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Endoreplication: polyploidy with purpose
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inferredcites →https://doi.org/10.1002/(sici)1520-6408(1997)21:1<21::aid-dvg3>3.0.co;2-aopenalex-snapshot
Developmental restriction of Mash2 expression in trophoblast correlates with potential activation of the Notch‐2 pathway
inferredcites →https://doi.org/10.1002/jcp.10035openalex-snapshot
Roads to polyploidy: The megakaryocyte example
inferredcites →https://doi.org/10.1002/jez.b.21211openalex-snapshot
Hepatic endopolyploidy as a cellular consequence of age‐specific selection for rate of development in mice
inferredcites →https://doi.org/10.1002/stem.160001openalex-snapshot
Hematopoietic Deficiencies in c‐mpl and TPO Knockout Mice
inferredcites →https://doi.org/10.1006/dbio.1998.8914openalex-snapshot
The Transition to Endoreduplication in Trophoblast Giant Cells Is Regulated by the mSNA Zinc Finger Transcription Factor
inferredcites →https://doi.org/10.1006/meth.1999.0799openalex-snapshot
Chorion Gene Amplification in Drosophila: A Model for Metazoan Origins of DNA Replication and S-Phase Control
inferredcites →https://doi.org/10.1006/scdb.2000.0156openalex-snapshot
Genetic insights into trophoblast differentiation and placental morphogenesis
inferredcites →https://doi.org/10.1007/400_023openalex-snapshot
Mouse Models of Cell Cycle Regulators: New Paradigms
inferredcites →https://doi.org/10.1007/s00412-008-0192-2openalex-snapshot
CAF-1 is required for efficient replication of euchromatic DNA in Drosophila larval endocycling cells
inferredcites →https://doi.org/10.1007/s004120050256openalex-snapshot
Mitosis-specific phosphorylation of histone H3 initiates primarily within pericentromeric heterochromatin during G2 and spreads in an ordered fashion coincident with mitotic chromosome condensation
inferredcites →https://doi.org/10.1016/0012-1606(85)90381-1openalex-snapshot
Polyploid tissues in the nematode Caenorhabditis elegans
inferredcites →https://doi.org/10.1016/0092-8674(94)90239-9openalex-snapshot
Cyclin E controls S phase progression and its down-regulation during Drosophila embryogenesis is required for the arrest of cell proliferation
inferredcites →https://doi.org/10.1016/0925-5710(95)00379-7openalex-snapshot
Thrombopoietin: basic biology, clinical promise.
inferredcites →https://doi.org/10.1016/j.bbadis.2008.06.008openalex-snapshot
Notch signaling and diseases: An evolutionary journey from a simple beginning to complex outcomes
inferredcites →https://doi.org/10.1016/j.cancergencyto.2006.09.013openalex-snapshot
Bipolar genome reductional division of human near-senescent, polyploid fibroblast cells
inferredcites →https://doi.org/10.1016/j.cardiores.2005.02.017openalex-snapshot
Endomitosis and polyploidization of myocardial cells in the periphery of human acute myocardial infarction
inferredcites →https://doi.org/10.1016/j.cellbi.2005.10.005openalex-snapshot
Mitotic catastrophe and endomitosis in tumour cells: An evolutionary key to a molecular solution
inferredcites →https://doi.org/10.1016/j.cellbi.2005.10.008openalex-snapshot
Segregation of genomes in polyploid tumour cells following mitotic catastrophe
inferredcites →https://doi.org/10.1016/j.cellbi.2005.10.015openalex-snapshot
Cell reproduction and genome multiplication in the proliferative and invasive trophoblast cell populations of mammalian placenta
inferredcites →https://doi.org/10.1016/j.cellbi.2007.06.015openalex-snapshot
Origin of diplochromosomal polyploidy in near‐senescent fibroblast cultures: Heterochromatin, telomeres and chromosomal instability (CIN)
inferredcites →https://doi.org/10.1016/j.cellbi.2008.04.021openalex-snapshot
Tumor cells can escape DNA‐damaging cisplatin through DNA endoreduplication and reversible polyploidy
inferredcites →https://doi.org/10.1016/j.cub.2004.03.040openalex-snapshot
Notch-Dependent Fizzy-Related/Hec1/Cdh1 Expression Is Required for the Mitotic-to-Endocycle Transition in Drosophila Follicle Cells
inferredcites →https://doi.org/10.1016/j.cub.2004.12.038openalex-snapshot
The DP-E2F-like Gene DEL1 Controls the Endocycle in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.cub.2006.01.048openalex-snapshot
Regulation of Growth by Ploidy in Caenorhabditis elegans
inferredcites →https://doi.org/10.1016/j.devcel.2007.02.003openalex-snapshot
Hindsight Mediates the Role of Notch in Suppressing Hedgehog Signaling and Cell Proliferation
inferredcites →https://doi.org/10.1016/j.devcel.2008.10.003openalex-snapshot
Intrinsic Negative Cell Cycle Regulation Provided by PIP Box- and Cul4Cdt2-Mediated Destruction of E2f1 during S Phase
inferredcites →https://doi.org/10.1016/j.febslet.2004.04.075openalex-snapshot
Endoreduplication and activation of the anaphase-promoting complex during symbiotic cell development
inferredcites →https://doi.org/10.1016/j.gde.2008.07.013openalex-snapshot
Modulating Notch signaling by pathway-intrinsic and pathway-extrinsic mechanisms
inferredcites →https://doi.org/10.1016/j.molcel.2009.05.012openalex-snapshot
Docking of a Specialized PIP Box onto Chromatin-Bound PCNA Creates a Degron for the Ubiquitin Ligase CRL4Cdt2
inferredcites →https://doi.org/10.1016/j.pbi.2003.09.009openalex-snapshot
“Big it up”: endoreduplication and cell-size control in plants
inferredcites →https://doi.org/10.1016/j.pbi.2004.09.015openalex-snapshot
Cell cycle and differentiation
inferredcites →https://doi.org/10.1016/j.placenta.2005.01.015openalex-snapshot
How to make a placenta: Mechanisms of trophoblast cell differentiation in mice – A Review
inferredcites →https://doi.org/10.1016/j.stem.2008.07.010openalex-snapshot
Notch Signaling Specifies Megakaryocyte Development from Hematopoietic Stem Cells
inferredcites →https://doi.org/10.1016/j.tcb.2007.04.002openalex-snapshot
A key role for the GINS complex at DNA replication forks
inferredcites →https://doi.org/10.1016/j.tcb.2009.01.002openalex-snapshot
Atypical E2Fs: new players in the E2F transcription factor family
inferredcites →https://doi.org/10.1016/j.yexcr.2009.05.011openalex-snapshot
The role of meiotic cohesin REC8 in chromosome segregation in γ irradiation-induced endopolyploid tumour cells
inferredcites →https://doi.org/10.1016/j.ygeno.2006.08.014openalex-snapshot
Genome multiplication as adaptation to tissue survival: Evidence from gene expression in mammalian heart and liver
inferredcites →https://doi.org/10.1016/s0074-7696(08)61053-0openalex-snapshot
Pattern Formation and Cell Differentiation: Trichomes in Arabidopsis as a Genetic Model System
inferredcites →https://doi.org/10.1016/s0092-8674(00)80528-0openalex-snapshot
Drosophila fizzy-related Down-Regulates Mitotic Cyclins and Is Required for Cell Proliferation Arrest and Entry into Endocycles
inferredcites →https://doi.org/10.1016/s0092-8674(00)81209-xopenalex-snapshot
Geminin, an Inhibitor of DNA Replication, Is Degraded during Mitosis
inferredcites →https://doi.org/10.1016/s0092-8674(01)00334-8openalex-snapshot
Endoreplication Cell Cycles
inferredcites →https://doi.org/10.1016/s0092-8674(03)00645-7openalex-snapshot
Cyclin E Ablation in the Mouse
inferredcites →https://doi.org/10.1016/s0165-4608(01)00572-6openalex-snapshot
The origin of transformed cells
inferredcites →https://doi.org/10.1016/s0303-7207(01)00703-1openalex-snapshot
Trophoblast functions, angiogenesis and remodeling of the maternal vasculature in the placenta
inferredcites →https://doi.org/10.1016/s0896-6273(00)80752-7openalex-snapshot
latheo Encodes a Subunit of the Origin Recognition Complex and Disrupts Neuronal Proliferation and Adult Olfactory Memory When Mutant
inferredcites →https://doi.org/10.1016/s0925-4773(00)00435-4openalex-snapshot
Expression of the cyclin-dependent kinase inhibitor Dacapo is regulated by Cyclin E
inferredcites →https://doi.org/10.1016/s0925-4773(02)00388-xopenalex-snapshot
The E2F cell cycle regulator is required for Drosophila nurse cell DNA replication and apoptosis
inferredcites →https://doi.org/10.1016/s0960-9822(01)00043-4openalex-snapshot
Arabidopsis genome: Life without Notch
inferredcites →https://doi.org/10.1016/s0960-9822(98)70089-2openalex-snapshot
Fluctuations in Cyclin E levels are required for multiple rounds of endocycle S phase in Drosophila
inferredcites →https://doi.org/10.1016/s0960-9822(98)70090-9openalex-snapshot
Continuous Cyclin E expression inhibits progression through endoreduplication cycles in Drosophila
inferredcites →https://doi.org/10.1016/s0962-8924(01)02203-6openalex-snapshot
Replication licensing — Origin licensing: defining the proliferative state?
inferredcites →https://doi.org/10.1016/s1097-2765(04)00256-4openalex-snapshot
Telomere Shortening Triggers Senescence of Human Cells through a Pathway Involving ATM, p53, and p21CIP1, but Not p16INK4a
inferredcites →https://doi.org/10.1016/s1369-5266(00)00118-7openalex-snapshot
Plant cell-size control: growing by ploidy?
inferredcites →https://doi.org/10.1016/s1534-5807(02)00117-xopenalex-snapshot
Drosophila's Insulin/PI3-Kinase Pathway Coordinates Cellular Metabolism with Nutritional Conditions
inferredcites →https://doi.org/10.1016/s1534-5807(03)00398-8openalex-snapshot
Gene Amplification as a Developmental Strategy
inferredcites →https://doi.org/10.1023/a:1006446417196openalex-snapshot
Endoreduplication in higher plants
inferredcites →https://doi.org/10.1038/35080570openalex-snapshot
Placental development: Lessons from mouse mutants
inferredcites →https://doi.org/10.1038/35095068openalex-snapshot
Archipelago regulates Cyclin E levels in Drosophila and is mutated in human cancer cell lines
inferredcites →https://doi.org/10.1038/35095076openalex-snapshot
Human F-box protein hCdc4 targets cyclin E for proteolysis and is mutated in a breast cancer cell line
inferredcites →https://doi.org/10.1038/369568a0openalex-snapshot
Promotion of megakaryocyte progenitor expansion and differentiation by the c-Mpl ligand thrombopoietin
inferredcites →https://doi.org/10.1038/nature01747openalex-snapshot
CUL-4 ubiquitin ligase maintains genome stability by restraining DNA-replication licensing
inferredcites →https://doi.org/10.1038/nature04333openalex-snapshot
The adult Drosophila posterior midgut is maintained by pluripotent stem cells
inferredcites →https://doi.org/10.1038/nature04371openalex-snapshot
Evidence that stem cells reside in the adult Drosophila midgut epithelium
inferredcites →https://doi.org/10.1038/nature06046openalex-snapshot
Cdk1 is sufficient to drive the mammalian cell cycle
inferredcites →https://doi.org/10.1038/ncb1284openalex-snapshot
Cdc2–cyclin E complexes regulate the G1/S phase transition
inferredcites →https://doi.org/10.1038/ncb1346openalex-snapshot
PCNA functions as a molecular platform to trigger Cdt1 destruction and prevent re-replication
inferredcites →https://doi.org/10.1038/ncb1742openalex-snapshot
Genomic stability and tumour suppression by the APC/C cofactor Cdh1
inferredcites →https://doi.org/10.1038/ncb813openalex-snapshot
Distinct roles for cyclins E and A during DNA replication complex assembly and activation
inferredcites →https://doi.org/10.1038/nrm1276openalex-snapshot
From polyploidy to aneuploidy, genome instability and cancer
inferredcites →https://doi.org/10.1038/nrm2469openalex-snapshot
Conserved functions of the pRB and E2F families
inferredcites →https://doi.org/10.1038/onc.2008.77openalex-snapshot
Fbw7 regulates the activity of endoreduplication mediators and the p53 pathway to prevent drug-induced polyploidy
inferredcites →https://doi.org/10.1038/sj.emboj.7601648openalex-snapshot
The cyclin‐dependent kinase inhibitor Dacapo promotes replication licensing during Drosophila endocycles
inferredcites →https://doi.org/10.1038/sj.onc.1203494openalex-snapshot
Ectopic expression of cyclin E allows non-endomitotic megakaryoblastic K562 cells to establish re-replication cycles
inferredcites →https://doi.org/10.1038/sj.onc.1203630openalex-snapshot
Normal and c-Myc-promoted human keratinocyte differentiation both occur via a novel cell cycle involving cellular growth and endoreplication
inferredcites →https://doi.org/10.1038/sj.onc.1208610openalex-snapshot
New insights into cell cycle control from the Drosophila endocycle
inferredcites →https://doi.org/10.1038/sj.onc.1208612openalex-snapshot
The E2F transcriptional network: old acquaintances with new faces
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00030.xopenalex-snapshot
Phytochrome controls the number of endoreduplication cycles in the Arabidopsis thaliana hypocotyl
inferredcites →https://doi.org/10.1073/pnas.0307875101openalex-snapshot
Defective cardiovascular development and elevated cyclin E and Notch proteins in mice lacking the Fbw7 F-box protein
inferredcites →https://doi.org/10.1073/pnas.0805189105openalex-snapshot
The origin recognition complex is dispensable for endoreplication in Drosophila
inferredcites →https://doi.org/10.1073/pnas.0806510105openalex-snapshot
Atypical E2F activity restrains APC/C CCS52A2 function obligatory for endocycle onset
inferredcites →https://doi.org/10.1073/pnas.24.2.56openalex-snapshot
A Cytological Study of Colchicine Effects in the Induction of Polyploidy in Plants
inferredcites →https://doi.org/10.1073/pnas.92.15.7070openalex-snapshot
Dynamics of maize endosperm development and DNA endoreduplication.
inferredcites →https://doi.org/10.1073/pnas.96.6.3132openalex-snapshot
Identification of mutations in the c-mpl gene in congenital amegakaryocytic thrombocytopenia
inferredcites →https://doi.org/10.1073/pnas.97.10.5285openalex-snapshot
Somatic polyploidization and cellular proliferation drive body size evolution in nematodes
inferredcites →https://doi.org/10.1073/pnas.97.13.6941openalex-snapshot
Variation and evolution in plants and microorganisms: Toward a new synthesis 50 years after Stebbins
inferredcites →https://doi.org/10.1074/jbc.271.8.4266openalex-snapshot
The Cell Cycle in Polyploid Megakaryocytes Is Associated with Reduced Activity of Cyclin B1-dependent Cdc2 Kinase
inferredcites →https://doi.org/10.1074/jbc.274.19.13480openalex-snapshot
Thrombopoietin Signal Transduction Requires Functional JAK2, Not TYK2
inferredcites →https://doi.org/10.1074/jbc.275.8.5553openalex-snapshot
Increased D-type Cyclin Expression Together with Decreased cdc2 Activity Confers Megakaryocytic Differentiation of a Human Thrombopoietin-dependent Hematopoietic Cell Line
inferredcites →https://doi.org/10.1074/jbc.c500464200openalex-snapshot
An Evolutionarily Conserved Function of Proliferating Cell Nuclear Antigen for Cdt1 Degradation by the Cul4-Ddb1 Ubiquitin Ligase in Response to DNA Damage
inferredcites →https://doi.org/10.1074/jbc.m106006200openalex-snapshot
Heterologous Expression of the Transcriptional Regulator Escargot Inhibits Megakaryocytic Endomitosis
inferredcites →https://doi.org/10.1074/jbc.m512705200openalex-snapshot
PCNA Is a Cofactor for Cdt1 Degradation by CUL4/DDB1-mediated N-terminal Ubiquitination
inferredcites →https://doi.org/10.1083/jcb.130.4.755openalex-snapshot
Early events in DNA replication require cyclin E and are blocked by p21CIP1.
inferredcites →https://doi.org/10.1083/jcb.139.2.449openalex-snapshot
Thrombopoietin-induced Polyploidization of Bone Marrow Megakaryocytes Is Due to a Unique Regulatory Mechanism in Late Mitosis
inferredcites →https://doi.org/10.1083/jcb.140.3.451openalex-snapshot
Chromosome Association of Minichromosome Maintenance Proteins in Drosophila Endoreplication Cycles
inferredcites →https://doi.org/10.1083/jcb.200104035openalex-snapshot
The NEDD8 system is essential for cell cycle progression and morphogenetic pathway in mice
inferredcites →https://doi.org/10.1083/jcb.200802084openalex-snapshot
Regulation of the endocycle/gene amplification switch by Notch and ecdysone signaling
inferredcites →https://doi.org/10.1091/mbc.11.3.1037openalex-snapshot
Periodic Expression of the Cyclin-dependent Kinase Inhibitor p57 Kip2 in Trophoblast Giant Cells Defines a G2-like Gap Phase of the Endocycle
inferredcites →https://doi.org/10.1091/mbc.12.7.2023openalex-snapshot
Telomere Dysfunction Triggers Developmentally Regulated Germ Cell Apoptosis
inferredcites →https://doi.org/10.1091/mbc.7.2.209openalex-snapshot
Novel alterations in CDK1/cyclin B1 kinase complex formation occur during the acquisition of a polyploid DNA content.
inferredcites →https://doi.org/10.1091/mbc.e02-04-0217openalex-snapshot
Regulation of CDC6, Geminin, and CDT1 in Human Cells that Undergo Polyploidization
inferredcites →https://doi.org/10.1093/emboj/18.16.4476openalex-snapshot
The mitotic inhibitor ccs52 is required for endoreduplication and ploidy‐dependent cell enlargement in plants
inferredcites →https://doi.org/10.1093/emboj/18.4.916openalex-snapshot
The role of RBF in the introduction of G1 regulation during Drosophila embryogenesis
inferredcites →https://doi.org/10.1093/emboj/cdg373openalex-snapshot
Critical role of active repression by E2F and Rb proteins in endoreplication during Drosophila development
inferredcites →https://doi.org/10.1093/emboj/cdg482openalex-snapshot
Cyclins E1 and E2 are required for endoreplication in placental trophoblast giant cells
inferredcites →https://doi.org/10.1093/emboj/cdg573openalex-snapshot
Degradation of origin recognition complex large subunit by the anaphase‐promoting complex in Drosophila
inferredcites →https://doi.org/10.1093/genetics/155.1.233openalex-snapshot
A Screen for Modifiers of Cyclin E Function in Drosophila melanogaster Identifies Cdk2 Mutations, Revealing the Insignificance of Putative Phosphorylation Sites in Cdk2
inferredcites →https://doi.org/10.1093/nar/gkh981openalex-snapshot
A novel E2 box-GATA element modulates Cdc6 transcription during human cells polyploidization
inferredcites →https://doi.org/10.1093/nar/gki854openalex-snapshot
The genes encoding Arabidopsis ORC subunits are E2F targets and the two ORC1 genes are differently expressed in proliferating and endoreplicating cells
inferredcites →https://doi.org/10.1097/00000658-192504000-00016openalex-snapshot
MICROSCOPIC EXAMINATION OF FRESH TISSUE, AND NECROPSY SERVICE IN RELATION TO SURGERY
inferredcites →https://doi.org/10.1101/gad.10.10.1206openalex-snapshot
RBF, a novel RB-related gene that regulates E2F activity and interacts with cyclin E in Drosophila.
inferredcites →https://doi.org/10.1101/gad.10.19.2514openalex-snapshot
The Drosophila endocycle is controlled by Cyclin E and lacks a checkpoint ensuring S-phase completion.
inferredcites →https://doi.org/10.1101/gad.11.15.1999openalex-snapshot
Mutations in Drosophila DP and E2F distinguish G1–S progression from an associated transcriptional program
inferredcites →https://doi.org/10.1101/gad.12.5.734openalex-snapshot
Cell cycle control of chorion gene amplification
inferredcites →https://doi.org/10.1101/gad.1361905openalex-snapshot
A novel motif governs APC-dependent degradation of Drosophila ORC1 in vivo
inferredcites →https://doi.org/10.1101/gad.1453606openalex-snapshot
Hepatocytes with extensive telomere deprotection and fusion remain viable and regenerate liver mass through endoreduplication
inferredcites →https://doi.org/10.1101/gad.1508907openalex-snapshot
Strength in numbers: preventing rereplication via multiple mechanisms in eukaryotic cells
inferredcites →https://doi.org/10.1101/gad.1710208openalex-snapshot
Endocycling cells do not apoptose in response to DNA rereplication genotoxic stress
inferredcites →https://doi.org/10.1101/gad.1718108openalex-snapshot
Differentiation of trophoblast stem cells into giant cells is triggered by p57/Kip2 inhibition of CDK1 activity
inferredcites →https://doi.org/10.1101/gad.1822409openalex-snapshot
Drosophila Minus is required for cell proliferation and influences Cyclin E turnover
inferredcites →https://doi.org/10.1101/gad.200901openalex-snapshot
Delta signaling from the germ line controls the proliferation and differentiation of the somatic follicle cells during Drosophila oogenesis
inferredcites →https://doi.org/10.1101/gad.379706openalex-snapshot
Geminin is essential to prevent endoreduplication and to form pluripotent cells during mammalian development
inferredcites →https://doi.org/10.1101/gad.469108openalex-snapshot
The anaphase-promoting complex/cyclosome (APC/C) is required for rereplication control in endoreplication cycles
inferredcites →https://doi.org/10.1101/gad.8.19.2270openalex-snapshot
Diploidy of Drosophila imaginal cells is maintained by a transcriptional repressor encoded by escargot.
inferredcites →https://doi.org/10.1101/gad.9.11.1327openalex-snapshot
Distinct modes of cyclin E/cdc2c kinase regulation and S-phase control in mitotic and endoreduplication cycles of Drosophila embryogenesis.
inferredcites →https://doi.org/10.1101/gad.9.12.1445openalex-snapshot
The transcription factor E2F is required for S phase during Drosophila embryogenesis.
inferredcites →https://doi.org/10.1101/gad.9.12.1456openalex-snapshot
Developmental control of the G1 to S transition in Drosophila: cyclin Eis a limiting downstream target of E2F.
inferredcites →https://doi.org/10.1101/gad.903901openalex-snapshot
Functional antagonism between E2F family members
inferredcites →https://doi.org/10.1104/pp.020002openalex-snapshot
SPINDLY Is a Nuclear-Localized Repressor of Gibberellin Signal Transduction Expressed throughout the Plant
inferredcites →https://doi.org/10.1104/pp.109.140269openalex-snapshot
CDKB1;1 Forms a Functional Complex with CYCA2;3 to Suppress Endocycle Onset
inferredcites →https://doi.org/10.1104/pp.124.2.553openalex-snapshot
Hormonal Interactions in the Control of Arabidopsis Hypocotyl Elongation
inferredcites →https://doi.org/10.1104/pp.96.3.985openalex-snapshot
Systemic Endopolyploidy in Arabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.010329openalex-snapshot
Expression and Stability of Arabidopsis CDC6 Are Associated with Endoreplication
inferredcites →https://doi.org/10.1105/tpc.022178openalex-snapshot
A Dominant Negative Mutant of Cyclin-Dependent Kinase A Reduces Endoreduplication but Not Cell Size or Gene Expression in Maize Endosperm
inferredcites →https://doi.org/10.1105/tpc.104.024398openalex-snapshot
The Plant-Specific Cyclin-Dependent Kinase CDKB1;1 and Transcription Factor E2Fa-DPa Control the Balance of Mitotically Dividing and Endoreduplicating Cells in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.105.037309openalex-snapshot
The A-Type Cyclin CYCA2;3 Is a Key Regulator of Ploidy Levels in Arabidopsis Endoreduplication
inferredcites →https://doi.org/10.1105/tpc.105.039651openalex-snapshot
The Balance between Cell Division and Endoreplication Depends on E2FC-DPB, Transcription Factors Regulated by the Ubiquitin-SCFSKP2A Pathway inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.5.10.1371openalex-snapshot
Embryogenesis in Angiosperms: Development of the Suspensor
inferredcites →https://doi.org/10.1111/j.1365-2443.2006.01019.xopenalex-snapshot
Geminin is essential for the development of preimplantation mouse embryos
inferredcites →https://doi.org/10.1111/j.1365-3040.2006.01506.xopenalex-snapshot
Cell and leaf size plasticity in Arabidopsis: what is the role of endoreduplication?
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02361.xopenalex-snapshot
Retinoblastoma protein regulates cell proliferation, differentiation, and endoreduplication in plants
inferredcites →https://doi.org/10.1111/j.1538-7836.2005.01428.xopenalex-snapshot
Qualitative disorders of platelets and megakaryocytes
inferredcites →https://doi.org/10.1126/science.1065203openalex-snapshot
Phosphorylation-Dependent Ubiquitination of Cyclin E by the SCF Fbw7 Ubiquitin Ligase
inferredcites →https://doi.org/10.1126/science.1142618openalex-snapshot
An Ancient Mechanism Controls the Development of Cells with a Rooting Function in Land Plants
inferredcites →https://doi.org/10.1126/science.269.5228.1262openalex-snapshot
Endoreduplication in Maize Endosperm: Involvement of M Phase—Promoting Factor Inhibition and Induction of S Phase—Related Kinases
inferredcites →https://doi.org/10.1126/science.282.5394.1721openalex-snapshot
Control of Cyclin Ubiquitination by CDK-Regulated Binding of Hct1 to the Anaphase Promoting Complex
inferredcites →https://doi.org/10.1126/science.290.5500.2309openalex-snapshot
Inhibition of Eukaryotic DNA Replication by Geminin Binding to Cdt1
inferredcites →https://doi.org/10.1126/science.8073287openalex-snapshot
Thrombocytopenia in c-mpl-deficient mice
inferredcites →https://doi.org/10.1128/.20.17.6308-6316.2000openalex-snapshot
Replication of Heterochromatin and Structure of Polytene Chromosomes
inferredcites →https://doi.org/10.1128/mcb.18.1.141openalex-snapshot
Mutations of the Drosophila dDP , dE2F , and cyclin E Genes Reveal Distinct Roles for the E2F-DP Transcription Factor and Cyclin E during the G 1 -S Transition
inferredcites →https://doi.org/10.1128/mcb.20.2.507-515.2000openalex-snapshot
Role of the Distal Half of the c-Mpl Intracellular Domain in Control of Platelet Production by Thrombopoietin In Vivo
inferredcites →https://doi.org/10.1128/mcb.26.9.3468-3477.2006openalex-snapshot
Specific Role of the SR Protein Splicing Factor B52 in Cell Cycle Control in Drosophila
inferredcites →https://doi.org/10.1146/annurev.biochem.71.110601.135425openalex-snapshot
DNA Replication in Eukaryotic Cells
inferredcites →https://doi.org/10.1146/annurev.genet.37.110801.143851openalex-snapshot
Developmental Gene Amplification and Origin Regulation
inferredcites →https://doi.org/10.1146/annurev.genet.40.110405.090431openalex-snapshot
Cell Cycle Regulation in Plant Development
inferredcites →https://doi.org/10.1146/annurev.genet.41.110306.130308openalex-snapshot
Cell Cycle Regulation of DNA Replication
inferredcites →https://doi.org/10.1158/0008-5472.can-08-3364openalex-snapshot
Activation of Meiosis-Specific Genes Is Associated with Depolyploidization of Human Tumor Cells following Radiation-Induced Mitotic Catastrophe
inferredcites →https://doi.org/10.1172/jci26674openalex-snapshot
The molecular mechanisms that control thrombopoiesis
inferredcites →https://doi.org/10.1172/jci26720openalex-snapshot
Megakaryocyte biology and related disorders
inferredcites →https://doi.org/10.1182/blood-2007-05-088500openalex-snapshot
Historical review: megakaryopoiesis and thrombopoiesis
inferredcites →https://doi.org/10.1182/blood.v74.2.594.594openalex-snapshot
Flow cytometric analysis of megakaryocytes from patients with abnormal platelet counts
inferredcites →https://doi.org/10.1182/blood.v87.6.2162.bloodjournal8762162openalex-snapshot
Deficiencies in progenitor cells of multiple hematopoietic lineages and defective megakaryocytopoiesis in mice lacking the thrombopoietic receptor c-Mpl
inferredcites →https://doi.org/10.1182/blood.v89.11.3980openalex-snapshot
Polyploidization and Functional Maturation Are Two Distinct Processes During Megakaryocytic Differentiation: Involvement of Cyclin-Dependent Kinase Inhibitor p21 in Polyploidization
inferredcites →https://doi.org/10.1182/blood.v91.10.3711openalex-snapshot
Endomitosis of Human Megakaryocytes Are Due to Abortive Mitosis
inferredcites →https://doi.org/10.1182/blood.v92.1.4.413k38_4_10openalex-snapshot
Role of c-mpl in Early Hematopoiesis
inferredcites →https://doi.org/10.1182/blood.v94.4.1273openalex-snapshot
Thrombopoietin-Induced Activation of the Mitogen-Activated Protein Kinase (MAPK) Pathway in Normal Megakaryocytes: Role in Endomitosis
inferredcites →https://doi.org/10.1186/1471-213x-6-16openalex-snapshot
Notch signaling through Tramtrack bypasses the mitosis promoting activity of the JNK pathway in the mitotic-to-endocycle transition of Drosophila follicle cells
inferredcites →https://doi.org/10.1242/dev.00355openalex-snapshot
Dp1is required for extra-embryonic development
inferredcites →https://doi.org/10.1242/dev.00932openalex-snapshot
Drosophila dMyc is required for ovary cell growth and endoreplication
inferredcites →https://doi.org/10.1242/dev.01108openalex-snapshot
dMyc is required for larval growth and endoreplication in Drosophila
inferredcites →https://doi.org/10.1242/dev.01172openalex-snapshot
The mitotic-to-endocycle switch inDrosophilafollicle cells is executed by Notch-dependent regulation of G1/S, G2/M and M/G1 cell-cycle transitions
inferredcites →https://doi.org/10.1242/dev.016295openalex-snapshot
APC/CFzr/Cdh1 promotes cell cycle progression during theDrosophilaendocycle
inferredcites →https://doi.org/10.1242/dev.01797openalex-snapshot
Cell cycle diversity involves differential regulation of Cyclin E activity in theDrosophilabristle cell lineage
inferredcites →https://doi.org/10.1242/dev.02015openalex-snapshot
Notch-dependent downregulation of the homeodomain gene cut is required for the mitotic cycle/endocycle switch and cell differentiation inDrosophilafollicle cells
inferredcites →https://doi.org/10.1242/dev.112.4.997openalex-snapshot
The regulation of the cell cycle during Drosophila embryogenesis: the transition to polyteny
inferredcites →https://doi.org/10.1242/dev.118.1.105openalex-snapshot
Control of imaginal cell development by the escargot gene of Drosophila
inferredcites →https://doi.org/10.1242/dev.122.4.1051openalex-snapshot
A Cdc2 dependent checkpoint maintains diploidy in Drosophila
inferredcites →https://doi.org/10.1242/dev.124.18.3555openalex-snapshot
Cell cycle progression, growth and patterning in imaginal discs despite inhibition of cell division after inactivation of Drosophila Cdc2 kinase
inferredcites →https://doi.org/10.1242/dev.125.11.2149openalex-snapshot
Environmental control of the cell cycle in Drosophila: nutrition activates mitotic and endoreplicative cells by distinct mechanisms
inferredcites →https://doi.org/10.1242/dev.126.2.293openalex-snapshot
The endocycle controls nurse cell polytene chromosome structure during Drosophila oogenesis
inferredcites →https://doi.org/10.1242/dev.127.10.2165openalex-snapshot
Regulation of cell proliferation and patterning in Drosophila oogenesis by Hedgehog signaling
inferredcites →https://doi.org/10.1242/dev.127.18.3931openalex-snapshot
SIAMESE, a gene controlling the endoreduplication cell cycle in Arabidopsis thaliana trichomes
inferredcites →https://doi.org/10.1242/dev.127.2.367openalex-snapshot
Suppression of the rbf null mutants by a de2f1 allele that lacks transactivation domain
inferredcites →https://doi.org/10.1242/dev.128.23.4737openalex-snapshot
Notch-Delta signaling induces a transition from mitotic cell cycle to endocycle inDrosophilafollicle cells
inferredcites →https://doi.org/10.1242/dev.128.9.1697openalex-snapshot
Orc mutants arrest in metaphase with abnormally condensed chromosomes
inferredcites →https://doi.org/10.1242/jcs.00740openalex-snapshot
Endopolyploid cells produced after severe genotoxic damage have the potential to repair DNA double strand breaks
inferredcites →https://doi.org/10.1242/jcs.035683openalex-snapshot
The molecular logic of Notch signaling – a structural and biochemical perspective
inferredcites →https://doi.org/10.1371/journal.pgen.1000385openalex-snapshot
Ploidy Reductions in Murine Fusion-Derived Hepatocytes
inferredcites →https://doi.org/10.1667/rr3009openalex-snapshot
Computerized Video Time-Lapse (CVTL) Analysis of the Fate of Giant Cells Produced by X-Irradiating EJ30 Human Bladder Carcinoma Cells
inferredcites →https://doi.org/10.2135/cropsci2001.4141114xopenalex-snapshot
DNA Endoreduplication in Maize Endosperm Cells is Reduced by High Temperature During the Mitotic Phase
inferredcites →https://doi.org/10.2174/1566524010606070739openalex-snapshot
Distinct and Overlapping Roles for E2F Family Members in Transcription, Proliferation and Apoptosis
inferredcites →https://doi.org/10.4161/cc.5.15.3149openalex-snapshot
L2DTL/CDT2 Interacts with the CUL4/DDB1 Complex and PCNA and Regulates CDT1 Proteolysis in Response to DNA Damage
inferredcites →https://doi.org/10.4161/cc.7.1.5228openalex-snapshot
Cell cycle switch to endocycle: The nucleolus lends a hand
inferredcites →https://doi.org/10.4161/cc.8.10.8325openalex-snapshot
Developmentally programmed endoreduplication in animals
inferredcites →https://doi.org/10.4161/fly.8087openalex-snapshot
Endoreplication: The advantage to initiating DNA replication without the ORC?
What points at this work
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inferred← citeshttps://doi.org/10.1016/j.asd.2012.09.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ejcb.2025.151529openalex-snapshot
Polyploid giant cancer cells: A novel target in future cancer therapy
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2018.06.026openalex-snapshot
Cell cycle regulation in different leaves of Arabidopsis thaliana plants grown under control and cadmium-exposed conditions
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.104963openalex-snapshot
Tomato UVI4 homologue modulates cell expansion to participate heat-stimulated hypocotyl elongation
inferred← citeshttps://doi.org/10.1016/j.gene.2011.12.056openalex-snapshot
Differential requirement for the N-terminal catalytic domain of the DNA polymerase ε p255 subunit in the mitotic cell cycle and the endocycle
inferred← citeshttps://doi.org/10.1016/j.ibmb.2018.09.002openalex-snapshot
Juvenile hormone promotes locust fat body cell polyploidization and vitellogenesis by activating the transcription of Cdk6 and E2f1
inferred← citeshttps://doi.org/10.1016/j.ibmb.2019.103241openalex-snapshot
Telomerase activity is upregulated in the fat bodies of pre-diapause bumblebee queens (Bombus terrestris)
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.124931openalex-snapshot
A novel transcription factor, BmZFP67, regulates endomitosis switch by controlling the expression of cyclin B in silk glands
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.131706openalex-snapshot
Characterization of polyploidy in cancer: Current status and future perspectives
inferred← citeshttps://doi.org/10.1016/j.isci.2024.111311openalex-snapshot
Resistance to spindle inhibitors in glioblastoma depends on STAT3 and therapy induced senescence
inferred← citeshttps://doi.org/10.1016/j.jarmap.2024.100612openalex-snapshot
Optimized flow cytometry protocol for assessing DNA content in Vanilla (Orchidaceae) species: Insights into crop wild relatives and a commercial hybrid
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2019.01.016openalex-snapshot
Physiological alterations of GS-CHO cells in response to adenosine monophosphate treatment
inferred← citeshttps://doi.org/10.1016/j.jcmgh.2020.09.016openalex-snapshot
Controversies Surrounding the Origin of Hepatocytes in Adult Livers and the in Vitro Generation or Propagation of Hepatocytes
inferred← citeshttps://doi.org/10.1016/j.jcs.2011.09.006openalex-snapshot
Replicate and die for your own good: Endoreduplication and cell death in the cereal endosperm
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2022.104367openalex-snapshot
Molecular pathogenesis of dengue virus infection in Aedes mosquitoes
inferred← citeshttps://doi.org/10.1016/j.jori.2026.100031openalex-snapshot
Plasticity of the endoreplication in insects: Multifaceted roles in development and adaptation
inferred← citeshttps://doi.org/10.1016/j.jtbi.2014.01.031openalex-snapshot
Modelling cell division and endoreduplication in tomato fruit pericarp
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2015.02.011openalex-snapshot
Temperature and developmental responses of body and cell size in Drosophila; effects of polyploidy and genome configuration
inferred← citeshttps://doi.org/10.1016/j.mbs.2026.109646openalex-snapshot
A Wheel of Fortune: The eukaryotic cell cycle as a tetra-stable excitable system
inferred← citeshttps://doi.org/10.1016/j.molbiopara.2012.11.005openalex-snapshot
Evaluation of drugs and stationary growth on the cell cycle of Giardia intestinalis
inferred← citeshttps://doi.org/10.1016/j.molcel.2022.07.017openalex-snapshot
Increasing cell size remodels the proteome and promotes senescence
inferred← citeshttps://doi.org/10.1016/j.molmed.2019.02.006openalex-snapshot
Surviving Acute Organ Failure: Cell Polyploidization and Progenitor Proliferation
inferred← citeshttps://doi.org/10.1016/j.mrrev.2018.01.001openalex-snapshot
Integrating plant and animal biology for the search of novel DNA damage biomarkers
inferred← citeshttps://doi.org/10.1016/j.neo.2024.101014openalex-snapshot
Aurkin-A, a TPX2-Aurora A small molecule inhibitor disrupts Alisertib-induced polyploidy in aggressive diffuse large B cell lymphoma
inferred← citeshttps://doi.org/10.1016/j.neo.2025.101268openalex-snapshot
Polyploid cisplatin-resistant cancer cells have altered nuclear organization and epigenomic status
inferred← citeshttps://doi.org/10.1016/j.pbi.2013.11.007openalex-snapshot
Endocycling in the path of plant development
inferred← citeshttps://doi.org/10.1016/j.pbi.2020.02.006openalex-snapshot
Endoreplication — a means to an end in cell growth and stress response
inferred← citeshttps://doi.org/10.1016/j.placenta.2015.05.017openalex-snapshot
ERBB2 gene amplification increases during the transition of proximal EGFR+ to distal HLA-G+ first trimester cell column trophoblasts
inferred← citeshttps://doi.org/10.1016/j.plantsci.2012.11.006openalex-snapshot
Evaluation of ploidy level and endoreduplication in carnation (Dianthus spp.)
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.06.006openalex-snapshot
Glutathione: A key player in metal chelation, nutrient homeostasis, cell cycle regulation and the DNA damage response in cadmium-exposed Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108804openalex-snapshot
FvUVI4 inhibits cell division and cell expansion to modulate fruit development in Fragaria vesca
inferred← citeshttps://doi.org/10.1016/j.prp.2024.155162openalex-snapshot
Beyond typical histology of BAP1-inactivated melanocytoma
inferred← citeshttps://doi.org/10.1016/j.semcancer.2019.09.005openalex-snapshot
The “life code”: A theory that unifies the human life cycle and the origin of human tumors
inferred← citeshttps://doi.org/10.1016/j.semcancer.2020.11.016openalex-snapshot
Cancer cells employ an evolutionarily conserved polyploidization program to resist therapy
inferred← citeshttps://doi.org/10.1016/j.semcancer.2021.03.003openalex-snapshot
Polyploidy formation in cancer cells: How a Trojan horse is born
inferred← citeshttps://doi.org/10.1016/j.semcancer.2021.04.005openalex-snapshot
Human cell polyploidization: The good and the evil
inferred← citeshttps://doi.org/10.1016/j.semcdb.2011.03.012openalex-snapshot
The emerging role of APC/CCdh1 in development
inferred← citeshttps://doi.org/10.1016/j.tcb.2013.03.005openalex-snapshot
Coordination of organ growth: principles and outstanding questions from the world of insects
inferred← citeshttps://doi.org/10.1016/j.tcb.2013.06.002openalex-snapshot
Physiological significance of polyploidization in mammalian cells
inferred← citeshttps://doi.org/10.1016/j.tcb.2018.02.006openalex-snapshot
Endoreplication: The Good, the Bad, and the Ugly
inferred← citeshttps://doi.org/10.1016/j.tem.2019.05.006openalex-snapshot
Adult Cardiomyocyte Cell Cycle Detour: Off-ramp to Quiescent Destinations
inferred← citeshttps://doi.org/10.1016/j.tig.2011.07.003openalex-snapshot
The aneuploidy paradox: costs and benefits of an incorrect karyotype
inferred← citeshttps://doi.org/10.1016/j.tig.2012.07.003openalex-snapshot
Coordinating genome expression with cell size
inferred← citeshttps://doi.org/10.1016/j.tig.2015.03.011openalex-snapshot
When bigger is better: the role of polyploidy in organogenesis
inferred← citeshttps://doi.org/10.1016/j.tpb.2022.03.004openalex-snapshot
Amitosis as a strategy of cell division—Insight from the proliferation of Tetrahymena thermophila macronuclei
inferred← citeshttps://doi.org/10.1016/j.tplants.2011.07.001openalex-snapshot
Molecular control and function of endoreplication in development and physiology
inferred← citeshttps://doi.org/10.1016/j.tplants.2014.11.007openalex-snapshot
Plasticity in ploidy: a generalized response to stress
inferred← citeshttps://doi.org/10.1016/j.xplc.2022.100330openalex-snapshot
A chromosome-level, haplotype-phased Vanilla planifolia genome highlights the challenge of partial endoreplication for accurate whole-genome assembly
inferred← citeshttps://doi.org/10.1016/j.ydbio.2020.09.002openalex-snapshot
Dynamic optima in cell sizes during early development enable normal gastrulation in zebrafish embryos
inferred← citeshttps://doi.org/10.1016/j.yexcr.2010.04.030openalex-snapshot
Up-regulation of the embryonic self-renewal network through reversible polyploidy in irradiated p53-mutant tumour cells
inferred← citeshttps://doi.org/10.1016/j.yexcr.2013.07.006openalex-snapshot
Chorion formation in panoistic ovaries requires windei and trimethylation of histone 3 lysine 9
inferred← citeshttps://doi.org/10.1016/j.yexcr.2021.112951openalex-snapshot
Geminin is essential for DNA re-replication in the silk gland cells of silkworms
inferred← citeshttps://doi.org/10.1016/j.ymben.2023.11.005openalex-snapshot
Directed evolution of biomass intensive CHO cells by adaptation to sub-physiological temperature
inferred← citeshttps://doi.org/10.1016/j.ymeth.2019.06.001openalex-snapshot
Next-generation transcriptome assembly and analysis: Impact of ploidy
inferred← citeshttps://doi.org/10.1017/s0960258520000148openalex-snapshot
Endosperm variability: from endoreduplication within a seed to higher ploidy across species, and its competence
inferred← citeshttps://doi.org/10.1038/bjc.2017.78openalex-snapshot
Multinucleated polyploidy drives resistance to Docetaxel chemotherapy in prostate cancer
inferred← citeshttps://doi.org/10.1038/bmt.2015.347openalex-snapshot
Conjunctival polyploid cells and donor-derived myofibroblasts in ocular GvHD
inferred← citeshttps://doi.org/10.1038/cdd.2010.145openalex-snapshot
Illicit survival of cancer cells during polyploidization and depolyploidization
inferred← citeshttps://doi.org/10.1038/emboj.2010.313openalex-snapshot
Atypical E2F activity coordinates PHR1 photolyase gene transcription with endoreduplication onset
inferred← citeshttps://doi.org/10.1038/emboj.2012.13openalex-snapshot
Arabidopsis E2FA stimulates proliferation and endocycle separately through RBR‐bound and RBR‐free complexes
inferred← citeshttps://doi.org/10.1038/emboj.2012.294openalex-snapshot
Transcriptional repression of the APC/C activator CCS52A1 promotes active termination of cell growth
inferred← citeshttps://doi.org/10.1038/ncb2585openalex-snapshot
E2F8 is essential for polyploidization in mammalian cells
inferred← citeshttps://doi.org/10.1038/ncb2595openalex-snapshot
Canonical and atypical E2Fs regulate the mammalian endocycle
inferred← citeshttps://doi.org/10.1038/ncb2609openalex-snapshot
Atypical E2Fs drive atypical cell cycles
inferred← citeshttps://doi.org/10.1038/ncomms8668openalex-snapshot
Aneuploidy generates proteotoxic stress and DNA damage concurrently with p53-mediated post-mitotic apoptosis in SAC-impaired cells
inferred← citeshttps://doi.org/10.1038/nrm3228openalex-snapshot
All tangled up: how cells direct, manage and exploit topoisomerase function
inferred← citeshttps://doi.org/10.1038/onc.2010.310openalex-snapshot
MOS, aneuploidy and the ploidy cycle of cancer cells
inferred← citeshttps://doi.org/10.1038/onc.2013.96openalex-snapshot
Generation of cancer stem-like cells through the formation of polyploid giant cancer cells
inferred← citeshttps://doi.org/10.1038/s41388-018-0272-6openalex-snapshot
Multi-nucleated cells use ROS to induce breast cancer chemo-resistance in vitro and in vivo
inferred← citeshttps://doi.org/10.1038/s41419-018-0413-4openalex-snapshot
Pan-class I PI3-kinase inhibitor BKM120 induces MEK1/2-dependent mitotic catastrophe in non-Hodgkin lymphoma leading to apoptosis or polyploidy determined by Bax/Bak and p53
inferred← citeshttps://doi.org/10.1038/s41419-026-09305-9openalex-snapshot
Mitotic bypass and continued endocycling promote cancer cell survival after genotoxic chemotherapy
inferred← citeshttps://doi.org/10.1038/s41467-021-22815-8openalex-snapshot
An Arabidopsis AT-hook motif nuclear protein mediates somatic embryogenesis and coinciding genome duplication
inferred← citeshttps://doi.org/10.1038/s41467-023-36968-1openalex-snapshot
DNA replication initiation factor RECQ4 possesses a role in antagonizing DNA replication initiation
inferred← citeshttps://doi.org/10.1038/s41467-025-62194-yopenalex-snapshot
Genetic architecture of a light-temperature coincidence detector
inferred← citeshttps://doi.org/10.1038/s41575-020-0284-xopenalex-snapshot
Polyploidy in liver development, homeostasis and disease
inferred← citeshttps://doi.org/10.1038/s41598-017-04602-yopenalex-snapshot
Self-diploidization of human haploid parthenogenetic embryos through the Rho pathway regulates endomitosis and failed cytokinesis
inferred← citeshttps://doi.org/10.1038/s41598-017-17275-4openalex-snapshot
Reduced cell size, chromosomal aberration and altered proliferation rates are characteristics and confounding factors in the STHdh cell model of Huntington disease
inferred← citeshttps://doi.org/10.1038/s41598-018-36036-5openalex-snapshot
Reversible senescence of human colon cancer cells after blockage of mitosis/cytokinesis caused by the CNF1 cyclomodulin from Escherichia coli
inferred← citeshttps://doi.org/10.1038/s41598-020-76350-5openalex-snapshot
Dengue virus infection impedes megakaryopoiesis in MEG-01 cells where the virus envelope protein interacts with the transcription factor TAL-1
inferred← citeshttps://doi.org/10.1038/s41598-020-79912-9openalex-snapshot
Seasonality in telomerase activity in relation to cell size, DNA replication, and nutrients in the fat body of Apis mellifera
inferred← citeshttps://doi.org/10.1038/s41598-021-91293-1openalex-snapshot
RETRACTED ARTICLE: SOG1 transcription factor promotes the onset of endoreduplication under salinity stress in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41598-022-12836-8openalex-snapshot
Ploidy dynamics in aphid host cells harboring bacterial symbionts
inferred← citeshttps://doi.org/10.1038/s41598-022-18137-4openalex-snapshot
A life history model of the ecological and evolutionary dynamics of polyaneuploid cancer cells
inferred← citeshttps://doi.org/10.1038/s41598-023-39880-2openalex-snapshot
IL-1β is involved in docetaxel chemoresistance by regulating the formation of polyploid giant cancer cells in non-small cell lung cancer
inferred← citeshttps://doi.org/10.1038/s41598-024-78278-6openalex-snapshot
Gradual chromosomal lagging drive programmed genome elimination in hemiclonal fishes from the genus Hypseleotris
inferred← citeshttps://doi.org/10.1038/s41598-025-02640-5openalex-snapshot
Dengue virus modulates critical cell cycle regulatory proteins in human megakaryocyte cells
inferred← citeshttps://doi.org/10.1038/s41598-025-24871-2openalex-snapshot
Hybridization and embryological patterns underpinning reproductive barriers in Dactylorhiza (Orchidaceae)
inferred← citeshttps://doi.org/10.1038/s42003-019-0453-zopenalex-snapshot
Cardiac interstitial tetraploid cells can escape replicative senescence in rodents but not large mammals
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