Meuse, L.3
-
78
-
-
0031722263
-
Hepatocyte growth factor induces hepatocyte proliferation in vivo and allows for efficient retroviral-mediated gene transfer in mice
-
Patijn GA, Lieber A, Schowalter DB, et al. 1998. Hepatocyte growth factor induces hepatocyte proliferation in vivo and allows for efficient retroviral-mediated gene transfer in mice. Hepatology 28:707-716.
-
(1998)
Hepatology
, vol.28
, pp. 707-716
-
-
Patijn, G.A.1
Lieber, A.2
Schowalter, D.B.3
-
79
-
-
0023787380
-
Retroviral-mediated gene transfer and expression of human phenylalanine hydroxylase in primary mouse hepatocytes
-
Peng H, Armentano D, MacKenzie-Graham L, et al. 1988. Retroviral-mediated gene transfer and expression of human phenylalanine hydroxylase in primary mouse hepatocytes. Proc Natl Acad Sci USA 85:8146-8150.
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 8146-8150
-
-
Peng, H.1
Armentano, D.2
MacKenzie-Graham, L.3
-
80
-
-
0031953134
-
Efficient transduction of nondividing human cells by feline immunodeficiency virus lentiviral vectors
-
Poeschla EM, Wong-Staal F, Looney DJ. 1998. Efficient transduction of nondividing human cells by feline immunodeficiency virus lentiviral vectors. Nat Med 4:354-357.
-
(1998)
Nat Med
, vol.4
, pp. 354-357
-
-
Poeschla, E.M.1
Wong-Staal, F.2
Looney, D.J.3
-
81
-
-
0026031297
-
Mouse hepatocytes migrate to liver parenchyma and function indefinitely after intrasplenic transplantation
-
Ponder K, Gupta S, Leland F, et al. 1991. Mouse hepatocytes migrate to liver parenchyma and function indefinitely after intrasplenic transplantation. Proc Natl Acad Sci USA 88:1217-1221.
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 1217-1221
-
-
Ponder, K.1
Gupta, S.2
Leland, F.3
-
82
-
-
0025848772
-
Adenovirus-mediated transfer of a recombinant alpha 1-antitrypsin gene to the lung epithelium in vivo
-
Rosenfeld MA, Siegfried W, Yoshimura K, et al. 1991. Adenovirus-mediated transfer of a recombinant alpha 1-antitrypsin gene to the lung epithelium in vivo. Science 252:431-434.
-
(1991)
Science
, vol.252
, pp. 431-434
-
-
Rosenfeld, M.A.1
Siegfried, W.2
Yoshimura, K.3
-
83
-
-
0031916435
-
Genomic DNA transfer with a high-capacity adenovirus vector results in improved in vivo gene expression and decreased toxicity
-
Schiedner G, Morral N, Parks RJ, et al. 1998. Genomic DNA transfer with a high-capacity adenovirus vector results in improved in vivo gene expression and decreased toxicity Nat Genet 18:180-183.
-
(1998)
Nat Genet
, vol.18
, pp. 180-183
-
-
Schiedner, G.1
Morral, N.2
Parks, R.J.3
-
84
-
-
0000059155
-
The hyperphenylalaninemias
-
Scriver CR, Beaudet AL, Sly WS, Valle D, editors. 7th ed. New York: McGraw-Hill.
-
Scriver CR, Kaufman S, Eisensmith RC, et al. 1995. The hyperphenylalaninemias. In: Scriver CR, Beaudet AL, Sly WS, Valle D, editors. The metabolic and molecular bases of inherited disease, Volume 1, 7th ed. New York: McGraw-Hill. p 1015-1075.
-
(1995)
The Metabolic and Molecular Bases of Inherited Disease
, vol.1
, pp. 1015-1075
-
-
Scriver, C.R.1
Kaufman, S.2
Eisensmith, R.C.3
-
85
-
-
0027742271
-
The biology of macrophages: I. General principles and properties
-
Seljelid R, Eskeland T. 1993. The biology of macrophages: I. general principles and properties. Eur J Haematol 51:267-275.
-
(1993)
Eur J Haematol
, vol.51
, pp. 267-275
-
-
Seljelid, R.1
Eskeland, T.2
-
86
-
-
0027295348
-
Mouse models of human phenylketonuria
-
Shedlovsky A, McDonald JD, Symula D, et al. 1993. Mouse models of human phenylketonuria. Genetics 134;1205-1210.
-
(1993)
Genetics
, vol.134
, pp. 1205-1210
-
-
Shedlovsky, A.1
McDonald, J.D.2
Symula, D.3
-
87
-
-
0000557447
-
Adenoviridae: The viruses and their replication
-
Fields BN, Knipe DM, Howley PM, editors. Philadelphia: Lippencott-Raven
-
Shenk T. 1996. Adenoviridae: the viruses and their replication. In: Fields BN, Knipe DM, Howley PM, editors. Virology. Philadelphia: Lippencott-Raven. p 2111-2148.
-
(1996)
Virology
, pp. 2111-2148
-
-
Shenk, T.1
-
88
-
-
0018180640
-
Effect of stopping low-phenylalanine diet on intellectual progress of children with phenylketonuria
-
Smith I, Lobascher ME, Stevenson JE, et al. 1978. Effect of stopping low-phenylalanine diet on intellectual progress of children with phenylketonuria. Br Med J 2:723-726.
-
(1978)
Br Med J
, vol.2
, pp. 723-726
-
-
Smith, I.1
Lobascher, M.E.2
Stevenson, J.E.3
-
89
-
-
0030997346
-
Persistent and therapeutic concentrations or human factor IX in mice after hepatic gene transfer of recombinant AAV vectors
-
Snyder RO, Miao CH, Patijn GA, et al. 1997. Persistent and therapeutic concentrations or human factor IX in mice after hepatic gene transfer of recombinant AAV vectors. Nat Genet 16:270-276.
-
(1997)
Nat Genet
, vol.16
, pp. 270-276
-
-
Snyder, R.O.1
Miao, C.H.2
Patijn, G.A.3
-
90
-
-
0031942297
-
Effects of macrophage depletion and anti-CD40 ligand on transgene expression and redosing with recombinant adenovirus
-
Stein CS, Pemberton JL, van Rooijen N, et al. 1998. Effects of macrophage depletion and anti-CD40 ligand on transgene expression and redosing with recombinant adenovirus. Gene Ther 5:431-439.
-
(1998)
Gene Ther
, vol.5
, pp. 431-439
-
-
Stein, C.S.1
Pemberton, J.L.2
Van Rooijen, N.3
-
91
-
-
0025487393
-
Evaluation of the transfer and expression in mice of an enzyme-encoding gene using a human adenovirus vector
-
Stratford-Perricaudet LD, Levrero M, Chasse JF, et al. 1990. Evaluation of the transfer and expression in mice of an enzyme-encoding gene using a human adenovirus vector. Hum Gene Ther 1:241-256.
-
(1990)
Hum Gene Ther
, vol.1
, pp. 241-256
-
-
Stratford-Perricaudet, L.D.1
Levrero, M.2
Chasse, J.F.3
-
92
-
-
0025853937
-
Magnetic resonance imaging changes in early treated patients with phenylketonuria
-
Thompson AJ, Smith I, Kendall BE, et al. 1991. Magnetic resonance imaging changes in early treated patients with phenylketonuria. Lancet 337:1224.
-
(1991)
Lancet
, vol.337
, pp. 1224
-
-
Thompson, A.J.1
Smith, I.2
Kendall, B.E.3
-
93
-
-
0029052716
-
Immunomodulation to enhance gene therapy
-
Wilson C, Kay MA. 1995. Immunomodulation to enhance gene therapy [comment]. Nat Med 1:887-889.
-
(1995)
Nat Med
, vol.1
, pp. 887-889
-
-
Wilson, C.1
Kay, M.A.2
-
94
-
-
0031060294
-
Enhancement of in vivo adenovirus-mediated gene transfer and expression by prior depletion of tissue macrophages in the target organ
-
Wolff G, Worgall S, van Rooijen N, et al. 1997. Enhancement of in vivo adenovirus-mediated gene transfer and expression by prior depletion of tissue macrophages in the target organ. J Virol 71:624-629.
-
(1997)
J Virol
, vol.71
, pp. 624-629
-
-
Wolff, G.1
Worgall, S.2
Van Rooijen, N.3
-
95
-
-
0029843596
-
Efficient long-term gene transfer into muscle tissue of immunocompetent mice by adeno-associated virus vector
-
Xiao X, Li J, Samulski RJ. 1996. Efficient long-term gene transfer into muscle tissue of immunocompetent mice by adeno-associated virus vector. J Virol 70:8098-8108.
-
(1996)
J Virol
, vol.70
, pp. 8098-8108
-
-
Xiao, X.1
Li, J.2
Samulski, R.J.3
-
96
-
-
0028484704
-
MHC class I-restricted cytotoxic t lymphocytes to viral antigens destroy hepatocytes in mice infected with E1-deleted recombinant adenoviruses
-
Yang Y, Ertl HCJ, Wilson JM. 1994a. MHC class I-restricted cytotoxic T lymphocytes to viral antigens destroy hepatocytes in mice infected with E1-deleted recombinant adenoviruses. Immunity 1:433-142.
-
(1994)
Immunity
, vol.1
, pp. 433-1142
-
-
Yang, Y.1
Ertl, H.C.J.2
Wilson, J.M.3
-
97
-
-
0029944988
-
Transient immune blockade prevents formation of neutralizing antibody to recombinant adenovirus and allows repeated gene transfer to mouse liver
-
Yang Y, Greenough K, Wilson JM. 1996. Transient immune blockade prevents formation of neutralizing antibody to recombinant adenovirus and allows repeated gene transfer to mouse liver. Gene Ther 3:412-420.
-
(1996)
Gene Ther
, vol.3
, pp. 412-420
-
-
Yang, Y.1
Greenough, K.2
Wilson, J.M.3
-
98
-
-
0028328261
-
Cellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapy
-
Yang Y, Nunes FA, Berencsi K, et al. 1994b. 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
-
99
-
-
0028229147
-
Inactivation of E2a in reeombinant adenoviruses improves the prospect for gene therapy in cystic fibrosis
-
Yang Y, Nunes FA, Berencsi K, et al. 1994c. Inactivation of E2a in reeombinant adenoviruses improves the prospect for gene therapy in cystic fibrosis. Nat Genet 7:362-369.
-
(1994)
Nat Genet
, vol.7
, pp. 362-369
-
-
Yang, Y.1
Nunes, F.A.2
Berencsi, K.3
-
100
-
-
0028978493
-
Recombinant IL-12 prevents formation of blocking IgA antibodies to recombinant adenovirus and allows repeated gene therapy to mouse lung
-
Yang Y, Trinchieri G, Wilson JM. 1995. Recombinant IL-12 prevents formation of blocking IgA antibodies to recombinant adenovirus and allows repeated gene therapy to mouse lung. Nat Med 1:890-893.
-
(1995)
Nat Med
, vol.1
, pp. 890-893
-
-
Yang, Y.1
Trinchieri, G.2
Wilson, J.M.3
-
101
-
-
0032170692
-
Inhibition of tumor necrosis factor alpha decreases inflammation and prolongs adenovirus gene expression in lung and liver
-
Zhang HG, Zhou T, Yang P, et al. 1998. Inhibition of tumor necrosis factor alpha decreases inflammation and prolongs adenovirus gene expression in lung and liver. Hum Gene Ther 9:1875-1884.
-
(1998)
Hum Gene Ther
, vol.9
, pp. 1875-1884
-
-
Zhang, H.G.1
Zhou, T.2
Yang, P.3
-
102
-
-
0029843063
-
Development of a complementing cell line and a system for construction of adenovirus vectors with E1 and E2a deleted
-
Zhou H, O'Neal W, Morral N, et al. 1996. Development of a complementing cell line and a system for construction of adenovirus vectors with E1 and E2a deleted. J Virol 70:7030-7038.
-
(1996)
J Virol
, vol.70
, pp. 7030-7038
-
-
Zhou, H.1
O'Neal, W.2
Morral, N.3
-
103
-
-
0030819379
-
Multiply attenuated lentiviral vector achieves efficient gene delivery in vivo
-
Zufferey R, Nagy D, Mandel RJ, et al. 1997. Multiply attenuated lentiviral vector achieves efficient gene delivery in vivo. Nat Biotechnol 15:871-875.
-
(1997)
Nat Biotechnol
, vol.15
, pp. 871-875
-
-
Zufferey, R.1
Nagy, D.2
Mandel, R.J.3
|