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Stable gene transfer to the nervous system using a non-primate lentiviral vector

Gene therapy, 1999-11, Vol.6 (11), p.1808-1818

1999

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Potential oncogene activity of the woodchuck hepatitis post-transcriptional regulatory element (WPRE)

Gene therapy, 2005-01, Vol.12 (1), p.3-4

2005

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Multicistronic Lentiviral Vector-Mediated Striatal Gene Transfer of Aromatic L-Amino Acid Decarboxylase, Tyrosine Hydroxylase, and GTP Cyclohydrolase I Induces Sustained Transgene Expression, Dopamine Production, and Functional Improvement in a Rat Model of Parkinson's Disease

The Journal of neuroscience, 2002-12, Vol.22 (23), p.10302-10312

2002

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Rabies virus glycoprotein pseudotyping of lentiviral vectors enables retrograde axonal transport and access to the nervous system after peripheral delivery

Human molecular genetics, 2001-09, Vol.10 (19), p.2109-2121

2001

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Long-term transgene expression by administration of a lentivirus-based vector to the fetal circulation of immuno-competent mice

Gene therapy, 2003-08, Vol.10 (15), p.1234-1240

2003

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Analysis of factor VIII mediated suppression of lentiviral vector titres

Gene therapy, 2008-02, Vol.15 (4), p.289-297

2008

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Lentivirus-mediated gene transfer to the central nervous system: therapeutic and research applications

Human gene therapy, 2006-01, Vol.17 (1), p.1

2006

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Hypoxia-mediated tumour targeting

Gene therapy, 2003-04, Vol.10 (7), p.540-549

2003

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An adenoviral vector regulated by hypoxia for the treatment of ischaemic disease and cancer

Gene therapy, 1999-10, Vol.6 (10), p.1721-1727

1999

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Minimal Requirement for a Lentivirus Vector Based on Human Immunodeficiency Virus Type 1

Journal of Virology, 1998-01, Vol.72 (1), p.811-816

1998

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Functional dissection of the Moloney murine leukemia virus envelope protein gp70

Journal of Virology, 1997-03, Vol.71 (3), p.2092-2099

1997

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Identification of Potential Stroke Targets by Lentiviral Vector Mediated Overexpression of HIF-1α and HIF-2α in a Primary Neuronal Model of Hypoxia

Journal of cerebral blood flow and metabolism, 2004-02, Vol.24 (2), p.245-258

2004

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Human immunodeficiency virus type 1 integrase: effect on viral replication of mutations at highly conserved residues

Journal of Virology, 1994-08, Vol.68 (8), p.4768-4775

1994

Volltextzugriff (PDF)

Lentiviral vectors for treating and modeling human CNS disorders

The journal of gene medicine, 2004-09, Vol.6 (9), p.951-962

2004

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Structure-function studies of the human immunodeficiency virus type 1 matrix protein, p17

Journal of Virology, 1997-05, Vol.71 (5), p.3474-3483

1997

Volltextzugriff (PDF)

Cytochrome P450-based cancer gene therapy: current status

Expert opinion on biological therapy, 2002-12, Vol.2 (8), p.857-868

2002

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Effects of stoichiometry of retroviral components on virus production

Journal of general virology, 2000-09, Vol.81 (9), p.2195-2202

2000

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A replication competent lentivirus (RCL) assay for equine infectious anaemia virus (EIAV)-based lentiviral vectors

Gene therapy, 2006-02, Vol.13 (3), p.196-205

2006

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Direct retroviral delivery of human cytochrome P450 2B6 for gene-directed enzyme prodrug therapy of cancer

Cancer gene therapy, 2001-07, Vol.8 (7), p.473-482

2001

Volltextzugriff (PDF)

Transcriptional control of the Saccharomyces cerevisiae PGK gene by RAP1

Molecular and Cellular Biology, 1989-12, Vol.9 (12), p.5516-5524

1989

Volltextzugriff (PDF)

Real-time analysis of the transcriptional regulation of HIV and hCMV promoters in single mammalian cells

Journal of cell science, 1995-02, Vol.108 ( Pt 2) (2), p.441-455

1995

Volltextzugriff (PDF)

Retinoic acid receptor beta 2 and neurite outgrowth in the adult mouse spinal cord in vitro

Journal of cell science, 2002-10, Vol.115 (19), p.3779-3786

2002

Volltextzugriff (PDF)

Analysis of 4070A envelope levels in retroviral preparations and effect on target cell transduction efficiency

Human gene therapy, 2000-07, Vol.11 (10), p.1439-1451

2000

Volltextzugriff (PDF)

Neuroprotection in a rat Parkinson model by GDNF gene therapy using EIAV vector

Neuroreport, 2004-04, Vol.15 (6), p.985-990

2004

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Silencing mutant SOD1 using RNAi protects against neurodegeneration and extends survival in an ALS model

Nature medicine, 2005-04, Vol.11 (43), p.429-433

2005

Volltextzugriff (PDF)

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Stable gene transfer to the nervous system using a non-primate lentiviral vector

Potential oncogene activity of the woodchuck hepatitis post-transcriptional regulatory element (WPRE)

Multicistronic Lentiviral Vector-Mediated Striatal Gene Transfer of Aromatic L-Amino Acid Decarboxylase, Tyrosine Hydroxylase, and GTP Cyclohydrolase I Induces Sustained Transgene Expression, Dopamine Production, and Functional Improvement in a Rat Model of Parkinson's Disease

Rabies virus glycoprotein pseudotyping of lentiviral vectors enables retrograde axonal transport and access to the nervous system after peripheral delivery

Long-term transgene expression by administration of a lentivirus-based vector to the fetal circulation of immuno-competent mice

Analysis of factor VIII mediated suppression of lentiviral vector titres

Lentivirus-mediated gene transfer to the central nervous system: therapeutic and research applications

Hypoxia-mediated tumour targeting

An adenoviral vector regulated by hypoxia for the treatment of ischaemic disease and cancer

Minimal Requirement for a Lentivirus Vector Based on Human Immunodeficiency Virus Type 1

Functional dissection of the Moloney murine leukemia virus envelope protein gp70

Identification of Potential Stroke Targets by Lentiviral Vector Mediated Overexpression of HIF-1α and HIF-2α in a Primary Neuronal Model of Hypoxia

Human immunodeficiency virus type 1 integrase: effect on viral replication of mutations at highly conserved residues

Lentiviral vectors for treating and modeling human CNS disorders

Structure-function studies of the human immunodeficiency virus type 1 matrix protein, p17

Cytochrome P450-based cancer gene therapy: current status

Effects of stoichiometry of retroviral components on virus production

A replication competent lentivirus (RCL) assay for equine infectious anaemia virus (EIAV)-based lentiviral vectors

Direct retroviral delivery of human cytochrome P450 2B6 for gene-directed enzyme prodrug therapy of cancer

Transcriptional control of the Saccharomyces cerevisiae PGK gene by RAP1

Real-time analysis of the transcriptional regulation of HIV and hCMV promoters in single mammalian cells

Retinoic acid receptor beta 2 and neurite outgrowth in the adult mouse spinal cord in vitro

Analysis of 4070A envelope levels in retroviral preparations and effect on target cell transduction efficiency

Neuroprotection in a rat Parkinson model by GDNF gene therapy using EIAV vector

Silencing mutant SOD1 using RNAi protects against neurodegeneration and extends survival in an ALS model

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