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Gene therapy: trials and tribulations
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scholarly article
1 reference
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Europe PubMed Central
PubMed ID
11253666
retrieved
31 July 2017
review article
1 reference
stated in
Europe PubMed Central
title
Gene therapy: trials and tribulations
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
11253666
retrieved
31 July 2017
main subject
gene therapy
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author name string
Somia N
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
11253666
retrieved
31 July 2017
Verma IM
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
11253666
retrieved
31 July 2017
publication date
1 November 2000
1 reference
stated in
Europe PubMed Central
PubMed ID
11253666
retrieved
31 July 2017
published in
Nature Reviews Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
11253666
retrieved
31 July 2017
volume
1
1 reference
stated in
Europe PubMed Central
PubMed ID
11253666
retrieved
31 July 2017
page(s)
91-99
1 reference
stated in
Europe PubMed Central
PubMed ID
11253666
retrieved
31 July 2017
issue
2
1 reference
stated in
Europe PubMed Central
PubMed ID
11253666
retrieved
31 July 2017
exact match
https://scigraph.springernature.com/pub.10.1038/35038533
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Nonviral gene therapy: promises and challenges
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Gene Therapy
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A triploblast origin for Myxozoa?
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The basic science of gene therapy
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Human gene therapy comes of age.
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A safe packaging line for gene transfer: separating viral genes on two different plasmids
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Human gene therapy
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Multiply attenuated lentiviral vector achieves efficient gene delivery in vivo
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HIV-1 genome nuclear import is mediated by a central DNA flap
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Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences
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Woodchuck hepatitis virus posttranscriptional regulatory element enhances expression of transgenes delivered by retroviral vectors.
1 reference
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Development of a self-inactivating lentivirus vector.
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High-fidelity correction of mutations at multiple chromosomal positions by adeno-associated virus vectors.
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Membrane-associated heparan sulfate proteoglycan is a receptor for adeno-associated virus type 2 virions
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Genetic capsid modifications allow efficient re-targeting of adeno-associated virus type 2.
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Evidence for gene transfer and expression of factor IX in haemophilia B patients treated with an AAV vector.
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Trans-splicing vectors expand the utility of adeno-associated virus for gene therapy
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Increasing the size of rAAV-mediated expression cassettes in vivo by intermolecular joining of two complementary vectors
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Advances in adenoviral vectors: from genetic engineering to their biology
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A new adenoviral vector: Replacement of all viral coding sequences with 28 kb of DNA independently expressing both full-length dystrophin and beta-galactosidase
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A helper-dependent adenovirus vector system: removal of helper virus by Cre-mediated excision of the viral packaging signal
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Administration of helper-dependent adenoviral vectors and sequential delivery of different vector serotype for long-term liver-directed gene transfer in baboons
1 reference
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Cellular and humoral immune responses to adenoviral vectors containing factor IX gene: tolerization of factor IX and vector antigens allows for long-term expression
1 reference
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1 reference
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1 reference
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Crossref
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Crossref
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1 reference
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Crossref
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Role of vector in activation of T cell subsets in immune responses against the secreted transgene product factor IX.
1 reference
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Crossref
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1 reference
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1 reference
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Crossref
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1 reference
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Crossref
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inferred from DOI database lookup
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1 reference
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Crossref
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Transduction of human CD34+ cells that mediate long-term engraftment of NOD/SCID mice by HIV vectors
1 reference
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1 reference
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1 reference
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Crossref
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inferred from DOI database lookup
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1 reference
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Crossref
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1 reference
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1 reference
stated in
Crossref
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Identifiers
DOI
10.1038/35038533
1 reference
stated in
Europe PubMed Central
PubMed ID
11253666
retrieved
31 July 2017
Dimensions Publication ID
1012109533
0 references
PubMed ID
11253666
1 reference
stated in
Europe PubMed Central
PubMed ID
11253666
retrieved
31 July 2017
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