发表研究结果有使用 ab17995?请让我们知道,以便我们可以引用本数据表中的参考文章。

ab17995 被引用在 5 文献中.

  • 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
  • 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
  • Shrivastav M  et al. DNA-PKcs and ATM co-regulate DNA double-strand break repair. DNA Repair (Amst) 8:920-9 (2009). PubMed: 19535303

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"