DNA damage response and cellular senescence in tissues of aging mice
By Chunfang Wang, D. Jurk, M. Maddick, Glyn Nelson, C. Martin-Ruiz, T. von Zglinicki. Aging Cell, 2009
680 citations recorded by the source corpus.
Subfields: Dermatology, Endocrine and Autonomic Systems, Physiology
View Paper: https://www.semanticscholar.org/paper/35e76e0af7c3d83039e63961a23b8dfdd89c56aa
How researchers see this paper
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In Dermatology
In Endocrine and Autonomic Systems
In Physiology
- J. Campisi
- J. Kirkland
- M. Demaria
- T. Tchkonia
- Manuel Serrano
- Adam Freund
- Guido Kroemer
- Nathan K. LeBrasseur
Citations in the corpus
- The hallmarks of aging. (2013, background): “Similar results were obtained in the skin, lung, and spleen, but no changeswere observed in heart, skeletal muscle, and kidney (Wang et al., 2009).”
- Lamin B1 loss is a senescence-associated biomarker (2012, methodology): “We chose liver because previous reports showed an accumulation of senescent cells in this tissue (Paradis et al., 2001; Xue et al., 2007; Krizhanovsky et al., 2008; Wang et al., 2009; Le et al., 2010), and liver showed low background staining, allowing for accurate quantitation.”
- A senescent cell bystander effect: senescence-induced senescence (2012, methodology): “2F) and Sen-b-Gal (Wang et al., 2009, 2010) and allows clear cell boundary definition in the low magnification tiled images necessary for cluster analysis.”
- Cellular Senescence: Aging, Cancer, and Injury. (2019, background): “Various markers of senescence, including SA- -gal, p16, and DDR, accumulate in tissues of aged mammals including rodents (42, 189, 335), baboons (156, 168), and humans (67, 97, 211, 225, 267), suggesting that senescent cells CELLULAR SENESCENCE”
- JAK inhibition alleviates the cellular senescence-associated secretory phenotype and frailty in old age (2015, background): “Senescent cells accumulate with aging in the skin (13, 14), liver (15, 16), kidney (17), the cardiovascular system (18), and other tissues in various species (16).”
- Aging, Cellular Senescence, and Cancer (2012, background): “Persistent DNA damage foci are found in tissues that experience genotoxic stress (42) and in aging mouse and primate tissues (29, 30, 84).”