Anti-Blooms Syndrome蛋白Blm抗体(ab476)

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ab476 被引用在 28 文献中.

  • Hampp S  et al. DNA damage tolerance pathway involving DNA polymerase ? and the tumor suppressor p53 regulates DNA replication fork progression. Proc Natl Acad Sci U S A 113:E4311-9 (2016). WB ; Human . PubMed: 27407148
  • Yang Y  et al. Arginine methylation facilitates the recruitment of TOP3B to chromatin to prevent R loop accumulation. Mol Cell 53:484-97 (2014). PubMed: 24507716
  • Sturzenegger A  et al. DNA2 cooperates with the WRN and BLM RecQ helicases to mediate long-range DNA end resection in human cells. J Biol Chem 289:27314-26 (2014). WB . PubMed: 25122754
  • Chaudhury I  et al. FANCD2-controlled chromatin access of the Fanconi-associated nuclease FAN1 is crucial for the recovery of stalled replication forks. Mol Cell Biol 34:3939-54 (2014). PubMed: 25135477
  • Chaudhury I  et al. FANCD2 regulates BLM complex functions independently of FANCI to promote replication fork recovery. Nucleic Acids Res 41:6444-59 (2013). Human . PubMed: 23658231
  • Chandra S  et al. Enhancement of c-Myc degradation by BLM helicase leads to delayed tumor initiation. J Cell Sci 126:3782-95 (2013). PubMed: 23750012
  • Berti M  et al. Human RECQ1 promotes restart of replication forks reversed by DNA topoisomerase I inhibition. Nat Struct Mol Biol 20:347-54 (2013). WB ; Human . PubMed: 23396353
  • Tedeschi A  et al. Wapl is an essential regulator of chromatin structure and chromosome segregation. Nature 501:564-8 (2013). PubMed: 23975099
  • Böhringer M  et al. siRNA screening identifies differences in the Fanconi anemia pathway in BALB/c-Trp53+/- with susceptibility versus C57BL/6-Trp53+/- mice with resistance to mammary tumors. Oncogene : (2013). WB . PubMed: 23435420
  • Rouzeau S  et al. Bloom's Syndrome and PICH Helicases Cooperate with Topoisomerase IIa in Centromere Disjunction before Anaphase. PLoS One 7:e33905 (2012). ICC/IF . PubMed: 22563370
  • Laulier C  et al. The relative efficiency of homology-directed repair has distinct effects on proper anaphase chromosome separation. Nucleic Acids Res 39:5935-44 (2011). WB ; Human . PubMed: 21459848
  • Wang Y  et al. Depletion of the bloom syndrome helicase stimulates homology-dependent repair at double-strand breaks in human chromosomes. DNA Repair (Amst) 10:416-26 (2011). WB ; Human . PubMed: 21300576
  • Chabosseau P  et al. Pyrimidine pool imbalance induced by BLM helicase deficiency contributes to genetic instability in Bloom syndrome. Nat Commun 2:368 (2011). PubMed: 21712816
  • Lahkim Bennani-Belhaj K  et al. BLM Deficiency Is Not Associated with Sensitivity to Hydroxyurea-Induced Replication Stress. J Nucleic Acids 2010:N/A (2010). Human . PubMed: 20936166
  • Lahkim Bennani-Belhaj K  et al. The Bloom syndrome protein limits the lethality associated with RAD51 deficiency. Mol Cancer Res 8:385-94 (2010). WB, ICC/IF ; Human . PubMed: 20215422
  • Larocque JR & Jasin M Mechanisms of recombination between diverged sequences in wild-type and BLM-deficient mouse and human cells. Mol Cell Biol 30:1887-97 (2010). WB . PubMed: 20154148
  • Kusumoto R  et al. Werner protein cooperates with the XRCC4-DNA ligase IV complex in end-processing. Biochemistry 47:7548-56 (2008). PubMed: 18558713
  • Bussen W  et al. Holliday junction processing activity of the BLM-Topo IIIalpha-BLAP75 complex. J Biol Chem 282:31484-92 (2007). IP . PubMed: 17728255
  • So S  et al. Enhanced gene targeting efficiency by siRNA that silences the expression of the Bloom syndrome gene in human cells. Genes Cells 11:363-71 (2006). PubMed: 16611240
  • Raynard S  et al. A double Holliday junction dissolvasome comprising BLM, topoisomerase IIIalpha, and BLAP75. J Biol Chem 281:13861-4 (2006). WB ; Human . PubMed: 16595695
  • Yin J  et al. BLAP75, an essential component of Bloom's syndrome protein complexes that maintain genome integrity. EMBO J 24:1465-76 (2005). PubMed: 15775963
  • Stockinger P  et al. Neural circuitry that governs Drosophila male courtship behavior. Cell 121:795-807 (2005). PubMed: 15935765
  • Restle A  et al. Differences in the association of p53 phosphorylated on serine 15 and key enzymes of homologous recombination. Oncogene 24:4380-7 (2005). PubMed: 15806145
  • Jurvansuu J  et al. Viral transport of DNA damage that mimics a stalled replication fork. J Virol 79:569-80 (2005). PubMed: 15596849
  • Opresko PL  et al. POT1 stimulates RecQ helicases WRN and BLM to unwind telomeric DNA substrates. J Biol Chem 280:32069-80 (2005). PubMed: 16030011
  • So S  et al. Genetic interactions between BLM and DNA ligase IV in human cells. J Biol Chem 279:55433-42 (2004). PubMed: 15509577
  • Yusa K  et al. Genome-wide phenotype analysis in ES cells by regulated disruption of Bloom's syndrome gene. Nature 429:896-9 (2004). PubMed: 15215867
  • Bordi L  et al. Expression of Werner and Bloom syndrome genes is differentially regulated by in vitro HIV-1 infection of peripheral blood mononuclear cells. Clin Exp Immunol 138:251-8 (2004). PubMed: 15498034