Hepatic gene transfer in neonatal mice by adeno-associated virus serotype 8 vector. (Q35988663)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22098408%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

title

Hepatic gene transfer in neonatal mice by adeno-associated virus serotype 8 vector (English)

1 reference

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17 January 2020

0 references

5

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17 January 2020

author name string

Lili Wang

1

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17 January 2020

Huan Wang

2

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17 January 2020

Peter Bell

3

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17 January 2020

Deirdre McMenamin

4

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17 January 2020

publication date

8 February 2012

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17 January 2020

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17 January 2020

volume

23

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17 January 2020

issue

5

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17 January 2020

page(s)

533-539

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Sustained correction of OTC deficiency in spf( ash) mice using optimized self-complementary AAV2/8 vectors.

17 January 2020

cites work

1 reference

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AAV8-mediated hepatic gene transfer in infant rhesus monkeys (Macaca mulatta)

2 October 2017

1 reference

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Perinatal gene transfer to the liver

2 October 2017

1 reference

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Impact of pre-existing immunity on gene transfer to nonhuman primate liver with adeno-associated virus 8 vectors

2 October 2017

1 reference

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Neonatal helper-dependent adenoviral vector gene therapy mediates correction of hemophilia A and tolerance to human factor VIII

2 October 2017

1 reference

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Long-term amelioration of feline Mucopolysaccharidosis VI after AAV-mediated liver gene transfer

2 October 2017

1 reference

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Adeno-associated virus serotype 8 gene transfer rescues a neonatal lethal murine model of propionic acidemia

2 October 2017

1 reference

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RH10 provides superior transgene expression in mice when compared with natural AAV serotypes for neonatal gene therapy

2 October 2017

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Liver-directed recombinant adeno-associated viral gene delivery rescues a lethal mouse model of methylmalonic acidemia and provides long-term phenotypic correction

2 October 2017

1 reference

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Complete normalization of hepatic G6PC deficiency in murine glycogen storage disease type Ia using gene therapy

2 October 2017

1 reference

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Lymphomagenesis in SCID-X1 mice following lentivirus-mediated phenotype correction independent of insertional mutagenesis and gammac overexpression

2 October 2017

1 reference

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Adeno-associated virus-mediated correction of a canine model of glycogen storage disease type Ia.

2 October 2017

1 reference

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Long-term rescue of a lethal murine model of methylmalonic acidemia using adeno-associated viral gene therapy

2 October 2017

1 reference

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Systematic evaluation of AAV vectors for liver directed gene transfer in murine models.

2 October 2017

1 reference

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Enhancing transduction of the liver by adeno-associated viral vectors

2 October 2017

1 reference

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Insertional oncogenesis in 4 patients after retrovirus-mediated gene therapy of SCID-X1

2 October 2017

1 reference

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Gene delivery to the juvenile mouse liver using AAV2/8 vectors

2 October 2017

1 reference

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Immunology of neonatal gene transfer

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3360497

Correction of clinical manifestations of canine mucopolysaccharidosis I with neonatal retroviral vector gene therapy

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3360497

Neonatal gene therapy of MPS I mice by intravenous injection of a lentiviral vector

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3360497

Bioluminescent imaging of a marking transgene and correction of Fabry mice by neonatal injection of recombinant lentiviral vectors

2 October 2017

1 reference

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Fetal and neonatal gene therapy: benefits and pitfalls

2 October 2017

1 reference

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Clades of Adeno-associated viruses are widely disseminated in human tissues.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3360497

Rapid and highly efficient transduction by double-stranded adeno-associated virus vectors in vitro and in vivo

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3360497

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3360497

Worldwide epidemiology of neutralizing antibodies to adeno-associated viruses.

2 October 2017

1 reference

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Analysis of tumors arising in male B6C3F1 mice with and without AAV vector delivery to liver.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3360497

High levels of persistent expression of alpha1-antitrypsin mediated by the nonhuman primate serotype rh.10 adeno-associated virus despite preexisting immunity to common human adeno-associated viruses

24 September 2018

1 reference

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Biology of AAV serotype vectors in liver-directed gene transfer to nonhuman primates.

24 September 2018

1 reference

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Adeno-associated virus serotype 8 efficiently delivers genes to muscle and heart

24 September 2018

1 reference

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AAV-mediated gene transfer to the liver

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3360497

Neonatal gene transfer with a retroviral vector results in tolerance to human factor IX in mice and dogs

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3360497

Prevention of systemic clinical disease in MPS VII mice following AAV-mediated neonatal gene transfer

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3360497

In Vivo Transduction by Intravenous Injection of a Lentiviral Vector Expressing Human ADA into Neonatal ADA Gene Knockout Mice: A Novel Form of Enzyme Replacement Therapy for ADA Deficiency

24 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22098408

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1089/HUM.2011.183

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22098408%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22098408%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

1 reference