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Oxygen sensitivity severely limits the replicative lifespan of murine fibroblasts
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/excr.2001.5182openalex-snapshot
Uncoupling the Senescent Phenotype from Telomere Shortening in Hydrogen Peroxide-Treated Fibroblasts
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Establishment of mouse embryo cells in vitro
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Induction and repair of benzo[a]pyrene-DNA adducts in C57BL/6 and BALB/c mice: association with aging and longevity
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Ku86-Deficient Mice Exhibit Severe Combined Immunodeficiency and Defective Processing of V(D)J Recombination Intermediates
inferredcites →https://doi.org/10.1016/s0092-8674(00)80452-3openalex-snapshot
Tumor Suppression at the Mouse INK4a Locus Mediated by the Alternative Reading Frame Product p19
inferredcites →https://doi.org/10.1016/s0092-8674(01)80006-4openalex-snapshot
Telomere Shortening and Tumor Formation by Mouse Cells Lacking Telomerase RNA
inferredcites →https://doi.org/10.1016/s0955-0674(00)00278-7openalex-snapshot
Putting the stress on senescence
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Oxygen Metabolism Causes Chromosome Breaks and Is Associated with the Neuronal Apoptosis Observed in DNA Double-Strand Break Repair Mutants
inferredcites →https://doi.org/10.1016/s0960-9822(99)80420-5openalex-snapshot
Microarray analysis of replicative senescence
inferredcites →https://doi.org/10.1016/s0962-8924(01)02151-1openalex-snapshot
Cellular senescence as a tumor-suppressor mechanism
inferredcites →https://doi.org/10.1016/s0962-8924(01)82148-6openalex-snapshot
Cellular senescence as a tumor-suppressor mechanism
inferredcites →https://doi.org/10.1016/s1383-5718(99)00232-6openalex-snapshot
A public domain image-analysis program for the single-cell gel-electrophoresis (comet) assay
inferredcites →https://doi.org/10.1038/25870openalex-snapshot
p19ARF links the tumour suppressor p53 to Ras
inferredcites →https://doi.org/10.1038/35092592openalex-snapshot
Loss of p16Ink4a with retention of p19Arf predisposes mice to tumorigenesis
inferredcites →https://doi.org/10.1038/377169a0openalex-snapshot
Increased susceptibility to ultraviolet-B and carcinogens of mice lacking the DNA excision repair gene XPA
inferredcites →https://doi.org/10.1038/78592openalex-snapshot
Telomere dynamics in cancer progression and prevention: fundamental differences in human and mouse telomere biology
inferredcites →https://doi.org/10.1038/sj.onc.1201862openalex-snapshot
Agents that cause DNA double strand breaks lead to p16INK4a enrichment and the premature senescence of normal fibroblasts
inferredcites →https://doi.org/10.1073/pnas.93.19.10309openalex-snapshot
Use of genetic suppressor elements to dissect distinct biological effects of separate p53 domains.
inferredcites →https://doi.org/10.1073/pnas.96.4.1403openalex-snapshot
Catalytic subunit of DNA-dependent protein kinase: Impact on lymphocyte development and tumorigenesis
inferredcites →https://doi.org/10.1074/jbc.m203747200openalex-snapshot
Reversible Manipulation of Telomerase Expression and Telomere Length
inferredcites →https://doi.org/10.1083/jcb.144.4.589openalex-snapshot
Telomere Length Dynamics and Chromosomal Instability in Cells Derived from Telomerase Null Mice
inferredcites →https://doi.org/10.1083/jcb.17.2.299openalex-snapshot
QUANTITATIVE STUDIES OF THE GROWTH OF MOUSE EMBRYO CELLS IN CULTURE AND THEIR DEVELOPMENT INTO ESTABLISHED LINES
inferredcites →https://doi.org/10.1093/carcin/14.9.1733openalex-snapshot
Direct enzymic detection of endogenous oxidative base damage in human lymphocyte DNA
inferredcites →https://doi.org/10.1101/gad.13.8.916openalex-snapshot
The DNA-dependent protein kinase
inferredcites →https://doi.org/10.1126/science.2104680openalex-snapshot
Repression of c- fos Transcription and an Altered Genetic Program in Senescent Human Fibroblasts
inferredcites →https://doi.org/10.1128/mcb.20.1.273-285.2000openalex-snapshot
Regulation of a Senescence Checkpoint Response by the E2F1 Transcription Factor and p14 ARF Tumor Suppressor
inferredcites →https://doi.org/10.1128/mcb.21.11.3642-3651.2001openalex-snapshot
The Absence of the DNA-Dependent Protein Kinase Catalytic Subunit in Mice Results in Anaphase Bridges and in Increased Telomeric Fusions with Normal Telomere Length and G-Strand Overhang
inferredcites →https://doi.org/10.1667/0033-7587(2001)155[0254:ccdslg]2.0.co;2openalex-snapshot
Culture Condition-Dependent Senescence-Like Growth Arrest and Immortalization in Rodent Embryo Cells
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Oncogene-Induced Senescence and its Role in Tumor Suppression
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ROS-mediated activation of AKT induces apoptosis via pVHL in prostate cancer cells
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Transcriptional activation of p21WAF1/CIP1 is mediated by increased DNA binding activity and increased interaction between p53 and Sp1 via phosphorylation during replicative senescence of human embryonic fibroblasts
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Rodents for comparative aging studies: from mice to beavers
inferred← citeshttps://doi.org/10.1007/s11357-010-9149-5openalex-snapshot
Effects of oxygen, growth state, and senescence on the antioxidant responses of WI-38 fibroblasts
inferred← citeshttps://doi.org/10.1007/s11357-012-9452-4openalex-snapshot
A role for c-Abl in cell senescence and spontaneous immortalization
inferred← citeshttps://doi.org/10.1007/s11357-016-9922-1openalex-snapshot
Cristacarpin promotes ER stress-mediated ROS generation leading to premature senescence by activation of p21waf-1
inferred← citeshttps://doi.org/10.1007/s11357-020-00183-3openalex-snapshot
Regulation of senescence traits by MAPKs
inferred← citeshttps://doi.org/10.1007/s11357-024-01297-8openalex-snapshot
Judith Campisi (1948–2024): tribute and personal memory
inferred← citeshttps://doi.org/10.1007/s11357-024-01420-9openalex-snapshot
Establishment of primary and immortalized fibroblasts reveals resistance to cytotoxic agents and loss of necroptosis-inducing ability in long-lived Damaraland mole-rats
inferred← citeshttps://doi.org/10.1007/s11626-015-9943-6openalex-snapshot
Expression of human cell cycle regulators in the primary cell line of the African savannah elephant (loxodonta africana) increases proliferation until senescence, but does not induce immortalization
inferred← citeshttps://doi.org/10.1007/s11745-011-3633-2openalex-snapshot
Quantitation of Multiple Sphingolipid Classes Using Normal and Reversed‐Phase LC–ESI–MS/MS: Comparative Profiling of Two Cell Lines
inferred← citeshttps://doi.org/10.1007/s11926-014-0473-0openalex-snapshot
Role of Cellular Senescence and NOX4-Mediated Oxidative Stress in Systemic Sclerosis Pathogenesis
inferred← citeshttps://doi.org/10.1007/s12015-016-9652-xopenalex-snapshot
Chemical and Physical Approaches to Extend the Replicative and Differentiation Potential of Stem Cells
inferred← citeshttps://doi.org/10.1007/s12015-017-9728-2openalex-snapshot
Prolonged Growth Hormone/Insulin/Insulin-like Growth Factor Nutrient Response Signaling Pathway as a Silent Killer of Stem Cells and a Culprit in Aging
inferred← citeshttps://doi.org/10.1007/s12094-010-0528-2openalex-snapshot
Bypassing cellular senescence by genetic screening tools
inferred← citeshttps://doi.org/10.1007/s12257-025-00210-0openalex-snapshot
Camellia japonica seed extract promotes hair growth by preventing dermal papilla cell senescence and activating hair follicle stem cells
inferred← citeshttps://doi.org/10.1007/s13577-015-0110-xopenalex-snapshot
Cellular senescence: a hitchhiker’s guide
inferred← citeshttps://doi.org/10.1007/s13577-024-01151-1openalex-snapshot
Establishment of a novel benign meningioma cell line spontaneously immortalized under hypoxic conditions
inferred← citeshttps://doi.org/10.1007/s13671-020-00320-3openalex-snapshot
Clinical Implications of Cellular Senescence on Wound Healing
inferred← citeshttps://doi.org/10.1007/s40495-016-0050-5openalex-snapshot
Oxidative Stress Under Ambient and Physiological Oxygen Tension in Tissue Culture
inferred← citeshttps://doi.org/10.1016/b978-0-08-101103-4.00006-5openalex-snapshot
Cell preparation for 3D bioprinting
inferred← citeshttps://doi.org/10.1016/b978-0-12-373866-0.00021-6openalex-snapshot
Free Radicals as Atherosclerotic Risk in Relation to Nitric Oxide
inferred← citeshttps://doi.org/10.1016/b978-0-12-378638-8.00007-5openalex-snapshot
Leukocyte Telomere Dynamics, Human Aging, and Life Span
inferred← citeshttps://doi.org/10.1016/b978-0-12-380916-2.00003-6openalex-snapshot
MDM2 and MDMX in Cancer and Development
inferred← citeshttps://doi.org/10.1016/b978-0-12-397157-9.00026-6openalex-snapshot
Oral Mucosal Keratinocyte Stem Cells
inferred← citeshttps://doi.org/10.1016/b978-0-12-398358-9.00081-1openalex-snapshot
Tissue-Engineered Skin Products
inferred← citeshttps://doi.org/10.1016/b978-0-12-800540-8.00002-8openalex-snapshot
In Situ Normoxia versus “Hypoxia”
inferred← citeshttps://doi.org/10.1016/b978-0-12-800540-8.00004-1openalex-snapshot
Low O2 Concentrations and the Maintenance of Stem Cells Ex Vivo
inferred← citeshttps://doi.org/10.1016/b978-0-12-804274-8.00023-0openalex-snapshot
The Role of Senescence in Hepatic Diseases
inferred← citeshttps://doi.org/10.1016/b978-0-12-818422-6.00081-2openalex-snapshot
Tissue-engineered skin products
inferred← citeshttps://doi.org/10.1016/b978-0-323-95488-4.00216-3openalex-snapshot
Mutational Signatures in Cancer Genomics and Toxicology
inferred← citeshttps://doi.org/10.1016/b978-012088387-5/50009-1openalex-snapshot
p53 and Mouse Aging Models
inferred← citeshttps://doi.org/10.1016/b978-012370615-7/50083-4openalex-snapshot
Tissue-Engineered Skin Products
inferred← citeshttps://doi.org/10.1016/bs.armc.2020.06.004openalex-snapshot
Fundamentals of G-quadruplex biology
inferred← citeshttps://doi.org/10.1016/j.abb.2013.06.008openalex-snapshot
Differential responses of SOD1-deficient mouse embryonic fibroblasts to oxygen concentrations
inferred← citeshttps://doi.org/10.1016/j.abb.2015.01.029openalex-snapshot
Mechanisms of oxidative stress resistance in the brain: Lessons learned from hypoxia tolerant extremophilic vertebrates
inferred← citeshttps://doi.org/10.1016/j.abb.2016.04.004openalex-snapshot
Reflections on the role of senescence during development and aging
inferred← citeshttps://doi.org/10.1016/j.actbio.2010.11.016openalex-snapshot
Senescence in cells in aseptic loosening after total hip replacement
inferred← citeshttps://doi.org/10.1016/j.acthis.2021.151841openalex-snapshot
A new insight into cell biological and biochemical changes through aging
inferred← citeshttps://doi.org/10.1016/j.acthis.2024.152185openalex-snapshot
Cryopreservation and passaging optimization for Galea spixii (Wagler, 1831) adult skin fibroblast lines: A step forward in species management and genetic studies
inferred← citeshttps://doi.org/10.1016/j.addr.2024.115216openalex-snapshot
The interaction between particles and vascular endothelium in blood flow
inferred← citeshttps://doi.org/10.1016/j.ajpath.2014.10.027openalex-snapshot
Functional Role of Cellular Senescence in Biliary Injury
inferred← citeshttps://doi.org/10.1016/j.ajpath.2019.07.009openalex-snapshot
The Inability of the Choroid to Revascularize in Oxygen-Induced Retinopathy Results from Increased p53/miR-Let-7b Activity
inferred← citeshttps://doi.org/10.1016/j.apsb.2020.01.011openalex-snapshot
Conditional reprogramming: next generation cell culture
inferred← citeshttps://doi.org/10.1016/j.arr.2010.01.002openalex-snapshot
Comparative cellular biogerontology: Primer and prospectus
inferred← citeshttps://doi.org/10.1016/j.arr.2010.10.002openalex-snapshot
Impact of cellular senescence signature on ageing research
inferred← citeshttps://doi.org/10.1016/j.arr.2011.06.001openalex-snapshot
MicroRNAs as a novel cellular senescence regulator
inferred← citeshttps://doi.org/10.1016/j.arr.2012.01.005openalex-snapshot
General RBP expression in human tissues as a function of age
inferred← citeshttps://doi.org/10.1016/j.arr.2015.03.004openalex-snapshot
Biomolecular bases of the senescence process and cancer. A new approach to oncological treatment linked to ageing
inferred← citeshttps://doi.org/10.1016/j.arr.2017.10.004openalex-snapshot
The role of cellular senescence in aging through the prism of Koch-like criteria
inferred← citeshttps://doi.org/10.1016/j.arr.2020.101154openalex-snapshot
Fight to the bitter end: DNA repair and aging
inferred← citeshttps://doi.org/10.1016/j.arr.2021.101267openalex-snapshot
To breathe or not to breathe: Understanding how oxygen sensing contributes to age-related phenotypes
inferred← citeshttps://doi.org/10.1016/j.arr.2022.101634openalex-snapshot
Assessment of cell cycle regulators in human peripheral blood cells as markers of cellular senescence
inferred← citeshttps://doi.org/10.1016/j.arr.2025.102760openalex-snapshot
The context-dependent effect of cellular senescence: From embryogenesis and wound healing to aging
inferred← citeshttps://doi.org/10.1016/j.arr.2025.102813openalex-snapshot
Cellular senescence in chronic obstructive pulmonary disease: Molecular mechanisms and therapeutic interventions
inferred← citeshttps://doi.org/10.1016/j.arr.2026.103115openalex-snapshot
Epigenetic remodeling induced by fatty acids: Chromatin modifications and cellular senescence during lipid overload
inferred← citeshttps://doi.org/10.1016/j.asr.2012.02.001openalex-snapshot
X-ray induced alterations in the differentiation and mineralization potential of murine preosteoblastic cells
inferred← citeshttps://doi.org/10.1016/j.bbadis.2009.02.003openalex-snapshot
Pathway analysis of senescence-associated miRNA targets reveals common processes to different senescence induction mechanisms
inferred← citeshttps://doi.org/10.1016/j.bbagen.2014.03.015openalex-snapshot
p19INK4d is involved in the cellular senescence mechanism contributing to heterochromatin formation
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2011.04.003openalex-snapshot
The PKB/FOXO switch in aging and cancer
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2012.01.016openalex-snapshot
Role of BI-1 (TEGT)-mediated ERK1/2 activation in mitochondria-mediated apoptosis and splenomegaly in BI-1 transgenic mice
inferred← citeshttps://doi.org/10.1016/j.bbcan.2005.08.008openalex-snapshot
The flexible evolutionary anchorage-dependent Pardee's restriction point of mammalian cells. How its deregulation may lead to cancer
inferred← citeshttps://doi.org/10.1016/j.bbcan.2009.11.001openalex-snapshot
A new generation of proto-oncogenes: Cold-inducible RNA binding proteins
inferred← citeshttps://doi.org/10.1016/j.bbrc.2006.12.112openalex-snapshot
Telomerase activation induces elongation of the telomeric single-stranded overhang, but does not prevent chromosome aberrations in human vascular endothelial cells
inferred← citeshttps://doi.org/10.1016/j.bbrc.2007.04.211openalex-snapshot
Hyaluronan preserves the proliferation and differentiation potentials of long-term cultured murine adipose-derived stromal cells
inferred← citeshttps://doi.org/10.1016/j.bbrc.2008.06.011openalex-snapshot
Monolayer expansion induces an oxidative metabolism and ROS in chondrocytes
inferred← citeshttps://doi.org/10.1016/j.bbrc.2011.04.145openalex-snapshot
Random mtDNA mutations modulate proliferation capacity in mouse embryonic fibroblasts
inferred← citeshttps://doi.org/10.1016/j.bbrc.2011.10.103openalex-snapshot
The hsa-miR-5787 represses cellular growth by targeting eukaryotic translation initiation factor 5 (eIF5) in fibroblasts
inferred← citeshttps://doi.org/10.1016/j.bbrc.2014.04.139openalex-snapshot
Glutathione peroxidase-1 is required for self-renewal of murine embryonic stem cells
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