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Subject Areas on Research
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A compensatory base change in human U2 snRNA can suppress a branch site mutation.
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A strong effect of AT mutational bias on amino acid usage in Buchnera is mitigated at high-expression genes.
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A transcription factor affinity-based code for mammalian transcription initiation.
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Accelerated deamination of cytosine residues in UV-induced cyclobutane pyrimidine dimers leads to CC-->TT transitions.
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Base composition of mononucleotide runs affects DNA polymerase slippage and removal of frameshift intermediates by mismatch repair in Saccharomyces cerevisiae.
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Bidirectional excision in methyl-directed mismatch repair.
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Characteristics of Rhizobium tianshanense sp. nov., a moderately and slowly growing root nodule bacterium isolated from an arid saline environment in Xinjiang, People's Republic of China.
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Complete genomic nucleotide sequence of the temperate bacteriophage Aa Phi 23 of Actinobacillus actinomycetemcomitans.
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Computational analysis of core promoters in the Drosophila genome.
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Context dependence of meiotic recombination hotspots in yeast: the relationship between recombination activity of a reporter construct and base composition.
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Coordination of replication and transcription along a Drosophila chromosome.
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Crystal structure and sequence-dependent conformation of the A.G mispaired oligonucleotide d(CGCAAGCTGGCG).
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Cutting of M13mp7 phage DNA and excision of cloned single-stranded sequences by restriction endonucleases.
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Cytosine deamination in mismatched base pairs.
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DNA base modification: ionized base pairs and mutagenesis.
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DNA bending near the replication origin of IncFII plasmid NR1.
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DNA mismatch correction.
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DNA polymerase delta is required for human mismatch repair in vitro.
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DNA structural features that lead to strand breakage by eukaryotic type-I topoisomerase.
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Dynamic evolution of base composition: causes and consequences in avian phylogenomics.
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Effect of isopropyl-beta-D-thiogalactopyranosid induction of the lac operon on the specificity of spontaneous and doxorubicin-induced mutations in Escherichia coli.
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Escherichia coli mutS-encoded protein binds to mismatched DNA base pairs.
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Escherichia coli mutY gene encodes an adenine glycosylase active on G-A mispairs.
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Escherichia coli mutY gene product is required for specific A-G----C.G mismatch correction.
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Evidence for GC-biased gene conversion as a driver of between-lineage differences in avian base composition.
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Exaggerated CpH methylation in the autism-affected brain.
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False gene and chromosome losses in genome assemblies caused by GC content variation and repeats.
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Functionality of the TOL plasmid under varying environmental conditions following conjugal transfer.
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GC content elevates mutation and recombination rates in the yeast Saccharomyces cerevisiae.
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GC sequence specific recognition by an N-formamido, C-terminus-modified and imidazole-containing analogue of netropsin.
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Gene conversion occurs within the mating-type locus of Cryptococcus neoformans during sexual reproduction.
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Gene expression level influences amino acid usage, but not codon usage, in the tsetse fly endosymbiont Wigglesworthia.
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Genes translocated into the plastid inverted repeat show decelerated substitution rates and elevated GC content
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Genetic bioaugmentation as an effective method for in situ bioremediation: functionality of catabolic plasmids following conjugal transfers.
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Genomic organization of rat rDNA.
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Hel-N1, an RNA-binding protein, is a ligand for an A + U rich region of the GLUT1 3' UTR.
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Human MutSalpha recognizes damaged DNA base pairs containing O6-methylguanine, O4-methylthymine, or the cisplatin-d(GpG) adduct.
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Human colonic sulfomucin identified by a specific monoclonal antibody.
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Human strand-specific mismatch repair occurs by a bidirectional mechanism similar to that of the bacterial reaction.
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Immunostimulatory properties of genomic DNA from different bacterial species.
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Improvements to the differential display method for gene analysis.
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Increased transversions in a novel mutator colon cancer cell line.
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Initial sequencing and comparative analysis of the mouse genome.
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Isolation and characterization of a human pro alpha 2(I) collagen gene segment.
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Isolation of MutSbeta from human cells and comparison of the mismatch repair specificities of MutSbeta and MutSalpha.
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Isolation of an hMSH2-p160 heterodimer that restores DNA mismatch repair to tumor cells.
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Isolation of two E-box binding factors that interact with the rat tyrosine hydroxylase enhancer.
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Methyl-directed DNA mismatch repair in Escherichia coli.
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Methyl-directed mismatch repair is bidirectional.
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Methyl-directed repair of DNA base-pair mismatches in vitro.
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Misincorporation and mispaired primer extension by human immunodeficiency virus reverse transcriptase.
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Mismatch repair, genetic stability, and cancer.
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Mismatch-, MutS-, MutL-, and helicase II-dependent unwinding from the single-strand break of an incised heteroduplex.
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Mispair specificity of methyl-directed DNA mismatch correction in vitro.
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Molecular evolutionary dynamics of cytochrome b in strepsirrhine primates: the phylogenetic significance of third-position transversions.
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Multifactorial determinants of protein expression in prokaryotic open reading frames.
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Multiple potential regulatory elements in the 5' flanking region of the human alpha 1a-adrenergic receptor.
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Mutation exposed: a neutral explanation for extreme base composition of an endosymbiont genome.
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Nucleotide bias of DCL and AGO in plant anti-virus gene silencing.
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OligoCalc: an online oligonucleotide properties calculator.
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Optimal self-cleavage activity of the hepatitis delta virus RNA is dependent on a homopurine base pair in the ribozyme core.
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Phage T3 DNA contains an exact copy of the 23 base-pair phage T7 RNA polymerase promoter sequence.
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Predicting cell-type-specific gene expression from regions of open chromatin.
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Protonated base pairs explain the ambiguous pairing properties of O6-methylguanine.
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Quadruplex DNA formation in a region of the tRNA gene supF associated with hydrogen peroxide mediated mutations.
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Rapid DNA sequencing of more than 1000 bases per run by capillary electrophoresis using replaceable linear polyacrylamide solutions.
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Recombination hotspots flank the Cryptococcus mating-type locus: implications for the evolution of a fungal sex chromosome.
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Repair of specific base pair mismatches formed during meiotic recombination in the yeast Saccharomyces cerevisiae.
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Resolving Arthropod Phylogeny: Exploring Phylogenetic Signal within 41 kb of Protein-Coding Nuclear Gene Sequence
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Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples.
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Retrotransposons Are the Major Contributors to the Expansion of the Drosophila ananassae Muller F Element.
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Secondary structure of the self-cleaving RNA of hepatitis delta virus: applications to catalytic RNA design.
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Sequence analysis of the cDNA encoding human liver glycogen phosphorylase reveals tissue-specific codon usage.
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Sequencing of double-stranded polymerase chain reaction products for mutation analysis.
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Structural relationships in glycogen phosphorylases.
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Structure of a G.T.A triplet in an intramolecular DNA triplex.
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Structure of the genes encoding transcription factor IIB and TATA box-binding protein from Drosophila melanogaster.
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Substrate spectrum of human excinuclease: repair of abasic sites, methylated bases, mismatches, and bulky adducts.
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The 5'-untranslated region of the N-methyl-D-aspartate receptor NR2A subunit controls efficiency of translation.
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The Ashbya gossypii genome as a tool for mapping the ancient Saccharomyces cerevisiae genome.
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The complete mitochondrial genome sequence of the Canada goose (Branta canadensis).
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The hydrogen bonding of cytosine with guanine: calorimetric and 1H-nmr analysis of the molecular interactions of nucleic acid bases.
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The western painted turtle genome, a model for the evolution of extreme physiological adaptations in a slowly evolving lineage.
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Transposon Tn5 target specificity: preference for insertion at G/C pairs.
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Two mouse early embryonic beta-globin gene sequences. Evolution of the nonadult beta-globins.
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Unprecedented loss of ammonia assimilation capability in a urease-encoding bacterial mutualist.
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Variable temperature infrared spectroscopy of cytosine-guanine base pairs: tautomerism versus polarization.
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Variation in modes and rates of evolution in nuclear and mitochondrial ribosomal DNA in the mushroom genus Amanita (Agaricales, Basidiomycota): phylogenetic implications.
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Keywords of People