Human immunodeficiency virus vectors for inducible expression of foreign genes. - Wikidata - wikimedia - TriplyDB

Human immunodeficiency virus vectors for inducible expression of foreign genes.

Human immunodeficiency virus vectors for inducible expression of foreign genes.

http://www.wikidata.org/entity/Q40065232

about

Construction and molecular analysis of gene transfer systems derived from bovine immunodeficiency virus Structural determinants and mechanism of HIV-1 genome packaging Comparison of 5' and 3' long terminal repeat promoter function in human immunodeficiency virus Efficient encapsidation of human immunodeficiency virus type 1 vectors and further characterization of cis elements required for encapsidation Position dependence of functional hairpins important for human immunodeficiency virus type 1 RNA encapsidation in vivo Role of the DIS hairpin in replication of human immunodeficiency virus type 1 The human immunodeficiency virus type 1 encapsidation site is a multipartite RNA element composed of functional hairpin structures The bovine leukemia virus encapsidation signal is discontinuous and extends into the 5' end of the gag gene A third-generation lentivirus vector with a conditional packaging system Lower in vivo mutation rate of human immunodeficiency virus type 1 than that predicted from the fidelity of purified reverse transcriptase Infectious molecular clones with the nonhomologous dimer initiation sequences found in different subtypes of human immunodeficiency virus type 1 can recombine and initiate a spreading infection in vitro.A packaging cell line for lentivirus vectors.The bovine leukemia virus encapsidation signal is composed of RNA secondary structures.High-titer human immunodeficiency virus type 1-based vector systems for gene delivery into nondividing cells.Separable mechanisms of attachment and cell uptake during retrovirus infection.Marking and gene expression by a lentivirus vector in transplanted human and nonhuman primate CD34(+) cells An Mpsi-containing heterologous RNA, but not env mRNA, is efficiently packaged into avian retroviral particles.The inside out of lentiviral vectors Mapping the RNA binding sites for human immunodeficiency virus type-1 gag and NC proteins within the complete HIV-1 and -2 untranslated leader regions.Effects of second-site mutations on dominant interference by a human immunodeficiency virus type 1 envelope glycoprotein mutant.RNA secondary structure and binding sites for gag gene products in the 5' packaging signal of human immunodeficiency virus type 1.Inducible and conditional inhibition of human immunodeficiency virus proviral expression by vesicular stomatitis virus matrix protein.Selective infection of human T-lymphotropic virus type 1 (HTLV-1)-infected cells by chimeric human immunodeficiency viruses containing HTLV-1 tax response elements in the long terminal repeat.Gene transfer into mammalian cells by a Rous sarcoma virus-based retroviral vector with the host range of the amphotropic murine leukemia virus Inducible human immunodeficiency virus type 1 packaging cell lines A conserved hairpin motif in the R-U5 region of the human immunodeficiency virus type 1 RNA genome is essential for replication Truncation of the human immunodeficiency virus type 1 envelope glycoprotein allows efficient pseudotyping of Moloney murine leukemia virus particles and gene transfer into CD4+ cells Mutations in the kissing-loop hairpin of human immunodeficiency virus type 1 reduce viral infectivity as well as genomic RNA packaging and dimerization.Beyond plasma membrane targeting: role of the MA domain of Gag in retroviral genome encapsidation.Efficient gene transfer by a human immunodeficiency virus type 1 (HIV-1)-derived vector utilizing a stable HIV packaging cell line.Transduction of human immunodeficiency virus type 1 vectors lacking encapsidation and dimerization signals.Mutational analysis of cis-acting packaging signals in human immunodeficiency virus type 1 RNA.Analysis in human immunodeficiency virus type 1 vectors of cis-acting sequences that affect gene transfer into human lymphocytes.Simian immunodeficiency virus RNA is efficiently encapsidated by human immunodeficiency virus type 1 particles Packaging of human immunodeficiency virus type 1 RNA requires cis-acting sequences outside the 5' leader region.Specific binding of human immunodeficiency virus type 1 gag polyprotein and nucleocapsid protein to viral RNAs detected by RNA mobility shift assays.Exploring Ty1 retrotransposon RNA structure within virus-like particles Transduction of nondividing cells using pseudotyped defective high-titer HIV type 1 particles.Efficient transfer, integration, and sustained long-term expression of the transgene in adult rat brains injected with a lentiviral vector.Development of HIV vectors for anti-HIV gene therapy.

P2860

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P2860

Human immunodeficiency virus vectors for inducible expression of foreign genes.

http://www.wikidata.org/entity/Q40065232

description

1992 nî lūn-bûn

@nan

1992年の論文

@ja

1992年論文

@yue

1992年論文

@zh-hant

1992年論文

@zh-hk

1992年論文

@zh-mo

1992年論文

@zh-tw

1992年论文

@wuu

1992年论文

@zh

1992年论文

@zh-cn

name

Human immunodeficiency virus vectors for inducible expression of foreign genes.

@en

type

label

Human immunodeficiency virus vectors for inducible expression of foreign genes.

@en

prefLabel

Human immunodeficiency virus vectors for inducible expression of foreign genes.

@en

P1433

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P932

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P1433

Journal of Virology

P1476

Human immunodeficiency virus vectors for inducible expression of foreign genes.

@en

P2093

A T Panganiban

http://www.w3.org/2001/XMLSchema#string

G L Buchschacher

http://www.w3.org/2001/XMLSchema#string

P2860

Identification of a sequence required for efficient packaging of human immunodeficiency virus type 1 RNA into virions

Gene transfer into human lymphocytes by a defective human immunodeficiency virus type 1 vector

A new technique for the assay of infectivity of human adenovirus 5 DNA

Production of acquired immunodeficiency syndrome-associated retrovirus in human and nonhuman cells transfected with an infectious molecular clone

The T4 gene encodes the AIDS virus receptor and is expressed in the immune system and the brain

Use of eukaryotic expression technology in the functional analysis of cloned genes

Cellular uptake of the tat protein from human immunodeficiency virus

Selective induction of toxicity to human cells expressing human immunodeficiency virus type 1 Tat by a conditionally cytotoxic adenovirus vector.

HIV causes AIDS.

Gene transfer into humans--immunotherapy of patients with advanced melanoma, using tumor-infiltrating lymphocytes modified by retroviral gene transduction.

P304

2731-2739

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P31

scholarly article

P407

P433

5

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P478

66

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P577

1992-05-01T00:00:00Z

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P698

1560523

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P921

vector-borne disease

P932

241028

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