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Christie N. Jones, Ph.D. - Publications

Affiliations: 
2008 Chemistry University of North Carolina, Chapel Hill, Chapel Hill, NC 
Area:
Protein Synthesis of Mammalian Mitochondria
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7 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2013 Nallagatla SR, Jones CN, Ghosh SK, Sharma SD, Cameron CE, Spremulli LL, Bevilacqua PC. Native tertiary structure and nucleoside modifications suppress tRNA's intrinsic ability to activate the innate immune sensor PKR. Plos One. 8: e57905. PMID 23483938 DOI: 10.1371/Journal.Pone.0057905  0.593
2011 Bilbille Y, Gustilo EM, Harris KA, Jones CN, Lusic H, Kaiser RJ, Delaney MO, Spremulli LL, Deiters A, Agris PF. The human mitochondrial tRNAMet: structure/function relationship of a unique modification in the decoding of unconventional codons. Journal of Molecular Biology. 406: 257-74. PMID 21168417 DOI: 10.1016/J.Jmb.2010.11.042  0.636
2010 Akama K, Christian BE, Jones CN, Ueda T, Takeuchi N, Spremulli LL. Analysis of the functional consequences of lethal mutations in mitochondrial translational elongation factors. Biochimica Et Biophysica Acta. 1802: 692-8. PMID 20435138 DOI: 10.1016/J.Bbadis.2010.04.003  0.585
2009 Jones CN, Miller C, Tenenbaum A, Spremulli LL, Saada A. Antibiotic effects on mitochondrial translation and in patients with mitochondrial translational defects. Mitochondrion. 9: 429-37. PMID 19671450 DOI: 10.1016/J.Mito.2009.08.001  0.66
2008 Jones CN, Jones CI, Graham WD, Agris PF, Spremulli LL. A disease-causing point mutation in human mitochondrial tRNAMet rsults in tRNA misfolding leading to defects in translational initiation and elongation. The Journal of Biological Chemistry. 283: 34445-56. PMID 18835817 DOI: 10.1074/Jbc.M806992200  0.716
2008 Jones CN, Wilkinson KA, Hung KT, Weeks KM, Spremulli LL. Lack of secondary structure characterizes the 5' ends of mammalian mitochondrial mRNAs. Rna (New York, N.Y.). 14: 862-71. PMID 18367717 DOI: 10.1261/Rna.909208  0.64
2007 Jones CN, Spremulli LL, Agris PF. Structural and biochemical investigation of disease causing mutations in human mitochondrial tRNA Met The Faseb Journal. 21. DOI: 10.1096/Fasebj.21.5.A279-B  0.683
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