Academic literature on the topic 'Hayflick's limit'

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Journal articles on the topic "Hayflick's limit"

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Chen, Jun, and Michael S. Goligorsky. "Premature senescence of endothelial cells: Methusaleh's dilemma." American Journal of Physiology-Heart and Circulatory Physiology 290, no. 5 (2006): H1729—H1739. http://dx.doi.org/10.1152/ajpheart.01103.2005.

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Senescence has been considered a programmed cellular response, parallel to apoptosis, that is turned on when a cell reaches Hayflick's limit. Once cells enter the senescence program, they cease to proliferate and undergo a series of morphological and functional changes. Studies support a central role for Rb protein in controlling this process after it receives senescent signals from the p53 and p16 pathways. Cellular senescence is considered an essential contributor to the aging process and has been shown to be an important tumor suppression mechanism. In addition, emerging evidence suggests t
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Gillooly, James F., April Hayward, Chen Hou, and J. Gordon Burleigh. "Explaining differences in the lifespan and replicative capacity of cells: a general model and comparative analysis of vertebrates." Proceedings of the Royal Society B: Biological Sciences 279, no. 1744 (2012): 3976–80. http://dx.doi.org/10.1098/rspb.2012.1129.

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A better understanding of the factors that govern individual cell lifespan and the replicative capacity of cells (i.e. Hayflick's limit) is important for addressing disease progression and ageing. Estimates of cell lifespan in vivo and the replicative capacity of cell lines in culture vary substantially both within and across species, but the underlying reasons for this variability remain unclear. Here, we address this issue by presenting a quantitative model of cell lifespan and cell replicative capacity. The model is based on the relationship between cell mortality and metabolic rate, which
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Franken, Jessica. "The Hayflick Limit." River Teeth: A Journal of Nonfiction Narrative 22, no. 2 (2021): 107–11. http://dx.doi.org/10.1353/rvt.2021.0010.

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Luft, Friedrich C. "Approaching the Hayflick limit." Trends in Cardiovascular Medicine 25, no. 3 (2015): 240–42. http://dx.doi.org/10.1016/j.tcm.2014.12.008.

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Shay, Jerry W., and Woodring E. Wright. "Hayflick, his limit, and cellular ageing." Nature Reviews Molecular Cell Biology 1, no. 1 (2000): 72–76. http://dx.doi.org/10.1038/35036093.

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Griffiths, Paul D. "Herpesviruses and the Hayflick Limit In Vivo." Journal of Infectious Diseases 216, no. 5 (2017): 511–13. http://dx.doi.org/10.1093/infdis/jix256.

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Gill, Zoe, Martin Nieuwoudt, and Wilfred Ndifon. "The Hayflick Limit and Age-Related Adaptive Immune Deficiency." Gerontology 64, no. 2 (2017): 135–39. http://dx.doi.org/10.1159/000478091.

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The adaptive immune system (AIS) acquires significant deficiency during chronological ageing, making older individuals more susceptible to infections and less responsive to vaccines compared to younger individuals. At the cellular level, one of the most striking features of this ageing-related immune deficiency is the dramatic loss of T-cell diversity that occurs in elderly humans. After the age of 70 years, there is a sharp decline in the diversity of naïve T cells, including a >10-fold decrease in the CD4+ compartment and a >100-fold decrease in the CD8+ compartment. Such changes are d
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Watts, Geoff. "Leonard Hayflick and the limits of ageing." Lancet 377, no. 9783 (2011): 2075. http://dx.doi.org/10.1016/s0140-6736(11)60908-2.

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Migliaccio, Giovanni, Massimo Sanchez, Francesca Masiello та ін. "the γ Isoform of the Glucocorticoid Receptor Is Ontogenetically Activated and Predicts Poor Ex-Vivo Expansion of Erythroid Cells From Adult Blood." Blood 114, № 22 (2009): 642. http://dx.doi.org/10.1182/blood.v114.22.642.642.

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Abstract Abstract 642 Ex-vivo generated erythroblasts (EBs) represent alternative transfusion products. Adult blood (AB) contains numbers of progenitor cells comparable to those present in cord blood (CB) (106 vs 1.8×106 CD34pos cells in average AB and CB donations) but generates lower numbers of erythroblasts (EBs) (∼4.8×108 vs 6.6×1010, respectively) and, in spite of its numerous advantages, is not considered suitable for ex-vivo EB production. To assess the potential of AB to generate EBs ex-vivo, the growth factors [stem cell factor (SCF), interleukin-3 (IL-3) and erythropoietin (EPO)] and
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Ndifon, Wilfred, and Jonathan Dushoff. "The Hayflick Limit May Determine the Effective Clonal Diversity of Naive T Cells." Journal of Immunology 196, no. 12 (2016): 4999–5004. http://dx.doi.org/10.4049/jimmunol.1502343.

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Dissertations / Theses on the topic "Hayflick's limit"

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Suchánek, Jakub. "Kmenové buňky zubní pulpy." Doctoral thesis, 2011. http://www.nusl.cz/ntk/nusl-296114.

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The aim of this dissertation study was to optimize the isolation and long term cultivation protocols for human dental pulp stem cells. The protocols which showed best results were used for cultivation of dental pulp stem cell isolated from exfoliated teeth (SHED). Additional aims were to characterize DPSC and SHED and prove their ability to proliferate over Hayflick's limit and differentiate into mature cell lines (osteoblasts, chondroblasts and adipocytes). In order to find optimal protocols for isolation of dental pulp from tooth, we tried three different approaches. During optimization of c
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Carriço, Diogo André Fonseca. "Telomerase: a sua relevância no envelhecimento e cancro." Master's thesis, 2016. http://hdl.handle.net/10316/33724.

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Trabalho de revisão do 6º ano médico com vista à atribuição do grau de mestre (área científica de medicina geriatria) no âmbito do ciclo de estudos de Mestrado Integrado em Medicina.<br>Este trabalho tem como objetivo explorar a relevância da telomerase em tratamentos futuros e revelar semelhanças da fisiopatologia do envelhecimento e cancro. Fiz uma breve revisão de vários artigos na área de geriatria, oncologia e gerontologia. Utilizei a rede privada virtual da Universidade de Coimbra. A telomerase é ativa em células estaminais e outras de alta taxa de divisão, encontra-se ativa também em 90
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Books on the topic "Hayflick's limit"

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Tierney, Matthew Frederick. The hayflick limit. Coach House Books, 2009.

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The hayflick limit. Coach House Books, 2009.

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Tomasetta, Leonardo. Il limite di Hayflick. Robin, 2005.

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Tierney, Matthew. Hayflick Limit. Coach House Books, 2009.

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Book chapters on the topic "Hayflick's limit"

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Rattan, Suresh I. S. "Origins of the Hayflick System, the Phenomenon and the Limit." In Cellular Ageing and Replicative Senescence. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-26239-0_1.

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"Hayflick's Limit." In Encyclopedia of Genetics, Genomics, Proteomics and Informatics. Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6754-9_7376.

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Hal, Stephen S. "Human Cloning and Stem Cells." In A Field Guide for Science Writers. Oxford University Press, 2005. http://dx.doi.org/10.1093/oso/9780195174991.003.0036.

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Of the countless interviews I have conducted with scientists over the years, only once has a question prompted something of a striptease. In December of 1999, I found myself in the elegant parlor of the Union Club in New York City, chatting with a biologist named Leonard Hayflick. Although hardly a household name to the general public, Hayflick is that rare scientist whose name is permanently attached to a biological phenomenon. It is known as the “Hayflick limit,” and it derives from experiments he did in the late 19505 and early 19605 showing that human cells grown in Petri dishes will predictably replicate for a certain number of cell divisions, but then hit a wall and stop dividing. This has obvious implications for cell biology, aging, and immortality (of the in vitro sort), and indeed the Hayflick limit has been the seed around which a spirited biological debate about the biology of aging has swirled, without definitive resolution, for about four decades now. Because of this history, Hayflick has closely followed the recent work on the biology of aging and regenerative medicine, which in turn has made him a front-row spectator in the more recent controversies involving human embryonic stem cell research and “therapeutic cloning.” At the time of my conversation with Hayflick, his longtime friend Michael West was attempting to obtain human embryonic stem cells through cloning—in a particularly controversial way, by putting human cells into egg cells from ... cows. Almost as an aside, I asked Hayflick what he thought about West's experiments. Hayflick replied by rolling up his pants leg. He bared enough skin to be able to point out a tiny dimple on his right knee. “The human cells he's using for the cow work came from here,” he said. I had to stand up and lean over to see it, but there was undeniably a tiny divot in Hayflick's skin. The implications were stunning: Leonard Hayflick, the father of cellular senescence and one of the elder statesmen of gerontology, was allowing himself, in a manner of speaking, to be cloned. In addition to making the obvious point that even the most innocuous question can elicit a startling answer, Hayflick's reply offered another lesson, too: that colorful characters can provide a narrative thread for bringing a controversy to life.
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