-
1
-
-
0034672304
-
Towards a neuroprotective gene therapy for Parkinson's disease: Use of adenovirus, AAV and lentivirus vectors for gene transfer of GDNF to the nigrostriatal system in the rat Parkinson model
-
Björklund A et al. Towards a neuroprotective gene therapy for Parkinson's disease: use of adenovirus, AAV and lentivirus vectors for gene transfer of GDNF to the nigrostriatal system in the rat Parkinson model. Brain Res 2000; 886: 82-98.
-
(2000)
Brain Res.
, vol.886
, pp. 82-98
-
-
Björklund, A.1
-
2
-
-
0032215712
-
Immunologic complexity in neurons
-
Darnell RB. Immunologic complexity in neurons. Neuron 1998; 21: 947-950.
-
(1998)
Neuron
, vol.21
, pp. 947-950
-
-
Darnell, R.B.1
-
3
-
-
0034094220
-
The role of CD8(+) T cells and major histocompatibility complex class I expression in the central nervous system of mice infected with neurovirulent Sindbis virus
-
Kimura T, Griffin DE. The role of CD8(+) T cells and major histocompatibility complex class I expression in the central nervous system of mice infected with neurovirulent Sindbis virus. J Virol 2000;74: 6117-6125.
-
(2000)
J. Virol.
, vol.74
, pp. 6117-6125
-
-
Kimura, T.1
Griffin, D.E.2
-
4
-
-
0031465261
-
Long-term gene therapy in the CNS: Reversal of hypothalamic diabetes insipidus in the Brattleboro rat by using an adenovirus expressing arginine vasopressin
-
Geddes BJ, Harding TC, Lightman SL, Uney JB. Long-term gene therapy in the CNS: reversal of hypothalamic diabetes insipidus in the Brattleboro rat by using an adenovirus expressing arginine vasopressin. Nat Med 1997; 3: 1402-1404.
-
(1997)
Nat. Med.
, vol.3
, pp. 1402-1404
-
-
Geddes, B.J.1
Harding, T.C.2
Lightman, S.L.3
Uney, J.B.4
-
5
-
-
0034294843
-
Strong promoters are the key to highly efficient, noninflammatory and noncytotoxic adenoviral-mediated transgene delivery into the brain in vivo
-
Gerdes CA, Castro MG, Lowenstein PR. Strong promoters are the key to highly efficient, noninflammatory and noncytotoxic adenoviral-mediated transgene delivery into the brain in vivo. Mol Ther 2000; 2: 330-338.
-
(2000)
Mol. Ther.
, vol.2
, pp. 330-338
-
-
Gerdes, C.A.1
Castro, M.G.2
Lowenstein, P.R.3
-
6
-
-
0034986065
-
Acute direct adenoviral vector cytotoxicity and chronic, but not acute, inflammatory responses correlate with decreased vector-mediated transgene expression in the brain
-
Thomas CE et al. Acute direct adenoviral vector cytotoxicity and chronic, but not acute, inflammatory responses correlate with decreased vector-mediated transgene expression in the brain. Mol Ther 2001; 3: 36-46.
-
(2001)
Mol. Ther.
, vol.3
, pp. 36-46
-
-
Thomas, C.E.1
-
7
-
-
0032758671
-
Efficient gene transfer and long-term expression in neurons using a recombinant adenovirus with a neuron-specific promoter
-
Navarro V et al. Efficient gene transfer and long-term expression in neurons using a recombinant adenovirus with a neuron-specific promoter. Gene Ther 1999; 6: 1884-1892.
-
(1999)
Gene Ther.
, vol.6
, pp. 1884-1892
-
-
Navarro, V.1
-
8
-
-
0032832363
-
Neuron-restrictive silencer elements mediate neuron specificity of adenoviral gene expression
-
Millecamps S et al., Neuron-restrictive silencer elements mediate neuron specificity of adenoviral gene expression. Nat Biotechnol 1999; 17: 865-869.
-
(1999)
Nat. Biotechnol.
, vol.17
, pp. 865-869
-
-
Millecamps, S.1
-
9
-
-
0033516876
-
Neuron-targeted gene transfer by adenovirus carrying neural-restrictive silencer element
-
Miyaguchi K et al. Neuron-targeted gene transfer by adenovirus carrying neural-restrictive silencer element. Neuroreport 1999; 10: 2349-2353.
-
(1999)
Neuroreport
, vol.10
, pp. 2349-2353
-
-
Miyaguchi, K.1
-
10
-
-
0035151061
-
Neuron-specific expression of therapeutic proteins: Evaluation of different cellular promoters in recombinant adenoviral vectors
-
Kügler S et al. Neuron-specific expression of therapeutic proteins: evaluation of different cellular promoters in recombinant adenoviral vectors. Mol Cell Neurosci 2001; 17: 78-96.
-
(2001)
Mol. Cell Neurosci.
, vol.17
, pp. 78-96
-
-
Kügler, S.1
-
11
-
-
17644432519
-
Transduction of axotomized retinal ganglion cells by adenoviral vector administration at the optic nerve stump: An in vivo model system for the inhibition of neuronal apoptotic cell death
-
Kügler S et al. Transduction of axotomized retinal ganglion cells by adenoviral vector administration at the optic nerve stump: an in vivo model system for the inhibition of neuronal apoptotic cell death. Gene Ther 1999; 6: 1759-1767.
-
(1999)
Gene Ther.
, vol.6
, pp. 1759-1767
-
-
Kügler, S.1
-
12
-
-
0034671450
-
Protection by synergistic effects of adenovirus-mediated X-chromosome-linked inhibitor of apoptosis and glial cell line-derived neurotrophic factor gene transfer in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine model of Parkinson's disease
-
Eberhardt O et al. Protection by synergistic effects of adenovirus-mediated X-chromosome-linked inhibitor of apoptosis and glial cell line-derived neurotrophic factor gene transfer in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine model of Parkinson's disease. J Neurosci 2000; 20: 9126-9134.
-
(2000)
J. Neurosci.
, vol.20
, pp. 9126-9134
-
-
Eberhardt, O.1
-
13
-
-
0036302541
-
Binding of adenovirus to its receptors in mouse astrocytes induces c-fos proto-oncogene and apoptosis
-
Rubio N, Martin-Clemente B. Binding of adenovirus to its receptors in mouse astrocytes induces c-fos proto-oncogene and apoptosis. Virology 2002; 297: 211-219.
-
(2002)
Virology
, vol.297
, pp. 211-219
-
-
Rubio, N.1
Martin-Clemente, B.2
-
14
-
-
0037123716
-
Modification of a fiber protein in an adenovirus vector improves in vitro gene transfer efficiency to the mouse microglial cell line
-
Omori N et al. Modification of a fiber protein in an adenovirus vector improves in vitro gene transfer efficiency to the mouse microglial cell line. Neurosci Lett 2002; 324: 145-148.
-
(2002)
Neurosci. Lett.
, vol.324
, pp. 145-148
-
-
Omori, N.1
-
15
-
-
0029760296
-
Role of T cells in inflammation caused by adenovirus vectors in the brain
-
Byrnes AP, Wood MJ, Charlton HM. Role of T cells in inflammation caused by adenovirus vectors in the brain. Gene Ther 1996; 3: 644-651.
-
(1996)
Gene Ther.
, vol.3
, pp. 644-651
-
-
Byrnes, A.P.1
Wood, M.J.2
Charlton, H.M.3
-
16
-
-
0036561265
-
Separating fact from fiction: Assessing the potential of modified adenovirus vectors for use in human gene therapy
-
Amalfitano A, Parks RJ. Separating fact from fiction: assessing the potential of modified adenovirus vectors for use in human gene therapy. Curr Gene Ther 2002;2: 111-133.
-
(2002)
Curr. Gene Ther.
, vol.2
, pp. 111-133
-
-
Amalfitano, A.1
Parks, R.J.2
-
18
-
-
0036109543
-
Adenoviral-mediated, high-level, cell-specific transgene expression: A syn1-wpre cassette mediates increased transgene expression with no loss of neuron specificity
-
Glover CP et al. Adenoviral-mediated, high-level, cell-specific transgene expression: a syn1-wpre cassette mediates increased transgene expression with no loss of neuron specificity. Mol Ther 2002; 5: 509-516.
-
(2002)
Mol. Ther.
, vol.5
, pp. 509-516
-
-
Glover, C.P.1
-
19
-
-
0036316170
-
Inhibition of chemokine expression by adenovirus early region three (E3) genes
-
Lesokhin AM, Delgado-Lopez F, Horwitz MS. Inhibition of chemokine expression by adenovirus early region three (E3) genes. J Virol 2002; 76: 8236-8243.
-
(2002)
J. Virol.
, vol.76
, pp. 8236-8243
-
-
Lesokhin, A.M.1
Delgado-Lopez, F.2
Horwitz, M.S.3
-
20
-
-
0035936954
-
Intravitreal adenoviral gene transfer evokes an immune response in the retina that is directed against the heterologous lacZ transgene product but does not limit transgene expression
-
Isenmann S et al. Intravitreal adenoviral gene transfer evokes an immune response in the retina that is directed against the heterologous lacZ transgene product but does not limit transgene expression. Brain Res 2001; 892: 229-240.
-
(2001)
Brain Res.
, vol.892
, pp. 229-240
-
-
Isenmann, S.1
-
21
-
-
0000735715
-
Substantia nigra
-
Paxínos G (ed.) 2nd ed. Academic Press: San Diego
-
Fallon JH, Loughlin SE. Substantia nigra, in: Paxínos G (ed.) The Rat Nervous System, 2nd ed. Academic Press: San Diego, 1995, pp. 215-237.
-
(1995)
The Rat Nervous System
, pp. 215-237
-
-
Fallon, J.H.1
Loughlin, S.E.2
-
22
-
-
0033587486
-
Diverse stabilities of expression in the rat brain from different cellular promoters in a helper virus-free herpes simplex virus type 1 vector system
-
Wang Y, Yu L, Geller AI. Diverse stabilities of expression in the rat brain from different cellular promoters in a helper virus-free herpes simplex virus type 1 vector system. Hum Gene Ther 1999; 10: 1763-1771.
-
(1999)
Hum. Gene Ther.
, vol.10
, pp. 1763-1771
-
-
Wang, Y.1
Yu, L.2
Geller, A.I.3
-
23
-
-
0031014887
-
Efficient transduction of green fluorescent protein in spinal cord neurons using adeno-associated virus vectors containing cell type- specific promoters
-
Peel AL et al. Efficient transduction of green fluorescent protein in spinal cord neurons using adeno-associated virus vectors containing cell type- specific promoters. Gene Ther 1997; 4: 16-24.
-
(1997)
Gene Ther.
, vol.4
, pp. 16-24
-
-
Peel, A.L.1
-
24
-
-
0034724209
-
Recombinant adeno-associated virus type 2, 4, and 5 vectors: Transduction of variant cell types and regions in the mammalian central nervous system
-
Davidson BL et al. Recombinant adeno-associated virus type 2, 4, and 5 vectors: transduction of variant cell types and regions in the mammalian central nervous system. Proc Natl Acad Sci USA 2000; 97: 3428-3432.
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 3428-3432
-
-
Davidson, B.L.1
-
25
-
-
0036140216
-
Cross-packaging of a single adeno-associated virus (AAV) type 2 vector genome into multiple AAV serotypes enables transduction with broad specificity
-
Rabinowitz JE et al. Cross-packaging of a single adeno-associated virus (AAV) type 2 vector genome into multiple AAV serotypes enables transduction with broad specificity. J Virol 2002; 76: 791-801.
-
(2002)
J. Virol.
, vol.76
, pp. 791-801
-
-
Rabinowitz, J.E.1
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