| Q92893014 | A comparison of strategies for immortalizing mouse embryonic fibroblasts |
| Q33532644 | A human-like senescence-associated secretory phenotype is conserved in mouse cells dependent on physiological oxygen |
| Q38596295 | Age-associated changes in regenerative capabilities of mesenchymal stem cell: impact on chronic wounds repair |
| Q35825021 | Analysis of gene expression during aging of CGNs in culture: implication of SLIT2 and NPY in senescence |
| Q34688159 | Are there roles for brain cell senescence in aging and neurodegenerative disorders? |
| Q37802011 | At the stem of youth and health |
| Q47634516 | Behead and live long or the tale of cathepsin L. |
| Q35093078 | Cellular senescence and aging: the role of B-MYB |
| Q51759405 | Copper accumulation in senescent cells: Interplay between copper transporters and impaired autophagy. |
| Q39521147 | Developmental arrest of T cells in Rpl22-deficient mice is dependent upon multiple p53 effectors |
| Q91933446 | Diet-induced leukocyte telomere shortening in a baboon model for early stage atherosclerosis |
| Q42130385 | Divergent cellular phenotypes of human and mouse cells lacking the Werner syndrome RecQ helicase |
| Q33728019 | Dual functions of ASCIZ in the DNA base damage response and pulmonary organogenesis |
| Q42494627 | E6AP is required for replicative and oncogene-induced senescence in mouse embryo fibroblasts |
| Q90016432 | Effects of continuous exposure to low concentration of ClO2 gas on the growth, viability, and maintenance of undifferentiated MSCs in long-term cultures |
| Q89026265 | Enhanced mitochondrial DNA repair of the common disease-associated variant, Ser326Cys, of hOGG1 through small molecule intervention |
| Q37492244 | Facilitating replication under stress: an oncogenic function of MYC? |
| Q38138557 | Friend or foe: emerging role of nuclear factor kappa-light-chain-enhancer of activated B cells in cell senescence |
| Q39126232 | Functional interplay between the DNA-damage-response kinase ATM and ARF tumour suppressor protein in human cancer |
| Q51340477 | Geminin Is Essential for Pluripotent Cell Viability During Teratoma Formation, but Not for Differentiated Cell Viability During Teratoma Expansion. |
| Q33557928 | Genetic deletion of Nrf2 promotes immortalization and decreases life span of murine embryonic fibroblasts |
| Q37843473 | Heterochromatin and the DNA damage response: the need to relax |
| Q28820756 | Identification of genes that are essential to restrict genome duplication to once per cell division |
| Q37676222 | Links between DNA Replication, Stem Cells and Cancer |
| Q21245465 | Main roads to melanoma |
| Q35674359 | Modulation of collagen synthesis and its gene expression in human skin fibroblasts by tocotrienol-rich fraction |
| Q42239715 | Molecular characterization of collaborator of ARF (CARF) as a DNA damage response and cell cycle checkpoint regulatory protein |
| Q35670683 | New Perspectives of "omics" Applications in Melanoma Research |
| Q50188872 | Nutrient sensing, growth and senescence |
| Q28512750 | Poldip2 knockout results in perinatal lethality, reduced cellular growth and increased autophagy of mouse embryonic fibroblasts |
| Q28572137 | Rapamycin induces pluripotent genes associated with avoidance of replicative senescence |
| Q30366115 | Reversible p53 inhibition prevents cisplatin ototoxicity without blocking chemotherapeutic efficacy |
| Q34634340 | Selenoprotein H suppresses cellular senescence through genome maintenance and redox regulation |
| Q51734443 | Stanniocalcin-1 acts in a negative feedback loop in the prosurvival ERK1/2 signaling pathway during oxidative stress. |
| Q50968575 | The B-cell receptor controls fitness of MYC-driven lymphoma cells via GSK3β inhibition. |
| Q33685413 | The regulation of the p53-mediated stress response by MDM2 and MDM4. |
| Q35116715 | The tumor suppressor PML specifically accumulates at RPA/Rad51-containing DNA damage repair foci but is nonessential for DNA damage-induced fibroblast senescence |
| Q37698893 | Wild-type p53-induced phosphatase 1 (Wip1) forestalls cellular premature senescence at physiological oxygen levels by regulating DNA damage response signaling during DNA replication |
| Q92542931 | mTORC1-Rps15 Axis Contributes to the Mechanisms Underlying Global Translation Reduction During Senescence of Mouse Embryonic Fibroblasts |
| Q37062834 | p19(Arf) is required for the cellular response to chronic DNA damage |