Retrovirus recombination depends on the length of sequence identity and is not error prone
about
Accurately measuring recombination between closely related HIV-1 genomesIdentifying the important HIV-1 recombination breakpoints.RNA structures facilitate recombination-mediated gene swapping in HIV-1Lentiviral vectors can be used for full-length dystrophin gene therapyStructural determinants of murine leukemia virus reverse transcriptase that affect the frequency of template switchingRecombination between two identical sequences within the same retroviral RNA molecule.Effect of distance between homologous sequences and 3' homology on the frequency of retroviral reverse transcriptase template switching.The kissing-loop motif is a preferred site of 5' leader recombination during replication of SL3-3 murine leukemia viruses in mice.Effects of homology length in the repeat region on minus-strand DNA transfer and retroviral replication.Determination of the site of first strand transfer during Moloney murine leukemia virus reverse transcription and identification of strand transfer-associated reverse transcriptase errors.Analysis of the 5' junctions of R2 insertions with the 28S gene: implications for non-LTR retrotranspositionComplex recombination patterns arising during geminivirus coinfections preserve and demarcate biologically important intra-genome interaction networks.Why do RNA viruses recombine?Pausing during reverse transcription increases the rate of retroviral recombinationHuman immunodeficiency virus type 1 genetic recombination is more frequent than that of Moloney murine leukemia virus despite similar template switching rates.Mechanisms and factors that influence high frequency retroviral recombinationThe dimerization/packaging sequence is dispensable for both the formation of high-molecular-weight RNA complexes within retroviral particles and the synthesis of proviruses of normal structure.High-titer packaging cells producing recombinant retroviruses resistant to human serumThe recombination rate is not increased when retroviral RNA is missing an encapsidation sequenceThe remarkable frequency of human immunodeficiency virus type 1 genetic recombinationReplication infidelity during a single cycle of Ty1 retrotransposition.Recombination leads to the rapid emergence of HIV-1 dually resistant mutants under selective drug pressure.Productive replication and evolution of HIV-1 in ferret cells.Sequence determinants of breakpoint location during HIV-1 intersubtype recombination.Recombination in the 5' leader of murine leukemia virus is accurate and influenced by sequence identity with a strong bias toward the kissing-loop dimerization region.Structure-based moloney murine leukemia virus reverse transcriptase mutants with altered intracellular direct-repeat deletion frequencies.Altering the intracellular environment increases the frequency of tandem repeat deletion during Moloney murine leukemia virus reverse transcription.Persistence of pathogenic challenge virus in macaques protected by simian immunodeficiency virus SIVmacDeltanef.Evidence for retroviral intramolecular recombinations.Effects of limiting homology at the site of intermolecular recombinogenic template switching during Moloney murine leukemia virus replicationRetroviral recombination rates do not increase linearly with marker distance and are limited by the size of the recombining subpopulation.Long terminal repeat enhancer core sequences in proviruses adjacent to c-myc in T-cell lymphomas induced by a murine retrovirus.Utilization of nonhomologous minus-strand DNA transfer to generate recombinant retroviruses.Pseudodiploid genome organization AIDS full-length human immunodeficiency virus type 1 DNA synthesis.Deep Sequencing Details the Cross-over Map of Chimeric Genes in Two Porcine Reproductive and Respiratory Syndrome Virus Infectious Clones.Effects of identity minimization on Moloney murine leukemia virus template recognition and frequent tertiary template-directed insertions during nonhomologous recombination.Recombination in HIV: an important viral evolutionary strategy.RNA motifs mediating in vivo site-specific nonhomologous recombination in (+) RNA virus enforce in vitro nonhomologous crossovers with HIV-1 reverse transcriptase.Genetic diversity and molecular evolution of Plum bark necrosis stem pitting-associated virus from ChinaLentiviral vectors can be used for full-length dystrophin gene therapy.
P2860
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P2860
Retrovirus recombination depends on the length of sequence identity and is not error prone
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Retrovirus recombination depen ...... dentity and is not error prone
@ast
Retrovirus recombination depen ...... dentity and is not error prone
@en
type
label
Retrovirus recombination depen ...... dentity and is not error prone
@ast
Retrovirus recombination depen ...... dentity and is not error prone
@en
prefLabel
Retrovirus recombination depen ...... dentity and is not error prone
@ast
Retrovirus recombination depen ...... dentity and is not error prone
@en
P2860
P1433
P1476
Retrovirus recombination depen ...... dentity and is not error prone
@en
P2093
P2860
P304
P407
P577
1994-04-01T00:00:00Z