pcDNA3.1-ccdB-3xFLAG-V5 Citations (6)
Originally described in: Quantitative analysis of HSP90-client interactions reveals principles of substrate recognition.Taipale M, Krykbaeva I, Koeva M, Kayatekin C, Westover KD, Karras GI, Lindquist S Cell. 2012 Aug 31;150(5):987-1001. doi: 10.1016/j.cell.2012.06.047. PubMed Journal
Articles Citing pcDNA3.1-ccdB-3xFLAG-V5
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| Proteome Instability Is a Therapeutic Vulnerability in Mismatch Repair-Deficient Cancer. McGrail DJ, Garnett J, Yin J, Dai H, Shih DJH, Lam TNA, Li Y, Sun C, Li Y, Schmandt R, Wu JY, Hu L, Liang Y, Peng G, Jonasch E, Menter D, Yates MS, Kopetz S, Lu KH, Broaddus R, Mills GB, Sahni N, Lin SY. Cancer Cell. 2020 Mar 16;37(3):371-386.e12. doi: 10.1016/j.ccell.2020.01.011. Epub 2020 Feb 27. PubMed |
| Identification and functional characterization of transcriptional activators in human cells. Alerasool N, Leng H, Lin ZY, Gingras AC, Taipale M. Mol Cell. 2022 Feb 3;82(3):677-695.e7. doi: 10.1016/j.molcel.2021.12.008. Epub 2022 Jan 10. PubMed |
Recruitment of a splicing factor to the nuclear lamina for its inactivation.
Vester K, Preussner M, Holton N, Feng S, Schultz C, Heyd F, Wahl MC.
Commun Biol. 2022 Jul 22;5(1):736. doi: 10.1038/s42003-022-03689-y.
PubMed
Associated Plasmids |
| A central chaperone-like role for 14-3-3 proteins in human cells. Segal D, Maier S, Mastromarco GJ, Qian WW, Nabeel-Shah S, Lee H, Moore G, Lacoste J, Larsen B, Lin ZY, Selvabaskaran A, Liu K, Smibert C, Zhang Z, Greenblatt J, Peng J, Lee HO, Gingras AC, Taipale M. Mol Cell. 2023 Mar 16;83(6):974-993.e15. doi: 10.1016/j.molcel.2023.02.018. PubMed |
| Pervasive mislocalization of pathogenic coding variants underlying human disorders. Lacoste J, Haghighi M, Haider S, Reno C, Lin ZY, Segal D, Qian WW, Xiong X, Teelucksingh T, Miglietta E, Shafqat-Abbasi H, Ryder PV, Senft R, Cimini BA, Murray RR, Nyirakanani C, Hao T, McClain GG, Roth FP, Calderwood MA, Hill DE, Vidal M, Yi SS, Sahni N, Peng J, Gingras AC, Singh S, Carpenter AE, Taipale M. Cell. 2024 Nov 14;187(23):6725-6741.e13. doi: 10.1016/j.cell.2024.09.003. Epub 2024 Sep 30. PubMed |
| Parkinson's disease-linked Kir4.2 mutation R28C leads to loss of ion channel function. Chen X, Finol-Urdaneta RK, Chen M, Sykes AM, Gao B, Iqbal J, Adams DJ, Mellick GD, Ma L. J Physiol. 2025 Jun;603(12):3499-3518. doi: 10.1113/JP287046. Epub 2025 Jun 25. PubMed |
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