Oge Arum, Ph.D.
Affiliations: | 2005 | University of Colorado, Boulder, Boulder, CO, United States |
Area:
Genetics, Molecular Biology, Cell BiologyGoogle:
"Oge Arum"Mean distance: (not calculated yet)
Parents
Sign in to add mentorThomas E. Johnson | grad student | 2005 | CU Boulder | |
(On the discovery and elucidation of the mechanism via which repression of the Caenorhabditis elegans p53 ortholog cep-1 results in longevity.) |
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Publications
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Boparai RK, Arum O, Miquet JG, et al. (2015) Resistance to the Beneficial Metabolic Effects and Hepatic Antioxidant Defense Actions of Fibroblast Growth Factor 21 Treatment in Growth Hormone-Overexpressing Transgenic Mice. International Journal of Endocrinology. 2015: 282375 |
Hill CM, Arum O, Boparai RK, et al. (2015) Female PAPP-A knockout mice are resistant to metabolic dysfunction induced by high-fat/high-sucrose feeding at middle age. Age (Dordrecht, Netherlands). 37: 9765 |
Arum O, Dawson JA, Smith DL, et al. (2015) Do altered energy metabolism or spontaneous locomotion 'mediate' decelerated senescence? Aging Cell. 14: 483-90 |
Martinez CS, Piazza VG, Díaz ME, et al. (2015) GH/STAT5 signaling during the growth period in livers of mice overexpressing GH. Journal of Molecular Endocrinology. 54: 171-84 |
Arum O, Saleh J, Boparai R, et al. (2014) Interaction of growth hormone receptor/binding protein gene disruption and caloric restriction for insulin sensitivity and attenuated aging. F1000research. 3: 256 |
Arum O, Boparai RK, Saleh JK, et al. (2014) Specific suppression of insulin sensitivity in growth hormone receptor gene-disrupted (GHR-KO) mice attenuates phenotypic features of slow aging. Aging Cell. 13: 981-1000 |
Arum O, Saleh JK, Boparai RK, et al. (2014) Preservation of blood glucose homeostasis in slow-senescing somatotrophism-deficient mice subjected to intermittent fasting begun at middle or old age. Age (Dordrecht, Netherlands). 36: 9651 |
Westbrook R, Bonkowski MS, Arum O, et al. (2014) Metabolic alterations due to caloric restriction and every other day feeding in normal and growth hormone receptor knockout mice. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. 69: 25-33 |
Arum O, Rickman DJ, Kopchick JJ, et al. (2014) The slow-aging growth hormone receptor/binding protein gene-disrupted (GHR-KO) mouse is protected from aging-resultant neuromusculoskeletal frailty. Age (Dordrecht, Netherlands). 36: 117-27 |
Arum O, Rasche ZA, Rickman DJ, et al. (2013) Prevention of neuromusculoskeletal frailty in slow-aging ames dwarf mice: longitudinal investigation of interaction of longevity genes and caloric restriction. Plos One. 8: e72255 |