| scholarly article | Q13442814 |
| P819 | ADS bibcode | 1984PNAS...81..512G |
| P356 | DOI | 10.1073/PNAS.81.2.512 |
| P932 | PMC publication ID | 344708 |
| P698 | PubMed publication ID | 6582506 |
| P5875 | ResearchGate publication ID | 16612820 |
| P2093 | author name string | Glickman BW | |
| Ripley LS | |||
| P2860 | cites work | ON THE TOPOGRAPHY OF THE GENETIC FINE STRUCTURE | Q24644905 |
| The structure and evolution of the human beta-globin gene family | Q29618222 | ||
| Frameshift mutations and the genetic code. This paper is dedicated to Professor Theodosius Dobzhansky on the occasion of his 66th birthday | Q34229913 | ||
| cDNA sequence of a new chicken embryonic rho-globin | Q35454319 | ||
| Template-directed pausing in in vitro DNA synthesis by DNA polymerase a from Drosophila melanogaster embryos | Q36281358 | ||
| Cloning of adeno-associated virus into pBR322: rescue of intact virus from the recombinant plasmid in human cells | Q36288360 | ||
| Mutational specificity of UV light in Escherichia coli: indications for a role of DNA secondary structure | Q36302324 | ||
| Model for the participation of quasi-palindromic DNA sequences in frameshift mutation | Q36302363 | ||
| Studies on the mechanism of enzymatic DNA elongation by Escherichia coli DNA polymerase II. | Q39396194 | ||
| Deletions and DNA rearrangements within the transposable DNA element IS2. A model for the creation of palindromic DNA by DNA repair synthesis | Q40482880 | ||
| DNA Sequence of the mini-insertion IS2–6 and its relation to the sequence of IS2 | Q40947684 | ||
| Genetic studies of the lac repressor. VII. On the molecular nature of spontaneous hotspots in the lacI gene of Escherichia coli | Q41008292 | ||
| Complete nucleotide sequence of an influenza virus haemagglutinin gene from cloned DNA | Q41541813 | ||
| Identification of a structural hairpin in the filamentous chimeric phage M13Gori1 | Q44647841 | ||
| Nucleotide sequence of the lysozyme gene of bacteriophage T4. Analysis of mutations involving repeated sequences | Q48399057 | ||
| Comparison of Total Sequence of a Cloned Rabbit β-Globin Gene and Its Flanking Regions with a Homologous Mouse Sequence | Q48414889 | ||
| Recombination between short DNA homologies causes tandem duplication. | Q54533116 | ||
| On the formation of spontaneous deletions: The importance of short sequence homologies in the generation of large deletions | Q56521354 | ||
| Cruciform structures in supercoiled DNA | Q59049726 | ||
| In vivo consequences of plasmid topology | Q59085240 | ||
| DNA structure and gene regulation | Q67260763 | ||
| Unique self-complementarity of palindromic sequences provides DNA structural intermediates for mutation | Q70262252 | ||
| Mutator versus antimutator activity of a T4 DNA polymerase mutant distinguishes two different frameshifting mechanisms | Q70903751 | ||
| Molecular mechanisms of nucleotide-sequences rearrangement in cDNA clones of human fibroblast interferon mRNA | Q72649620 | ||
| Instability of palindromic DNA in Escherichia coli | Q72911645 | ||
| T4 endonuclease VII cleaves holliday structures | Q72949848 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 512-516 | |
| P577 | publication date | 1984-01-01 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Structural intermediates of deletion mutagenesis: a role for palindromic DNA | |
| P478 | volume | 81 |
| Q42280286 | A 140-bp-Long Palindromic Sequence Induces Double-Strand Breaks During Meiosis in the Yeast Saccharomyces cerevisiae |
| Q54403108 | A coding RNA segment that enhances the ribosomal recruitment of chicken ccn1 mRNA. |
| Q41348516 | A hotspot for novel amplification joints in a mosaic of Alu-like repeats and palindromic A + T-rich DNA. |
| Q40535788 | A mechanism for deletion formation in DNA by human cell extracts: the involvement of short sequence repeats |
| Q33635836 | Alternative DNA structure formation in the mutagenic human c-MYC promoter |
| Q50464071 | Analysis of chloroplast promoters using bidirectional transcription vectors |
| Q36305477 | Analysis of plasmid deletional instability in Bacillus subtilis |
| Q69251959 | Analysis of structural and biological parameters affecting plasmid deletion formation in Bacillus subtilis |
| Q35619388 | Apparent and real recombination frequencies in multicopy plasmids: the need for a novel approach in frequency determination |
| Q54762750 | Asymmetric cytosine deamination revealed by spontaneous mutational specificity in an Ung- strain of Escherichia coli. |
| Q37480732 | Base substitutions, frameshifts, and small deletions constitute ionizing radiation-induced point mutations in mammalian cells |
| Q40819665 | Breakage--reunion and copy choice mechanisms of recombination between short homologous sequences |
| Q36438389 | C1 inhibitor gene sequence facilitates frameshift mutations |
| Q33953906 | Changes in DNA base sequence induced by gamma-ray mutagenesis of lambda phage and prophage |
| Q43523106 | Characterization of putative membrane protein genes of the 'Candidatus Phytoplasma asteris', chrysanthemum yellows isolate |
| Q33245667 | Chromosomal deletion and rearrangement in Streptomyces glaucescens |
| Q35626219 | Cloning and characterization of the region III flagellar operons of the four Shigella subgroups: genetic defects that cause loss of flagella of Shigella boydii and Shigella sonnei |
| Q64390072 | Cluster of point mutations predetermined by a quasipalindromic nucleotide sequence in plasmid pBR322 DNA |
| Q72286532 | Contiguous deletion and duplication mutations resulting in type 1 hereditary angioneurotic edema |
| Q52546083 | DNA base sequence changes induced by diethyl sulfate in postmeiotic male germ cells of Drosophila melanogaster. |
| Q37051064 | DNA secondary structures: stability and function of G-quadruplex structures |
| Q54765345 | DNA sequence analysis of spontaneous mutation in a PolA1 strain of Escherichia coli indicates sequence-specific effects. |
| Q40658984 | DNA sequence analysis of spontaneous mutations at the aprt locus of hamster cells |
| Q72089392 | Deletion between direct repeats in bacteriophage T7 gene 1.2 |
| Q36125840 | Deletion mutagenesis independent of recombination in bacteriophage T7 |
| Q36676852 | Deletion of the UL4 gene sequence of equine herpesvirus 1 precludes the generation of defective interfering particles |
| Q33957696 | Deletions in plasmid pBR322: replication slippage involving leading and lagging strands |
| Q35591486 | Differential DNA secondary structure-mediated deletion mutation in the leading and lagging strands |
| Q34616458 | Dissecting the fidelity of bacteriophage RB69 DNA polymerase: site-specific modulation of fidelity by polymerase accessory proteins |
| Q34245117 | Down-regulation of the antisense mitochondrial non-coding RNAs (ncRNAs) is a unique vulnerability of cancer cells and a potential target for cancer therapy |
| Q42146770 | Endonuclease VII resolves Y-junctions in branched DNA in vitro |
| Q42132539 | Evidence for two mechanisms of palindrome-stimulated deletion in Escherichia coli: single-strand annealing and replication slipped mispairing. |
| Q48073230 | Evolution of a repeat sequence in the parathyroid hormone-related peptide gene in primates |
| Q48383539 | Evolution of two actin genes in the sea urchin Strongylocentrotus franciscanus |
| Q41948688 | Expression of a novel non-coding mitochondrial RNA in human proliferating cells. |
| Q69705868 | Extremely large chromosomal deletions are intimately involved in genetic instability and genomic rearrangements in Streptomyces glaucescens |
| Q34604021 | Factors affecting inverted repeat stimulation of recombination and deletion in Saccharomyces cerevisiae |
| Q33888422 | Filler DNA is associated with spontaneous deletions in maize |
| Q36105241 | Formation of large deletions by illegitimate recombination in the HPRT gene of primary human fibroblasts |
| Q36568343 | Frameshift intermediates in homopolymer runs are removed efficiently by yeast mismatch repair proteins |
| Q37399577 | Frameshift mutations produced by proflavin in bacteriophage T4: specificity within a hotspot |
| Q71265030 | Gene conversion as a focusing mechanism for correlated mutations: a hypothesis |
| Q41182021 | Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment |
| Q37688594 | Generation of a dominant 8-MDa deletion at the left terminus of vaccinia virus DNA |
| Q69355202 | Genetic deletions between directly repeated sequences in bacteriophage T7 |
| Q41886362 | Genetic instability within monotonous runs of CpG sequences in Escherichia coli |
| Q35579976 | Hemophilia B (factor IXSeattle 2) due to a single nucleotide deletion in the gene for factor IX. |
| Q74697501 | High and low UV-dose responses in SOS-induction of the precise excision of transposons tn1, Tn5 and Tn10 in Escherichia coli |
| Q52177319 | Identification of a large region of secondary structure in the 3'-untranslated region of chicken elastin mRNA with implications for the regulation of mRNA stability. |
| Q35197051 | Identification of a splice-site mutation in the aldolase B gene from an individual with hereditary fructose intolerance |
| Q40390619 | Identification of an X-ray induced deletion mutant flanked by direct repeats |
| Q83820790 | Identification of secondary structure in the 5'-untranslated region of the human adrenomedullin mRNA with implications for the regulation of mRNA translation |
| Q35605677 | Illegitimate recombination at the replication origin of bacteriophage M13. |
| Q40555599 | Illegitimate recombination in the histone multigenic family generates circular DNAs in Drosophila embryos |
| Q33552539 | Illegitimate recombination induced by benzo[a]pyrene diol epoxide in Escherichia coli |
| Q54619398 | In vivo cloning of a carboxy-terminal rpoB allele which confers altered transcriptional properties. |
| Q48899776 | Influence of nucleotide excision repair and of dose on the types of vermilion mutations induced by diethyl sulfate in postmeiotic male germ cells of Drosophila. |
| Q42963887 | Instability of a plasmid-borne inverted repeat in Saccharomyces cerevisiae |
| Q37096065 | Instability of repetitive DNA sequences: the role of replication in multiple mechanisms |
| Q38684190 | Left-handed Z-DNA and genetic recombination. |
| Q36128701 | Limits to the role of palindromy in deletion formation |
| Q42959914 | Local DNA sequence control of deletion formation in Escherichia coli plasmid pBR322. |
| Q34608413 | Long inverted repeats are an at-risk motif for recombination in mammalian cells |
| Q39452796 | Long palindromic sequences induce double-strand breaks during meiosis in yeast. |
| Q82667285 | Long sequence duplications, repeats, and palindromes in HIV-1 gp120: length variation in V4 as the product of misalignment mechanism |
| Q53670055 | Looking backward on a century of mutation research. |
| Q40762839 | Loss of critical palindromic transgene promoter sequence in chemically induced Tg.AC mouse skin papillomas expressing transgene-derived mRNA. |
| Q34278779 | Mitochondrial DNA deletions are associated with non-B DNA conformations |
| Q44076843 | Molecular aspects of genetic instability of an artificial 68 bp perfect palindrome in Escherichia coli |
| Q34514876 | Molecular characteristics of spontaneous deletions in the hyperthermophilic archaeon Sulfolobus acidocaldarius |
| Q36835999 | Molecular characterization of 15 rearrangements among 90 human in vivo somatic mutants shows that deletions predominate |
| Q33287807 | Multiple homoplasious insertions and deletions of a Triticeae (Poaceae) DNA transposon: a phylogenetic perspective |
| Q22254326 | Multiple mutations and frameshifts are the hallmark of defective hPMS2 in pZ189-transfected human tumor cells |
| Q40486494 | Multiple pathways of deletion formation in Escherichia coli |
| Q57011519 | Mutational spectra at the hypoxanthine–guanine phosphoribosyltransferase (HPRT) locus in T-lymphocytes of nonsmoking and smoking lung cancer patients |
| Q41875983 | Nearest neighbor affects G:C to A:T transitions induced by alkylating agents |
| Q24611196 | Non-B DB: a database of predicted non-B DNA-forming motifs in mammalian genomes |
| Q34473652 | Non-B DNA structure-induced genetic instability and evolution |
| Q64897533 | Noncanonical secondary structures arising from non-B DNA motifs are determinants of mutagenesis. |
| Q74181220 | Novel deletional mutation of the MEN 1 gene in a kindred with multiple endocrine neoplasia type 1 |
| Q35496410 | 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. |
| Q36902758 | Nucleotide sequence and structural features of a novel US-a junction present in a defective herpes simplex virus genome. |
| Q58998172 | Palindromic sequences in heteroduplex DNA inhibit mismatch repair in yeast |
| Q54244726 | Participation of the SOS system in producing deletions in E. coli plasmids |
| Q33952719 | Patterns of somatic mutations in immunoglobulin variable genes |
| Q33273876 | Plastidic trnFUUC pseudogenes in North American genus Boechera (Brassicaceae): mechanistic aspects of evolution. |
| Q34604333 | Plastome mutator-induced alterations arise in Oenothera chloroplast DNA through template slippage |
| Q28333820 | Potential DNA slippage structures acquired during evolutionary divergence of Acinetobacter calcoaceticus chromosomal benABC and Pseudomonas putida TOL pWW0 plasmid xylXYZ, genes encoding benzoate dioxygenases |
| Q54693237 | Preferential DNA secondary structure mutagenesis in the lagging strand of replication in E. coli |
| Q68914922 | Protein engineering and site-directed mutagenesis. Patents and literature |
| Q36483459 | RETRACTED: In vivo and in vitro evidence for slipped mispairing in mammalian mitochondria |
| Q41824013 | RecA-dependent increased precise excision of Tn10 in Salmonella typhimurium |
| Q74669213 | RecBC and RecF recombination pathways and the induced precise excision of Tn10 in Escherichia coli |
| Q54625080 | Recombination between repeats in Escherichia coli by a recA-independent, proximity-sensitive mechanism. |
| Q33924800 | Recombination resulting in unusual features in the polyomavirus genome isolated from a murine tumor cell line. |
| Q36365130 | Regulatory region of the divergent Klebsiella pneumoniae lac operon |
| Q35221861 | Replication errors may contribute to the generation of large deletions and duplications in the dystrophin gene |
| Q31058320 | Role of direct repeat and stem-loop motifs in mtDNA deletions: cause or coincidence? |
| Q40470860 | S1-sensitive sites in the supercoiled double-stranded form of tomato golden mosaic virus DNA component B: identification of regions of potential alternative secondary structure and regulatory function. |
| Q41552163 | Selection for spontaneous null mutations in a chromosomally-integrated HSV-1 thymidine kinase gene yields deletions and a mutation caused by intragenic illegitimate recombination |
| Q40112244 | Sequence specificities in the interactions of chemicals and radiations with DNA. |
| Q37540329 | Sequence-directed mutagenesis: evidence from a phylogenetic history of human alpha-interferon genes |
| Q33962893 | Sequences with the potential to form stem-and-loop structures are associated with coding-region duplications in animal mitochondrial DNA. |
| Q49606909 | Short inverted repeats contribute to localized mutability in human somatic cells |
| Q34045705 | 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 function |
| Q48345437 | Specificity of bacteriophage Mu excision |
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| Q33574499 | Spectrum of spontaneous mutation at the APRT locus of Chinese hamster ovary cells: an analysis at the DNA sequence level |
| Q69443581 | Spectrum of spontaneous mutations in a cDNA of the human hprt gene integrated in chromosomal DNA |
| Q36272882 | Spontaneous and mutagen-induced deletions: mechanistic studies in Salmonella tester strain TA102 |
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| Q37608909 | Spontaneous deletion formation within the beta-galactosidase gene of Lactobacillus bulgaricus |
| Q33952945 | Spontaneous microdeletions and microinsertions in a transgenic mouse mutation detection system: analysis of age, tissue, and sequence specificity |
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| Q48160126 | Structural analysis of length mutations in a hot-spot region of wheat chloroplast DNAs |
| Q70403332 | Structural plasmid instability in Bacillus subtilis: effect of direct and inverted repeats |
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| Q41106861 | Study of arsenic mutagenesis using the plasmid shuttle vector pZ189 propagated in DNA repair proficient human cells |
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| Q33964465 | The cross-linking agent hexamethylphosphoramide predominantly induces intra-locus and multi-locus deletions in postmeiotic germ cells of Drosophila. |
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| Q41170350 | The factor IX gene as a model for analysis of human germline mutations: an update |
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