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pLX301 Citations (13)

Plasmid Article: A public genome-scale lentiviral expression library of human ORFs.
Yang X, Boehm JS, Yang X, Salehi-Ashtiani K, Hao T, Shen Y, Lubonja R, Thomas SR, Alkan O, Bhimdi T, Green TM, Johannessen CM, Silver SJ, Nguyen C, Murray RR, Hieronymus H, Balcha D, Fan C, Lin C, Ghamsari L, Vidal M, Hahn WC, Hill DE, Root DE Nat Methods. 2011 Jun 26. ():.
PubMed Journal

Articles Citing pLX301

Articles
Reversible and adaptive resistance to BRAF(V600E) inhibition in melanoma. Sun C, Wang L, Huang S, Heynen GJ, Prahallad A, Robert C, Haanen J, Blank C, Wesseling J, Willems SM, Zecchin D, Hobor S, Bajpe PK, Lieftink C, Mateus C, Vagner S, Grernrum W, Hofland I, Schlicker A, Wessels LF, Beijersbergen RL, Bardelli A, Di Nicolantonio F, Eggermont AM, Bernards R. Nature. 2014 Apr 3;508(7494):118-22. doi: 10.1038/nature13121. Epub 2014 Mar 26. PubMed
The RNA binding protein quaking regulates formation of circRNAs. Conn SJ, Pillman KA, Toubia J, Conn VM, Salmanidis M, Phillips CA, Roslan S, Schreiber AW, Gregory PA, Goodall GJ. Cell. 2015 Mar 12;160(6):1125-34. doi: 10.1016/j.cell.2015.02.014. PubMed
Dynamic Changes in Cytosolic ATP Levels in Cultured Glutamatergic Neurons During NMDA-Induced Synaptic Activity Supported by Glucose or Lactate. Lange SC, Winkler U, Andresen L, Byhro M, Waagepetersen HS, Hirrlinger J, Bak LK. Neurochem Res. 2015 Dec;40(12):2517-26. doi: 10.1007/s11064-015-1651-9. Epub 2015 Jul 17. PubMed
Poly(A)-specific ribonuclease (PARN) mediates 3'-end maturation of the telomerase RNA component. Moon DH, Segal M, Boyraz B, Guinan E, Hofmann I, Cahan P, Tai AK, Agarwal S. Nat Genet. 2015 Dec;47(12):1482-8. doi: 10.1038/ng.3423. Epub 2015 Oct 19. PubMed
Zic2 mutation causes holoprosencephaly via disruption of NODAL signalling. Houtmeyers R, Tchouate Gainkam O, Glanville-Jones HA, Van den Bosch B, Chappell A, Barratt KS, Souopgui J, Tejpar S, Arkell RM. Hum Mol Genet. 2016 Jul 27. pii: ddw235. PubMed
KANK1 inhibits cell growth by inducing apoptosis though regulating CXXC5 in human malignant peripheral nerve sheath tumors. Cui Z, Shen Y, Chen KH, Mittal SK, Yang JY, Zhang G. Sci Rep. 2017 Jan 9;7:40325. doi: 10.1038/srep40325. PubMed
Migration against the direction of flow is LFA-1-dependent in human hematopoietic stem and progenitor cells. Buffone A Jr, Anderson NR, Hammer DA. J Cell Sci. 2018 Jan 10;131(1). pii: jcs.205575. doi: 10.1242/jcs.205575. PubMed
The mTOR inhibitor AZD8055 overcomes tamoxifen resistance in breast cancer cells by down-regulating HSPB8. Shi JJ, Chen SM, Guo CL, Li YX, Ding J, Meng LH. Acta Pharmacol Sin. 2018 Jan 18. pii: aps2017181. doi: 10.1038/aps.2017.181. PubMed
Upregulation of tryptophanyl-tRNA synthethase adapts human cancer cells to nutritional stress caused by tryptophan degradation. Adam I, Dewi DL, Mooiweer J, Sadik A, Mohapatra SR, Berdel B, Keil M, Sonner JK, Thedieck K, Rose AJ, Platten M, Heiland I, Trump S, Opitz CA. Oncoimmunology. 2018 Sep 5;7(12):e1486353. doi: 10.1080/2162402X.2018.1486353. eCollection 2018. PubMed
Discovery of a novel long noncoding RNA overlapping the LCK gene that regulates prostate cancer cell growth. Ta HQ, Whitworth H, Yin Y, Conaway M, Frierson HF Jr, Campbell MJ, Raj GV, Gioeli D. Mol Cancer. 2019 Jun 28;18(1):113. doi: 10.1186/s12943-019-1039-6. PubMed
Hotspot SF3B1 mutations induce metabolic reprogramming and vulnerability to serine deprivation. Dalton WB, Helmenstine E, Walsh N, Gondek LP, Kelkar DS, Read A, Natrajan R, Christenson ES, Roman B, Das S, Zhao L, Leone RD, Shinn D, Groginski T, Madugundu AK, Patil A, Zabransky DJ, Medford A, Lee J, Cole AJ, Rosen M, Thakar M, Ambinder A, Donaldson J, DeZern AE, Cravero K, Chu D, Madero-Marroquin R, Pandey A, Hurley PJ, Lauring J, Park BH. J Clin Invest. 2019 Aug 8;130:4708-4723. doi: 10.1172/JCI125022. PubMed
Challenges and Reinterpretation of Antibody-Based Research on Phosphorylation of Tyr(307) on PP2Ac. Mazhar S, Leonard D, Sosa A, Schlatzer D, Thomas D, Narla G. Cell Rep. 2020 Mar 3;30(9):3164-3170.e3. doi: 10.1016/j.celrep.2020.02.012. PubMed
Mutations in the exocyst component EXOC2 cause severe defects in human brain development. Van Bergen NJ, Ahmed SM, Collins F, Cowley M, Vetro A, Dale RC, Hock DH, de Caestecker C, Menezes M, Massey S, Ho G, Pisano T, Glover S, Gusman J, Stroud DA, Dinger M, Guerrini R, Macara IG, Christodoulou J. J Exp Med. 2020 Oct 5;217(10). pii: 151928. doi: 10.1084/jem.20192040. PubMed

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