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Aging and Death in an Organism That Reproduces by Morphologically Symmetric Division
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1097-0061(199910)15:14<1511::aid-yea482>3.0.co;2-yopenalex-snapshot
Replicative ageing in the fission yeast Schizosaccharomyces pombe
inferredcites →https://doi.org/10.1016/0014-4827(61)90192-6openalex-snapshot
The serial cultivation of human diploid cell strains
inferredcites →https://doi.org/10.1016/0014-4827(62)90150-7openalex-snapshot
Normal distribution of cell generation rate
inferredcites →https://doi.org/10.1016/s0047-6374(02)00023-4openalex-snapshot
Paradigms and pitfalls of yeast longevity research
inferredcites →https://doi.org/10.1016/s0092-8674(00)80493-6openalex-snapshot
Extrachromosomal rDNA Circles— A Cause of Aging in Yeast
inferredcites →https://doi.org/10.1016/s1534-5807(01)00098-3openalex-snapshot
Model Organisms as a Guide to Mammalian Aging
inferredcites →https://doi.org/10.1038/2091039a0openalex-snapshot
Normal Distribution of Cell Generation Rates
inferredcites →https://doi.org/10.1038/362305a0openalex-snapshot
Optimally, mutation and the evolution of ageing
inferredcites →https://doi.org/10.1083/jcb.127.6.1985openalex-snapshot
Daughter cells of Saccharomyces cerevisiae from old mothers display a reduced life span.
inferredcites →https://doi.org/10.1085/jgp.15.3.257openalex-snapshot
A CHEMICAL EXPLANATION OF THE VARIABILITY OF THE GROWTH RATE
inferredcites →https://doi.org/10.1093/genetics/141.2.571openalex-snapshot
Evidence for an inducible repair-recombination system in the female germ line of Drosophila melanogaster. I. Induction by inhibitors of nucleotide synthesis and by gamma rays.
inferredcites →https://doi.org/10.1093/genetics/162.1.73openalex-snapshot
A Mutation in the ATP2 Gene Abrogates the Age Asymmetry Between Mother and Daughter Cells of the Yeast Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1098/rspb.1979.0083openalex-snapshot
The evolution of ageing and longevity
inferredcites →https://doi.org/10.1099/00221287-29-3-421openalex-snapshot
Growth, Cell and Nuclear Divisions in some Bacteria
inferredcites →https://doi.org/10.1099/00221287-31-2-315openalex-snapshot
Generation Times of Individual Bacteria: Some Corroborative Measurements
inferredcites →https://doi.org/10.1126/science.1070919openalex-snapshot
Stochastic Gene Expression in a Single Cell
inferredcites →https://doi.org/10.1126/science.1072163openalex-snapshot
Generating and Exploiting Polarity in Bacteria
inferredcites →https://doi.org/10.1126/science.1082358openalex-snapshot
Genetics and the Specificity of the Aging Process
inferredcites →https://doi.org/10.1126/science.1083532openalex-snapshot
Senescence in a Bacterium with Asymmetric Division
inferredcites →https://doi.org/10.1126/science.1099390openalex-snapshot
Bacterial Persistence as a Phenotypic Switch
inferredcites →https://doi.org/10.1126/science.277.5331.1453openalex-snapshot
The Complete Genome Sequence of Escherichia coli K-12
inferredcites →https://doi.org/10.1128/jb.108.1.375-385.1971openalex-snapshot
On the Process of Cellular Division in Escherichia coli VI. Use of a Methocel-Autoradiographic Method for the Study of Cellular Division in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.171.1.37-42.1989openalex-snapshot
Evidence for the involvement of a cytoplasmic factor in the aging of the yeast Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1128/jb.179.9.2823-2834.1997openalex-snapshot
Murein segregation in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.183.11.3261-3267.2001openalex-snapshot
Polarity in Action: Asymmetric Protein Localization in Bacteria
inferredcites →https://doi.org/10.1146/annurev.micro.56.012302.160830openalex-snapshot
Growing Old: Metabolic Control and Yeast Aging
inferredcites →https://doi.org/10.2307/4613openalex-snapshot
Physiological Ecology: An Evolutionary Approach to Resource Use
What points at this work
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inferred← citeshttps://doi.org/10.2139/ssrn.4661747openalex-extracted
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inferred← citeshttps://doi.org/10.1002/9780470015902.a0001419.pub2openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780470015902.a0021988openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781118108062.ch13openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781118845363.ch4openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781119751939.ch2openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9783527647064.ch33openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201005461openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201005461openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/bies.200800224openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/bies.200900001openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/bies.201100148openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/bies.201500132openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/bies.201800038openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/bies.201900246openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/bies.202400099openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/bies.20295openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/bies.70003openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/bit.23226openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cbic.201000412openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cbic.201000602openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/eji.202250225openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/elsc.201400089openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/smll.201303724openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/11731177_30openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-1-0716-5535-1_13openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-1-4939-2450-9_14openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-1-59745-327-1_1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-1-62703-239-1_28openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-030-22009-9_40openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-030-25241-0_7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-030-46886-6_4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-030-60173-7_8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-031-14417-2_12openalex-snapshot
Ontology (2) Death Programs and Their Discontents
inferred← citeshttps://doi.org/10.1007/978-3-031-64995-0_2openalex-snapshot
The Origin of Life, Immortality, and Aging
inferred← citeshttps://doi.org/10.1007/978-3-319-21711-6_8openalex-snapshot
Splitting Feller Diffusion for Cell Division with Parasite Infection
inferred← citeshttps://doi.org/10.1007/978-3-319-21819-9_1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-319-26239-0_4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-319-42111-7_25openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-319-69892-2_40-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-476-05762-4_22openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-540-74231-9_3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-540-74921-9_12openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-540-77587-4_279openalex-snapshot
Microcolony Growth Procedures
inferred← citeshttps://doi.org/10.1007/978-3-540-92916-1_10openalex-snapshot
Processing of Information Microgranules within an Individual’s Society
inferred← citeshttps://doi.org/10.1007/978-3-658-21966-6_15openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-96-0077-9_17openalex-snapshot
Cell Regulation and the Early Evolution of Autonomous Control
inferred← citeshttps://doi.org/10.1007/s00018-010-0344-4openalex-snapshot
Protein folding and aggregation in bacteria
inferred← citeshttps://doi.org/10.1007/s00018-010-0417-4openalex-snapshot
Bacterial aging: from mechanistic basis to evolutionary perspective
inferred← citeshttps://doi.org/10.1007/s00018-020-03658-wopenalex-snapshot
Nontraditional systems in aging research: an update
inferred← citeshttps://doi.org/10.1007/s00203-021-02508-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00253-010-2824-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00253-010-2895-6openalex-snapshot
Non-linear population dynamics in chemostats associated with live–dead cell cycling in Escherichia coli strain K12-MG1655
inferred← citeshttps://doi.org/10.1007/s00253-011-3697-1openalex-snapshot
Conditional confined oscillatory dynamics of Escherichia coli strain K12-MG1655 in chemostat systems
inferred← citeshttps://doi.org/10.1007/s00253-015-6877-6openalex-snapshot
Modeling microbial growth and dynamics
inferred← citeshttps://doi.org/10.1007/s00285-007-0147-xopenalex-snapshot
An age-and-cyclin-structured cell population model for healthy and tumoral tissues
inferred← citeshttps://doi.org/10.1007/s00285-008-0243-6openalex-snapshot
Failure of antibiotic treatment in microbial populations
inferred← citeshttps://doi.org/10.1007/s00285-009-0302-7openalex-snapshot
Senescence and antibiotic resistance in an age-structured population model
inferred← citeshttps://doi.org/10.1007/s00285-021-01695-yopenalex-snapshot
Long-time behavior and Darwinian optimality for an asymmetric size-structured branching process
inferred← citeshttps://doi.org/10.1007/s00294-019-01041-2openalex-snapshot
Nucleoid-mediated positioning and transport in bacteria
inferred← citeshttps://doi.org/10.1007/s00500-014-1319-4openalex-snapshot
Bacterially inspired evolution of intelligent systems under constantly changing environments
inferred← citeshttps://doi.org/10.1007/s10522-006-9025-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10522-008-9171-5openalex-snapshot
Natural selection and immortality
inferred← citeshttps://doi.org/10.1007/s10522-010-9278-3openalex-snapshot
Let’s stop overlooking bacterial aging
inferred← citeshttps://doi.org/10.1007/s10522-010-9305-4openalex-snapshot
Linking cell polarity, aging and rejuvenation
inferred← citeshttps://doi.org/10.1007/s10539-010-9232-4openalex-snapshot
What’s transmitted? Inherited information.
inferred← citeshttps://doi.org/10.1007/s10539-019-9687-xopenalex-snapshot
Measurement in biology is methodized by theory
inferred← citeshttps://doi.org/10.1007/s10959-020-01033-wopenalex-snapshot
A Phase Transition for Large Values of Bifurcating Autoregressive Models
inferred← citeshttps://doi.org/10.1007/s10967-023-09095-wopenalex-snapshot
Fe spin states and redox processes in Schiff base type complexes
inferred← citeshttps://doi.org/10.1007/s10973-016-5591-7openalex-snapshot
Synthesis, physico-chemical characterization and bacteriostatic study of Pt complexes with substituted amine ligands
inferred← citeshttps://doi.org/10.1007/s10973-025-15080-0openalex-snapshot
Novel Schiff base-type platinum(II) complexes: syntheses, physical–chemical characterization and biological activities
inferred← citeshttps://doi.org/10.1007/s11047-006-9030-8openalex-snapshot
Modeling individual’s aging within a bacterial population using a pi-calculus paradigm
inferred← citeshttps://doi.org/10.1007/s11203-016-9140-6openalex-snapshot
Autoregressive functions estimation in nonlinear bifurcating autoregressive models
inferred← citeshttps://doi.org/10.1007/s11357-025-01769-5openalex-snapshot
Gene expression and co-expression heterogeneity patterns and biodemography analyses during the cell cycle encourage aging studies in archaea
inferred← citeshttps://doi.org/10.1007/s11692-013-9236-5openalex-snapshot
Making Young from Old: How is Sex Designed to Help?
inferred← citeshttps://doi.org/10.1007/s12304-011-9122-4openalex-snapshot
Stasis is an Inevitable Consequence of Every Successful Evolution
inferred← citeshttps://doi.org/10.1007/s40843-024-2932-3openalex-snapshot
Two-dimensional ultrathin vanadium oxide nanosheets as catalytic bactericide
inferred← citeshttps://doi.org/10.1016/b978-0-12-378638-8.00010-5openalex-snapshot
Comparative Genetics of Aging
inferred← citeshttps://doi.org/10.1016/b978-0-12-417029-2.00002-9openalex-snapshot
Constraints in the Design of the Synthetic Bacterial Chassis
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.11327-3openalex-snapshot
Evolutionary Theories of Aging
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.11394-7openalex-snapshot
Chance Events in Aging
inferred← citeshttps://doi.org/10.1016/b978-0-12-822105-1.00009-3openalex-snapshot
Pharmaceuticals/biotechnology—engineered proteins, vaccines, DNA vaccines
inferred← citeshttps://doi.org/10.1016/b978-0-443-21712-8.00009-0openalex-snapshot
The structure of pili under electron and atomic force microscopy
inferred← citeshttps://doi.org/10.1016/bs.apcsb.2023.03.003openalex-snapshot
Mitochondria-associated cellular senescence mechanisms: Biochemical and pharmacological perspectives
inferred← citeshttps://doi.org/10.1016/bs.mim.2016.10.002openalex-snapshot
Microfluidics for bacterial imaging
inferred← citeshttps://doi.org/10.1016/j.addr.2025.115740openalex-snapshot
Microbial heterogeneity-mediated treatment evasion and the potential for engineered live biotherapeutic products
inferred← citeshttps://doi.org/10.1016/j.algal.2013.03.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.archger.2024.105665openalex-snapshot
Five-factor theory of aging and death due to aging
inferred← citeshttps://doi.org/10.1016/j.arr.2008.04.001openalex-snapshot
Detoxification reactions: Relevance to aging
inferred← citeshttps://doi.org/10.1016/j.arr.2009.09.003openalex-snapshot
Circadian clocks and antiaging: Do non-aging microalgae like Euglena reveal anything?
inferred← citeshttps://doi.org/10.1016/j.arr.2013.07.001openalex-snapshot
Ageing of trees: Application of general ageing theories
inferred← citeshttps://doi.org/10.1016/j.arr.2016.10.007openalex-snapshot
The origin of life at the origin of ageing?
inferred← citeshttps://doi.org/10.1016/j.arr.2020.101064openalex-snapshot
Ancestral germen/soma distinction in microbes: Expanding the disposable soma theory of aging to all unicellular lineages
inferred← citeshttps://doi.org/10.1016/j.arr.2021.101375openalex-snapshot
Interspecific interactions that affect ageing: Age-distorters manipulate host ageing to their own evolutionary benefits
inferred← citeshttps://doi.org/10.1016/j.arr.2023.101982openalex-snapshot
Expanding evolutionary theories of ageing to better account for symbioses and interactions throughout the Web of Life
inferred← citeshttps://doi.org/10.1016/j.arr.2026.103304openalex-snapshot
Aging's competing paradigms: Another decade of investigation into damage-driven versus programmed theories
inferred← citeshttps://doi.org/10.1016/j.asoc.2012.10.012openalex-snapshot
Bacterially inspired evolving system with an application to time series prediction
inferred← citeshttps://doi.org/10.1016/j.bbadis.2017.05.028openalex-snapshot
Aging across the tree of life: The importance of a comparative perspective for the use of animal models in aging
inferred← citeshttps://doi.org/10.1016/j.bbagen.2009.06.005openalex-snapshot
Protein aggregation as a paradigm of aging
inferred← citeshttps://doi.org/10.1016/j.bbagen.2009.07.010openalex-snapshot
Integrating evolutionary and molecular genetics of aging
inferred← citeshttps://doi.org/10.1016/j.biosystems.2013.03.014openalex-snapshot
Robustness and aging—A systems-level perspective
inferred← citeshttps://doi.org/10.1016/j.biosystems.2020.104154openalex-snapshot
Stochastic models coupling gene expression and partitioning in cell division in Escherichia coli
inferred← citeshttps://doi.org/10.1016/j.bpj.2014.03.015openalex-snapshot
Variable Cell Morphology Approach for Individual-Based Modeling of Microbial Communities
inferred← citeshttps://doi.org/10.1016/j.bpj.2014.03.035openalex-snapshot
In Vivo Kinetics of Segregation and Polar Retention of MS2-GFP-RNA Complexes in Escherichia coli
inferred← citeshttps://doi.org/10.1016/j.bpj.2014.05.004openalex-snapshot
Contributions of Cell Growth and Biochemical Reactions to Nongenetic Variability of Cells
inferred← citeshttps://doi.org/10.1016/j.bpj.2015.07.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bpj.2017.09.033openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bpj.2018.07.021openalex-snapshot
Optimal Allocation of Bacterial Protein Resources under Nonlethal Protein Maturation Stress
inferred← citeshttps://doi.org/10.1016/j.cell.2005.01.027openalex-snapshot
Understanding the Odd Science of Aging
inferred← citeshttps://doi.org/10.1016/j.cell.2005.09.042openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cell.2008.11.006openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cell.2009.12.031openalex-snapshot
The Polarisome Is Required for Segregation and Retrograde Transport of Protein Aggregates
inferred← citeshttps://doi.org/10.1016/j.cell.2014.03.007openalex-snapshot
Differential Scales of Protein Quality Control
inferred← citeshttps://doi.org/10.1016/j.cels.2016.06.008openalex-snapshot
Asymmetric Damage Segregation Constitutes an Emergent Population-Level Stress Response
inferred← citeshttps://doi.org/10.1016/j.cels.2017.08.015openalex-snapshot
The Effects of Stochasticity at the Single-Cell Level and Cell Size Control on the Population Growth
inferred← citeshttps://doi.org/10.1016/j.colsurfb.2016.02.006openalex-snapshot
Morphological and nanostructural surface changes in Escherichia coli over time, monitored by atomic force microscopy
inferred← citeshttps://doi.org/10.1016/j.copbio.2005.11.001openalex-snapshot
Information from single-cell bacterial biosensors: what is it good for?
inferred← citeshttps://doi.org/10.1016/j.copbio.2010.01.002openalex-snapshot
Origin and analysis of microbial population heterogeneity in bioprocesses
inferred← citeshttps://doi.org/10.1016/j.copbio.2010.10.004openalex-snapshot
Studying transcriptional interactions in single cells at sufficient resolution
inferred← citeshttps://doi.org/10.1016/j.csda.2013.07.025openalex-snapshot
Statistical study of asymmetry in cell lineage data
inferred← citeshttps://doi.org/10.1016/j.cub.2005.04.006openalex-snapshot
Senescence: Even Bacteria Get Old
inferred← citeshttps://doi.org/10.1016/j.cub.2010.04.045openalex-snapshot
Robust Growth of Escherichia coli
inferred← citeshttps://doi.org/10.1016/j.cub.2010.06.071openalex-snapshot
Seeing Mutations in Living Cells
inferred← citeshttps://doi.org/10.1016/j.cub.2011.09.018openalex-snapshot
Temporal Dynamics of Bacterial Aging and Rejuvenation
inferred← citeshttps://doi.org/10.1016/j.cub.2013.07.084openalex-snapshot
Fission Yeast Does Not Age under Favorable Conditions, but Does So after Stress
inferred← citeshttps://doi.org/10.1016/j.cub.2013.08.013openalex-snapshot
Cellular Aging: Symmetry Evades Senescence
inferred← citeshttps://doi.org/10.1016/j.cub.2015.11.067openalex-snapshot
Single-Cell Analysis of Growth in Budding Yeast and Bacteria Reveals a Common Size Regulation Strategy
inferred← citeshttps://doi.org/10.1016/j.cub.2019.08.074openalex-snapshot
Spatial Organization of Expanding Bacterial Colonies Is Affected by Contact-Dependent Growth Inhibition
inferred← citeshttps://doi.org/10.1016/j.cub.2022.07.035openalex-snapshot
Connecting single-cell ATP dynamics to overflow metabolism, cell growth, and the cell cycle in Escherichia coli
inferred← citeshttps://doi.org/10.1016/j.devcel.2012.01.016openalex-snapshot
Asymmetric Cell Division: A Persistent Issue?
inferred← citeshttps://doi.org/10.1016/j.ecolmodel.2015.01.024openalex-snapshot
From protein damage to cell aging to population fitness in E. coli: Insights from a multi-level agent-based model
inferred← citeshttps://doi.org/10.1016/j.exger.2010.03.016openalex-snapshot
Quantitation of (a)symmetric inheritance of functional and of oxidatively damaged mitochondrial aconitase in the cell division of old yeast mother cells
inferred← citeshttps://doi.org/10.1016/j.exger.2010.03.017openalex-snapshot
Declining asexual reproduction is suggestive of senescence in hydra: Comment on Martinez, D., “Mortality patterns suggest lack of senescence in hydra.” Exp Gerontol 33, 217–25
inferred← citeshttps://doi.org/10.1016/j.exger.2013.05.062openalex-snapshot
Noise-driven onset time of biodemographic aging
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2011.07.003openalex-snapshot
Effects of electron beam irradiation on the variability in survivor number and duration of lag phase of four food-borne organisms
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2018.07.002openalex-snapshot
Characterization of damage on Listeria innocua surviving to pulsed light: Effect on growth, DNA and proteome
inferred← citeshttps://doi.org/10.1016/j.isci.2018.08.011openalex-snapshot
Fundamental Characteristics of Single-Cell Aging in Diploid Yeast
inferred← citeshttps://doi.org/10.1016/j.jmb.2009.07.009openalex-snapshot
E. coli Transports Aggregated Proteins to the Poles by a Specific and Energy-Dependent Process
inferred← citeshttps://doi.org/10.1016/j.jspi.2023.106138openalex-snapshot
Kernel estimation of the transition density in bifurcating Markov chains
inferred← citeshttps://doi.org/10.1016/j.jtbi.2007.05.021openalex-snapshot
Incorporating toxin hypothesis into a mathematical model of persister formation and dynamics
inferred← citeshttps://doi.org/10.1016/j.jtbi.2010.01.020openalex-snapshot
Birth, growth and death as structuring operators in bacterial population dynamics
inferred← citeshttps://doi.org/10.1016/j.jtbi.2013.12.001openalex-snapshot
A novel method to study aging in bacteria that reproduce by morphologically symmetric fission
inferred← citeshttps://doi.org/10.1016/j.jtbi.2019.04.005openalex-snapshot
Adaptive damage retention mechanism enables healthier yeast population
inferred← citeshttps://doi.org/10.1016/j.jtbi.2020.110331openalex-snapshot
Aging a little: On the optimality of limited senescence in Escherichia coli
inferred← citeshttps://doi.org/10.1016/j.mad.2005.02.001openalex-snapshot
Asymmetry and the origins of ageing
inferred← citeshttps://doi.org/10.1016/j.mad.2005.03.021openalex-snapshot
Food restriction, evolution and ageing
inferred← citeshttps://doi.org/10.1016/j.mad.2006.05.001openalex-snapshot
Sex-specific regulation of aging and apoptosis
inferred← citeshttps://doi.org/10.1016/j.mad.2006.07.004openalex-snapshot
Life histories and the evolution of aging in bacteria and other single-celled organisms
inferred← citeshttps://doi.org/10.1016/j.mad.2017.08.006openalex-snapshot
Aging and immortality in unicellular species
inferred← citeshttps://doi.org/10.1016/j.mad.2025.112146openalex-snapshot
How to measure, analyze, and interpret age-related changes in Caenorhabditis elegans: Lessons for mechanistic and evolutionary theories of aging
inferred← citeshttps://doi.org/10.1016/j.mbs.2018.06.006openalex-snapshot
Fluctuation analysis on mutation models with birth-date dependence
inferred← citeshttps://doi.org/10.1016/j.mbs.2023.108980openalex-snapshot
Statistical theory of asymmetric damage segregation in clonal cell populations
inferred← citeshttps://doi.org/10.1016/j.mcm.2007.06.008openalex-snapshot
Analysis of a molecular structured population model with possible polynomial growth for the cell division cycle
inferred← citeshttps://doi.org/10.1016/j.mib.2006.10.010openalex-snapshot
Conditional and replicative senescence in Escherichia coli
inferred← citeshttps://doi.org/10.1016/j.mib.2006.12.007openalex-snapshot
Microbial phenotypic heterogeneity and antibiotic tolerance
inferred← citeshttps://doi.org/10.1016/j.mib.2009.09.006openalex-snapshot
Signals of growth regulation in bacteria
inferred← citeshttps://doi.org/10.1016/j.micres.2018.02.002openalex-snapshot
Physiologically distinct subpopulations formed in Escherichia coli cultures in response to heat shock
inferred← citeshttps://doi.org/10.1016/j.mimet.2020.105984openalex-snapshot
Screening for a suitable cell membrane anchoring tag for Pseudomonas aeruginosa and applying it in cell membrane real-time tracking to investigate membrane aging
inferred← citeshttps://doi.org/10.1016/j.mlong.2010.06.002openalex-snapshot
An organismal view of cellular aging
inferred← citeshttps://doi.org/10.1016/j.molcel.2005.10.035openalex-snapshot
Coherence and Timing of Cell Cycle Start Examined at Single-Cell Resolution
inferred← citeshttps://doi.org/10.1016/j.pocean.2024.103312openalex-snapshot
Dynamic population modeling of bacterioplankton community response to gelatinous marine zooplankton bloom collapse and its impact on marine nutrient balance
inferred← citeshttps://doi.org/10.1016/j.ppees.2018.10.002openalex-snapshot
Ageing in trees: Role of body size optimization in demographic senescence
inferred← citeshttps://doi.org/10.1016/j.rechem.2024.101365openalex-snapshot
Synergistic antimicrobial potential: Exploring the efficacy of poly methacrylic acid (PMAA) polymers, CuO NPs, and pomegranate peel extract against bacterial pathogens
inferred← citeshttps://doi.org/10.1016/j.sbi.2015.10.007openalex-snapshot
Protein–protein interactions and the spatiotemporal dynamics of bacterial outer membrane proteins
inferred← citeshttps://doi.org/10.1016/j.semcdb.2011.06.006openalex-snapshot
Polarity and the diversity of growth mechanisms in bacteria
inferred← citeshttps://doi.org/10.1016/j.semcdb.2013.05.006openalex-snapshot
The mortal strand hypothesis: Non-random chromosome inheritance and the biased segregation of damaged DNA
inferred← citeshttps://doi.org/10.1016/j.semcdb.2017.05.013openalex-snapshot
Evolutionary perspectives on ageing
inferred← citeshttps://doi.org/10.1016/j.shpsc.2020.101265openalex-snapshot
Asexual organisms, identity and vertical gene transfer
inferred← citeshttps://doi.org/10.1016/j.snb.2019.127540openalex-snapshot
Application of an optically induced dielectrophoresis (ODEP)-based microfluidic system for the detection and isolation of bacteria with heterogeneity of antibiotic susceptibility
inferred← citeshttps://doi.org/10.1016/j.spa.2010.07.002openalex-snapshot
Detection of cellular aging in a Galton–Watson process
inferred← citeshttps://doi.org/10.1016/j.spa.2014.10.006openalex-snapshot
A Rademacher–Menchov approach for random coefficient bifurcating autoregressive processes
inferred← citeshttps://doi.org/10.1016/j.spa.2023.104262openalex-snapshot
Spread of parasites affecting death and division rates in a cell population
inferred← citeshttps://doi.org/10.1016/j.spl.2012.04.003openalex-snapshot
Asymmetry tests for bifurcating auto-regressive processes with missing data
inferred← citeshttps://doi.org/10.1016/j.stem.2012.09.003openalex-snapshot
Asymmetric Stem Cell Division: Precision for Robustness
inferred← citeshttps://doi.org/10.1016/j.tcb.2025.06.006openalex-snapshot
Lessons in longevity from blood stem cells under protein stress
inferred← citeshttps://doi.org/10.1016/j.tem.2025.04.001openalex-snapshot
Dietary and pharmacological energy restriction and exercise for healthspan extension
inferred← citeshttps://doi.org/10.1016/j.tpb.2007.02.004openalex-snapshot
Damage segregation at fissioning may increase growth rates: A superprocess model
inferred← citeshttps://doi.org/10.1016/j.tree.2007.07.003openalex-snapshot
All paths to fitness lead through demography
inferred← citeshttps://doi.org/10.1016/j.tree.2021.11.007openalex-snapshot
Reproductive value and the evolution of altruism
inferred← citeshttps://doi.org/10.1016/j.virs.2025.07.001openalex-snapshot
Identification of a novel ectromelia virus from rodent: Implications for use as an in vivo infection model for vaccine and antiviral research
inferred← citeshttps://doi.org/10.1016/s0076-6879(07)23022-8openalex-snapshot
Single‐Cell Analysis of Gene Expression by Fluorescence Microscopy
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