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Allsopp, Richard
One or more keywords matched the following items that are connected to Allsopp, Richard
Item TypeName
Academic Article Genetic analysis of TOR complex gene variation with human longevity: a nested case-control study of American men of Japanese ancestry.
Academic Article Genetic variation in the raptor gene is associated with overweight but not hypertension in American men of Japanese ancestry.
Academic Article Longevity-Associated FOXO3 Genotype and its Impact on Coronary Artery Disease Mortality in Japanese, Whites, and Blacks: A Prospective Study of Three American Populations.
Academic Article Association of Polymorphisms in Connective Tissue Growth Factor and Epidermal Growth Factor Receptor Genes With Human Longevity.
Academic Article FOXO3 longevity interactome on chromosome 6.
Academic Article FOXO3 and Exceptional Longevity: Insights From Hydra to Humans.
Academic Article Analysis of Polymorphisms in 59 Potential Candidate Genes for Association With Human Longevity.
Academic Article Minimal Shortening of Leukocyte Telomere Length Across Age Groups in a Cross-Sectional Study for Carriers of a Longevity-Associated FOXO3 Allele.
Concept Polymorphism, Single Nucleotide
Academic Article FOXO3 longevity genotype mitigates the increased mortality risk in men with a cardiometabolic disease.
Academic Article Lifespan extension conferred by mitogen-activated protein kinase kinase kinase 5 (MAP3K5) longevity-associated gene variation is confined to at-risk men with a cardiometabolic disease.
Academic Article Association of growth hormone receptor gene variant with longevity in men is due to amelioration of increased mortality risk from hypertension.
Academic Article The Association Between Longevity-Associated FOXO3 Allele and Heart Disease in Septuagenarians and Octogenarians: The SONIC Study.
Academic Article Extreme longevity variants at the FOXO3 locus may moderate FOXO3 isoform levels.
Academic Article Forkhead box O3 longevity genotype may attenuate the impact of hypertension on risk of intracerebral haemorrhage.
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  • Polymorphism Single Nucleotide
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