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Journal of Biological Chemistry, ISSN 0021-9258, 07/2017, Volume 292, Issue 28, pp. 11702 - 11713
Journal Article
Nature Cell Biology, ISSN 1465-7392, 08/2009, Volume 11, Issue 8, pp. 980 - 987
The ends of linear eukaryotic chromosomes are protected by telomeres, which serve to ensure proper chromosome replication and to prevent spurious recombination... 
REPAIR | KU HETERODIMER | COLOCALIZATION | DYSFUNCTIONAL TELOMERES | DOUBLE-STRAND BREAKS | S-PHASE | YEAST TELOMERES | BINDING PROTEIN | SACCHAROMYCES-CEREVISIAE | G-TAILS | CELL BIOLOGY | Saccharomyces cerevisiae - genetics | Recombinant Fusion Proteins - metabolism | DNA, Single-Stranded - genetics | Nuclear Pore Complex Proteins - genetics | Saccharomyces cerevisiae - metabolism | Haploidy | Telomere-Binding Proteins - genetics | Telomerase - genetics | Chromatin Immunoprecipitation | Rad52 DNA Repair and Recombination Protein - metabolism | Replication Protein A - genetics | S Phase | Cell Cycle Proteins - genetics | G2 Phase | Telomerase - metabolism | Telomere - metabolism | Telomere-Binding Proteins - metabolism | Telomere - genetics | Nuclear Pore Complex Proteins - metabolism | Cell Cycle Proteins - metabolism | Replication Protein A - metabolism | Saccharomyces cerevisiae Proteins - genetics | Nuclear Pore - metabolism | Rad52 DNA Repair and Recombination Protein - genetics | DNA Repair | Adaptor Proteins, Signal Transducing - genetics | Saccharomyces cerevisiae Proteins - metabolism | Recombinant Fusion Proteins - genetics | Luminescent Proteins - genetics | DNA Damage | Mutation | Adaptor Proteins, Signal Transducing - metabolism | Microscopy, Fluorescence | Luminescent Proteins - metabolism | Physiological aspects | DNA replication | Research | Telomerase | DNA damage | Index Medicus
Journal Article
Journal Article
The EMBO Journal, ISSN 0261-4189, 08/2011, Volume 30, Issue 16, pp. 3322 - 3336
The spindle assembly checkpoint (SAC) restrains anaphase until all chromosomes become bi‐oriented on the mitotic spindle. The SAC protein Mad2 can fold into... 
p31comet | Mad2 template model | mitotic timing | closed‐Mad2 | spindle assembly checkpoint | RAD52 | c-ABL | tyrosine phosphorylation | ssDNA annealing | DNA repair | ANAPHASE-PROMOTING COMPLEX | PROTEIN BUBR1 | BIOCHEMISTRY & MOLECULAR BIOLOGY | CONFORMATIONAL DIMERIZATION | MONOCLONAL-ANTIBODY | MAD2 ACTIVATION | CORE COMPLEX | CELL BIOLOGY | CDC20 | MITOSIS | closed-Mad2 | BINDING | UNATTACHED KINETOCHORES | Humans | Cell Cycle Proteins - chemistry | Repressor Proteins - physiology | Cell Cycle Proteins - immunology | Time Factors | Calcium-Binding Proteins - immunology | Adaptor Proteins, Signal Transducing - immunology | Mad2 Proteins | Cdc20 Proteins | Spindle Apparatus - physiology | Dimerization | Antibodies, Monoclonal - immunology | Calcium-Binding Proteins - chemistry | Rabbits | Repressor Proteins - chemistry | Kinetochores - metabolism | RNA, Small Interfering - pharmacology | Anaphase - physiology | Nuclear Pore - metabolism | Nuclear Proteins - chemistry | Nuclear Proteins - immunology | Protein Folding | Macromolecular Substances | Protein Interaction Mapping | Adaptor Proteins, Signal Transducing - physiology | Animals | Mitosis - drug effects | Mitosis - physiology | Calcium-Binding Proteins - physiology | Repressor Proteins - immunology | Protein Conformation | Mice | Mice, Inbred BALB C | Nuclear Proteins - physiology | Cell Cycle Proteins - physiology | Proteins | Cell division | Molecular biology | Signal to noise ratio
Journal Article
Oncogene, ISSN 0950-9232, 05/2013, Volume 32, Issue 19, pp. 2452 - 2462
Journal Article
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 4115 - 12
Journal Article
Nature Cell Biology, ISSN 1465-7392, 05/2013, Volume 15, Issue 5, pp. 526 - +
Cdc48 (also known as p97), a conserved chaperone-like ATPase, plays a strategic role in the ubiquitin system(1-3). Empowered by ATP-driven conformational... 
UBIQUITIN-SELECTIVE SEGREGASE | COMPLEX | PROTEIN | RAD51 | PCNA | AAA-ATPASE | HOMOLOGOUS RECOMBINATION | DNA-REPAIR | BRCA2 | SUMOYLATION | CELL BIOLOGY | Immunoprecipitation | DNA, Fungal - genetics | Saccharomyces cerevisiae - genetics | Humans | Valosin Containing Protein | DNA Breaks, Double-Stranded | Saccharomyces cerevisiae - metabolism | Multiprotein Complexes - metabolism | Rad52 DNA Repair and Recombination Protein - metabolism | Proteolysis | Recombination, Genetic | Cell Cycle Proteins - genetics | Rad51 Recombinase - metabolism | Recombinant Proteins - metabolism | Rad51 Recombinase - genetics | Small Ubiquitin-Related Modifier Proteins - metabolism | Electrophoresis, Polyacrylamide Gel | Cell Cycle Proteins - metabolism | Adenosine Triphosphatases - metabolism | Recombinant Proteins - genetics | Saccharomyces cerevisiae Proteins - genetics | Blotting, Western | Rad52 DNA Repair and Recombination Protein - genetics | Protein Interaction Mapping - methods | Two-Hybrid System Techniques | Animals | Ubiquitin-Conjugating Enzymes - metabolism | DNA Repair | DNA, Fungal - metabolism | Saccharomyces cerevisiae Proteins - metabolism | Cell Line, Tumor | Protein Binding | Sumoylation | Adenosine Triphosphatases - genetics | SUMO-1 Protein - metabolism | Enzyme Activation | Cellular control mechanisms | Research | Ubiquitin-proteasome system | Observations | Properties | Adenosine triphosphatase | Testing
Journal Article
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 2791 - 14
Common fragile sites (CFSs) are prone to chromosomal breakage and are hotspots for chromosomal rearrangements in cancer cells. We uncovered a novel function of... 
ANEMIA CORE COMPLEX | DNA-DAMAGE RESPONSE | MULTIDISCIPLINARY SCIENCES | SYNTHETICALLY LETHAL | HOMOLOGOUS RECOMBINATION | ONCOGENE-INDUCED SENESCENCE | MAINTAIN GENOME STABILITY | REPLICATION STRESS | SACCHAROMYCES-CEREVISIAE | NEGATIVE BREAST-CANCER | CHROMOSOMAL INSTABILITY | RNA, Small Interfering - genetics | Colonic Neoplasms - genetics | Humans | Gene Expression Regulation, Neoplastic | DNA Breaks, Double-Stranded | Colonic Neoplasms - metabolism | DNA-Binding Proteins - metabolism | Rad52 DNA Repair and Recombination Protein - metabolism | Injections, Subcutaneous | Tumor Suppressor Proteins - genetics | HEK293 Cells | Apoptosis Regulatory Proteins - genetics | Female | Nuclear Proteins - genetics | DNA Helicases - genetics | Colonic Neoplasms - therapy | Recombinational DNA Repair | Tumor Suppressor Proteins - metabolism | Signal Transduction | HCT116 Cells | Chromosome Fragile Sites | Nuclear Proteins - metabolism | DNA - metabolism | DNA-Binding Proteins - genetics | Rad52 DNA Repair and Recombination Protein - genetics | Apoptosis Regulatory Proteins - metabolism | DNA - genetics | Xenograft Model Antitumor Assays | DNA Helicases - metabolism | Rad52 DNA Repair and Recombination Protein - antagonists & inhibitors | Animals | Mice, Nude | Colonic Neoplasms - pathology | Cell Line, Tumor | Mice | DNA Helicases - antagonists & inhibitors | RNA, Small Interfering - metabolism | Nucleotide sequence | Anemia | DNA damage | Homologous recombination | Homology | Lethality | Translocase | Double-strand break repair | Chromosome rearrangements | Fanconi syndrome | Gene sequencing | Mammalian cells | Proteins | Fragile sites | Breakage | Deoxyribonucleic acid--DNA | Rad52 protein | Tumors | Cancer
Journal Article
The Plant Journal, ISSN 0960-7412, 11/2012, Volume 72, Issue 3, pp. 423 - 435
Summary The plant mitochondrial DNA‐binding protein ODB1 was identified from a mitochondrial extract after DNA‐affinity purification. ODB1 (organellar... 
RAD52 | repair | recombination | Arabidopsis | mitochondrial DNA | ssDNA binding | ARABIDOPSIS-THALIANA | CHLOROPLASTS | GENOME STABILITY | BACTERIAL RECA | FAMILY | PLANT SCIENCES | MAINTENANCE | RNA-BINDING | WHIRLY PROTEINS | PLANT-MITOCHONDRIA | STRUCTURE PREDICTION | Flowers - metabolism | Plant Roots - genetics | Seedlings - genetics | Homologous Recombination | Mitochondrial Proteins - genetics | DNA Breaks, Double-Stranded | Arabidopsis Proteins - metabolism | DNA-Binding Proteins - metabolism | DNA, Mitochondrial - genetics | Mitochondria - genetics | Rad52 DNA Repair and Recombination Protein - metabolism | Mitochondrial Proteins - metabolism | Brassica - genetics | Plants, Genetically Modified | Plant Proteins - metabolism | DNA, Plant - genetics | Arabidopsis Proteins - genetics | Plant Roots - metabolism | Brassica - metabolism | Mitochondria - metabolism | DNA-Binding Proteins - genetics | Organ Specificity | Rad52 DNA Repair and Recombination Protein - genetics | Arabidopsis - metabolism | Arabidopsis - genetics | Plant Proteins - genetics | Chromatography, Affinity | Plant Leaves - genetics | Plant Leaves - metabolism | DNA Repair | DNA Damage | Mutation | Flowers - genetics | Seedlings - metabolism | Nylon | Peptides | RNA | DNA damage | Ferritin | Antibodies | Fluorescence | Genomes | Mitochondrial DNA | Recombinant proteins | DNA repair | Arabidopsis thaliana | Chemical properties | Nucleotide sequencing | Protein binding | Chlorophyll | DNA replication | Mitomycin | Chromatography | Cells | Viral antibodies | Anopheles | Analysis | Genetic research | Explosives | Ciprofloxacin | Binding proteins | DNA sequencing | Proteins | Plant biology | Genetic recombination | Binding sites | Mitochondria | DNA-binding protein | Nucleotide sequence | homologous recombination | Genotoxicity | protein purification | Nuclei | Plant extracts | Life Sciences | Molecular biology | Cellular Biology | Biochemistry, Molecular Biology
Journal Article
The EMBO Journal, ISSN 0261-4189, 04/2009, Volume 28, Issue 8, pp. 1121 - 1130
Recruitment of the homologous recombination machinery to sites of double‐strand breaks is a cell cycle‐regulated event requiring entry into S phase and CDK1... 
replication | checkpoints | recombination | DNA damage | Replication | Recombination | DNAdamage | Checkpoints | BUDDING YEAST | PROTEIN-KINASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | UBIQUITIN-LIGASE COMPLEX | DOUBLE-STRAND BREAKS | SACCHAROMYCES-CEREVISIAE | NUCLEOTIDE EXCISION-REPAIR | CELL BIOLOGY | CYCLIN-DEPENDENT KINASES | S-PHASE | CELL-CYCLE | HOMOLOGOUS RECOMBINATION | Saccharomyces cerevisiae - genetics | CDC2 Protein Kinase - metabolism | Saccharomyces cerevisiae - metabolism | Rad52 DNA Repair and Recombination Protein - metabolism | Recombination, Genetic | Cell Cycle Proteins - genetics | CDC28 Protein Kinase, S cerevisiae - metabolism | Protein-Serine-Threonine Kinases - metabolism | Caffeine - metabolism | CDC2 Protein Kinase - genetics | Enzyme Inhibitors - metabolism | F-Box Proteins - metabolism | Cell Cycle Proteins - metabolism | Protein-Serine-Threonine Kinases - genetics | Ubiquitin-Protein Ligases - metabolism | Intracellular Signaling Peptides and Proteins | CDC28 Protein Kinase, S cerevisiae - genetics | DNA Replication | Saccharomyces cerevisiae Proteins - genetics | Rad52 DNA Repair and Recombination Protein - genetics | Saccharomyces cerevisiae Proteins - metabolism | Cell Cycle - physiology | Checkpoint Kinase 2 | DNA Damage | Ubiquitin-Protein Ligases - genetics | F-Box Proteins - genetics | Hydroxyurea - metabolism | Genetic recombination | Kinases | Molecular biology | Genomics | Cell cycle
Journal Article