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2761por Zhong, Fangmin, Yang, Yulin, Yao, Fangyi, Liu, Jing, Yu, Xiajing, Wang, Xin-Lu, Huang, Bo, Wang, Xiao-Zhong“…Cellular senescence is closely related to the occurrence, development, and immune regulation of cancer. …”
Publicado 2023
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2762por Ting, Ka Ka, Coleman, Paul, Kim, Hani Jieun, Zhao, Yang, Mulangala, Jocelyne, Cheng, Ngan Ching, Li, Wan, Gunatilake, Dilini, Johnstone, Daniel M., Loo, Lipin, Neely, G. Gregory, Yang, Pengyi, Götz, Jürgen, Vadas, Mathew A., Gamble, Jennifer R.“…Here, we show for the first time the presence of senescent cells in the vasculature in AD patients and mouse models of AD. …”
Publicado 2023
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2763“…Consequently, the DNA damage remains unrepaired and TAZ::CAMTA1-expressing cells enter senescence. Knockout of Cdkn2a, the most common secondary mutation found in EHE, allows senescence bypass and uncontrolled growth. …”
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2764por Tan, Dunyong, Huang, Zeqi, Zhao, Zhe, Chen, Xiaoqiang, Liu, Jianquan, Wang, Daping, Deng, Zhiqin, Li, WencuiEnlace del recurso
Publicado 2023
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2765“…However, the involvement of cellular senescence in CC development is still unclear and requires further investigation. …”
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2766por Azam, Mahrukh, Lee, Julia Y., Abraham, Veena, Chanoux, Rebecca, Schoenly, Kimberly A., Johnson, F. Brad“…Here, we explore the protein sequences and genetic interactors of Sgs1p that function to slow the senescence of telomerase (tlc1) mutants. We find that the S-phase checkpoint function of Sgs1p is dispensable for preventing rapid senescence, but that Sgs1p sequences required for homologous recombination, including the helicase domain and topoisomerase III interaction domain, are essential. sgs1 and rad52 mutations are epistatic during senescence, indicating that Sgs1p participates in a RAD52-dependent recombinational pathway of telomere maintenance. …”
Publicado 2006
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2767“…Severe flower wilting occurs reproducibly within 36 hours, providing an excellent model for investigation of petal senescence and programmed cell death. Expression of a number of genes and various enzyme activities involved in the degradation and remobilization of macromolecules have been found to be upregulated during the early stages of petal senescence. …”
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2768por Lew, Virgilio L., Daw, Nuala, Etzion, Zipora, Tiffert, Teresa, Muoma, Adaeze, Vanagas, Laura, Bookchin, Robert M.“…The previously described subpopulation of high-Na(+), low-density RBCs had the highest Hb A1c levels, suggesting it represents a late homeostatic condition of senescent RBCs. Thus, the normal densification process of RBCs with age must undergo late reversal, requiring a membrane permeability increase with net NaCl gain exceeding KCl loss. …”
Publicado 2007
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2769por Mohler, Peter J., Healy, Jane A., Xue, Hui, Puca, Annibale A., Kline, Crystal F., Rand Allingham, R., Kranias, Evangelia G., Rockman, Howard A., Bennett, Vann“…Studies with the ankyrin-B(+/−) mouse reveal both benefits of enhanced cardiac contractility, as well as costs in earlier senescence and reduced lifespan. Together these findings suggest a constellation of traits that we term “ankyrin-B syndrome”, which may contribute to both aging-related disorders and enhanced cardiac function.…”
Publicado 2007
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2770Publicado 1975“…The [3H]thymidine labeling index of senescent fibroblast nuclei in heteropolykaryons was a function of the ratio of HeLa to senescent nuclei.…”
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2771Publicado 1992“…Human fibroblasts have a limited replicative life span when maintained in culture after which they become unresponsive to treatment with mitogens, a phenomenon most commonly called senescence. Experiments indicating that serum does not induce expression of the c-fos proto- oncogene in senescent fibroblasts raised the issue of a potential central role for c-fos in the phenotype of sustained growth arrest. …”
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2772por Alexopoulos, Evangelos C., Cominos, Xenophon, Trougakos, Ioannis P., Lourda, Magda, Gonos, Efstathios S., Makropoulos, Vassilios“…In vitro data showed that exposure of human diploid fibroblasts to hexavalent chromium (Cr(VI)) resulted in premature senescence and significant upregulation of the ApoJ/CLU protein. …”
Publicado 2008
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2773por Efeyan, Alejo, Murga, Matilde, Martinez-Pastor, Barbara, Ortega-Molina, Ana, Soria, Rebeca, Collado, Manuel, Fernandez-Capetillo, Oscar, Serrano, Manuel“…Moreover, lung adenomas initiated by endogenous levels of oncogenic K-Ras presented abundant senescent cells, but undetectable DNA damage signaling. …”
Publicado 2009
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2775“…This phenomenon was exhibited both during developmental leaf senescence and during senescence of detached leaves artificially induced by either darkness or phytohormones. …”
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2776“…Development of agents that suppress aging (aging suppressants) requires quantification of cellular senescence. Cellular senescence in vitro is characterized by a large cell morphology and permanent loss of proliferative potential. …”
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2777“…Thus, the senescence of cells, which was initially triggered by inflammatory stimuli, becomes a self-reinforcing stimulus for further inflammation and senescence. …”
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2778por Korotchkina, Lioubov G., Leontieva, Olga V., Bukreeva, Elena I., Demidenko, Zoya N., Gudkov, Andrei V., Blagosklonny, Mikhail V.“…In these senescence-prone cells, the mTOR inhibitor rapamycin converted nutlin-3a-induced senescence into quiescence. …”
Publicado 2010
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2779por Mallette, Frédérick A., Calabrese, Viviane, Ilangumaran, Subburaj, Ferbeyre, Gerardo“…Through this mechanism SOCS1 regulates the process of oncogene-induced senescence, which is a very important tumor suppressor response. …”
Publicado 2010
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2780“…The senescence-associated markers high mobility group (Hmg) A1 and heterochromatin protein 1 (HP1) are also upregulated in Dex-exposed NSCs, whereas Bmi1 (polycomb ring finger oncogene) and mitochondrial genes Nd3 (NADH dehydrogenase 3) and Cytb (cytochrome b) are downregulated. …”
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