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Telomere Biology and Human Phenotype
Cells · 2019 · Vol. 8(1) · pp. 73–73
Abstract
Telomeres are nucleoprotein structures that cap the end of each chromosome arm and function to maintain genome stability. The length of telomeres is known to shorten with each cell division and it is well-established that telomere attrition is related to replicative capacity in vitro. Moreover, telomere loss is also correlated with the process of aging in vivo. In this review, we discuss the mechanisms that lead to telomere shortening and summarise telomere homeostasis in humans throughout a lifetime. In addition, we discuss the available evidence that shows that telomere shortening is related to human aging and the onset of age-related disease.
Telomeres, Telomerase, and SenescenceMicroplastics and Plastic PollutionTelomereBiologyTelomere-binding proteinPhenotypeGeneticsCell divisionChromosomeCell biologyGenomeGenome instability
MeSH terms
AgingDNA ReplicationHomeostasisHumansPhenotypeTelomereTelomere Homeostasis
Citations
368
FWCI
22.84
field-weighted impact
References
188
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100%
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Citations per year
Cited by
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