On the public citation graph
Variation in the life history strategy of cells underlies tumor’s functional diversity
0 signed · 110 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-1-4614-6220-0openalex-snapshot
The Hippo Signaling Pathway and Cancer
inferredcites →https://doi.org/10.1007/bf00318088openalex-snapshot
Lotka-Volterra equation and replicator dynamics: A two-dimensional classification
inferredcites →https://doi.org/10.1007/bf00347974openalex-snapshot
The meanings of r- and K-selection
inferredcites →https://doi.org/10.1007/s00526-016-0964-0openalex-snapshot
Global dynamics of the Lotka–Volterra competition–diffusion system with equal amount of total resources, II
inferredcites →https://doi.org/10.1007/s00526-016-1084-6openalex-snapshot
Properties of optimizers of the principal eigenvalue with indefinite weight and Robin conditions
inferredcites →https://doi.org/10.1007/s10883-015-9276-5openalex-snapshot
On a Two Species Stochastic Lotka-Volterra Competition System
inferredcites →https://doi.org/10.1016/0020-7101(81)90050-7openalex-snapshot
Three-dimensional pattern generation applied to spheroidal tumor growth in a nutrient medium
inferredcites →https://doi.org/10.1016/j.bbcan.2009.11.002openalex-snapshot
Tumor heterogeneity: Causes and consequences
inferredcites →https://doi.org/10.1016/j.ccr.2006.06.001openalex-snapshot
Autophagy promotes tumor cell survival and restricts necrosis, inflammation, and tumorigenesis
inferredcites →https://doi.org/10.1016/j.cell.2011.02.013openalex-snapshot
Hallmarks of Cancer: The Next Generation
inferredcites →https://doi.org/10.1016/j.cell.2012.06.037openalex-snapshot
Regulation of the Hippo-YAP Pathway by G-Protein-Coupled Receptor Signaling
inferredcites →https://doi.org/10.1016/j.mehy.2005.12.010openalex-snapshot
No cancer in cancers: Evolutionary trade-off between successful viviparity and tumor escape from the adaptive immune system
inferredcites →https://doi.org/10.1016/j.molmed.2012.06.005openalex-snapshot
Hallmarks of cancer: of all cancer cells, all the time?
inferredcites →https://doi.org/10.1016/j.physleta.2004.12.068openalex-snapshot
Coexistence and chaos in complex ecologies
inferredcites →https://doi.org/10.1016/j.tree.2005.07.007openalex-snapshot
Evolutionary biology of cancer
inferredcites →https://doi.org/10.1016/s0022-1910(97)00014-0openalex-snapshot
The effects of reproduction on longevity and fertility in male Drosophila melanogaster
inferredcites →https://doi.org/10.1016/s0092-8674(00)80125-7openalex-snapshot
A Signaling Pathway to Translational Control
inferredcites →https://doi.org/10.1038/118558a0openalex-snapshot
Fluctuations in the Abundance of a Species considered Mathematically1
inferredcites →https://doi.org/10.1038/119012b0openalex-snapshot
Fluctuations in the Abundance of a Species considered Mathematically
inferredcites →https://doi.org/10.1038/311127a0openalex-snapshot
Antibodies to gap-junctional protein selectively disrupt junctional communication in the early amphibian embryo
inferredcites →https://doi.org/10.1038/hdy.2013.75openalex-snapshot
Key questions in the genetics and genomics of eco-evolutionary dynamics
inferredcites →https://doi.org/10.1038/nature03998openalex-snapshot
Regulated cell-to-cell variation in a cell-fate decision system
inferredcites →https://doi.org/10.1038/nature08012openalex-snapshot
Non-genetic origins of cell-to-cell variability in TRAIL-induced apoptosis
inferredcites →https://doi.org/10.1038/nature14971openalex-snapshot
A spatial model predicts that dispersal and cell turnover limit intratumour heterogeneity
inferredcites →https://doi.org/10.1038/ng.3315openalex-snapshot
Spatial genomic heterogeneity within localized, multifocal prostate cancer
inferredcites →https://doi.org/10.1038/ng.3683openalex-snapshot
Spatial intratumoral heterogeneity and temporal clonal evolution in esophageal squamous cell carcinoma
inferredcites →https://doi.org/10.1038/nprot.2008.211openalex-snapshot
Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources
inferredcites →https://doi.org/10.1038/nrc.2017.69openalex-snapshot
Classifying the evolutionary and ecological features of neoplasms
inferredcites →https://doi.org/10.1038/nrc2013openalex-snapshot
Cancer as an evolutionary and ecological process
inferredcites →https://doi.org/10.1038/nrc3261openalex-snapshot
Intra-tumour heterogeneity: a looking glass for cancer?
inferredcites →https://doi.org/10.1038/nrc3606openalex-snapshot
Life history trade-offs in cancer evolution
inferredcites →https://doi.org/10.1038/nrc3712openalex-snapshot
Turning ecology and evolution against cancer
inferredcites →https://doi.org/10.1038/nrg2398openalex-snapshot
Tuning gene expression to changing environments: from rapid responses to evolutionary adaptation
inferredcites →https://doi.org/10.1038/nrg2808openalex-snapshot
Mutational effects and the evolution of new protein functions
inferredcites →https://doi.org/10.1038/nrm2457openalex-snapshot
Nectins and nectin-like molecules: roles in contact inhibition of cell movement and proliferation
inferredcites →https://doi.org/10.1038/onc.2008.341openalex-snapshot
Control of tumourigenesis by the Scribble/Dlg/Lgl polarity module
inferredcites →https://doi.org/10.1038/s41586-018-0657-2openalex-snapshot
Gene expression variability across cells and species shapes innate immunity
inferredcites →https://doi.org/10.1053/j.gastro.2010.01.058openalex-snapshot
Inflammation and Colon Cancer
inferredcites →https://doi.org/10.1073/pnas.0407158101openalex-snapshot
A screen for genes that suppress loss of contact inhibition: Identification of ING4 as a candidate tumor suppressor gene in human cancer
inferredcites →https://doi.org/10.1073/pnas.1113882109openalex-snapshot
Tumor suppression by cell competition through regulation of the Hippo pathway
inferredcites →https://doi.org/10.1073/pnas.1512317112openalex-snapshot
Alfred J. Lotka and the origins of theoretical population ecology
inferredcites →https://doi.org/10.1073/pnas.1519556112openalex-snapshot
Extremely high genetic diversity in a single tumor points to prevalence of non-Darwinian cell evolution
inferredcites →https://doi.org/10.1073/pnas.1600151113openalex-snapshot
Correction for Ling et al., Extremely high genetic diversity in a single tumor points to prevalence of non-Darwinian cell evolution
inferredcites →https://doi.org/10.1073/pnas.18.2.172openalex-snapshot
Contribution to the Mathematical Theory of Capture
inferredcites →https://doi.org/10.1073/pnas.8.6.151openalex-snapshot
Natural Selection as a Physical Principle
inferredcites →https://doi.org/10.1080/19336934.2017.1336270openalex-snapshot
The dark side of hippo signaling: A cancer promoter role
inferredcites →https://doi.org/10.1086/282955openalex-snapshot
Ecological Strategies and Population Parameters
inferredcites →https://doi.org/10.1086/283488openalex-snapshot
Optimal Life Histories Under Age-Specific Predation
inferredcites →https://doi.org/10.1086/284890openalex-snapshot
Density-Dependent Population Growth and Natural Selection in Food-Limited Environments: The Drosophila Model
inferredcites →https://doi.org/10.1086/605963openalex-snapshot
Cost of Reproduction, Resource Quality, and Terminal Investment in a Burying Beetle
inferredcites →https://doi.org/10.1088/0951-7715/25/7/2151openalex-snapshot
A slow pushed front in a Lotka–Volterra competition model
inferredcites →https://doi.org/10.1091/mbc.e10-08-0721openalex-snapshot
Genome-wide analysis of yeast stress survival and tolerance acquisition to analyze the central trade-off between growth rate and cellular robustness
inferredcites →https://doi.org/10.1093/bioinformatics/btp692openalex-snapshot
RNA-Seq gene expression estimation with read mapping uncertainty
inferredcites →https://doi.org/10.1093/bioinformatics/btt087openalex-snapshot
EBSeq: an empirical Bayes hierarchical model for inference in RNA-seq experiments
inferredcites →https://doi.org/10.1093/genetics/76.3.567openalex-snapshot
THE EFFECTS OF r- AND K-SELECTION ON COMPONENTS OF VARIANCE FOR TWO QUANTITATIVE TRAITS
inferredcites →https://doi.org/10.1093/jb/mvr021openalex-snapshot
Mammalian Hippo pathway: from development to cancer and beyond
inferredcites →https://doi.org/10.1093/molbev/msx115openalex-snapshot
A Direct Test of Selection in Cell Populations Using the Diversity in Gene Expression within Tumors
inferredcites →https://doi.org/10.1093/nar/gkn923openalex-snapshot
Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists
inferredcites →https://doi.org/10.1093/nar/gkp829openalex-snapshot
Sequence-non-specific effects of RNA interference triggers and microRNA regulators
inferredcites →https://doi.org/10.1093/nar/gkq622openalex-snapshot
MapSplice: Accurate mapping of RNA-seq reads for splice junction discovery
inferredcites →https://doi.org/10.1098/rsfs.2013.0020openalex-snapshot
Exploiting ecological principles to better understand cancer progression and treatment
inferredcites →https://doi.org/10.1098/rstl.1825.0026openalex-snapshot
XXIV. On the nature of the function expressive of the law of human mortality, and on a new mode of determining the value of life contingencies. In a letter to Francis Baily, Esq. F. R. S. &c
inferredcites →https://doi.org/10.1099/0022-1317-80-7-1725openalex-snapshot
Nucleotide sequences and further characterization of human papillomavirus DNA present in the CaSki, SiHa and HeLa cervical carcinoma cell lines.
inferredcites →https://doi.org/10.1101/270900openalex-snapshot
The dynamic tumor ecosystem: how cell turnover and trade-offs affect cancer evolution
inferredcites →https://doi.org/10.1101/gad.1909210openalex-snapshot
The Hippo–YAP pathway in organ size control and tumorigenesis: an updated version
inferredcites →https://doi.org/10.1101/gad.2000111openalex-snapshot
Angiomotin is a novel Hippo pathway component that inhibits YAP oncoprotein
inferredcites →https://doi.org/10.1101/gad.210773.112openalex-snapshot
The Hippo pathway: regulators and regulations
inferredcites →https://doi.org/10.1109/tsmc.1980.4308502openalex-snapshot
Spatial Structure of Tumor Growth: A Simulation Study
inferredcites →https://doi.org/10.1111/eva.12444openalex-snapshot
Cancer: A disease at the crossroads of trade‐offs
inferredcites →https://doi.org/10.1111/j.1558-5646.1957.tb02911.xopenalex-snapshot
PLEIOTROPY, NATURAL SELECTION, AND THE EVOLUTION OF SENESCENCE
inferredcites →https://doi.org/10.1111/j.1752-4571.2008.00063.xopenalex-snapshot
SYNTHESIS: Cancer research meets evolutionary biology
inferredcites →https://doi.org/10.1126/science.1222361openalex-snapshot
Heterogeneity and Tumor History
inferredcites →https://doi.org/10.1126/science.131.3409.1292openalex-snapshot
The Competitive Exclusion Principle
inferredcites →https://doi.org/10.1126/science.159.3810.71openalex-snapshot
Biogeography and Ecology in a New Setting: The Theory of Island Biogeography . Robert H. MacArthur and Edward O. Wilson. Princeton University Press, Princeton, N.J., 1967. 215 pp., illus. Cloth, $8; paper, $3.95. Monographs in Population Biology, No. 1.
inferredcites →https://doi.org/10.1126/science.959840openalex-snapshot
The Clonal Evolution of Tumor Cell Populations
inferredcites →https://doi.org/10.1146/annurev-genet-102808-114910openalex-snapshot
Regulation Mechanisms and Signaling Pathways of Autophagy
inferredcites →https://doi.org/10.1146/annurev-genet-112414-054842openalex-snapshot
The Ecology and Evolution of Cancer: The Ultra-Microevolutionary Process
inferredcites →https://doi.org/10.1146/annurev.es.08.110177.001045openalex-snapshot
The Evolution of Life History Traits: A Critique of the Theory and a Review of the Data
inferredcites →https://doi.org/10.1158/0008-5472.can-14-1428openalex-snapshot
Impact of Metabolic Heterogeneity on Tumor Growth, Invasion, and Treatment Outcomes
inferredcites →https://doi.org/10.1186/1423-0127-17-36openalex-snapshot
Trypsin-induced proteome alteration during cell subculture in mammalian cells
inferredcites →https://doi.org/10.1186/1471-2105-10-1openalex-snapshot
Regularized gene selection in cancer microarray meta-analysis
inferredcites →https://doi.org/10.1186/1471-2105-10-161openalex-snapshot
GAGE: generally applicable gene set enrichment for pathway analysis
inferredcites →https://doi.org/10.1186/1471-2105-12-323openalex-snapshot
RSEM: accurate transcript quantification from RNA-Seq data with or without a reference genome
inferredcites →https://doi.org/10.1242/dev.045500openalex-snapshot
Hippo signaling: growth control and beyond
inferredcites →https://doi.org/10.1242/jcs.140103openalex-snapshot
The Hippo-YAP signaling pathway and contact inhibition of growth
inferredcites →https://doi.org/10.1371/journal.pone.0017933openalex-snapshot
Solving the Puzzle of Metastasis: The Evolution of Cell Migration in Neoplasms
inferredcites →https://doi.org/10.1371/journal.pone.0083962openalex-snapshot
Computational Modeling of 3D Tumor Growth and Angiogenesis for Chemotherapy Evaluation
inferredcites →https://doi.org/10.1371/journal.pone.0089680openalex-snapshot
A Selected Core Microbiome Drives the Early Stages of Three Popular Italian Cheese Manufactures
inferredcites →https://doi.org/10.1515/9781400881376openalex-snapshot
The Theory of Island Biogeography
inferredcites →https://doi.org/10.1890/0012-9658(1999)080[1168:etouco]2.0.co;2openalex-snapshot
EVOLUTIONARY TRADE-OFFS UNDER CONDITIONS OF RESOURCE ABUNDANCE AND SCARCITY: EXPERIMENTS WITH BACTERIA
inferredcites →https://doi.org/10.1890/0012-9658(2002)083[1509:raksrt]2.0.co;2openalex-snapshot
r- ANDK-SELECTION REVISITED: THE ROLE OF POPULATION REGULATION IN LIFE-HISTORY EVOLUTION
inferredcites →https://doi.org/10.1890/04-0508openalex-snapshot
IMPACTS OF DENSITY-INDEPENDENT MORTALITY AND PRODUCTIVITY ON THE STRENGTH AND OUTCOME OF COMPETITION
inferredcites →https://doi.org/10.2307/2095875openalex-snapshot
Density Dependence in the Evolution of Populations of Newspaper Organizations
inferredcites →https://doi.org/10.2307/2406060openalex-snapshot
Pleiotropy, Natural Selection, and the Evolution of Senescence
inferredcites →https://doi.org/10.2307/3863openalex-snapshot
Density-Dependence in Single-Species Populations
inferredcites →https://doi.org/10.3389/fonc.2013.00045openalex-snapshot
Tumor Evolution in Space: The Effects of Competition Colonization Tradeoffs on Tumor Invasion Dynamics
inferredcites →https://doi.org/10.3389/fonc.2013.00133openalex-snapshot
Single Cell Functional Proteomics for Assessing Immune Response in Cancer Therapy: Technology, Methods, and Applications
inferredcites →https://doi.org/10.3406/marb.1845.3438openalex-snapshot
Recherches mathématiques sur la loi d’accroissement de la population
inferredcites →https://doi.org/10.5860/choice.43-5886openalex-snapshot
Demons in Eden: the paradox of plant diversity
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1101/2020.09.01.277848openalex-snapshot
Many are called but few are chosen – Multiple clonal origins greatly elevate the functional heterogeneity of tumors
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.