Structural intermediates of deletion mutagenesis: a role for palindromic DNA
about
Multiple mutations and frameshifts are the hallmark of defective hPMS2 in pZ189-transfected human tumor cellsNon-B DB: a database of predicted non-B DNA-forming motifs in mammalian genomesUnusually long palindromes are abundant in mitochondrial control regions of insects and nematodesPotential DNA slippage structures acquired during evolutionary divergence of Acinetobacter calcoaceticus chromosomal benABC and Pseudomonas putida TOL pWW0 plasmid xylXYZ, genes encoding benzoate dioxygenasesRole of direct repeat and stem-loop motifs in mtDNA deletions: cause or coincidence?Chromosomal deletion and rearrangement in Streptomyces glaucescens.Plastidic trnFUUC pseudogenes in North American genus Boechera (Brassicaceae): mechanistic aspects of evolution.Multiple homoplasious insertions and deletions of a Triticeae (Poaceae) DNA transposon: a phylogenetic perspective.Illegitimate recombination induced by benzo[a]pyrene diol epoxide in Escherichia coli.Spectrum of spontaneous mutation at the APRT locus of Chinese hamster ovary cells: an analysis at the DNA sequence levelAlternative DNA structure formation in the mutagenic human c-MYC promoter.Spontaneous deletion formation at the aprt locus of hamster cells: the presence of short sequence homologies and dyad symmetries at deletion termini.Filler DNA is associated with spontaneous deletions in maize.Recombination resulting in unusual features in the polyomavirus genome isolated from a murine tumor cell line.Patterns of somatic mutations in immunoglobulin variable genesSpontaneous microdeletions and microinsertions in a transgenic mouse mutation detection system: analysis of age, tissue, and sequence specificity.Changes in DNA base sequence induced by gamma-ray mutagenesis of lambda phage and prophage.Deletions in plasmid pBR322: replication slippage involving leading and lagging strands.The influence of local DNA sequence and DNA repair background on the mutational specificity of 1-nitroso-8-nitropyrene in Escherichia coli: inferences for mutagenic mechanisms.The influence of primary and secondary DNA structure in deletion and duplication between direct repeats in Escherichia coli.Sequences with the potential to form stem-and-loop structures are associated with coding-region duplications in animal mitochondrial DNA.The cross-linking agent hexamethylphosphoramide predominantly induces intra-locus and multi-locus deletions in postmeiotic germ cells of Drosophila.Site-directed mutagenesis of large DNA palindromes: construction and in vitro characterization of herpes simplex virus type 1 mutants containing point mutations that eliminate the oriL or oriS initiation functionDown-regulation of the antisense mitochondrial non-coding RNAs (ncRNAs) is a unique vulnerability of cancer cells and a potential target for cancer therapy.Mitochondrial DNA deletions are associated with non-B DNA conformationsNon-B DNA structure-induced genetic instability and evolution.Molecular characteristics of spontaneous deletions in the hyperthermophilic archaeon Sulfolobus acidocaldarius.Factors affecting inverted repeat stimulation of recombination and deletion in Saccharomyces cerevisiaePlastome mutator-induced alterations arise in Oenothera chloroplast DNA through template slippageLong inverted repeats are an at-risk motif for recombination in mammalian cells.Stability of an inverted repeat in a human fibrosarcoma cell.Dissecting the fidelity of bacteriophage RB69 DNA polymerase: site-specific modulation of fidelity by polymerase accessory proteinsUse of denaturing-gradient gel electrophoresis to study chromium-induced point mutations in human cellsIdentification of a splice-site mutation in the aldolase B gene from an individual with hereditary fructose intolerance.Nucleotide sequence and expression of the gene encoding the major 25-kilodalton outer membrane protein of Brucella ovis: Evidence for antigenic shift, compared with other Brucella species, due to a deletion in the gene.Hemophilia B (factor IXSeattle 2) due to a single nucleotide deletion in the gene for factor IX.Spontaneous mutations in pcaH and -G, structural genes for protocatechuate 3,4-dioxygenase in Acinetobacter calcoaceticusDifferential DNA secondary structure-mediated deletion mutation in the leading and lagging strands.Illegitimate recombination at the replication origin of bacteriophage M13.Apparent and real recombination frequencies in multicopy plasmids: the need for a novel approach in frequency determination
P2860
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P2860
Structural intermediates of deletion mutagenesis: a role for palindromic DNA
description
1984 nî lūn-bûn
@nan
1984年の論文
@ja
1984年学术文章
@wuu
1984年学术文章
@zh-cn
1984年学术文章
@zh-hans
1984年学术文章
@zh-my
1984年学术文章
@zh-sg
1984年學術文章
@yue
1984年學術文章
@zh
1984年學術文章
@zh-hant
name
Structural intermediates of deletion mutagenesis: a role for palindromic DNA
@ast
Structural intermediates of deletion mutagenesis: a role for palindromic DNA
@en
type
label
Structural intermediates of deletion mutagenesis: a role for palindromic DNA
@ast
Structural intermediates of deletion mutagenesis: a role for palindromic DNA
@en
prefLabel
Structural intermediates of deletion mutagenesis: a role for palindromic DNA
@ast
Structural intermediates of deletion mutagenesis: a role for palindromic DNA
@en
P2860
P356
P1476
Structural intermediates of deletion mutagenesis: a role for palindromic DNA
@en
P2093
Glickman BW
P2860
P304
P356
10.1073/PNAS.81.2.512
P407
P577
1984-01-01T00:00:00Z