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Lloye M. Dillon, Ph.D. - Publications

Affiliations: 
2012 Molecular Cell and Developmental Biology (Medicine) University of Miami, Coral Gables, FL 
Area:
Cell Biology, Molecular Biology, Aging
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12 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
2016 Pinto M, Pickrell AM, Wang X, Bacman SR, Yu A, Hida A, Dillon LM, Morton PD, Malek TR, Williams SL, Moraes CT. Transient mitochondrial DNA double strand breaks in mice cause accelerated aging phenotypes in a ROS-dependent but p53/p21-independent manner. Cell Death and Differentiation. PMID 27911443 DOI: 10.1038/Cdd.2016.123  0.711
2013 Wang X, Pickrell AM, Rossi SG, Pinto M, Dillon LM, Hida A, Rotundo RL, Moraes CT. Transient systemic mtDNA damage leads to muscle wasting by reducing the satellite cell pool. Human Molecular Genetics. 22: 3976-86. PMID 23760083 DOI: 10.1093/Hmg/Ddt251  0.723
2013 Noe N, Dillon L, Lellek V, Diaz F, Hida A, Moraes CT, Wenz T. Bezafibrate improves mitochondrial function in the CNS of a mouse model of mitochondrial encephalopathy. Mitochondrion. 13: 417-26. PMID 23261681 DOI: 10.1016/J.Mito.2012.12.003  0.68
2012 Dillon LM, Hida A, Garcia S, Prolla TA, Moraes CT. Long-term bezafibrate treatment improves skin and spleen phenotypes of the mtDNA mutator mouse. Plos One. 7: e44335. PMID 22962610 DOI: 10.1371/Journal.Pone.0044335  0.683
2012 Dillon LM, Williams SL, Hida A, Peacock JD, Prolla TA, Lincoln J, Moraes CT. Increased mitochondrial biogenesis in muscle improves aging phenotypes in the mtDNA mutator mouse. Human Molecular Genetics. 21: 2288-97. PMID 22357654 DOI: 10.1093/Hmg/Dds049  0.713
2012 Dillon LM, Rebelo AP, Moraes CT. The role of PGC-1 coactivators in aging skeletal muscle and heart. Iubmb Life. 64: 231-41. PMID 22279035 DOI: 10.1002/Iub.608  0.746
2012 Williams S, Pickrell A, Dillon L, Bacman S, Mash D, Zϋchner S, Moraes CT. Towards a clearer picture of somatic mitochondrial DNA mutation spectrums using next generation sequencing Mitochondrion. 12: 566. DOI: 10.1016/J.Mito.2012.07.042  0.729
2012 Pickrell AM, Wang X, Pinto M, Bacman SR, Yu A, Hida A, Dillon LM, Morton PD, Malek TR, Williams SL, Moraes CT. Mitochondrial DNA damage contributes to premature aging through p53-dependent response mechanisms Mitochondrion. 12: 565-566. DOI: 10.1016/J.Mito.2012.07.040  0.736
2011 Rebelo AP, Dillon LM, Moraes CT. Mitochondrial DNA transcription regulation and nucleoid organization. Journal of Inherited Metabolic Disease. 34: 941-51. PMID 21541724 DOI: 10.1007/S10545-011-9330-8  0.728
2011 Williams⁎ SL, Huang J, Edwards Y, Ulla R, Pickrell A, Dillon L, Bacman S, Vance J, Zuchner S, Moraes CT. Next generation sequencing as a means to detect low frequency mtDNA variants Mitochondrion. 11: 653. DOI: 10.1016/J.Mito.2011.03.056  0.654
2011 Dillon⁎ LM, Prolla TA, Moraes CT. The effect of increased mitochondrial biogenesis on premature aging Mitochondrion. 11: 646. DOI: 10.1016/J.Mito.2011.03.036  0.691
2010 Williams SL, Huang J, Edwards YJ, Ulloa RH, Dillon LM, Prolla TA, Vance JM, Moraes CT, Züchner S. The mtDNA mutation spectrum of the progeroid Polg mutator mouse includes abundant control region multimers. Cell Metabolism. 12: 675-82. PMID 21109200 DOI: 10.1016/J.Cmet.2010.11.012  0.612
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