Isolation of cloned Moloney murine leukemia virus reverse transcriptase lacking ribonuclease H activity.
about
Thermostable DNA polymerase from a viral metagenome is a potent RT-PCR enzymeRNase H activity: structure, specificity, and function in reverse transcriptionPhylogenetic relationships among highly virulent Newcastle disease virus isolates obtained from exotic birds and poultry from 1989 to 1996Primer Extension Enrichment Reaction (PEER): a new subtraction method for identification of genetic differences between biological specimensCharacterization of Newcastle disease virus isolates by reverse transcription PCR coupled to direct nucleotide sequencing and development of sequence database for pathotype prediction and molecular epidemiological analysisDetection of hepatitis C virus RNA by a combined reverse transcription-polymerase chain reaction assayInfluence of the RNase H domain of retroviral reverse transcriptases on the metal specificity and substrate selection of their polymerase domainsNovel mutations in Moloney Murine Leukemia Virus reverse transcriptase increase thermostability through tighter binding to template-primer.Phylogenetic relationships among virulent Newcastle disease virus isolates from the 2002-2003 outbreak in California and other recent outbreaks in North America.Replication of phenotypically mixed human immunodeficiency virus type 1 virions containing catalytically active and catalytically inactive reverse transcriptase.Dynamic copy choice: steady state between murine leukemia virus polymerase and polymerase-dependent RNase H activity determines frequency of in vivo template switching.Use of a heteroduplex mobility assay to detect differences in the fusion protein cleavage site coding sequence among Newcastle disease virus isolates.Molecular epidemiology of subgroup C avian pneumoviruses isolated in the United States and comparison with subgroup a and B viruses.HIV-1 RT-associated ribonuclease H displays both endonuclease and 3'----5' exonuclease activitySolid phase assays for the detection of inhibitors of HIV reverse transcriptaseRNase H domain of Moloney murine leukemia virus reverse transcriptase retains activity but requires the polymerase domain for specificity.Signal transmission in the parallel fiber-Purkinje cell system visualized by high-resolution imaging.Stable expression of a functional GluR6 homomeric glutamate receptor channel in mammalian cells.RNase H domain mutations affect the interaction between Moloney murine leukemia virus reverse transcriptase and its primer-templateStrand displacement synthesis capability of Moloney murine leukemia virus reverse transcriptase.Cassette mutagenesis of the reverse transcriptase of human immunodeficiency virus type 1.RNase H activity associated with reverse transcriptase from feline immunodeficiency virusTemplate switching by reverse transcriptase during DNA synthesis.Specificities involved in the initiation of retroviral plus-strand DNA.Functional organization of the murine leukemia virus reverse transcriptase: characterization of a bacterially expressed AKR DNA polymerase deficient in RNase H activity.Reconstitution in vitro of RNase H activity by using purified N-terminal and C-terminal domains of human immunodeficiency virus type 1 reverse transcriptase.Expression of the cystic fibrosis transmembrane conductance regulator gene in the respiratory tract of normal individuals and individuals with cystic fibrosis.Sulphydryl groups in the template-primer-binding domain of murine leukaemia virus reverse transcriptase. Identification and functional analysis of cysteine-90.Polypurine tract primer generation and utilization by Moloney murine leukemia virus reverse transcriptase.Alanine-scanning mutations in the "primer grip" of p66 HIV-1 reverse transcriptase result in selective loss of RNA priming activity.The role of template-primer in protection of reverse transcriptase from thermal inactivation.Defects in Moloney murine leukemia virus replication caused by a reverse transcriptase mutation modeled on the structure of Escherichia coli RNase H.Detection of enteroviruses in cell cultures by using in situ transcription.Evolutionarily conserved elements in the 5' untranslated region of beta globin mRNA mediate site-specific priming of a unique hairpin structure during cDNA synthesis.Site-directed mutagenesis of the conserved Asp-443 and Asp-498 carboxy-terminal residues of HIV-1 reverse transcriptase.Functional differences between the human LINE retrotransposon and retroviral reverse transcriptases for in vivo mRNA reverse transcriptionPoint mutations in conserved amino acid residues within the C-terminal domain of HIV-1 reverse transcriptase specifically repress RNase H function.Purification and characterization of the RNase H domain of HIV-1 reverse transcriptase expressed in recombinant Escherichia coli.Comparison of the thermal stabilities of reverse transcriptases from avian myeloblastosis virus and Moloney murine leukaemia virus.Generation and characterization of new highly thermostable and processive M-MuLV reverse transcriptase variants.
P2860
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P2860
Isolation of cloned Moloney murine leukemia virus reverse transcriptase lacking ribonuclease H activity.
description
1988 nî lūn-bûn
@nan
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
1988年论文
@zh
1988年论文
@zh-cn
name
Isolation of cloned Moloney mu ...... cking ribonuclease H activity.
@en
type
label
Isolation of cloned Moloney mu ...... cking ribonuclease H activity.
@en
prefLabel
Isolation of cloned Moloney mu ...... cking ribonuclease H activity.
@en
P2093
P2860
P356
P1476
Isolation of cloned Moloney mu ...... cking ribonuclease H activity.
@en
P2093
D'Alessio JM
Kotewicz ML
Sampson CM
P2860
P304
P356
10.1093/NAR/16.1.265
P577
1988-01-01T00:00:00Z