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Subject Areas on Research
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A circular trans-acting hepatitis delta virus ribozyme.
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A nuclease-resistant RNA aptamer specifically inhibits angiopoietin-1-mediated Tie2 activation and function.
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Association and interactions between DNA repair gene polymorphisms and adult glioma.
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Association between the ERCC5 Asp1104His polymorphism and cancer risk: a meta-analysis.
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Beta-thalassemia resulting from a single nucleotide substitution in an acceptor splice site.
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Cas9 loosens its grip on off-target sites.
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Characterization of reaction intermediates of human excision repair nuclease.
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Chromosome aberrations resulting from double-strand DNA breaks at a naturally occurring yeast fragile site composed of inverted ty elements are independent of Mre11p and Sae2p.
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Clinical and Genetic Risk Prediction of Subsequent CNS Tumors in Survivors of Childhood Cancer: A Report From the COG ALTE03N1 Study.
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Clinical application of whole-genome sequencing in patients with primary immunodeficiency.
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Correction of dystrophin expression in cells from Duchenne muscular dystrophy patients through genomic excision of exon 51 by zinc finger nucleases.
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Correlation of DNA fragmentation and chromatin condensation in apoptotic nuclei of the Ser 6 mouse retina.
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Cyanobacterial ribosomal RNA genes with multiple, endonuclease-encoding group I introns
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DNA polymerase zeta introduces multiple mutations when bypassing spontaneous DNA damage in Saccharomyces cerevisiae.
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DNA repair gene ERCC1 and ERCC2/XPD polymorphisms and risk of squamous cell carcinoma of the head and neck.
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Diagnosis of 22q11.2 deletion syndrome and artemis deficiency in two children with T-B-NK+ immunodeficiency.
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Differential staining of actin in metaphase spindles with 7-nitrobenz-2-oxa-1,3-diazole-phallacidin and fluorescent DNase: is actin involved in chromosomal movement?
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Direct carrier testing in 14 families with haemophilia B.
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ERCC1 and ERCC2 polymorphisms predict clinical outcomes of oxaliplatin-based chemotherapies in gastric and colorectal cancer: a systemic review and meta-analysis.
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ERCC1 and ERCC2 variants predict survival in gastric cancer patients.
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ERCC1 protein expression is associated with differential survival in oropharyngeal head and neck squamous cell carcinoma.
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EcoRI endonuclease. Physical and catalytic properties of the homogenous enzyme.
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Effects of hexavalent chromium on the survival and cell cycle distribution of DNA repair-deficient S. cerevisiae.
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Efficient generation of targeted and controlled mutational events in porcine cells using nuclease-directed homologous recombination.
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EndoU is a novel regulator of AICD during peripheral B cell selection.
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Endonuclease-independent DNA mismatch repair processes on the lagging strand.
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Evidence that non-caspase proteases are required for chromatin degradation during apoptosis.
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Evolution of Pleopsidium (lichenized Ascomycota) S943 group I introns and the phylogeography of an intron-encoded putative homing endonuclease.
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Expression of nucleotide excision repair genes and the risk for squamous cell carcinoma of the head and neck.
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Functional genetic variants of XRCC4 and ERCC1 predict survival of gastric cancer patients treated with chemotherapy by regulating the gene expression.
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Genetic polymorphisms of selected DNA repair genes, estrogen and progesterone receptor status, and breast cancer risk.
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Genetic variants in ERCC1 and XPC predict survival outcome of non-small cell lung cancer patients treated with platinum-based therapy.
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Genome-editing Technologies for Gene and Cell Therapy.
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Genotypes and haplotypes of ERCC1 and ERCC2/XPD genes predict levels of benzo[a]pyrene diol epoxide-induced DNA adducts in cultured primary lymphocytes from healthy individuals: a genotype-phenotype correlation analysis.
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High gene expression of TS1, GSTP1, and ERCC1 are risk factors for survival in patients treated with trimodality therapy for esophageal cancer.
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Highly active zinc-finger nucleases by extended modular assembly.
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Human MutLγ, the MLH1-MLH3 heterodimer, is an endonuclease that promotes DNA expansion.
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Improving the clinical risk score: an analysis of molecular biomarkers in the era of modern chemotherapy for resectable hepatic colorectal cancer metastases.
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In Vivo Zinc Finger Nuclease-mediated Targeted Integration of a Glucose-6-phosphatase Transgene Promotes Survival in Mice With Glycogen Storage Disease Type IA.
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In vitro maturation of circular bacteriophage P2 DNA. Purification of ter components and characterization of the reaction.
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In vivo activity of nuclease-resistant siRNAs.
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In vivo repair of alkylating and oxidative DNA damage in the mitochondrial and nuclear genomes of wild-type and glycosylase-deficient Caenorhabditis elegans
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Inactivation of the human papillomavirus E6 or E7 gene in cervical carcinoma cells by using a bacterial CRISPR/Cas RNA-guided endonuclease.
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Interplay between structure-specific endonucleases for crossover control during Caenorhabditis elegans meiosis.
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Interplay of catalysis, fidelity, threading, and processivity in the exo- and endonucleolytic reactions of human exonuclease I.
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Isolation and characterization of the Escherichia coli mutH gene product.
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Machine Learning Approach to Classify Cardiovascular Disease in Patients With Nonalcoholic Fatty Liver Disease in the UK Biobank Cohort.
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Meiotic recombination involving heterozygous large insertions in Saccharomyces cerevisiae: formation and repair of large, unpaired DNA loops.
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Mre11-Sae2 and RPA Collaborate to Prevent Palindromic Gene Amplification.
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Multiple DNA repair mechanisms and alkylator resistance in the human medulloblastoma cell line D-283 Med (4-HCR).
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No evidence of an association of ERCC1 and ERCC2 polymorphisms with clinical outcomes of platinum-based chemotherapies in non-small cell lung cancer: a meta-analysis.
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Overlapping specificities of base excision repair, nucleotide excision repair, recombination, and translesion synthesis pathways for DNA base damage in Saccharomyces cerevisiae.
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PCNA function in the activation and strand direction of MutLα endonuclease in mismatch repair.
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PMS2 endonuclease activity has distinct biological functions and is essential for genome maintenance.
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Polymorphisms in ERCC1 and XPF genes and risk of gastric cancer in an eastern Chinese population.
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Polymorphisms in the DNA repair genes XPC, XPD, and XPG and risk of cutaneous melanoma: a case-control analysis.
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Polymorphisms in the ERCC5 gene and risk of esophageal squamous cell carcinoma (ESCC) in Eastern Chinese populations.
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Polymorphisms in the XPG gene and risk of gastric cancer in Chinese populations.
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Polymorphisms of XPG/ERCC5 and risk of squamous cell carcinoma of the head and neck.
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Polymorphisms of nucleotide excision repair genes predict melanoma survival.
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Potentially functional variants in the core nucleotide excision repair genes predict survival in Japanese gastric cancer patients.
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Prognostic significance of mucin and p53 expression in stage IB non-small cell lung cancer: a laboratory companion study to CALGB 9633.
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RGEN Editing of RNA and DNA: The Long and Winding Road from Catalytic RNAs to CRISPR to the Clinic.
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RNA-guided transcriptional silencing in vivo with S. aureus CRISPR-Cas9 repressors.
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Reaction mechanism of human DNA repair excision nuclease.
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Reading frame correction by targeted genome editing restores dystrophin expression in cells from Duchenne muscular dystrophy patients.
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Recognition sequence of the dam methylase of Escherichia coli K12 and mode of cleavage of Dpn I endonuclease.
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Recombination between homologous chromosomes induced by unrepaired UV-generated DNA damage requires Mus81p and is suppressed by Mms2p.
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Recombinational Repair of Nuclease-Generated Mitotic Double-Strand Breaks with Different End Structures in Yeast.
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Reduced expression levels of nucleotide excision repair genes in lung cancer: a case-control analysis.
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RelB cellular regulation and transcriptional activity are regulated by p100.
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Repair of DNA loops involves DNA-mismatch and nucleotide-excision repair proteins.
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Resveratrol prevents protein nitration and release of endonucleases from mitochondria during acetaminophen hepatotoxicity.
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Saccharomyces cerevisiae MutLalpha is a mismatch repair endonuclease.
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Sequence variations in DNA repair gene XPC is associated with lung cancer risk in a Chinese population: a case-control study.
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Some properties of a DNA-unwinding protein unique to lymphocytes from chronic lymphocytic leukemia.
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Structure of the endonuclease domain of MutL: unlicensed to cut.
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Structure of the eukaryotic transcription apparatus: features of the gene for the largest subunit of Drosophila RNA polymerase II.
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Structures and mechanisms of DNA restriction and modification enzymes.
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Structures of human exonuclease 1 DNA complexes suggest a unified mechanism for nuclease family.
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Tagging single nucleotide polymorphisms in excision repair cross-complementing group 1 (ERCC1) and risk of primary lung cancer in a Chinese population.
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Temporal and tissue-specific expression of distinct retrovirus-like (VL30) elements during mouse development.
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The evolution of homing endonuclease genes and group I introns in nuclear rDNA.
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The next generation of CRISPR-Cas technologies and applications.
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Two restriction-like enzymes from Xanthomonas malvacearum.
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Variants in nucleotide excision repair core genes and susceptibility to recurrence of squamous cell carcinoma of the oropharynx.
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Wogonin and fisetin induce apoptosis in human promyeloleukemic cells, accompanied by a decrease of reactive oxygen species, and activation of caspase 3 and Ca(2+)-dependent endonuclease.
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Yeast base excision repair: interconnections and networks.
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α-synucleinopathy exerts sex-dimorphic effects on the multipurpose DNA repair/redox protein APE1 in mice and humans.