Stable in vivo gene transduction via a novel adenoviral/retroviral chimeric vector (Q41083246)

26 September 2017

Stable in vivo gene transduction via a novel adenoviral/retroviral chimeric vector (English)

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26 September 2017

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Curiel DT

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26 September 2017

Feng M

1

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26 September 2017

Jackson WH Jr

2

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26 September 2017

Goldman CK

3

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26 September 2017

Rancourt C

4

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26 September 2017

Wang M

5

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26 September 2017

Dusing SK

6

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26 September 2017

Siegal G

7

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26 September 2017

1 September 1997

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26 September 2017

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26 September 2017

15

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26 September 2017

866-870

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26 September 2017

9

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https://scigraph.springernature.com/pub.10.1038/nbt0997-866

26 September 2017

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Recent advances in the application of gene therapy to human disease

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Cellular gene therapy: an overview

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Gene therapy via primary myoblasts: long-term expression of factor IX protein following transplantation in vivo

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Gene therapy for cystic fibrosis: challenges and future directions

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7 January 2021

Gene therapy for cystic fibrosis

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7 January 2021

Cardiovascular gene therapy: current concepts

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7 January 2021

Gene therapy and the hemophilias

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7 January 2021

Adenovirus-mediated in vivo gene transfer and expression in normal rat liver

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7 January 2021

Adenovirus mediated expression of therapeutic plasma levels of human factor IX in mice

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7 January 2021

Efficient adenoviral-mediated ornithine transcarbamylase expression in deficient mouse and human hepatocytes

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7 January 2021

Adenovirus-mediated transfer of low density lipoprotein receptor gene acutely accelerates cholesterol clearance in normal mice

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7 January 2021

Adenovirus-mediated correction of the genetic defect in hepatocytes from patients with familial hypercholesterolemia

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7 January 2021

Hypercholesterolemia in low density lipoprotein receptor knockout mice and its reversal by adenovirus-mediated gene delivery

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7 January 2021

Effective treatment of familial hypercholesterolaemia in the mouse model using adenovirus-mediated transfer of the VLDL receptor gene

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7 January 2021

Prolonged metabolic correction in adult ornithine transcarbamylase-deficient mice with adenoviral vectors

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7 January 2021

Cellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapy

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7 January 2021

MHC class I-restricted cytotoxic T lymphocytes to viral antigens destroy hepatocytes in mice infected with E1-deleted recombinant adenoviruses.

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https://api.crossref.org/works/10.1038%2FNBT0997-866

7 January 2021

Cellular and humoral immune responses to viral antigens create barriers to lung-directed gene therapy with recombinant adenoviruses

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https://api.crossref.org/works/10.1038%2FNBT0997-866

7 January 2021

Retroviral-mediated gene transfer into hepatocytes in vivo

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https://api.crossref.org/works/10.1038%2FNBT0997-866

7 January 2021

Hepatic gene therapy: efficient retroviral-mediated gene transfer into rat hepatocytes in vivo

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https://api.crossref.org/works/10.1038%2FNBT0997-866

7 January 2021

Direct retroviral-mediated transfer of a dystrophin minigene into mdx mouse muscle in vivo

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https://api.crossref.org/works/10.1038%2FNBT0997-866

7 January 2021

Gene delivery to glioma cells in rat brain by grafting of a retrovirus packaging cell line

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7 January 2021

In Vivo Gene Transfer with Retroviral Vector-Producer Cells for Treatment of Experimental Brain Tumors

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7 January 2021

An experimental model of retrovirus gene therapy for malignant brain tumors

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7 January 2021

Toxicity studies of retroviral-mediated gene transfer for the treatment of brain tumors

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7 January 2021

Retroviruses as vectors

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https://api.crossref.org/works/10.1038%2FNBT0997-866

7 January 2021

Retroviral vector producer cell killing in human serum is mediated by natural antibody and complement: strategies for evading the humoral immune response

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https://api.crossref.org/works/10.1038%2FNBT0997-866

7 January 2021

Production of high-titer helper-free retroviruses by transient transfection

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https://api.crossref.org/works/10.1038%2FNBT0997-866

7 January 2021

Virofection: a one-step procedure for using replication-defective retrovirus vectors

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https://api.crossref.org/works/10.1038%2FNBT0997-866

7 January 2021

Plasmoviruses: nonviral/viral vectors for gene therapy.

1 reference

https://api.crossref.org/works/10.1038%2FNBT0997-866

7 January 2021

An efficient and flexible system for construction of adenovirus vectors with insertions or deletions in early regions 1 and 3.

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https://api.crossref.org/works/10.1038%2FNBT0997-866

7 January 2021

A novel adenovirus-adeno-associated virus hybrid vector that displays efficient rescue and delivery of the AAV genome

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https://api.crossref.org/works/10.1038%2FNBT0997-866

7 January 2021

Identifiers

DOI

10.1038/NBT0997-866

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26 September 2017

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