Aaron M. Domina, Ph.D. - Publications
Affiliations: | 2001 | Dartmouth College, Hanover, NH, United States |
Area:
Pharmacology, Molecular Biology, Cell BiologyYear | Citation | Score | |||
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2012 | Nifoussi SK, Vrana JA, Domina AM, De Biasio A, Gui J, Gregory MA, Hann SR, Craig RW. Thr 163 phosphorylation causes Mcl-1 stabilization when degradation is independent of the adjacent GSK3-targeted phosphodegron, promoting drug resistance in cancer. Plos One. 7: e47060. PMID 23056582 DOI: 10.1371/Journal.Pone.0047060 | 0.65 | |||
2007 | De Biasio A, Vrana JA, Zhou P, Qian L, Bieszczad CK, Braley KE, Domina AM, Weintraub SJ, Neveu JM, Lane WS, Craig RW. N-terminal truncation of antiapoptotic MCL1, but not G2/M-induced phosphorylation, is associated with stabilization and abundant expression in tumor cells. The Journal of Biological Chemistry. 282: 23919-36. PMID 17561513 DOI: 10.1074/Jbc.M700938200 | 0.623 | |||
2004 | Domina AM, Vrana JA, Gregory MA, Hann SR, Craig RW. MCL1 is phosphorylated in the PEST region and stabilized upon ERK activation in viable cells, and at additional sites with cytotoxic okadaic acid or taxol. Oncogene. 23: 5301-15. PMID 15241487 DOI: 10.1038/Sj.Onc.1207692 | 0.646 | |||
2000 | Domina AM, Smith JH, Craig RW. Myeloid cell leukemia 1 is phosphorylated through two distinct pathways, one associated with extracellular signal-regulated kinase activation and the other with G2/M accumulation or protein phosphatase 1/2A inhibition. The Journal of Biological Chemistry. 275: 21688-94. PMID 10777489 DOI: 10.1074/Jbc.M000915200 | 0.648 | |||
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