Lloye M. Dillon, Ph.D.
Affiliations: | 2012 | Molecular Cell and Developmental Biology (Medicine) | University of Miami, Coral Gables, FL |
Area:
Cell Biology, Molecular Biology, AgingGoogle:
"Lloye Dillon"Mean distance: 23.34
Parents
Sign in to add mentor| Carlos T. Moraes | grad student | 2012 | University of Miami | |
| (The effect of increased mitochondrial biogenesis and activation of PPAR pathways in a mouse model of aging.) | ||||
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Publications
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| Pinto M, Pickrell AM, Wang X, et al. (2016) 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 |
| Wang X, Pickrell AM, Rossi SG, et al. (2013) Transient systemic mtDNA damage leads to muscle wasting by reducing the satellite cell pool. Human Molecular Genetics. 22: 3976-86 |
| Noe N, Dillon L, Lellek V, et al. (2013) Bezafibrate improves mitochondrial function in the CNS of a mouse model of mitochondrial encephalopathy. Mitochondrion. 13: 417-26 |
| Dillon LM, Hida A, Garcia S, et al. (2012) Long-term bezafibrate treatment improves skin and spleen phenotypes of the mtDNA mutator mouse. Plos One. 7: e44335 |
| Dillon LM, Williams SL, Hida A, et al. (2012) Increased mitochondrial biogenesis in muscle improves aging phenotypes in the mtDNA mutator mouse. Human Molecular Genetics. 21: 2288-97 |
| Dillon LM, Rebelo AP, Moraes CT. (2012) The role of PGC-1 coactivators in aging skeletal muscle and heart. Iubmb Life. 64: 231-41 |
| Williams S, Pickrell A, Dillon L, et al. (2012) Towards a clearer picture of somatic mitochondrial DNA mutation spectrums using next generation sequencing Mitochondrion. 12: 566 |
| Pickrell AM, Wang X, Pinto M, et al. (2012) Mitochondrial DNA damage contributes to premature aging through p53-dependent response mechanisms Mitochondrion. 12: 565-566 |
| Rebelo AP, Dillon LM, Moraes CT. (2011) Mitochondrial DNA transcription regulation and nucleoid organization. Journal of Inherited Metabolic Disease. 34: 941-51 |
| Williams⁎ SL, Huang J, Edwards Y, et al. (2011) Next generation sequencing as a means to detect low frequency mtDNA variants Mitochondrion. 11: 653 |