ab63801 を使用した論文を発表された方は、こちらまでお知らせください。データシートに掲載させていただきます。

ab63801 は 18 報の論文で使用されています。

  • Marin-Vicente C  et al. RRP6/EXOSC10 is required for the repair of DNA double-strand breaks by homologous recombination. J Cell Sci 128:1097-107 (2015). PubMed: 25632158
  • Danilowicz C  et al. The differential extension in dsDNA bound to Rad51 filaments may play important roles in homology recognition and strand exchange. Nucleic Acids Res 42:526-33 (2014). PubMed: 24084082
  • Vidi PA  et al. NuMA promotes homologous recombination repair by regulating the accumulation of the ISWI ATPase SNF2h at DNA breaks. Nucleic Acids Res 42:6365-79 (2014). WB, ICC/IF . PubMed: 24753406
  • Nikolova T  et al. The ?H2AX Assay for Genotoxic and Nongenotoxic Agents: Comparison of H2AX Phosphorylation with Cell Death Response. Toxicol Sci 140:103-17 (2014). PubMed: 24743697
  • Zhang H  et al. Mechanisms controlling the smooth muscle cell death in progeria via down-regulation of poly(ADP-ribose) polymerase 1. Proc Natl Acad Sci U S A 111:E2261-70 (2014). PubMed: 24843141
  • Ensminger M  et al. DNA breaks and chromosomal aberrations arise when replication meets base excision repair. J Cell Biol 206:29-43 (2014). PubMed: 24982429
  • Hunter FW  et al. Dual targeting of hypoxia and homologous recombination repair dysfunction in triple-negative breast cancer. Mol Cancer Ther 13:2501-14 (2014). PubMed: 25193512
  • Qiao B  et al. Imatinib radiosensitizes bladder cancer by targeting homologous recombination. Cancer Res 73:1611-20 (2013). PubMed: 23302228
  • Lai XY & Egan LJ Suppression of radiation-induced DNA double-strand break repair by MyD88 is accompanied by apoptosis and crypt loss in mouse colon. Oncogenesis 2:e62 (2013). ICC/IF ; Mouse . PubMed: 23939014
  • Geuting V  et al. ATM release at resected double-strand breaks provides heterochromatin reconstitution to facilitate homologous recombination. PLoS Genet 9:e1003667 (2013). ICC/IF ; Human . PubMed: 23935532
  • Horn HF  et al. A mammalian KASH domain protein coupling meiotic chromosomes to the cytoskeleton. J Cell Biol 202:1023-39 (2013). PubMed: 24062341
  • Osorio A  et al. Predominance of pathogenic missense variants in the RAD51C gene occurring in breast and ovarian cancer families. Hum Mol Genet : (2012). ICC/IF ; Human . PubMed: 22451500
  • Islam MN  et al. A Variant of the Breast Cancer Type 2 Susceptibility Protein (BRC) Repeat Is Essential for the RECQL5 Helicase to Interact with RAD51 Recombinase for Genome Stabilization. J Biol Chem 287:23808-18 (2012). WB . PubMed: 22645136
  • Knies K  et al. Genotyping of fanconi anemia patients by whole exome sequencing: advantages and challenges. PLoS One 7:e52648 (2012). WB ; Human . PubMed: 23285130
  • Stoepker C  et al. SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype. Nat Genet 43:138-41 (2011). ICC/IF ; Human . PubMed: 21240277
  • Quennet V  et al. CtIP and MRN promote non-homologous end-joining of etoposide-induced DNA double-strand breaks in G1. Nucleic Acids Res 39:2144-52 (2011). WB ; Human . PubMed: 21087997
  • Weis E  et al. Reduced mRNA and Protein Expression of the Genomic Caretaker RAD9A in Primary Fibroblasts of Individuals with Childhood and Independent Second Cancer. PLoS One 6:e25750 (2011). Dot Blot ; Human . PubMed: 21991345
  • Vaz F  et al. Mutation of the RAD51C gene in a Fanconi anemia-like disorder. Nat Genet 42:406-9 (2010). ICC/IF ; Human . PubMed: 20400963