-
1
-
-
0034650348
-
Cardiovascular gene therapy
-
Ylä-Herttuala S., Martin J.F. Cardiovascular gene therapy. Lancet. 355:2000;213-222.
-
(2000)
Lancet
, vol.355
, pp. 213-222
-
-
Ylä-Herttuala, S.1
Martin, J.F.2
-
3
-
-
0033554866
-
Images in cardiovascular medicine: Percutaneous myocardial gene transfer of phVEGF-2
-
Vale P.R., Losordo D.W., Milliken C.E., et al. Images in cardiovascular medicine: percutaneous myocardial gene transfer of phVEGF-2. Circulation. 100:1999;2462-2463.
-
(1999)
Circulation
, vol.100
, pp. 2462-2463
-
-
Vale, P.R.1
Losordo, D.W.2
Milliken, C.E.3
-
4
-
-
0035030237
-
Myocardial Doppler tissue velocity improves following myocardial gene therapy with VEGF-A165 plasmid in patients with inoperable angina pectoris
-
Sylven C., Sarkar N., Ruck A., et al. Myocardial Doppler tissue velocity improves following myocardial gene therapy with VEGF-A165 plasmid in patients with inoperable angina pectoris. Coron Artery Dis. 12:2001;239-243.
-
(2001)
Coron Artery Dis
, vol.12
, pp. 239-243
-
-
Sylven, C.1
Sarkar, N.2
Ruck, A.3
-
5
-
-
0034688216
-
Catheter-mediated VEGF gene transfer to human coronary arteries after angioplasty
-
Laitinen M., Hartikainen J., Hiltunen M.O., et al. Catheter-mediated VEGF gene transfer to human coronary arteries after angioplasty. Hum Gene Ther. 11:2000;263-270.
-
(2000)
Hum Gene Ther
, vol.11
, pp. 263-270
-
-
Laitinen, M.1
Hartikainen, J.2
Hiltunen, M.O.3
-
6
-
-
0034654128
-
Electromagnetic guidance for catheter-based transendocardial injection: A platform for intramyocardial angiogenesis therapy
-
Kornovski R., Leon M.B., Fuchs S., et al. Electromagnetic guidance for catheter-based transendocardial injection: a platform for intramyocardial angiogenesis therapy. J Am Coll Cardiol. 35:2000;1031-1039.
-
(2000)
J Am Coll Cardiol
, vol.35
, pp. 1031-1039
-
-
Kornovski, R.1
Leon, M.B.2
Fuchs, S.3
-
7
-
-
0033503798
-
Six-month assessment of a phase I trial of angiogenic gene therapy for the treatment of coronary artery disease using direct intramyocardial administration of an adenovirus vector expressing the VEGF121 cDNA
-
Rosengart T.K., Lee L.Y., Patel S.R., et al. Six-month assessment of a phase I trial of angiogenic gene therapy for the treatment of coronary artery disease using direct intramyocardial administration of an adenovirus vector expressing the VEGF121 cDNA. Ann Surg. 230:1999;466-470.
-
(1999)
Ann Surg
, vol.230
, pp. 466-470
-
-
Rosengart, T.K.1
Lee, L.Y.2
Patel, S.R.3
-
8
-
-
0000410720
-
Catheter-mediated VEGF gene transfer to human lower limb arteries after PTA
-
Mäkinen K., Laitinin M., Manninen H., Matsi P., Alhava E., Ylä-Herttuala S. Catheter-mediated VEGF gene transfer to human lower limb arteries after PTA. Circulation. 100:1999;I-770.
-
(1999)
Circulation
, vol.100
, pp. 770
-
-
Mäkinen, K.1
Laitinin, M.2
Manninen, H.3
Matsi, P.4
Alhava, E.5
Ylä-Herttuala, S.6
-
10
-
-
0032583951
-
165 after intramuscular gene transfer promotes collateral vessel development in patients with critical limb ischemia
-
165 after intramuscular gene transfer promotes collateral vessel development in patients with critical limb ischemia. Circulation. 97:1998;1114-1123.
-
(1998)
Circulation
, vol.97
, pp. 1114-1123
-
-
Baumgartner, I.1
Pieczek, A.2
Manor, O.3
-
11
-
-
0025607319
-
Expression of recombinant genes in myocardium in vivo after direct injection of DNA
-
Lin H., Parmacek M.S., Morle G., Bolling S., Leiden J.M. Expression of recombinant genes in myocardium in vivo after direct injection of DNA. Circulation. 82:1990;2217-2221.
-
(1990)
Circulation
, vol.82
, pp. 2217-2221
-
-
Lin, H.1
Parmacek, M.S.2
Morle, G.3
Bolling, S.4
Leiden, J.M.5
-
12
-
-
0035040977
-
In vivo myocardial gene transfer: Optimization, evaluation and direct comparison of gene transfer vectors
-
Wright M.J., Wightmann L.M.L., Lilley C., et al. In vivo myocardial gene transfer: optimization, evaluation and direct comparison of gene transfer vectors. Basic Res Cardiol. 96:2001;227-236.
-
(2001)
Basic Res Cardiol
, vol.96
, pp. 227-236
-
-
Wright, M.J.1
Wightmann, L.M.L.2
Lilley, C.3
-
13
-
-
0027527177
-
Efficient gene transfer into myocardium by direct injection of adenovirus vectors
-
Guzman R.J., Lemarchand P., Crystal R.G., Epstein S.E., Finkel T. Efficient gene transfer into myocardium by direct injection of adenovirus vectors. Circ Res. 73:1993;1202-1207.
-
(1993)
Circ Res
, vol.73
, pp. 1202-1207
-
-
Guzman, R.J.1
Lemarchand, P.2
Crystal, R.G.3
Epstein, S.E.4
Finkel, T.5
-
14
-
-
0029095454
-
Endothelium-specific in vivo gene transfer
-
Schulick A.H., Dong G., Newman K.D., Virmani R., Dichek D.A. Endothelium-specific in vivo gene transfer. Circ Res. 77:1995;475-485.
-
(1995)
Circ Res
, vol.77
, pp. 475-485
-
-
Schulick, A.H.1
Dong, G.2
Newman, K.D.3
Virmani, R.4
Dichek, D.A.5
-
15
-
-
16244410439
-
A mouse model of arterial gene transfer: Antigen-specific immunity is a minor determinant of the early loss of adenovirus-mediated transgene expression
-
Vassalli G., Agah R., Qiao R., Aguilar C., Dichek D.A. A mouse model of arterial gene transfer: antigen-specific immunity is a minor determinant of the early loss of adenovirus-mediated transgene expression. Circ Res. 85:1999;e25-e32.
-
(1999)
Circ Res
, vol.85
-
-
Vassalli, G.1
Agah, R.2
Qiao, R.3
Aguilar, C.4
Dichek, D.A.5
-
16
-
-
0031923328
-
Cytotoxic T-lymphocyte target proteins and their major histocompatibility complex class I restriction in response to adenovirus vectors delivered to mouse liver
-
Jooss K., Ertl H.C., Wilson J.M. Cytotoxic T-lymphocyte target proteins and their major histocompatibility complex class I restriction in response to adenovirus vectors delivered to mouse liver. J Virol. 72:1998;2945-2954.
-
(1998)
J Virol
, vol.72
, pp. 2945-2954
-
-
Jooss, K.1
Ertl, H.C.2
Wilson, J.M.3
-
17
-
-
0029936764
-
Immune responses to transgene-encoded proteins limit the stability of gene expression after injection of replication-defective adenovirus vectors
-
Tripathy S.K., Black H.B., Goldwasser E., Leiden J.M. Immune responses to transgene-encoded proteins limit the stability of gene expression after injection of replication-defective adenovirus vectors. Nat Med. 2:1996;545-550.
-
(1996)
Nat Med
, vol.2
, pp. 545-550
-
-
Tripathy, S.K.1
Black, H.B.2
Goldwasser, E.3
Leiden, J.M.4
-
18
-
-
0029242185
-
AAV as a viral vector for human gene therapy: Generation of a recombinant virus
-
Rolling F., Samuslki R.J. AAV as a viral vector for human gene therapy: generation of a recombinant virus. Mol Biotechnol. 3:1995;9-15.
-
(1995)
Mol Biotechnol
, vol.3
, pp. 9-15
-
-
Rolling, F.1
Samuslki, R.J.2
-
19
-
-
0032064006
-
The kinetics of rAAV integration in the liver
-
Miao C.H., Snyder R.O., Schowalter D.B., et al. The kinetics of rAAV integration in the liver. Nat Genet. 19:1998;13-15.
-
(1998)
Nat Genet
, vol.19
, pp. 13-15
-
-
Miao, C.H.1
Snyder, R.O.2
Schowalter, D.B.3
-
20
-
-
0030997346
-
Persistent and therapeutic concentrations of human factor IX in mice after hepatic gene transfer of recombinant AAV vectors
-
Snyder R.O., Miao C.H., Patijn G.A., et al. Persistent and therapeutic concentrations of human factor IX in mice after hepatic gene transfer of recombinant AAV vectors. Nat Genet. 16:1997;270-276.
-
(1997)
Nat Genet
, vol.16
, pp. 270-276
-
-
Snyder, R.O.1
Miao, C.H.2
Patijn, G.A.3
-
21
-
-
0030451214
-
Gene delivery to skeletal muscle results in sustained expression and systemic delivery of a therapeutic protein
-
Kessler P.D., Podsakoff G.M., Chen X., et al. Gene delivery to skeletal muscle results in sustained expression and systemic delivery of a therapeutic protein. Proc Natl Acad Sci USA. 93:1996;14082-14087.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 14082-14087
-
-
Kessler, P.D.1
Podsakoff, G.M.2
Chen, X.3
-
22
-
-
0030540970
-
Long-term gene transfer in porcine myocardium after coronary infusion of an adeno-associate virus vector
-
Kaplitt M.G., Xiao X., Samulski R.J., et al. Long-term gene transfer in porcine myocardium after coronary infusion of an adeno-associate virus vector. Ann Thorac Surg. 62:1996;1669-1676.
-
(1996)
Ann Thorac Surg
, vol.62
, pp. 1669-1676
-
-
Kaplitt, M.G.1
Xiao, X.2
Samulski, R.J.3
-
23
-
-
0032902054
-
Efficient and stable transduction of cardiomyocytes after intramyocardial injection or intracoronary perfusion with recombinant adeno-associated virus vectors
-
Svensson E.C., Marshall D.J., Woodard K., et al. Efficient and stable transduction of cardiomyocytes after intramyocardial injection or intracoronary perfusion with recombinant adeno-associated virus vectors. Circulation. 99:1999;201-205.
-
(1999)
Circulation
, vol.99
, pp. 201-205
-
-
Svensson, E.C.1
Marshall, D.J.2
Woodard, K.3
-
24
-
-
0031062452
-
Characterization of recombinant adeno-associated virus-2 as a vehicle for gene delivery and expression into vascular cells
-
Gnatenko D., Arnold T.E., Zolotukhin S., Nuovo G.J., Muzyczka N., Bahou W.F. Characterization of recombinant adeno-associated virus-2 as a vehicle for gene delivery and expression into vascular cells. J Invest Med. 45:1997;87-98.
-
(1997)
J Invest Med
, vol.45
, pp. 87-98
-
-
Gnatenko, D.1
Arnold, T.E.2
Zolotukhin, S.3
Nuovo, G.J.4
Muzyczka, N.5
Bahou, W.F.6
-
25
-
-
0030912001
-
Adeno-associated virus vectors for vascular gene delivery
-
Lynch C.M., Hara P.S., Leonard J.C., Williams J.K., Dean R.H., Geary R.L. Adeno-associated virus vectors for vascular gene delivery. Circ Res. 80:1997;497-505.
-
(1997)
Circ Res
, vol.80
, pp. 497-505
-
-
Lynch, C.M.1
Hara, P.S.2
Leonard, J.C.3
Williams, J.K.4
Dean, R.H.5
Geary, R.L.6
-
26
-
-
0030866312
-
Adeno-associated virus-mediated gene transfer into rat carotid arteries
-
Rolling F., Nong Z., Pisvin S., Collen D. Adeno-associated virus-mediated gene transfer into rat carotid arteries. Gene Ther. 4:1997;757-761.
-
(1997)
Gene Ther
, vol.4
, pp. 757-761
-
-
Rolling, F.1
Nong, Z.2
Pisvin, S.3
Collen, D.4
-
27
-
-
0024311525
-
Helper-free stocks of recombinant adeno-associated viruses: Normal integration does not require viral gene expression
-
Samulski R.J., Chang L.S., Shenk T. Helper-free stocks of recombinant adeno-associated viruses: normal integration does not require viral gene expression. J Virol. 63:1989;3822-3828.
-
(1989)
J Virol
, vol.63
, pp. 3822-3828
-
-
Samulski, R.J.1
Chang, L.S.2
Shenk, T.3
-
28
-
-
0028559768
-
An efficient and flexible system for construction of adenovirus vectors with insertions or deletions in early regions 1 and 3
-
Bett A.J., Haddara W., Prevec L., Graham F.L. An efficient and flexible system for construction of adenovirus vectors with insertions or deletions in early regions 1 and 3. Proc Natl Acad Sci USA. 91:1994;8802-8806.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 8802-8806
-
-
Bett, A.J.1
Haddara, W.2
Prevec, L.3
Graham, F.L.4
-
29
-
-
0033023881
-
Structure of adeno-associated virus vector DNA following transduction of the skeletal muscle
-
Vincent-Lacaze N., Snyder R.O., Gluzman R., Bohl D., Lagarde C., Danos O. Structure of adeno-associated virus vector DNA following transduction of the skeletal muscle. J Virol. 73:1999;1949-1955.
-
(1999)
J Virol
, vol.73
, pp. 1949-1955
-
-
Vincent-Lacaze, N.1
Snyder, R.O.2
Gluzman, R.3
Bohl, D.4
Lagarde, C.5
Danos, O.6
-
30
-
-
0029806827
-
Enhancer stimulation unmasks latent gene transfer after adenovirus-mediated gene delivery into human vascular smooth muscle cells
-
Clesham G.J., Browne H., Efstathiou S., Weissberg P.L. Enhancer stimulation unmasks latent gene transfer after adenovirus-mediated gene delivery into human vascular smooth muscle cells. Circ Res. 79:1996;1188-1195.
-
(1996)
Circ Res
, vol.79
, pp. 1188-1195
-
-
Clesham, G.J.1
Browne, H.2
Efstathiou, S.3
Weissberg, P.L.4
-
31
-
-
0033882190
-
CD40 ligand-dependent activation of cytotoxic T lymphocytes by adeno-associated virus vectors in vivo: Role of immature dendritic cells
-
Zhang Y., Chirmule N., Gao G.-P., Wilson J. CD40 ligand-dependent activation of cytotoxic T lymphocytes by adeno-associated virus vectors in vivo: role of immature dendritic cells. J Virol. 74:2000;8003-8010.
-
(2000)
J Virol
, vol.74
, pp. 8003-8010
-
-
Zhang, Y.1
Chirmule, N.2
Gao, G.-P.3
Wilson, J.4
-
32
-
-
0032812877
-
Immune response to green fluorescent protein: Implications for gene therapy
-
Stripecke R., Carmen Villacres M., et al. Immune response to green fluorescent protein: implications for gene therapy. Gene Ther. 6:1999;1305-1312.
-
(1999)
Gene Ther
, vol.6
, pp. 1305-1312
-
-
Stripecke, R.1
Carmen Villacres, M.2
-
33
-
-
0031969428
-
Transduction of dendritic cells by DNA viral vectors directs the immune response to transgene products in muscle fibers
-
Jooss K., Yang Y., Fisher K.J., Wilson J.M. Transduction of dendritic cells by DNA viral vectors directs the immune response to transgene products in muscle fibers. J Virol. 72:1998;4212-4223.
-
(1998)
J Virol
, vol.72
, pp. 4212-4223
-
-
Jooss, K.1
Yang, Y.2
Fisher, K.J.3
Wilson, J.M.4
-
34
-
-
0029923638
-
Second-strand synthesis is a rate-limiting step for efficient transduction by recombinant adeno-associated virus vectors
-
Ferrari F.K., Samulski T., Shenk T., Samulski R.J. Second-strand synthesis is a rate-limiting step for efficient transduction by recombinant adeno-associated virus vectors. J Virol. 70:1996;3227-3234.
-
(1996)
J Virol
, vol.70
, pp. 3227-3234
-
-
Ferrari, F.K.1
Samulski, T.2
Shenk, T.3
Samulski, R.J.4
-
35
-
-
0033775626
-
Gene transfer to hepatocellular carcinoma: Transduction efficacy and transgene expression kinetics by using retroviral and lentiviral vectors
-
Gerolami R., Uch R., Jordier F., et al. Gene transfer to hepatocellular carcinoma: transduction efficacy and transgene expression kinetics by using retroviral and lentiviral vectors. Cancer Gene Ther. 7:2000;1286-1292.
-
(2000)
Cancer Gene Ther
, vol.7
, pp. 1286-1292
-
-
Gerolami, R.1
Uch, R.2
Jordier, F.3
-
36
-
-
0033760062
-
Transcriptionally active drugs improve adenovirus vector performance in vitro and in vivo
-
Gaetano C., Catalano A., Palumbo R., et al. Transcriptionally active drugs improve adenovirus vector performance in vitro and in vivo. Gene Ther. 7:2000;1624-1630.
-
(2000)
Gene Ther
, vol.7
, pp. 1624-1630
-
-
Gaetano, C.1
Catalano, A.2
Palumbo, R.3
-
37
-
-
0033765020
-
Recombinant adeno-associated virus vectors efficiently transduce foreign gene into bovine aortic endothelial cells: Comparison with adenovirus vectors
-
Teramoto S., Ishii T., Matsuse T., Fukuchi Y. Recombinant adeno-associated virus vectors efficiently transduce foreign gene into bovine aortic endothelial cells: comparison with adenovirus vectors. Jpn J Pharmacol. 84:2000;206-212.
-
(2000)
Jpn J Pharmacol
, vol.84
, pp. 206-212
-
-
Teramoto, S.1
Ishii, T.2
Matsuse, T.3
Fukuchi, Y.4
-
38
-
-
2642642141
-
Production of high-titer recombinant adeno-associated virus vectors in the absence of helper adenovirus
-
Xiao X., Li J., Samuslki R.J. Production of high-titer recombinant adeno-associated virus vectors in the absence of helper adenovirus. J Virol. 72:1998;2224-2232.
-
(1998)
J Virol
, vol.72
, pp. 2224-2232
-
-
Xiao, X.1
Li, J.2
Samuslki, R.J.3
-
39
-
-
0032917854
-
Viral receptors and vector purification: New approaches for generating clinical-grade reagents
-
Summerford C., Samulski R.J. Viral receptors and vector purification: new approaches for generating clinical-grade reagents. Nat Med. 5:1999;587-588.
-
(1999)
Nat Med
, vol.5
, pp. 587-588
-
-
Summerford, C.1
Samulski, R.J.2
-
40
-
-
0033868530
-
Stimulatory and inhibitory action of cytokines in the regulation of hCMV-IE promoter activity in human endothelial cells
-
Ritter T., Brandt C., Prösch S., et al. Stimulatory and inhibitory action of cytokines in the regulation of hCMV-IE promoter activity in human endothelial cells. Cytokine. 12:2000;1163-1170.
-
(2000)
Cytokine
, vol.12
, pp. 1163-1170
-
-
Ritter, T.1
Brandt, C.2
Prösch, S.3
-
41
-
-
0033588867
-
A pressure-mediated non-viral method for efficient arterial gene and oligonucleotide transfer
-
Von der Leyen H.E., Braun-Dullaeus R., Mann M.J., Zhang L., Niebauer J., Dzau V. A pressure-mediated non-viral method for efficient arterial gene and oligonucleotide transfer. Hum Gene Ther. 10:1999;2355-2364.
-
(1999)
Hum Gene Ther
, vol.10
, pp. 2355-2364
-
-
Von Der Leyen, H.E.1
Braun-Dullaeus, R.2
Mann, M.J.3
Zhang, L.4
Niebauer, J.5
Dzau, V.6
-
42
-
-
0034610388
-
Adeno-associated virus vector-mediated vascular endothelial growth factor gene transfer induces neovascular formation in ischemic hearts
-
Su H., Lu R., Kan Y.W. Adeno-associated virus vector-mediated vascular endothelial growth factor gene transfer induces neovascular formation in ischemic hearts. Proc Natl Acad Sci USA. 97:2000;13801-13806.
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 13801-13806
-
-
Su, H.1
Lu, R.2
Kan, Y.W.3
-
43
-
-
0037022253
-
Gene therapy strategy for long-term myocardial protection using adeno-associated virus-mediated delivery of heme oxygenase gene
-
Melo L.G., Agrawal R., Zhang L., et al. Gene therapy strategy for long-term myocardial protection using adeno-associated virus-mediated delivery of heme oxygenase gene. Circulation. 105:2002;602-607.
-
(2002)
Circulation
, vol.105
, pp. 602-607
-
-
Melo, L.G.1
Agrawal, R.2
Zhang, L.3
-
44
-
-
0034641624
-
Clinical trials in coronary angiogenesis: Issues, problems, consensus. An expert panel summary
-
Simons M., Bonow R.O., Chronos N.A., et al. Clinical trials in coronary angiogenesis: issues, problems, consensus. An expert panel summary. Circulation. 102:2000;e73-e86.
-
(2000)
Circulation
, vol.102
-
-
Simons, M.1
Bonow, R.O.2
Chronos, N.A.3
-
45
-
-
0036098944
-
Enhanced secretion and uptake of beta-glucuronidase improves adeno-associated viral-mediated gene therapy of mucopolysaccharisosis type VII mice
-
Elliger S.S., Elliger C.A., Lang C., Watson G.L. Enhanced secretion and uptake of beta-glucuronidase improves adeno-associated viral-mediated gene therapy of mucopolysaccharisosis type VII mice. Mol Ther. 5:2002;617-626.
-
(2002)
Mol Ther
, vol.5
, pp. 617-626
-
-
Elliger, S.S.1
Elliger, C.A.2
Lang, C.3
Watson, G.L.4
-
46
-
-
0036099319
-
Correction of the enzymatic and functional deficits in a model of Pompe disease using adeno-associated virus vectors
-
Fraites T.J. Jr., Schleissing M.R., Shanely R.A., et al. Correction of the enzymatic and functional deficits in a model of Pompe disease using adeno-associated virus vectors. Mol Ther. 5:2002;571-578.
-
(2002)
Mol Ther
, vol.5
, pp. 571-578
-
-
Fraites T.J., Jr.1
Schleissing, M.R.2
Shanely, R.A.3
-
47
-
-
0028793489
-
A pilot study of ex vivo gene therapy for homozygous familial hypercholesterolaemia
-
Grossman M., Rader D.J., Mulller D.W., et al. A pilot study of ex vivo gene therapy for homozygous familial hypercholesterolaemia. Nat Med. 1:1995;1148-1154.
-
(1995)
Nat Med
, vol.1
, pp. 1148-1154
-
-
Grossman, M.1
Rader, D.J.2
Mulller, D.W.3
-
48
-
-
0031727714
-
Efficient coexpression and secretion of anti-atherogenic human apolipoprotein AI and lecithin-cholesterol acyltransferase by cultured muscle cells using adeno-associated virus plasmid vectors
-
Fan L., Drew J., Dunckley M.G., Owen J.S. Efficient coexpression and secretion of anti-atherogenic human apolipoprotein AI and lecithin-cholesterol acyltransferase by cultured muscle cells using adeno-associated virus plasmid vectors. Gene Ther. 5:1998;1434-1440.
-
(1998)
Gene Ther
, vol.5
, pp. 1434-1440
-
-
Fan, L.1
Drew, J.2
Dunckley, M.G.3
Owen, J.S.4
-
49
-
-
0001575125
-
Tolerance to cardiac allografts via local and systemic mechanisms after adenovirus-mediated CTLA4Ig expression
-
Guillot C., Mathieu P., Coathalem H., et al. Tolerance to cardiac allografts via local and systemic mechanisms after adenovirus-mediated CTLA4Ig expression. J Immunol. 164:2000;5258-5268.
-
(2000)
J Immunol
, vol.164
, pp. 5258-5268
-
-
Guillot, C.1
Mathieu, P.2
Coathalem, H.3
-
50
-
-
0033978147
-
AAV vectors. Is clinical success on the horizon?
-
Monahan P.E., Samulski R.J. AAV vectors. Is clinical success on the horizon? Gene Ther. 7:2000;24-30.
-
(2000)
Gene Ther
, vol.7
, pp. 24-30
-
-
Monahan, P.E.1
Samulski, R.J.2
-
51
-
-
19044388848
-
Avigen AAV trial continues
-
Bouchie A. Avigen AAV trial continues. Nat Biotechnol. 20:2002;119.
-
(2002)
Nat Biotechnol
, vol.20
, pp. 119
-
-
Bouchie, A.1
|