| scholarly article | Q13442814 |
| P356 | DOI | 10.1101/SQB.1966.031.01.014 |
| P698 | PubMed publication ID | 5237214 |
| P2093 | author name string | Tsugita A | |
| Okada Y | |||
| Newton J | |||
| Inouye M | |||
| Streisinger G | |||
| Emrich J | |||
| Terzaghi E | |||
| P304 | page(s) | 77-84 | |
| P577 | publication date | 1966-01-01 | |
| P1433 | published in | Cold Spring Harbor Symposia on Quantitative Biology | Q15758412 |
| P1476 | title | Frameshift mutations and the genetic code. This paper is dedicated to Professor Theodosius Dobzhansky on the occasion of his 66th birthday | |
| P478 | volume | 31 |
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| Q34606865 | Genetic factors affecting the impact of DNA polymerase delta proofreading activity on mutation avoidance in yeast. |
| Q41886362 | Genetic instability within monotonous runs of CpG sequences in Escherichia coli |
| Q24670186 | Genetic reconstruction of individual colorectal tumor histories |
| Q33993026 | Genetic studies of acridine-induced mutants in Streptococcus pneumoniae |
| Q34509955 | Genetic variation in the Vibrio vulnificus group 1 capsular polysaccharide operon |
| Q35560459 | Genetics and molecular biology of telomeres |
| Q35855629 | Genome Sequence of African Swine Fever Virus BA71, the Virulent Parental Strain of the Nonpathogenic and Tissue-Culture Adapted BA71V. |
| Q37943542 | Genome rearrangement and genetic instability in Streptomyces spp |
| Q36627910 | Genome-wide analysis of the specificity and mechanisms of replication infidelity driven by imbalanced dNTP pools. |
| Q46049171 | Genomic instability in repeated sequences is an early somatic event in colorectal tumorigenesis that persists after transformation |
| Q47942439 | Genomic rearrangements in the CFTR gene: extensive allelic heterogeneity and diverse mutational mechanisms |
| Q34983022 | Genotoxicity of 2-nitro-7-methoxy-naphtho[2,1-b]furan (R7000): a case study with some considerations on nitrofurantoin and nifuroxazide |
| Q80231263 | Genotyping of simple sequence repeats--factors implicated in shadow band generation revisited |
| Q37010270 | Germ-line mutations of the APC gene in 53 familial adenomatous polyposis patients |
| Q33938826 | Germline BHD-mutation spectrum and phenotype analysis of a large cohort of families with Birt-Hogg-Dubé syndrome |
| Q39136621 | Glutamine Synthetase Induction in Embryonic Neural Retina Interactions of Receptor-Hydrocortisone Complexes with Cell Nuclei |
| Q34743394 | Hairpin properties of single-stranded DNA containing a GC-rich triplet repeat: (CTG)15. |
| Q44419286 | Headwaters of the zebrafish -- emergence of a new model vertebrate |
| Q74127581 | Hemoglobin Phnom Penh [alpha117Phe(H1)-Ile-alpha118Thr(H2)]; evidence for a hotspot for insertion of residues in the third exon of the alpha1-globin gene |
| Q35988146 | Hemoglobin Wayne: a frameshift mutation detected in human hemoglobin alpha chains |
| Q35579976 | Hemophilia B (factor IXSeattle 2) due to a single nucleotide deletion in the gene for factor IX. |
| Q37062526 | Heteroduplex deoxyribonucleic acid base mismatch repair in bacteria |
| Q28762138 | Heterogeneous AVPR2 gene mutations in congenital nephrogenic diabetes insipidus |
| Q40388905 | High frequencies of short frameshifts in poly-CA/TG tandem repeats borne by bacteriophage M13 in Escherichia coli K-12. |
| Q24533135 | High frequency repeat-induced point mutation (RIP) is not associated with efficient recombination in Neurospora |
| Q36556609 | High-frequency illegitimate integration of transfected DNA at preintegrated target sites in a mammalian genome |
| Q36901646 | Highly mutable sites for ICR-170-induced frameshift mutations are associated with potential DNA hairpin structures: studies with SUP4 and other Saccharomyces cerevisiae genes |
| Q34964296 | Highly mutagenic replication by DNA polymerase V (UmuC) provides a mechanistic basis for SOS untargeted mutagenesis |
| Q48405786 | Homocopolymer sequences in the spacer of a sea urchin histone gene repeat are sensitive to S1 nuclease |
| Q73093633 | Homonucleotide tracts, short repeats and CpG/CpNpG motifs are frequent sites for heterogeneous mutations in the neurofibromatosis type 1 (NF1) tumour-suppressor gene |
| Q24792585 | Homopolymer tract length dependent enrichments in functional regions of 27 eukaryotes and their novel dependence on the organism DNA (G+C)% composition |
| Q24670499 | Human DNA polymerase kappa uses template-primer misalignment as a novel means for extending mispaired termini and for generating single-base deletions |
| Q34055705 | Human base excision repair creates a bias toward -1 frameshift mutations |
| Q41125504 | Human immunodeficiency virus type 1 reverse transcriptase and early events in reverse transcription |
| Q36814219 | Human polymerase kappa uses a template-slippage deletion mechanism, but can realign the slipped strands to favour base substitution mutations over deletions |
| Q36278152 | Hydrophobic core repacking and aromatic-aromatic interaction in the thermostable mutant of T4 lysozyme Ser 117-->Phe |
| Q36568353 | Hypermutability of homonucleotide runs in mismatch repair and DNA polymerase proofreading yeast mutants. |
| Q29541254 | Hypervariabflity of simple sequences as a general source for polymorphic DNA markers |
| Q33768667 | ICR-Induced Frameshift Mutations in the Histidine Operon of Salmonella |
| Q37138530 | Identification and characterization of a -1 reading frameshift in the heavy chain constant region of an IgG1 recombinant monoclonal antibody produced in CHO cells |
| Q38629504 | Identification of Nine New RAI1-Truncating Mutations in Smith-Magenis Syndrome Patients without 17p11.2 Deletions |
| Q24677160 | Identification of a frameshift mutation responsible for the silent phenotype of human serum cholinesterase, Gly 117 (GGT----GGAG) |
| Q28364152 | Identification of a mutant DNA polymerase delta in Saccharomyces cerevisiae with an antimutator phenotype for frameshift mutations |
| Q71937474 | Identification of a novel mutation causing aspartylglucosaminuria reveals a mutation hotspot region in the aspartylglucosaminidase gene |
| Q21261447 | Identification of the first intragenic deletion of the PITX2 gene causing an Axenfeld-Rieger Syndrome: case report |
| Q36206645 | Illegitimate recombination in an Escherichia coli plasmid: modulation by DNA damage and a new bacterial gene |
| Q41022147 | Impaired secretion of the elongated mutant of protein C (protein C-Nagoya). Molecular and cellular basis for hereditary protein C deficiency |
| Q54543256 | Implications of mismatch repair genes hMLH1 and hMSH2 in patients with sporadic renal cell carcinoma. |
| Q39716950 | In vitro expansion of GGC:GCC repeats: identification of the preferred strand of expansion. |
| Q33811519 | In vivo analysis of human T-cell leukemia virus type 1 reverse transcription accuracy |
| Q41432638 | In vivo transfer of genetic information between gram-positive and gram-negative bacteria |
| Q36175010 | Increased binding of ethidium bromide to polynucleotide duplexes containing mismatched bases |
| Q33782815 | Increased misincorporation fidelity observed for nucleoside analog resistance mutations M184V and E89G in human immunodeficiency virus type 1 reverse transcriptase does not correlate with the overall error rate measured in vitro |
| Q39455847 | Increased rates of genomic deletions generated by mutations in the yeast gene encoding DNA polymerase delta or by decreases in the cellular levels of DNA polymerase delta |
| Q66905310 | Increased spontaneous reversion of certain frameshift mutations in DNA polymerase I deficient strains of Escherichia coli |
| Q40316233 | Inducible repair systems and their implications for toxicology |
| Q43715473 | Induction of -2 frameshift mutations by 2-nitrofluorene, N-hydroxyacetylaminofluorene, and N-2-acetylaminofluorene in reversion assays in Escherichia coli strains differing in permeability and acetyltransferase activity |
| Q68203593 | Induction of mutations in the zebrafish with ultraviolet light |
| Q54564238 | Influence of nucleotide excision repair of Escherichia coli on radiation-induced mutagenesis of double-stranded M13 DNA. |
| Q35174364 | Inhibitors of HIV-1 reverse transcriptase and fidelity of in vitro DNA replication |
| Q38685600 | Insertion-and-deletion-derived tumour-specific neoantigens and the immunogenic phenotype: a pan-cancer analysis |
| Q35065478 | Insights into mutagenesis using Escherichia coli chromosomal lacZ strains that enable detection of a wide spectrum of mutational events. |
| Q37096065 | Instability of repetitive DNA sequences: the role of replication in multiple mechanisms |
| Q40655124 | Instability of simple sequence DNA in Saccharomyces cerevisiae |
| Q72727302 | Interacalation of ethidium ion into DNA and RNA oligonucleotides |
| Q31777720 | Interacting fidelity defects in the replicative DNA polymerase of bacteriophage RB69. |
| Q36355441 | Interaction and sequence diversity among T15 VH genes in CBA/J mice |
| Q39676094 | Interaction of acridine drugs with DNA and nucleotides |
| Q47581991 | Interaction of nick-directed DNA mismatch repair and loop repair in human cells |
| Q28652237 | Interaction-based evolution: how natural selection and nonrandom mutation work together |
| Q52684632 | Interactions of molecules with nucleic acids. XI. Generalization of techniques to generate nucleic acid structures with applications to intercalation sites and kinked structures. |
| Q68580138 | Intercalation into DNA |
| Q35829037 | Internal eliminated sequences are removed prior to chromosome fragmentation during development in Euplotes crassus |
| Q35763815 | Intestinal stem cell division and genetic diversity. A computer and experimental analysis. |
| Q57263800 | Intrachromosomal serial replication slippage intransgives rise to diverse genomic rearrangements involving inversions |
| Q33993172 | Intragenic suppression at the b2 locus in Ascobolus immersus. I. Identification of three distinct groups of suppression |
| Q50144014 | Involvement of umuDCST genes in nitropyrene-induced -CG frameshift mutagenesis at the repetitive CG sequence in the hisD3052 allele of Salmonella typhimurium. |
| Q38812569 | Isolating Escherichia coli strains for recombinant protein production |
| Q33772092 | Isolation and characterization of koi herpesvirus (KHV) from Indonesia: identification of a new genetic lineage. |
| Q41667440 | Kinds and locations of mutations arising spontaneously in the coding region of theHPRT gene of finite-life-span diploid human fibroblasts |
| Q71778278 | Kinetic and hydrodynamic studies of the complex of proflavine with poly A·poly U |
| Q35928339 | Kinking of DNA and RNA helices by bulged nucleotides observed by fluorescence resonance energy transfer |
| Q50513019 | LacI mutation spectra following benzo[a]pyrene treatment of Big Blue mice. |
| Q33958118 | Length and sequence variation in evening bat D-loop mtDNA. |
| Q35564351 | Length heterogeneity of a conserved displacement-loop sequence in human mitochondrial DNA. |
| Q24623930 | Lessons from the lysozyme of phage T4 |
| Q68695212 | Letter: Letter: Nucleotide distribution in bacterial DNA's differing in G plus C content |
| Q36549744 | Ligase-Defective Bacteriophage T4 I. Effects on Mutation Rates |
| 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. |
| Q34703806 | Low Activity of β-Galactosidase in Frameshift Mutants of Escherichia coli |
| Q43937118 | Low fidelity DNA synthesis by a y family DNA polymerase due to misalignment in the active site. |
| Q36740110 | Low-fidelity DNA synthesis by human DNA polymerase theta. |
| Q29619994 | Lower in vivo mutation rate of human immunodeficiency virus type 1 than that predicted from the fidelity of purified reverse transcriptase |
| Q89870636 | Machine learning of reverse transcription signatures of variegated polymerases allows mapping and discrimination of methylated purines in limited transcriptomes |
| Q27320576 | Mathematical and live meningococcal models for simple sequence repeat dynamics - coherent predictions and observations |
| Q70471224 | Mechanism of gene conversion in Ascobolus immersus. II. The relationships between the genetic alterations in b 1 or b 2 mutants and their conversion spectrum |
| Q36975128 | Mechanisms for human genomic rearrangements |
| Q39933360 | Mechanisms of Suppression |
| Q42044589 | Mechanisms of dinucleotide repeat instability in Escherichia coli |
| Q36319705 | Mechanisms of glycosylase induced genomic instability |
| Q57263975 | Mechanisms of insertional mutagenesis in human genes causing genetic disease |
| Q41252829 | Mechanisms of mutagenesis |
| Q33663239 | Mechanisms of mutagenesis in the Escherichia coli mutator mutD5: role of DNA mismatch repair |
| Q33692291 | Mechanisms of mutation in nondividing cells. Insights from the study of adaptive mutation in Escherichia coli |
| Q41879395 | Mechanisms of spontaneous and induced frameshift mutation in bacteriophage T4. |
| Q30912512 | Mechanistic aspects of CoII(HAPP)(TFA)2 in DNA bulge-specific recognition. |
| Q57263803 | Meta-Analysis of gross insertions causing human genetic disease: Novel mutational mechanisms and the role of replication slippage |
| Q57263827 | Meta-analysis of indels causing human genetic disease: mechanisms of mutagenesis and the role of local DNA sequence complexity |
| Q36184519 | Methyl-directed repair of frameshift heteroduplexes in cell extracts from Escherichia coli |
| Q33970339 | Microsatellite Instability in Yeast: Dependence on the Length of the Microsatellite |
| Q34723085 | Microsatellite instability and its relevance to cutaneous tumorigenesis |
| Q40022200 | Microsatellite instability in yeast: dependence on repeat unit size and DNA mismatch repair genes |
| Q44602861 | Microsatellite instability: the mutator that mutates the other mutator |
| Q37524598 | Microsatellite spreading in the human genome: evolutionary mechanisms and structural implications |
| Q77912101 | Mismatch extension by Escherichia coli DNA polymerase III holoenzyme |
| Q36839000 | Mismatch repair-independent tandem repeat sequence instability resulting from ribonucleotide incorporation by DNA polymerase ε. |
| Q70309830 | Missense and nonsense suppressors derived from a glycine tRNA by nucleotide insertion and deletion in vivo |
| Q41396233 | Mitochondrial acetoacetyl-coenzyme A thiolase gene: a novel 68-bp deletion involving 3' splice site of intron 7, causing exon 8 skipping in a Caucasian patient with beta-ketothiolase deficiency |
| Q41691083 | Mitochondrial genomes of African pangolins and insights into evolutionary patterns and phylogeny of the family Manidae |
| Q59087140 | Molecular Basis of a Mutational Hot Spot in the Lysozyme Gene of Bacteriophage T4 |
| Q34857173 | Molecular analysis of mutations induced at the hisD3052 allele of Salmonella by single chemicals and complex mixtures |
| Q50181372 | Molecular analysis of mutations induced by the intercalating agent ellipticine at the hisD3052 allele of Salmonella typhimurium TA98. |
| Q35197886 | Molecular analysis of the gene of the alpha 1-antitrypsin deficiency variant, Mnichinan |
| Q35661466 | Molecular analysis of type I-A (tyrosinase negative) oculocutaneous albinism |
| Q44076843 | Molecular aspects of genetic instability of an artificial 68 bp perfect palindrome in Escherichia coli |
| Q34572566 | Molecular basis for congenital deficiency of alpha 2-plasmin inhibitor. A frameshift mutation leading to elongation of the deduced amino acid sequence |
| Q70668885 | Molecular basis of type I (tyrosinase-related) oculocutaneous albinism: mutations and polymorphisms of the human tyrosinase gene |
| Q48081369 | Molecular characterization of multilocus deletions at a diploid locus in CHO cells: association with an intracisternal-A particle gene |
| Q37688089 | Molecular cloning and nucleotide sequence of the alpha and beta subunits of allophycocyanin from the cyanelle genome of Cyanophora paradoxa |
| Q34181756 | Molecular defect in siblings with prolidase deficiency and absence or presence of clinical symptoms. A 0.8-kb deletion with breakpoints at the short, direct repeat in the PEPD gene and synthesis of abnormal messenger RNA and inactive polypeptide |
| Q33909484 | Molecular epidemiology of Mycobacterium leprae as determined by structure-neighbor clustering |
| Q44891770 | Molecular evolution of two actin genes from carrot |
| Q35212075 | Molecular instability in the COII-tRNA(Lys) intergenic region of the human mitochondrial genome: multiple origins of the 9-bp deletion and heteroplasmy for expanded repeats. |
| Q33643628 | Molecular mechanisms of chromosomal rearrangement in fungi. |
| Q73457782 | Molecular mechanisms of mutagenesis by aromatic amines and amides |
| Q36464319 | Molecular mechanisms of oncogenic mutations in tumors from patients with bilateral and unilateral retinoblastoma |
| Q37953680 | Molecular mechanisms of oxygen radical carcinogenesis and mutagenesis: the role of DNA base damage |
| Q36019427 | Molecular nature of intrachromosomal deletions and base substitutions induced by environmental mutagens. |
| Q52453196 | Molecular structure of a naturally occurring alcohol dehydrogenase null activity allele in Drosophila melanogaster. |
| Q35763450 | Molecular tumor clocks and dynamic phenotype |
| Q36384107 | Mouse IgA heavy chain gene sequence: implications for evolution of immunoglobulin hinge axons |
| Q54625085 | MucAB but not UmuDC proteins enhance -2 frameshift mutagenesis induced by N-2-acetylaminofluorene at alternating GC sequences. |
| Q48074595 | Mucopolysaccharidosis type IVA: common double deletion in the N-acetylgalactosamine-6-sulfatase gene (GALNS) |
| Q33690962 | Multiple genetic switches spontaneously modulating bacterial mutability |
| Q36268081 | Multiple pathways of duplication formation with and without recombination (RecA) in Salmonella enterica. |
| Q52870975 | Multiple substitutions create biased estimates of divergence times and small increases in the variance to mean ratio. |
| Q37598519 | Mutagen-nucleic acid intercalative binding: structure of a 9-aminoacridine: 5-iodocytidylyl(3'-5')guanosine crystalline complex |
| Q37060983 | Mutagenesis and inducible responses to deoxyribonucleic acid damage in Escherichia coli |
| Q41647461 | Mutagenesis by apurinic sites in normal and ataxia telangiectasia human lymphoblastoid cells |
| Q36072151 | Mutagenesis induced by site specifically placed 4'-hydroxymethyl-4,5',8-trimethylpsoralen adducts |
| Q37553709 | Mutagenesis of the lac promoter region in M13 mp10 phage DNA by 4'-hydroxymethyl-4,5',8-trimethylpsoralen |
| Q40147358 | Mutagenic Effects of Nucleic Acid Modification and Repair Assessed by in Vitro Transcription |
| Q41824083 | Mutagenic spectra arising from replication bypass of the 2,6-diamino-4-hydroxy-N(5)-methyl formamidopyrimidine adduct in primate cells. |
| Q34798628 | Mutagenicity and pausing of HIV reverse transcriptase during HIV plus-strand DNA synthesis |
| Q44290766 | Mutagenicity test system based on a reporter gene assay for short-term detection of mutagens (MutaGen assay). |
| Q55670954 | Mutation analysis of PEX7 in 60 probands with rhizomelic chondrodysplasia punctata and functional correlations of genotype with phenotype |
| Q34465215 | Mutation frequency and spectrum of mutations vary at different chromosomal positions of Pseudomonas putida |
| Q36128650 | Mutation hot spots in yeast caused by long-range clustering of homopolymeric sequences |
| Q33933753 | Mutation spectra in supF: approaches to elucidating sequence context effects |
| Q50153888 | Mutation spectra of Glu-P-1 in Salmonella: induction of hotspot frameshifts and site-specific base substitutions |
| Q39686714 | Mutation spectra of herpes simplex virus type 1 thymidine kinase mutants |
| Q43785142 | Mutation spectrum of spontaneous frameshift revertants in yeast using double-strand gap repair |
| Q40278427 | Mutational dynamics in human tumors confirm the neutral intrinsic instability of the mitochondrial D-loop poly-cytidine repeat |
| Q43165547 | Mutational effects of different LET radiations in rpsL transgenic Arabidopsis |
| Q42913220 | Mutational effects of γ-rays and carbon ion beams on Arabidopsis seedlings |
| Q37264027 | Mutational inactivation of the proapoptotic gene BAX confers selective advantage during tumor clonal evolution |
| Q44770357 | Mutational specificity of a bacteriophage T4 DNA polymerase mutant, mel88. |
| Q54154876 | Mutational specificity of a conditional Escherichia coli mutator, mutD5 |
| Q38146054 | Mutational specificity of alkylating agents and the influence of DNA repair |
| Q41362645 | Mutational specificity of animal cell DNA polymerases |
| Q57011519 | Mutational spectra at the hypoxanthine–guanine phosphoribosyltransferase (HPRT) locus in T-lymphocytes of nonsmoking and smoking lung cancer patients |
| Q53461851 | Mutational spectra in the lacl gene in skin from 7,12-dimethylbenz[a]anthracene-treated and untreated transgenic mice. |
| Q72519717 | Mutational spectrum induced in Saccharomyces cerevisiae by the carcinogen N-2-acetylaminofluorene |
| Q41499457 | Mutational spectrum of ICR-191 at the hprt locus in human lymphoblastoid cells |
| Q71079191 | Mutations and the conformational stability of globular proteins |
| Q33960923 | Mutations in POL1 increase the mitotic instability of tandem inverted repeats in Saccharomyces cerevisiae |
| Q28219681 | Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dubé syndrome |
| Q33842093 | Mutations in the MSH3 gene preferentially lead to deletions within tracts of simple repetitive DNA in Saccharomyces cerevisiae |
| Q73019259 | Mutations in the primer grip region of HIV reverse transcriptase can increase replication fidelity |
| Q41465447 | Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy |
| Q44734045 | Mutations induced by 60Co gamma-irradiation in double-stranded M13 bacteriophage DNA in nitrous-oxide saturated solutions are characterized by a high specificity |
| Q40560826 | Mutations induced by DNA polymerase alpha upon in vitro replication of M13mp8(+) DNA. |
| Q73687941 | Mutations of p53 gene in human colorectal cancer: distinct frameshifts among populations |
| Q54315339 | Mutations produced by DNA polymerase III holoenzyme of Escherichia coli after in vitro synthesis in the absence of single-strand binding protein. |
| Q34919969 | Mutator phenotypes due to DNA replication infidelity. |
| Q70903751 | Mutator versus antimutator activity of a T4 DNA polymerase mutant distinguishes two different frameshifting mechanisms |
| Q55016019 | Muver, a computational framework for accurately calling accumulated mutations. |
| Q49874388 | Mycoplasma genitalium non-adherent phase variants arise by multiple mechanisms and escape antibody-dependent growth inhibition |
| Q34243740 | N-terminal domains of human DNA polymerase lambda promote primer realignment during translesion DNA synthesis. |
| Q36799068 | NMR data show that the carcinogen N-2-acetylaminofluorene stabilises an intermediate of -2 frameshift mutagenesis in a region of high mutation frequency |
| Q40401950 | NMR evidence of the stabilisation by the carcinogen N-2-acetylaminofluorene of a frameshift mutagenesis intermediate |
| Q35038542 | Natural history of transposition in the green alga Chlamydomonas reinhardtii: use of the AMT4 locus as an experimental system |
| Q32140481 | Nature of mutation in the human hprt gene following in vivo exposure to ionizing radiation of cesium-137. |
| Q35158302 | Nature of the hisD3018 frameshift mutation in Salmonella typhimurium |
| Q33681371 | Neurofibromatosis type 1 (NF1): a protein truncation assay yielding identification of mutations in 73% of patients |
| Q34718318 | Nicks 3' or 5' to AP sites or to mispaired bases, and one-nucleotide gaps can be sealed by T4 DNA ligase |
| Q36919036 | Nonhomologous recombination in the parvovirus chromosome: role for a CTATTTCT motif |
| Q74127812 | Novel 5 bp germline deletion in exon 11 of the BRCA1 gene |
| Q28763558 | Novel inherited mutations and variable expressivity of BRCA1 alleles, including the founder mutation 185delAG in Ashkenazi Jewish families |
| Q39716728 | Nucleotide Sequence of Human β Globin Messenger RNA |
| Q40707350 | Nucleotide insertion and primer extension at abasic template sites in different sequence contexts. |
| Q24817042 | Nucleotide modification at the gamma-phosphate leads to the improved fidelity of HIV-1 reverse transcriptase. |
| Q35542181 | Nucleotide sequence changes in thymidine kinase gene of herpes simplex virus type 2 clones from an isolate of a patient treated with acyclovir |
| Q48396847 | Nucleotide sequence of Escherichia coli pabA and its evolutionary relationship to trp (G) D |
| Q40463463 | Nucleotide sequence of Marchantia polymorpha chloroplast DNA: a region possibly encoding three tRNAs and three proteins including a homologue of E. coli ribosomal protein S14 |
| Q40489915 | Nucleotide sequence of the genetically labile repeated elements 5′ to the origin of mouse rRNA transcription |
| Q48345419 | Nucleotide sequence of the kanamycin resistance determinant of the pneumococcal transposon Tn1545: evolutionary relationships and transcriptional analysis of aphA-3 genes |
| Q36905981 | Nucleotide sequence of the vaccinia virus thymidine kinase gene and the nature of spontaneous frameshift mutations |
| Q36061920 | Nucleotide sequences of chimpanzee MHC class I alleles: evidence for trans-species mode of evolution |
| Q34635579 | O-antigen structural variation: mechanisms and possible roles in animal/plant-microbe interactions |
| Q33958860 | On the deletion of inverted repeated DNA in Escherichia coli: effects of length, thermal stability, and cruciform formation in vivo |
| Q70246357 | On the fidelity of DNA replication. Mechanisms of misincorporation by intercalating agents |
| Q33966750 | Opposing roles of the holliday junction processing systems of Escherichia coli in recombination-dependent adaptive mutation |
| Q33955188 | Palindromy and the location of deletion endpoints in Escherichia coli |
| Q33952719 | Patterns of somatic mutations in immunoglobulin variable genes |
| Q33405466 | PeakSeeker: a program for interpreting genotypes of mononucleotide repeats |
| Q35860526 | Peptide nucleic acid-targeted mutagenesis of a chromosomal gene in mouse cells |
| Q42028717 | Persistence of tandem arrays: implications for satellite and simple-sequence DNAs. |
| Q36139867 | Perspective on mutagenesis and repair: the standard model and alternate modes of mutagenesis |
| Q27732119 | Perturbation of Trp 138 in T4 lysozyme by mutations at Gln 105 used to correlate changes in structure, stability, solvation, and spectroscopic properties |
| Q39878061 | Phenotypic and genetic analysis of Lymantria dispar nucleopolyhedrovirus few polyhedra mutants: mutations in the 25K FP gene may be caused by DNA replication errors. |
| Q39951144 | Phosphate regulon in members of the family Enterobacteriaceae: comparison of the phoB-phoR operons of Escherichia coli, Shigella dysenteriae, and Klebsiella pneumoniae |
| Q40936615 | Photodynamic effects of dyes on bacteria. I. Mutagenesis by acridine orange in the dark in excision- and recombination-deficient strains of Escherichia coli |
| Q38563589 | Phylogenetic analysis of DNA length mutations in a repetitive region of the Hawaiian Drosophila yolk protein gene Yp2. |
| Q34482326 | Phylogenetic fate mapping |
| Q24805812 | Poly: a quantitative analysis tool for simple sequence repeat (SSR) tracts in DNA |
| Q86871027 | Polycyclic aromatic hydrocarbon concentrations, mutagenicity, and Microtox® acute toxicity testing of Peruvian crude oil and oil-contaminated water and sediment |
| Q57259961 | Polymorphism at the Hor 1 locus of barley (Hordeum vulgare L.) |
| Q48082107 | Polymorphism of the beta-globin region in apes: implications for the origin of human haplotypes. |
| Q47951603 | Pooled analysis of p53 mutations in hematological malignancies |
| Q71059980 | Possible mechanism for transition of viral RNA from polysome to replication complex |
| Q39656167 | Potentiation of the mutagenicity and recombinagenicity of bleomycin in yeast by unconventional intercalating agents |
| Q39972127 | Powerful mutator activity of the polA1 mutation within the histidine region of Escherichia coli K-12. |
| Q24629471 | Predicting DNA duplex stability from the base sequence |
| Q54693237 | Preferential DNA secondary structure mutagenesis in the lagging strand of replication in E. coli |
| Q34708963 | Preferential inhibition by proflavine of the hormonal induction of glutamine synthetase in embryonic neural retina |
| Q46738619 | Preferential occurrence of 1-2 microindels |
| Q54783731 | Probing DNA mismatched and bulged structures by using 19F NMR spectroscopy and oligodeoxynucleotides with an 19F-labeled nucleobase. |
| Q77206910 | Probing immunoglobulin gene hypermutation with microsatellites suggests a nonreplicative short patch DNA synthesis process |
| Q38099632 | Programmed heterogeneity: epigenetic mechanisms in bacteria |
| Q53062576 | Proper functioning of the GINS complex is important for the fidelity of DNA replication in yeast. |
| Q46595699 | Purification and properties of wild-type and exonuclease-deficient DNA polymerase II from Escherichia coli |
| Q51911464 | RAI1 point mutations, CAG repeat variation, and SNP analysis in non-deletion Smith-Magenis syndrome. |
| Q39979344 | RNA Polymerase and the Control of RNA Synthesis |
| Q40493867 | Rat mitochondrial DNA polymorphism: sequence analysis of a hypervariable site for insertions/deletions |
| Q36339832 | Rate and molecular spectrum of spontaneous mutations in the bacterium Escherichia coli as determined by whole-genome sequencing. |
| Q36248697 | Rearranged sequences of a human Kpn I element |
| Q36376072 | Recent Advances in DNA Sequence Analysi |
| Q54625080 | Recombination between repeats in Escherichia coli by a recA-independent, proximity-sensitive mechanism. |
| Q37586298 | Recombination by sequence repeats with formation of suppressive or residual mitochondrial DNA in Neurospora |
| Q44920681 | Reduced frameshift fidelity and processivity of HIV-1 reverse transcriptase mutants containing alanine substitutions in helix H of the thumb subdomain. |
| Q34604145 | Regulation of DNA polymerase exonucleolytic proofreading activity: studies of bacteriophage T4 "antimutator" DNA polymerases |
| Q34675873 | Reiterative dG addition by Euplotes crassus telomerase during extension of non-telomeric DNA. |
| Q35062359 | Relative rates of insertion and deletion mutations in a microsatellite sequence in cultured cells |
| Q33865368 | Removal of frameshift intermediates by mismatch repair proteins in Saccharomyces cerevisiae |
| Q40969083 | Repair of large insertion/deletion heterologies in human nuclear extracts is directed by a 5' single-strand break and is independent of the mismatch repair system |
| Q36839809 | Repair of single-stranded DNA nicks, gaps, and loops in mammalian cells |
| Q39719038 | Replication bypass and mutagenic effect of alpha-deoxyadenosine site-specifically incorporated into single-stranded vectors |
| Q43074239 | Replication bypass of N2-deoxyguanosine interstrand cross-links by human DNA polymerases η and ι. |
| Q35221861 | Replication errors may contribute to the generation of large deletions and duplications in the dystrophin gene |
| Q37621481 | Replication of acetylaminofluorene-adducted plasmids in human cells: spectrum of base substitutions and evidence of excision repair |
| Q36555338 | Replication slippage between distant short repeats in Saccharomyces cerevisiae depends on the direction of replication and the RAD50 and RAD52 genes. |
| Q77322177 | Resolving a fidelity paradox: why Escherichia coli DNA polymerase II makes more base substitution errors in AT- compared with GC-rich DNA |
| Q47783309 | Restoration of In-phase Translation by an Unlinked Suppressor of a Frameshift Mutation in Salmonella typhimurium |
| Q36439044 | Retrovirus variation and reverse transcription: abnormal strand transfers result in retrovirus genetic variation |
| Q36579145 | Reversion of Frameshift Mutations Stimulated by Lesions in Early Function Genes of Bacteriophage T4 |
| Q35913743 | Revertant mosaicism in a human skin fragility disorder results from slipped mispairing and mitotic recombination. |
| Q54442540 | Role of the 5' --> 3' exonuclease and Klenow fragment of Escherichia coli DNA polymerase I in base mismatch repair. |
| Q36687824 | Roles of DNA polymerases in replication, repair, and recombination in eukaryotes. |
| Q47973829 | Roles of the mutagenesis proteins SamA'B and MucA'B in chemically induced frameshift mutagenesis in Salmonella typhimurium hisD3052. |
| Q24554358 | Rsp5, a ubiquitin-protein ligase, is involved in degradation of the single-stranded-DNA binding protein rfa1 in Saccharomyces cerevisiae |
| Q33953638 | SOS mutator DNA polymerase IV functions in adaptive mutation and not adaptive amplification |
| Q36699247 | Saccharomyces cerevisiae RAD5-encoded DNA repair protein contains DNA helicase and zinc-binding sequence motifs and affects the stability of simple repetitive sequences in the genome |
| Q57570711 | Searching Parameter Values in Support Vector Machines Using DNA Genetic Algorithms |
| Q34318015 | Searching for the hereditary causes of renal-cell carcinoma |
| Q66944902 | Sensitivity of premeiotic and meiotic stages to spontaneous and induced mutations in barley and maize |
| Q48067268 | Sequence analysis and allelic designation of the two short tandem repeat loci D18S51 and D8S1179. |
| Q34624183 | Sequence analysis of spontaneous mutations in a shuttle vector gene integrated into mammalian chromosomal DNA |
| Q35815997 | Sequence and exon-intron organization of the DNA encoding the alpha I domain of human spectrin. Application to the study of mutations causing hereditary elliptocytosis |
| Q34610604 | Sequence composition and context effects on the generation and repair of frameshift intermediates in mononucleotide runs in Saccharomyces cerevisiae. |
| Q37420606 | Sequence context-specific mutagenesis and base excision repair |
| Q24657452 | Sequence variation in the Fanconi anemia gene FAA |
| Q37540329 | Sequence-directed mutagenesis: evidence from a phylogenetic history of human alpha-interferon genes |
| Q36949151 | Short Direct Repeats Mediate Spontaneous High-Frequency Deletions in DNA of Minute Virus of Mice |
| Q34286847 | Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene |
| Q36623645 | Simple DNA sequences of Drosophila virilis isolated by screening with RNA. |
| Q33228944 | Simultaneous genotyping of indels and SNPs by mass spectroscopy. |
| Q40566903 | Single base bulges in small RNA hairpins enhance ethidium binding and promote an allosteric transition |
| Q33929734 | Singlet oxygen-induced mutations in M13 lacZ phage DNA |
| Q34656824 | Site-specific targeting of aflatoxin adduction directed by triple helix formation in the major groove of oligodeoxyribonucleotides |
| Q33881162 | Slip into something more functional: selection maintains ancient frameshifts in homopolymeric sequences |
| Q39493764 | Slipped misalignment mechanisms of deletion formation: in vivo susceptibility to nucleases |
| Q59070212 | Slippery DNA and diseases |
| Q53445992 | Somatic frameshift mutations in the BAX gene in colon cancers of the microsatellite mutator phenotype. |
| Q24652779 | Somatic hypermutation introduces insertions and deletions into immunoglobulin V genes |
| Q35798579 | Somatic mitochondrial mutation in gastric cancer |
| Q34472144 | Somatic mosaicism in Fanconi anemia: evidence of genotypic reversion in lymphohematopoietic stem cells. |
| Q57978019 | Somatic mutations in mitochondrial DNA do not associate with nuclear microsatellite instability in gastrointestinal cancer |
| Q48945509 | Somatic mutations of synaptic cadherin (CNR family) transcripts in the nervous system |
| Q50134974 | Sources of spontaneous mutagenesis in bacteria. |
| Q36079605 | Specific binding of o-phenanthroline at a DNA structural lesion |
| Q33200551 | Specific recognition of DNA bulge structure by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry |
| Q67767339 | Specificity of recA441-mediated (tif-1) mutational events |
| Q34604252 | Spectra of spontaneous frameshift mutations at the hisD3052 allele of Salmonella typhimurium in four DNA repair backgrounds |
| Q34343418 | Spectra of spontaneous mutations in Escherichia coli strains defective in mismatch correction: the nature of in vivo DNA replication errors. |
| Q41582295 | Spectrum of spontaneous HPRT- mutations in TK6 human lymphoblasts |
| 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 |
| Q38321193 | Spi(-) selection: An efficient method to detect gamma-ray-induced deletions in transgenic mice |
| Q42628660 | Spontaneous and 9-aminoacridine-induced frameshift mutagenesis: second-site frameshift mutation within the N-terminal region of the lacI gene of Escherichia coli |
| Q70741889 | Spontaneous and induced host-range mutants of cyanophage N-1 |
| Q36272882 | Spontaneous and mutagen-induced deletions: mechanistic studies in Salmonella tester strain TA102 |
| Q34613326 | Spontaneous frameshift mutations in Saccharomyces cerevisiae: accumulation during DNA replication and removal by proofreading and mismatch repair activities. |
| Q33952945 | Spontaneous microdeletions and microinsertions in a transgenic mouse mutation detection system: analysis of age, tissue, and sequence specificity |
| Q33964164 | Spontaneous mutation during the sexual cycle of Neurospora crassa. |
| Q73606010 | Spontaneous mutation of the lacI transgene in rodents: absence of species, strain, and insertion-site influence |
| Q41445831 | Spontaneous mutations at aprt locus in a mammalian cell line defective in mismatch recognition |
| Q54490387 | Spontaneous transformations of a nicotinic mutant in Coprinus radiatus: study of nic-2 homothalic or diploid strains |
| Q36936784 | Spontaneous variation and synthesis in the U3 region of the long terminal repeat of an avian retrovirus |
| Q34599367 | Stability of intrastrand hairpin structures formed by the CAG/CTG class of DNA triplet repeats associated with neurological diseases |
| Q37489429 | Stabilization of diverged tandem repeats by mismatch repair: evidence for deletion formation via a misaligned replication intermediate. |
| Q42967686 | Stabilization of microsatellite sequences by variant repeats in the yeast Saccharomyces cerevisiae |
| Q74463085 | Stabilization of the intermediate in frameshift mutation |
| Q28507252 | Stepwise deletions of polyA sequences in mismatch repair-deficient colorectal cancers |
| Q73176036 | Strand asymmetry of +1 frameshift mutagenesis at a homopolymeric run by DNA polymerase III holoenzyme of Escherichia coli |
| Q58066694 | Strand misalignments lead to quasipalindrome correction |
| Q30382858 | Streptococcal M protein: molecular design and biological behavior. |
| Q40459862 | Stress-Induced Mutagenesis. |
| Q37428432 | Strong heterogeneity in mutation rate causes misleading hallmarks of natural selection on indel mutations in the human genome |
| Q38342796 | Strong structural effect of the position of a single acetylaminofluorene adduct within a mutation hot spot |
| Q27658910 | Structural Insight into Translesion Synthesis by DNA Pol II |
| Q45420674 | Structural determinants of slippage-mediated mutations by human immunodeficiency virus type 1 reverse transcriptase |
| Q36247516 | Structural intermediates of deletion mutagenesis: a role for palindromic DNA |
| Q27642304 | Structural study of DNA duplex containing an N-(2-deoxy- -D-erythro-pentofuranosyl) formamide frameshift by NMR and restrained molecular dynamics |
| Q42615301 | Structure and chromosomal assignment of a gene encoding the major protein of rat sperm outer dense fibres |
| Q28687676 | Structure and thermodynamic insights on acetylaminofluorene-modified deletion DNA duplexes as models for frameshift mutagenesis |
| Q26849468 | Structure-function studies of DNA polymerase λ |
| Q44312236 | Studies on the lysozyme from the bacteriophage T4 eJD7eJD4, carrying two frame shift mutations |
| Q37942291 | Study of mutational specificity in the lacl gene of Escherichia coli as a window on the mechanisms of mutation |
| Q27650171 | Substrate-induced DNA strand misalignment during catalytic cycling by DNA polymerase λ |
| Q36892771 | Suppressible and nonsuppressible +1 G-C base pair insertions induced by ICR-170 at the his4 locus in Saccharomyces cerevisiae |
| Q34411726 | TCOF1 mutation database: novel mutation in the alternatively spliced exon 6A and update in mutation nomenclature. |
| Q73947948 | Tandem duplication. A novel type of triplet repeat instability |
| Q34353810 | Tandem duplications in animal mitochondrial DNAs: variation in incidence and gene content among lizards |
| Q39731447 | Taq DNA polymerase slippage mutation rates measured by PCR and quasi-likelihood analysis: (CA/GT)n and (A/T)n microsatellites |
| Q54657595 | Template-directed pausing of DNA synthesis by HIV-1 reverse transcriptase during polymerization of HIV-1 sequences in vitro |
| Q92944033 | Tetranucleotide Microsatellite Mutational Behavior Assessed in Real Time: Implications for Future Microsatellite Panels |
| Q35037449 | The "A" rule revisited: polymerases as determinants of mutational specificity |
| Q37713424 | The 'A rule' of mutagen specificity: a consequence of DNA polymerase bypass of non-instructional lesions? |
| Q45035333 | The DNA gyrase of Escherichia coli participates in the formation of a spontaneous deletion by recA-independent recombination in vivo |
| Q34102902 | The Escherichia coli lacZ reversion mutagenicity assay |
| Q28551589 | The Eukaryotic Mismatch Recognition Complexes Track with the Replisome during DNA Synthesis |
| Q27930815 | The Saccharomyces cerevisiae Msh2 and Msh6 proteins form a complex that specifically binds to duplex oligonucleotides containing mismatched DNA base pairs |
| Q62594877 | The Spectrum of Replication Errors in the Absence of Error Correction Assayed Across the Whole Genome of |
| Q35129650 | The Three Dimensional Structure of the Lysozyme from Bacteriophage T4 |
| Q36248608 | The X family portrait: structural insights into biological functions of X family polymerases. |
| Q27667302 | The Y-Family DNA Polymerase Dpo4 Uses a Template Slippage Mechanism To Create Single-Base Deletions |
| Q40413967 | The adenomatous polyposis coli gene and human cancers |
| Q77172508 | The base substitution and frameshift fidelity of Escherichia coli DNA polymerase III holoenzyme in vitro |
| Q34416320 | The cadherin-related neuronal receptor family: a novel diversified cadherin family at the synapse |
| Q48068829 | The contribution of slippage-like processes to genome evolution |
| Q30252138 | The discovery, function and development of the variable number tandem repeats in different Mycobacterium species |
| Q33892878 | The early detection of frameshift mutations induced by a food-borne carcinogen in rats: a new tool for molecular epidemiology. |
| Q67482479 | The effect of dose and time on the induction of genetic alterations in Saccharomyces cerevisiae by aminoacridines in the presence and absence of visible light irradiation in comparison with the dose-effect-curves of mutagens with other type of action |
| Q35772796 | The effect of the length of direct repeats and the presence of palindromes on deletion between directly repeated DNA sequences in bacteriophage T7 |
| Q34807461 | The excess of small inverted repeats in prokaryotes |
| Q24544757 | The favorable features of tryptophan synthase for proving Beadle and Tatum's one gene-one enzyme hypothesis |
| Q24630867 | The fidelity of DNA synthesis by eukaryotic replicative and translesion synthesis polymerases |
| Q33257520 | The fidelity of DNA synthesis by yeast DNA polymerase zeta alone and with accessory proteins. |
| Q53653976 | The frameshift infidelity of human DNA polymerase lambda. Implications for function. |
| Q34462261 | The genome length of human parainfluenza virus type 2 follows the rule of six, and recombinant viruses recovered from non-polyhexameric-length antigenomic cDNAs contain a biased distribution of correcting mutations |
| Q34070278 | The genome sequence of ectromelia virus Naval and Cornell isolates from outbreaks in North America. |
| Q35064113 | The in vitro fidelity of yeast DNA polymerase δ and polymerase ε holoenzymes during dinucleotide microsatellite DNA synthesis |
| Q33961004 | The influence of primary and secondary DNA structure in deletion and duplication between direct repeats in Escherichia coli |
| Q34603883 | The lacI gene as a target for mutation in transgenic rodents and Escherichia coli |
| Q42617085 | The length of a tetranucleotide repeat tract in Haemophilus influenzae determines the phase variation rate of a gene with homology to type III DNA methyltransferases. |
| Q33904471 | The nucleotide composition of microsatellites impacts both replication fidelity and mismatch repair in human colorectal cells |
| Q36800421 | The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes |
| Q33968093 | The prevention of repeat-associated deletions in Saccharomyces cerevisiae by mismatch repair depends on size and origin of deletions. |
| Q40582018 | The return of copy-choice in DNA recombination |
| Q40838250 | The role of DNA repeats and associated secondary structures in genomic instability and neoplasia |
| Q40715324 | The role of the adenomatous polyposis coli (APC) gene in human cancers. |
| Q26998736 | The role of variable DNA tandem repeats in bacterial adaptation |
| Q34614165 | The roles of Klenow processing and flap processing activities of DNA polymerase I in chromosome instability in Escherichia coli K12 strains |
| Q42927218 | The specificity of topoisomerase-mediated DNA cleavage defines acridine-induced frameshift specificity within a hotspot in bacteriophage T4 |
| Q35951260 | The spectrum of mutations generated by passage of a hydrogen peroxide damaged shuttle vector plasmid through a mammalian host |
| Q43779743 | The synthetase gene of the RNA phages R17, MS2 and f2 has a single UAG terminator codon |
| Q39952732 | The temperature influence on the spontaneous mutation rate. I. Literature review |
| Q36119900 | The three faces of riboviral spontaneous mutation: spectrum, mode of genome replication, and mutation rate |
| Q34177189 | The three-dimensional structure of a DNA duplex containing looped-out bases |
| Q24609754 | The tryptophan repressor sequence is highly conserved among the Enterobacteriaceae |
| Q34218124 | Theoretical analysis of mutation hotspots and their DNA sequence context specificity |
| Q71767204 | Thermal Elution of Complementary Sequences of Nucleic Acids from Cellulose Columns with Covalently Attached Oligonucleotides of Known Length and Sequence |
| Q35196959 | Three different frameshift mutations of the tyrosinase gene in type IA oculocutaneous albinism |
| Q46375749 | To slip or skip, visualizing frameshift mutation dynamics for error-prone DNA polymerases |
| Q42575223 | Topical reversion at the HIS1 locus of Saccharomyces cerevisiae. A tale of three mutants. |
| Q35753529 | Tracing cell fates in human colorectal tumors from somatic microsatellite mutations: evidence of adenomas with stem cell architecture |
| Q72902049 | Transcribed heteroplasmic repeated sequences in the porcine mitochondrial DNA D-loop region |
| Q39956355 | Transcription of Genetic Information and Its Regulation by Protein Factors |
| Q40517580 | Transcriptional slippage occurs during elongation at runs of adenine or thymine in Escherichia coli |
| Q33851815 | Translational frameshifting: implications for the mechanism of translational frame maintenance |
| Q47903001 | Triplet repeat expansion generated by DNA slippage is suppressed by human flap endonuclease 1. |
| Q34995821 | Triplet repeats form secondary structures that escape DNA repair in yeast |
| Q66896674 | Tryptophan operon read-through. Isolation and characterization of an abnormally long tryptophan synthetase alpha subunit from a frame-shift mutant of Escherichia coli |
| Q42617783 | Two GC-rich DNA elements ofChlamydomonas reinhardtii with complex arrangements of directly repeated sequence motifs |
| Q39847637 | Two distinct models account for short and long deletions within sequence repeats in Escherichia coli |
| Q54131428 | Two new human hemoglobin variants caused by unusual mutational events: Hb Zaïre contains a five residue repetition within the alpha-chain and Hb Duino has two residues substituted in the beta-chain. |
| Q41566071 | UV-induced reversion of his4 frameshift mutations in rad6, rev1, and rev3 mutants of yeast |
| Q22122362 | Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis |
| Q99563521 | Ultrasensitive deletion detection links mitochondrial DNA replication, disease, and aging |
| Q33769444 | Ultraviolet-Induced Reversions of Salmonella his Frameshift Mutations |
| Q34003939 | UmuD(2) inhibits a non-covalent step during DinB-mediated template slippage on homopolymeric nucleotide runs. |
| Q37127515 | Unequal human immunodeficiency virus type 1 reverse transcriptase error rates with RNA and DNA templates |
| Q35498513 | Universal strategies for the DNA-encoding of libraries of small molecules using the chemical ligation of oligonucleotide tags |
| Q27622679 | Use of a non-rigid region in T4 lysozyme to design an adaptable metal-binding site |
| Q54307155 | Use of inverse PCR to amplify and sequence breakpoints of HPRT deletion and translocation mutations. |
| Q36066595 | V(D)J hypermutation and DNA mismatch repair: vexed by fixation |
| Q33854065 | Variation in efficiency of DNA mismatch repair at different sites in the yeast genome |
| Q36362654 | X-ray-structure of a cytidylyl-3',5'-adenosine-proflavine complex: a self-paired parallel-chain double helical dimer with an intercalated acridine dye. |
| Q34307496 | Z-DNA-forming sequences are spontaneous deletion hot spots |
| Q60043617 | Zebrafish: Development of a Vertebrate Model Organism |
| Q50046037 | mutL as a genetic switch of bacterial mutability: turned on or off through repeat copy number changes |
| Q28477333 | α,β-D-constrained nucleic acids are strong terminators of thermostable DNA polymerases in polymerase chain reaction |
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