17‐a‐estradiol late in life extends lifespan in aging UM‐HET3 male mice; nicotinamide riboside and three other drugs do not affect lifespan in either sex
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N. Rosenthal | L. Leng | R. Bucala | G. Cortopassi | M. Bogue | A. Salmon | M. Javors | R. Strong | Richard A. Miller | D. Harrison | Alessandro Bitto | James F. Nelson | K. Kavanagh | T. Stearns | K. Flurkey | Amy L. Sindler | F. Macchiarini | P. Reifsnyder | J. Nelson | M. Lopez-Cruzan | Elizabeth Fernandez | Navasuja Kumar
[1] Corrigendum to: 17‐a‐estradiol late in life extends lifespan in aging UM‐HET3 male mice; nicotinamide riboside and three other drugs do not affect lifespan in either sex , 2022, Aging cell.
[2] M. Bogue,et al. Rapamycin‐mediated mouse lifespan extension: Late‐life dosage regimes with sex‐specific effects , 2020, Aging cell.
[3] D. Allison,et al. Canagliflozin Extends Lifespan in Genetically Heterogeneous Male But Not Female Mice , 2020, bioRxiv.
[4] P. Khaitovich,et al. Identification and Application of Gene Expression Signatures Associated with Lifespan Extension. , 2019, Cell metabolism.
[5] Megan M. Sheehan,et al. Novel Role of Macrophage Migration Inhibitory Factor in Upstream Control of the Unfolded Protein Response After Ethanol Feeding in Mice. , 2019, Alcoholism, clinical and experimental research.
[6] J. C. Price,et al. Short-term calorie restriction and 17α-estradiol administration elicit divergent effects on proteostatic processes and protein content in metabolically active tissues. , 2019, The journals of gerontology. Series A, Biological sciences and medical sciences.
[7] T. Slaga,et al. Acarbose improves health and lifespan in aging HET3 mice , 2019, Aging cell.
[8] A. Galecki,et al. Male lifespan extension with 17‐α estradiol is linked to a sex‐specific metabolomic response modulated by gonadal hormones in mice , 2018, Aging cell.
[9] D. Sinclair,et al. Therapeutic Potential of NAD-Boosting Molecules: The In Vivo Evidence. , 2018, Cell metabolism.
[10] Mark S. Schmidt,et al. Nicotinamide Improves Aspects of Healthspan, but Not Lifespan, in Mice. , 2018, Cell metabolism.
[11] Richard A. Miller,et al. Sex differences in lifespan extension with acarbose and 17‐α estradiol: gonadal hormones underlie male‐specific improvements in glucose tolerance and mTORC2 signaling , 2017, Aging cell.
[12] J. Bernhagen,et al. MIF allele-dependent regulation of the MIF coreceptor CD44 and role in rheumatoid arthritis , 2016, Proceedings of the National Academy of Sciences.
[13] J. Auwerx,et al. NAD+ repletion improves muscle function in muscular dystrophy and counters global PARylation , 2016, Science Translational Medicine.
[14] Mark S. Schmidt,et al. Nicotinamide riboside is uniquely and orally bioavailable in mice and humans , 2016, Nature Communications.
[15] R. Aebersold,et al. NAD+ repletion improves mitochondrial and stem cell function and enhances life span in mice , 2016, Science.
[16] Dudley Lamming,et al. Longer lifespan in male mice treated with a weakly estrogenic agonist, an antioxidant, an α‐glucosidase inhibitor or a Nrf2‐inducer , 2016, Aging cell.
[17] G. Shulman,et al. 17α-Estradiol Alleviates Age-related Metabolic and Inflammatory Dysfunction in Male Mice Without Inducing Feminization , 2016, The journals of gerontology. Series A, Biological sciences and medical sciences.
[18] Marnie G Silverstein,et al. Inducing Muscle Heat Shock Protein 70 Improves Insulin Sensitivity and Muscular Performance in Aged Mice. , 2015, The journals of gerontology. Series A, Biological sciences and medical sciences.
[19] S. Austad,et al. Long-lived species have improved proteostasis compared to phylogenetically-related shorter-lived species. , 2015, Biochemical and biophysical research communications.
[20] Z. D. Sharp,et al. Rapamycin-mediated lifespan increase in mice is dose and sex dependent and metabolically distinct from dietary restriction , 2014, Aging cell.
[21] B. Ames,et al. Acarbose, 17-α-estradiol, and nordihydroguaiaretic acid extend mouse lifespan preferentially in males , 2013, Aging cell.
[22] J. Auwerx,et al. The NAD(+) precursor nicotinamide riboside enhances oxidative metabolism and protects against high-fat diet-induced obesity. , 2012, Cell metabolism.
[23] R. de Cabo,et al. Rapamycin, but not resveratrol or simvastatin, extends life span of genetically heterogeneous mice. , 2011, The journals of gerontology. Series A, Biological sciences and medical sciences.
[24] K. Flurkey,et al. Life extension by diet restriction and N-acetyl-L-cysteine in genetically heterogeneous mice. , 2010, The journals of gerontology. Series A, Biological sciences and medical sciences.
[25] J. Wilkinson,et al. Macrophage migration inhibitory factor‐knockout mice are long lived and respond to caloric restriction , 2010, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[26] Marco Pahor,et al. Rapamycin fed late in life extends lifespan in genetically heterogeneous mice , 2009, Nature.
[27] G. Remuzzi,et al. Disruption of the Ang II type 1 receptor promotes longevity in mice. , 2009, The Journal of clinical investigation.
[28] Kenneth L. Hensley,et al. Nordihydroguaiaretic acid and aspirin increase lifespan of genetically heterogeneous male mice , 2008, Aging cell.
[29] Tian Zhu,et al. HPLC-APCI-MS for the determination of teprenone in human plasma: method and clinical application. , 2007, Journal of Pharmaceutical and Biomedical Analysis.
[30] K. Node,et al. Effects of Candesartan for Middle-Aged and Elderly Women with Hypertension and Menopausal-Like Symptoms , 2006, Hypertension Research.
[31] A. Galecki,et al. Genetic Loci That Influence Cause of Death in a Heterogeneous Mouse Stock , 2004, The journals of gerontology. Series A, Biological sciences and medical sciences.
[32] David B. Allison,et al. Statistical methods for testing effects on “maximum lifespan” , 2004, Mechanisms of Ageing and Development.
[33] G. Mancia,et al. Comparative effects of candesartan and hydrochlorothiazide on blood pressure, insulin sensitivity, and sympathetic drive in obese hypertensive individuals: results of the CROSS study , 2003, Journal of hypertension.
[34] Richard A. Miller,et al. T Cell Subset Patterns That Predict Resistance to Spontaneous Lymphoma, Mammary Adenocarcinoma, and Fibrosarcoma in Mice1 , 2002, The Journal of Immunology.
[35] John A. Katzenellenbogen,et al. The estradiol pharmacophore: Ligand structure-estrogen receptor binding affinity relationships and a model for the receptor binding site , 1997, Steroids.
[36] C. Desjardins,et al. Luteinizing hormone and testosterone secretion in young and old male mice. , 1982, The American journal of physiology.
[37] T. Roderick. Selection for radiation resistance in mice. , 1963, Genetics.
[38] R. Strong,et al. NIA Interventions Testing Program: A collaborative approach for investigating interventions to promote healthy aging , 2021, Handbook of the Biology of Aging.
[39] F. Hoogstra-Berends,et al. Oral geranylgeranylacetone treatment increases heat shock protein expression in human atrial tissue. , 2019, Heart rhythm.