(Q40583540)

English

Recombinant adeno-associated virus serotype 4 mediates unique and exclusive long-term transduction of retinal pigmented epithelium in rat, dog, and nonhuman primate after subretinal delivery

scientific article published on June 2003

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scholarly article

1 reference

Europe PubMed Central

21 September 2017

Recombinant adeno-associated virus serotype 4 mediates unique and exclusive long-term transduction of retinal pigmented epithelium in rat, dog, and nonhuman primate after subretinal delivery (English)

1 reference

Europe PubMed Central

21 September 2017

Fabienne Rolling

11

object named as

Fabienne Rolling

0 references

author name string

Michel Weber

1

1 reference

Europe PubMed Central

21 September 2017

Joseph Rabinowitz

2

1 reference

Europe PubMed Central

21 September 2017

Nathalie Provost

3

1 reference

Europe PubMed Central

21 September 2017

Hervé Conrath

4

1 reference

Europe PubMed Central

21 September 2017

Sébastien Folliot

5

1 reference

Europe PubMed Central

21 September 2017

Delphine Briot

6

1 reference

Europe PubMed Central

21 September 2017

Yan Chérel

7

1 reference

Europe PubMed Central

21 September 2017

Pierre Chenuaud

8

1 reference

Europe PubMed Central

21 September 2017

Jude Samulski

9

1 reference

Europe PubMed Central

21 September 2017

Philippe Moullier

10

1 reference

Europe PubMed Central

21 September 2017

Fabienne Rolling

11

1 reference

Europe PubMed Central

21 September 2017

publication date

1 June 2003

1 reference

Europe PubMed Central

21 September 2017

Molecular Therapy

1 reference

Europe PubMed Central

21 September 2017

7

1 reference

Europe PubMed Central

21 September 2017

6

1 reference

Europe PubMed Central

21 September 2017

774-781

1 reference

Europe PubMed Central

21 September 2017

Long-term and significant correction of brain lesions in adult mucopolysaccharidosis type VII mice using recombinant AAV vectors.

1 reference

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7 January 2021

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Neonatal gene transfer leads to widespread correction of pathology in a murine model of lysosomal storage disease.

1 reference

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7 January 2021

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Elimination of lysosomal storage in brains of MPS VII mice treated by intrathecal administration of an adeno-associated virus vector

1 reference

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7 January 2021

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Adeno-associated viral vector-mediated gene transfer results in long-term enzymatic and functional correction in multiple organs of Fabry mice

1 reference

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7 January 2021

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Correction of hemophilia B in canine and murine models using recombinant adeno-associated viral vectors

1 reference

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7 January 2021

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Adeno-associated virus vector carrying human minidystrophin genes effectively ameliorates muscular dystrophy in mdx mouse model

1 reference

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7 January 2021

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Full functional rescue of a complete muscle (TA) in dystrophic hamsters by adeno-associated virus vector-directed gene therapy

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7 January 2021

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Nucleotide sequencing and generation of an infectious clone of adeno-associated virus 3.

1 reference

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7 January 2021

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Infectious clones and vectors derived from adeno-associated virus (AAV) serotypes other than AAV type 2.

1 reference

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7 January 2021

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Novel adeno-associated viruses from rhesus monkeys as vectors for human gene therapy

1 reference

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7 January 2021

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Several log increase in therapeutic transgene delivery by distinct adeno-associated viral serotype vectors

1 reference

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7 January 2021

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Sustained and complete phenotype correction of hemophilia B mice following intramuscular injection of AAV1 serotype vectors

1 reference

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7 January 2021

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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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7 January 2021

based on heuristic

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Adeno-associated virus type 5 (AAV5) but not AAV2 binds to the apical surfaces of airway epithelia and facilitates gene transfer

1 reference

https://api.crossref.org/works/10.1016%2FS1525-0016%2803%2900098-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Gene transfer into the mouse retina mediated by an adeno-associated viral vector

1 reference

https://api.crossref.org/works/10.1016%2FS1525-0016%2803%2900098-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Adeno-associated virus gene transfer to mouse retina

1 reference

https://api.crossref.org/works/10.1016%2FS1525-0016%2803%2900098-4

7 January 2021

based on heuristic

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Stable transgene expression in rod photoreceptors after recombinant adeno-associated virus-mediated gene transfer to monkey retina

1 reference

https://api.crossref.org/works/10.1016%2FS1525-0016%2803%2900098-4

7 January 2021

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Ribozyme rescue of photoreceptor cells in P23H transgenic rats: long-term survival and late-stage therapy.

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

AAV-mediated delivery of ciliary neurotrophic factor prolongs photoreceptor survival in the rhodopsin knockout mouse

1 reference

https://api.crossref.org/works/10.1016%2FS1525-0016%2803%2900098-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Restoration of photoreceptor ultrastructure and function in retinal degeneration slow mice by gene therapy.

1 reference

https://api.crossref.org/works/10.1016%2FS1525-0016%2803%2900098-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Two animal models of retinal degeneration are rescued by recombinant adeno-associated virus-mediated production of FGF-5 and FGF-18.

1 reference

https://api.crossref.org/works/10.1016%2FS1525-0016%2803%2900098-4

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS1525-0016%2803%2900098-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Exchange of surface proteins impacts on viral vector cellular specificity and transduction characteristics: the retina as a model

1 reference

https://api.crossref.org/works/10.1016%2FS1525-0016%2803%2900098-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Virus-mediated transduction of murine retina with adeno-associated virus: effects of viral capsid and genome size.

1 reference

https://api.crossref.org/works/10.1016%2FS1525-0016%2803%2900098-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Immediate and long-term safety of recombinant adeno-associated virus injection into the nonhuman primate muscle

1 reference

https://api.crossref.org/works/10.1016%2FS1525-0016%2803%2900098-4

7 January 2021

based on heuristic

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Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FS1525-0016%2803%2900098-4

7 January 2021

based on heuristic

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Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS1525-0016%2803%2900098-4

7 January 2021

based on heuristic

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Recombinant adeno-associated virus for muscle directed gene therapy

1 reference

https://api.crossref.org/works/10.1016%2FS1525-0016%2803%2900098-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Factors influencing in vivo transduction by recombinant adeno-associated viral vectors expressing the human factor IX cDNA.

1 reference

https://api.crossref.org/works/10.1016%2FS1525-0016%2803%2900098-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Long-term correction of canine hemophilia B by gene transfer of blood coagulation factor IX mediated by adeno-associated viral vector

1 reference

https://api.crossref.org/works/10.1016%2FS1525-0016%2803%2900098-4

7 January 2021

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Kinetics of recombinant adeno-associated virus-mediated gene transfer

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Transduction with recombinant adeno-associated virus for gene therapy is limited by leading-strand synthesis

1 reference

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7 January 2021

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Evidence for gene transfer and expression of factor IX in haemophilia B patients treated with an AAV vector.

1 reference

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A phase II, double-blind, randomized, placebo-controlled clinical trial of tgAAVCF using maxillary sinus delivery in patients with cystic fibrosis with antrostomies.

1 reference

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7 January 2021

based on heuristic

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Adeno-associated virus serotype 4 (AAV4) and AAV5 both require sialic acid binding for hemagglutination and efficient transduction but differ in sialic acid linkage specificity

1 reference

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7 January 2021

based on heuristic

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Factors influencing recombinant adeno-associated virus production

1 reference

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Five recombinant simian immunodeficiency virus pseudotypes lead to exclusive transduction of retinal pigmented epithelium in rat.

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Identifiers

10.1016/S1525-0016(03)00098-4

1 reference

Europe PubMed Central

21 September 2017

1 reference

Europe PubMed Central

21 September 2017

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