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BIBLIO ID Author and year Title Citations External link
0001Zhou et al. (1997)A mammalian model for Laron syndrome produced by targeted disruption of the mouse growth hormone receptor/binding protein gene (the Laron mouse)1PubMed
0002Kopchick and Laron (1999)Is the Laron mouse an accurate model of Laron syndrome?1PubMed
0003Coschigano et al. (2003)Deletion, but not antagonism, of the mouse growth hormone receptor results in severely decreased body weights, insulin, and insulin-like growth factor I levels and increased life span4PubMed
0004Coschigano et al. (2000)Assessment of growth parameters and life span of GHR/BP gene-disrupted mice1PubMed
0005Flurkey et al. (2001)Lifespan extension and delayed immune and collagen aging in mutant mice with defects in growth hormone production2PubMed
0006Migliaccio et al. (1999)The p66shc adaptor protein controls oxidative stress response and life span in mammals2PubMed
0007Nemoto and Finkel (2002)Redox regulation of forkhead proteins through a p66shc-dependent signaling pathway2PubMed
0008Trinei et al. (2002)A p53-p66Shc signalling pathway controls intracellular redox status, levels of oxidation-damaged DNA and oxidative stress-induced apoptosis2PubMed
0009Napoli et al. (2003)Deletion of the p66Shc longevity gene reduces systemic and tissue oxidative stress, vascular cell apoptosis, and early atherogenesis in mice fed a high-fat diet1PubMed
0010Brown-Borg et al. (1996)Dwarf mice and the ageing process1PubMed
0011Tyner et al. (2002)p53 mutant mice that display early ageing-associated phenotypes1PubMed
0012Wong et al. (2003)Telomere dysfunction and Atm deficiency compromises organ homeostasis and accelerates ageing2PubMed
0013Miskin and Masos (1997)Transgenic mice overexpressing urokinase-type plasminogen activator in the brain exhibit reduced food consumption, body weight and size, and increased longevity1PubMed
0014de Boer et al. (2002)Premature aging in mice deficient in DNA repair and transcription2PubMed
0015Henning et al. (1995)The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH2PubMed
0016Yu et al. (1996)Positional cloning of the Werner's syndrome gene1PubMed
0017Eriksson et al. (2003)Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome1PubMed
0018Holzenberger et al. (2003)IGF-1 receptor regulates lifespan and resistance to oxidative stress in mice2PubMed
0019Mitsui et al. (2002)Overexpression of human thioredoxin in transgenic mice controls oxidative stress and life span1PubMed
0020Kuro-o et al. (1997)Mutation of the mouse klotho gene leads to a syndrome resembling ageing1PubMed


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