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Circular Journal "Repair, Recombination and Mutagenesis"

Analysis for molecule pathology of nucleotide excision repair abnormality.
Establishment of mouse strain deprived of repairing function and analysis for molecule pathology of defect hereditary disease by the mouse strain.
Studies of repair enzyme for DNA strand breaks and base defficiency site.
Analysis for nucleotide excision repair mechanism by acellular DNA repair system.
Analysis for molecule pathology of mismatch repair mechanism.
Interaction between repair system and DNA damage recognition protein.
Stabilization of p53 protein in DNA double-strand breaks and ATM.
Analysis for three dimentional structure of complex between RPA of human XPA protein and damaged DNA.
Analysis for function of human MSH3 protein.
Analysis for DNA excision repair mechanism of Neurospora crassa.
Stadies for molecular mechanism of coupling between transfer and DNA repair.
Roles of photoreactive enzyme effective to photoproducts and human homologous protein in DNA repair mechanism.
Analysis for molecular mechanism in central neuron death by DNA repair gene deleting mouse.
Studies for function of endonuclease for excision repair and molecular pathology in defect.
Modification of function of antibody molecules peculiarly recognizing ultraviolet damaged DNA.
Stadies for mechanism on excision repair of 8-hydroxyguanine in human cell DNA.
Mechanism for dissociation of Holliday structure of recombination intermediates.
Analysis for function of RecQ family protein in eukaryotic cells.
Transition of transposon IS3 and Tn3 and the control mechanism.
Analysis for function of Mre11 in start of meiosis period recombination of budding yeast.
General mechanism in DNA recombination .
Site specificity of recombination in meiosis period on mice.
Analysis for mechanism in DNA homologous recombination by chicken B lymphocyte stocks triggering target integration.
Control of DNA recombination and the repair in meiosis period.
Biological response caused by blocking of replication fork.
Studies for recombination repairing mechanism by Rad51 and Dmc1 gene of mice.
Analysis for unstable mutation in higher plants by mobile genetic factors.
Studies for repairing of DNA double-strand breaks and Molecular mechanism of nonhomology recombination.
Molecular mechanism of genome restruction. With a view to chromosomal deletions.
DNA recombination in and near large tandem repeat sequence of higher animals.
Isolation of DNA binding protein of Bacillus subtilis effective to holiday structure and functional analysis of function in the protein.
Analysis for mechanism in effects of RAD24 gene on DNA damage checkpoints.
Studies for DNA repairing mechanism by poly(ADP-ribose) polymerase-deficient cells and mice.
Telomere control mechanism participated by recombination repairing system.
Studies for function and control of homologous recombination in yeast mitochondrial DNA.
DNA replication errors and the repairing mechanism.
Control mechanism of SOS mutagenesis in Escherichia coli.
DNA spontaneous damage caused by oxygen radicals and the mutagenicity.
Studies for target genes on carcinogenesis caused by DNA repair deficient.
Molecular pathology of mutation. Molecular pathology for conservation of genetic information and DNA instability.
Spontaneous mutation caused by oxidation of nucleic acid in mammal and the control mechanism.
Studies for mutation in mice by transgenic mice.
Molecular mechanism of mutagenesis caused by errable DNA repair.
Factorial analysis of instability in short tandem repeats in mammal cells.
Elongation of triplet repeat causing crisis of hereditary diseases.
Roles of DNA polymerase .EPSILON. of budding yeast and the cofactors in DNA repairing.
Analysis in molecular structure related to DNA repairing mechanism by thermophilic bacterium protein.
Vital phenomena caused by O6- methylguanine on genome DNA.
Molecular pathology of gene deficiency for mismatch repairing in human cancer.
Analysis for enzymes related to production and removal of mutagen in mammal in vivo.
Molecular pathology in Werner syndrome.
Analysis for function of 3D structure in 8 - oxo - dGTPase controling spontaneous mutation.
Molecular pathology for repairing enzyme deficiency in DNA dmage induced by reactive oxygen.