Djun

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Hooper, C., et al. (2007). Glycogen synthase kinase-3 inhibition is integral to long-term potentiation. Eur. J. Neurosci. 25: 81-86. PubMed Citation: 17241269

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Kardassis, D., et al. (1999). c-Jun transactivates the promoter of the human p21WAF1/Cip1 gene by acting as a superactivator of the ubiquitous transcription factor Sp1. J. Biol. Chem. 274: 29572-29581. PubMed Citation: 10506225

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Kawasaki, H., et al. (1998). p300 and ATF-2 are components of the DRF complex, which regulates retinoic acid- and E1A-mediated transcription of the c-jun gene in F9 cells. Genes Dev. 12: 233-245. PubMed Citation: 9436983

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Kim, S. M., et al. (2009). Fos and Jun potentiate individual release sites and mobilize the reserve synaptic-vesicle pool at the Drosophila larval motor synapse. Proc. Natl. Acad. Sci. 106(10): 4000-4005. PubMed Citation: 19228945

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Liberati, N. T., et al. (1999). Smads bind directly to the jun family of AP-1 transcription factors. Proc. Natl. Acad. Sci. 96(9): 4844-9. PubMed Citation: 10220381

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Lively, T. N., Nguyen, T. N., Galasinski, S. K. and Goodrich, J. A. (2004). The basic leucine zipper domain of c-Jun functions in transcriptional activation through interaction with the N terminus of human TATA-binding protein-associated factor-1 (human TAF(II)250). J. Biol. Chem. 279(25): 26257-65. Medline abstract: 15087451

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date revised: 28 October 2010

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