ab17995 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。

ab17995 は 9 報の論文で使用されています。

  • Jain N  et al. A phase I-II trial of fludarabine, bendamustine and rituximab (FBR) in previously treated patients with CLL. Oncotarget 8:22104-22112 (2017). WB ; Human . PubMed: 27655665
  • Tanikawa M  et al. The spliceosome U2 snRNP factors promote genome stability through distinct mechanisms; transcription of repair factors and R-loop processing. Oncogenesis 5:e280 (2016). WB ; Human . PubMed: 27991914
  • Nanetti L  et al. SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein. Orphanet J Rare Dis 8:123 (2013). WB ; Human . PubMed: 23941260
  • Cavalieri S  et al. Deep-intronic ATM mutation detected by genomic resequencing and corrected in vitro by antisense morpholino oligonucleotide (AMO). Eur J Hum Genet 21:774-8 (2013). PubMed: 23211698
  • Khalil HS  et al. Pharmacological inhibition of ATM by KU55933 stimulates ATM transcription. Exp Biol Med (Maywood) 237:622-34 (2012). PubMed: 22728709
  • Colnaghi L  et al. Patient-derived C-terminal mutation of FANCI causes protein mislocalization and reveals putative EDGE motif function in DNA repair. Blood 117:2247-56 (2011). WB ; Human . PubMed: 20971953
  • Dregalla RC  et al. Regulatory roles of tankyrase 1 at telomeres and in DNA repair: suppression of T-SCE and stabilization of DNA-PKcs. Aging (Albany NY) 2:691-708 (2010). WB ; Human . PubMed: 21037379
  • Chailleux C  et al. Physical interaction between the histone acetyl transferase Tip60 and the DNA double-strand breaks sensor MRN complex. Biochem J 426:365-71 (2010). PubMed: 20070254
  • Shrivastav M  et al. DNA-PKcs and ATM co-regulate DNA double-strand break repair. DNA Repair (Amst) 8:920-9 (2009). PubMed: 19535303

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