(Q45858691)

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Human synapsin 1 gene promoter confers highly neuron-specific long-term transgene expression from an adenoviral vector in the adult rat brain depending on the transduced area.

scientific article published in February 2003

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12595892%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

Human synapsin 1 gene promoter confers highly neuron-specific long-term transgene expression from an adenoviral vector in the adult rat brain depending on the transduced area (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12595892%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

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Sebastian Kügler

1

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31 October 2019

author name string

Kilic E

2

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31 October 2019

Bähr M

3

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31 October 2019

publication date

1 February 2003

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31 October 2019

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31 October 2019

10

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31 October 2019

4

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31 October 2019

337-347

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PubMed publication ID

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31 October 2019

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

1 reference

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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

1 reference

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21 January 2018

Long-term gene therapy in the CNS: reversal of hypothalamic diabetes insipidus in the Brattleboro rat by using an adenovirus expressing arginine vasopressin.

1 reference

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21 January 2018

Strong promoters are the key to highly efficient, noninflammatory and noncytotoxic adenoviral-mediated transgene delivery into the brain in vivo

1 reference

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21 January 2018

Acute direct adenoviral vector cytotoxicity and chronic, but not acute, inflammatory responses correlate with decreased vector-mediated transgene expression in the brain

1 reference

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21 January 2018

Efficient gene transfer and long-term expression in neurons using a recombinant adenovirus with a neuron-specific promoter

1 reference

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21 January 2018

Neuron-restrictive silencer elements mediate neuron specificity of adenoviral gene expression

1 reference

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21 January 2018

Neuron-specific expression of therapeutic proteins: evaluation of different cellular promoters in recombinant adenoviral vectors

1 reference

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21 January 2018

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.

1 reference

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21 January 2018

Binding of adenovirus to its receptors in mouse astrocytes induces c-fos proto-oncogene and apoptosis

1 reference

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21 January 2018

Modification of a fiber protein in an adenovirus vector improves in vitro gene transfer efficiency to the mouse microglial cell line

1 reference

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21 January 2018

Separating fact from fiction: assessing the potential of modified adenovirus vectors for use in human gene therapy

1 reference

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21 January 2018

Critical issues in gene therapy for neurologic disease

1 reference

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21 January 2018

Adenoviral-mediated, high-level, cell-specific transgene expression: a SYN1-WPRE cassette mediates increased transgene expression with no loss of neuron specificity

1 reference

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21 January 2018

Inhibition of chemokine expression by adenovirus early region three (E3) genes

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Diverse stabilities of expression in the rat brain from different cellular promoters in a helper virus-free herpes simplex virus type 1 vector system

1 reference

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21 January 2018

Efficient transduction of green fluorescent protein in spinal cord neurons using adeno-associated virus vectors containing cell type-specific promoters

1 reference

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21 January 2018

Recombinant adeno-associated virus type 2, 4, and 5 vectors: transduction of variant cell types and regions in the mammalian central nervous system.

1 reference

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21 January 2018

Cross-packaging of a single adeno-associated virus (AAV) type 2 vector genome into multiple AAV serotypes enables transduction with broad specificity

1 reference

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21 January 2018

Immunologic complexity in neurons

1 reference

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7 January 2021

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inferred from DOI database lookup

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.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301905

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.GT.3301905

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12595892%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

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1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12595892%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

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