Model for the participation of quasi-palindromic DNA sequences in frameshift mutation
about
Mechanisms of gene duplication and amplificationSolution structure of a two-base DNA bulge complexed with an enediyne cleaving analogIncreased mutagenesis and unique mutation signature associated with mitotic gene conversionIdentification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hypoparathyroidism.Transcription-associated mutagenesis increases protein sequence diversity more effectively than does random mutagenesis in Escherichia coliShort template switch events explain mutation clusters in the human genome.Break-induced replication is highly inaccurateSpontaneous microdeletions and microinsertions in a transgenic mouse mutation detection system: analysis of age, tissue, and sequence specificity.An in vitro assay for frameshift mutations: hotspots for deletions of 1 bp by Klenow-fragment polymerase share a consensus DNA sequenceRecombination and replication of plasmid-like derivatives of a short section of the mitochondrial chromosome of Neurospora crassa.The influence of primary and secondary DNA structure in deletion and duplication between direct repeats in Escherichia coli.DNA synthesis errors associated with double-strand-break repairThe distribution of inverted repeat sequences in the Saccharomyces cerevisiae genome.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 functionSynthesis-dependent microhomology-mediated end joining accounts for multiple types of repair junctions.Ribosomal protein gene sequence changes in erythromycin-resistant mutants of Escherichia coli.Evidence that a metabolic microcompartment contains and recycles private cofactor pools.Site-specific targeting of aflatoxin adduction directed by triple helix formation in the major groove of oligodeoxyribonucleotides.Insights into mutagenesis using Escherichia coli chromosomal lacZ strains that enable detection of a wide spectrum of mutational events.Differential DNA secondary structure-mediated deletion mutation in the leading and lagging strands.An absence of cutaneous neurofibromas associated with a 3-bp inframe deletion in exon 17 of the NF1 gene (c.2970-2972 delAAT): evidence of a clinically significant NF1 genotype-phenotype correlation.Azidothymidine and other chain terminators are mutagenic for template-switch-generated genetic mutations.Conformational transitions of synthetic DNA sequences with inserted bases, related to the dodecamer d(CGCGAATTCGCG).Perspective on mutagenesis and repair: the standard model and alternate modes of mutagenesis.Compensatory evolution of a precursor messenger RNA secondary structure in the Drosophila melanogaster Adh gene.Characterization of the defect in the Escherichia coli mutT1 mutator geneStructural intermediates of deletion mutagenesis: a role for palindromic DNAMutational specificity of depurinationC1 inhibitor gene sequence facilitates frameshift mutationsTemplated mutagenesis in bacteriophage T4 involving imperfect direct or indirect sequence repeats.A mutation allowing an mRNA secondary structure diminishes translation of Saccharomyces cerevisiae iso-1-cytochrome cInhibition of DNA synthesis facilitates expansion of low-complexity repeats: is strand slippage stimulated by transient local depletion of specific dNTPs?Distinguishing "looped-out" and "stacked-in" DNA bulge conformation using fluorescent 2-aminopurine replacing a purine base.Frameshift mutations produced by proflavin in bacteriophage T4: specificity within a hotspot.2-(N-acetoxy-N-acetylamino)fluorene mutagenesis in mammalian cells: sequence-specific hot spot.DNA polymerases ζ and Rev1 mediate error-prone bypass of non-B DNA structures.Sequence-directed mutagenesis: evidence from a phylogenetic history of human alpha-interferon genes.Demonstration of the production of frameshift and base-substitution mutations by quasipalindromic DNA sequencesMechanisms and consequences of mutation induction in mammalian cells.Short-range inversions: rethinking organelle genome stability: template switching events during DNA replication destabilize organelle genomes.
P2860
Q22065788-420F9C44-009E-438B-97F1-0CEC9081E23AQ27732813-AF10F500-ED9C-481E-A7A5-8B2E2A6E8976Q27934880-98FDF6ED-CEB9-48A8-A7F2-68964F43CD9DQ29568914-A69CA6D9-87E1-4D82-B9FD-6F4FDF5B8C65Q30982797-15B476FA-C637-4A1D-B76E-1693DFBB4C96Q33365166-D0A44263-CE4A-4994-846D-CD7157621C4EQ33828325-824741C0-D596-466D-8B9E-42FC49D28710Q33952945-96C0BEEA-E6F3-4DFB-BEDC-0FDBC0A6EC0EQ33953707-F4B4B1C4-4F55-4275-B989-9F43BA3D57BFQ33955212-2F4AB104-1CF4-4208-B08C-86E1BF3E6B74Q33961004-45B97F74-2618-4C5E-B6E6-A4A9EBAD057BQ33965497-C13C53AE-71EC-4B60-9204-2033F7B3170CQ34013441-3A3E4A70-91E5-4DAE-8F90-EA945E7E66DEQ34045705-86B839FC-3F03-4E77-8DE8-AFD470642972Q34146358-8A113E82-A4D3-4819-BC73-C114B189A069Q34323549-92F23F96-4DB8-4505-AB1B-8AC9F552EA42Q34339232-321F26A1-F6C1-4DFE-A5A2-FC99F62C8291Q34656824-1CAF8912-1174-4456-9474-C762A1EEAB6CQ35065478-9A005FDF-7832-41F6-A9DB-686AC7EF0741Q35591486-D2DD3F2B-A53E-42D9-A6A0-0B192842E22EQ35616603-C945CF0B-0F4C-4BC5-828B-97E788CDE7A3Q35924896-B6315410-A28B-4E8D-A7D2-90FBA25DB906Q36125983-98F6A070-7A4F-4873-BDA2-6A8A2350CF37Q36139867-9C1943E7-33AF-449F-B140-2807A4E1152EQ36161161-7A0D2CE4-D878-4BFD-9DE9-12004D2137A5Q36162829-7ACABFB1-B068-4D20-B4CA-E14FC3B54EF8Q36247516-ACB5D9E0-EB9F-4CCA-AA25-BCB77488C514Q36252034-9496E62F-2EBD-4391-B095-F6CA19D66C74Q36438389-7A86B385-3CFC-4192-8362-A3B7328A0E7FQ36470525-ADDF89DD-D3BE-4555-BD2A-7D577AF8D0F2Q36891464-DEE54E3C-7810-4BFE-8EE6-13D36590DB98Q37149212-28183072-DFC4-480A-B32C-2187BF88B6A7Q37267420-E19A9BC6-D3D0-4E2A-A4B3-75806CF9455FQ37399577-04BE44E7-14F8-48EF-B22B-86189E71F77FQ37411682-68A4F696-477E-449C-A5B3-A8168D25BD20Q37416977-542A56D9-0804-4F26-92AA-FFC62DB70645Q37540329-6FC3F4E8-2028-43BD-869C-8D4C589FEE6CQ37566558-E1F4B289-0F62-407C-B59D-C6D8621613A4Q37584299-CEE82AC8-3CDF-475E-A32E-15B60F5B39B8Q38556923-0CDCF657-9D0D-4B50-ADBA-FE3D664C2B1E
P2860
Model for the participation of quasi-palindromic DNA sequences in frameshift mutation
description
1982 nî lūn-bûn
@nan
1982年の論文
@ja
1982年学术文章
@wuu
1982年学术文章
@zh-cn
1982年学术文章
@zh-hans
1982年学术文章
@zh-my
1982年学术文章
@zh-sg
1982年學術文章
@yue
1982年學術文章
@zh
1982年學術文章
@zh-hant
name
Model for the participation of quasi-palindromic DNA sequences in frameshift mutation
@ast
Model for the participation of quasi-palindromic DNA sequences in frameshift mutation
@en
type
label
Model for the participation of quasi-palindromic DNA sequences in frameshift mutation
@ast
Model for the participation of quasi-palindromic DNA sequences in frameshift mutation
@en
prefLabel
Model for the participation of quasi-palindromic DNA sequences in frameshift mutation
@ast
Model for the participation of quasi-palindromic DNA sequences in frameshift mutation
@en
P2860
P356
P1476
Model for the participation of quasi-palindromic DNA sequences in frameshift mutation
@en
P2093
P2860
P304
P356
10.1073/PNAS.79.13.4128
P407
P577
1982-07-01T00:00:00Z