Aging cells accumulate somatic mutations, gross chromosomal rearrangements, aneuploidy, mtDNA mutations, and persistent DNA damage. Drivers include endogenous oxidative damage, replication errors, declining DNA-repair machinery (NER, BER,…
Aging cells accumulate somatic mutations, gross chromosomal rearrangements, aneuploidy, mtDNA mutations, and persistent DNA damage. Drivers include endogenous oxidative damage, replication errors, declining DNA-repair machinery (NER, BER,…