Linked from

The 28 pages that link to Cellular senescence, each with the reason it gives.

• AgingRelated: Senescent cells accumulate with age and can release signals that disrupt nearby tissues.

• Stem cellRelated: Senescence can limit stem-cell function and complicate long-term tissue regeneration.

• Cell biologyRelated: Its roles in aging, tissue repair, and disease remain active areas of investigation.

• DNA damageRelated: Persistent damage signals can induce senescence and alter tissue environments.

• CarcinogenesisRelated: Senescence can prevent damaged cells from continuing to proliferate.

• TelomereRelated: Critically short telomeres can trigger senescence by activating DNA-damage signaling.

• DNA damage responseRelated: Persistent damage can impose senescence, limiting proliferation while changing tissue signaling.

• p53Related: p53 can help establish senescence when continued proliferation would be harmful.

• Cell-cycle checkpointRelated: Persistent checkpoint signaling can drive an irreversible proliferative arrest.

• LongevityRelated: Senescent cells accumulate with age and can disrupt tissue function.

• TelomeraseRelated: Telomere shortening can contribute to senescence when chromosome ends become critically short.

• Elizabeth BlackburnRelated: Telomere shortening can trigger senescence in some cells, connecting chromosome maintenance to aging biology.

• Somatic cellRelated: Some somatic cells enter this state after damage or repeated division.

• Carol W. GreiderRelated: Telomere shortening can trigger senescence, linking Greider’s research to limits on cell division.

• Jack W. SzostakRelated: Telomere shortening can contribute to senescence, a consequence of chromosome-end biology.

• ProgeriaRelated: Progerin can promote senescence, contributing to tissue dysfunction.

• SupercentenarianRelated: Senescent cells accumulate with age and are studied in longevity research.

• Werner syndromeRelated: DNA damage and telomere dysfunction can push cells toward senescence in Werner syndrome.

• Cell Physiological PhenomenaRelated: Its varied effects raise questions about aging, tissue repair, and disease.

• Oxyphil cells (parathyroid)Related: Age-related accumulation has prompted proposals that oxyphil cells represent altered or senescent cells.

• Pancreatic stellate cellsRelated: Whether senescent stellate cells limit or worsen pancreatic fibrosis depends on their signals and context.