On the public citation graph

ESCRT-III accumulates in micronuclei with ruptured nuclear envelopes

https://doi.org/10.1101/476630
0 signed · 58 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.
Claim with ORCID
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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/(sici)1098-2264(199607)16:3<189::aid-gcc6>3.0.co;2-vopenalex-snapshot
Loss of heterozygosity from the short arm of chromosome 8 is associated with invasive behavior in breast cancer
inferredcites →https://doi.org/10.1007/s00204-016-1818-4openalex-snapshot
Impaired nuclear functions in micronuclei results in genome instability and chromothripsis
inferredcites →https://doi.org/10.1016/j.ccell.2016.04.003openalex-snapshot
Loss of Chromosome 8p Governs Tumor Progression and Drug Response by Altering Lipid Metabolism
inferredcites →https://doi.org/10.1016/j.ceb.2016.03.001openalex-snapshot
Closing a gap in the nuclear envelope
inferredcites →https://doi.org/10.1016/j.cell.2013.06.007openalex-snapshot
Catastrophic Nuclear Envelope Collapse in Cancer Cell Micronuclei
inferredcites →https://doi.org/10.1016/j.cell.2018.08.027openalex-snapshot
The Multifaceted Role of Chromosomal Instability in Cancer and Its Microenvironment
inferredcites →https://doi.org/10.1016/j.cub.2011.06.028openalex-snapshot
UBAP1 Is a Component of an Endosome-Specific ESCRT-I Complex that Is Essential for MVB Sorting
inferredcites →https://doi.org/10.1016/j.cub.2014.01.019openalex-snapshot
The mitotic origin of chromosomal instability
inferredcites →https://doi.org/10.1016/j.cub.2016.07.039openalex-snapshot
Membrane Binding by CHMP7 Coordinates ESCRT-III-Dependent Nuclear Envelope Reformation
inferredcites →https://doi.org/10.1016/j.mrfmmm.2011.09.003openalex-snapshot
Nuclear envelope defects impede a proper response to micronuclear DNA lesions
inferredcites →https://doi.org/10.1016/j.tcb.2013.04.006openalex-snapshot
Knowing when to cut and run: mechanisms that control cytokinetic abscission
inferredcites →https://doi.org/10.1016/j.tcb.2017.02.008openalex-snapshot
Bursting the Bubble – Nuclear Envelope Rupture as a Path to Genomic Instability?
inferredcites →https://doi.org/10.1038/nature10802openalex-snapshot
DNA breaks and chromosome pulverization from errors in mitosis
inferredcites →https://doi.org/10.1038/nature12305openalex-snapshot
Structural mechanism of cytosolic DNA sensing by cGAS
inferredcites →https://doi.org/10.1038/nature14408openalex-snapshot
Spastin and ESCRT-III coordinate mitotic spindle disassembly and nuclear envelope sealing
inferredcites →https://doi.org/10.1038/nature14493openalex-snapshot
Chromothripsis from DNA damage in micronuclei
inferredcites →https://doi.org/10.1038/nature14503openalex-snapshot
ESCRT-III controls nuclear envelope reformation
inferredcites →https://doi.org/10.1038/nature23449openalex-snapshot
cGAS surveillance of micronuclei links genome instability to innate immunity
inferredcites →https://doi.org/10.1038/nature23470openalex-snapshot
Mitotic progression following DNA damage enables pattern recognition within micronuclei
inferredcites →https://doi.org/10.1038/nature25432openalex-snapshot
Chromosomal instability drives metastasis through a cytosolic DNA response
inferredcites →https://doi.org/10.1038/ncb2959openalex-snapshot
ANCHR mediates Aurora-B-dependent abscission checkpoint control through retention of VPS4
inferredcites →https://doi.org/10.1038/ncb3450openalex-snapshot
Selective Y centromere inactivation triggers chromosome shattering in micronuclei and repair by non-homologous end joining
inferredcites →https://doi.org/10.1038/ncb3586openalex-snapshot
Innate immune sensing of cytosolic chromatin fragments through cGAS promotes senescence
inferredcites →https://doi.org/10.1038/ncomms11752openalex-snapshot
RPA and Rad51 constitute a cell intrinsic mechanism to protect the cytosol from self DNA
inferredcites →https://doi.org/10.1038/ni.3558openalex-snapshot
Regulation and function of the cGAS–STING pathway of cytosolic DNA sensing
inferredcites →https://doi.org/10.1038/nmeth.2019openalex-snapshot
Fiji: an open-source platform for biological-image analysis
inferredcites →https://doi.org/10.1038/nprot.2007.77openalex-snapshot
Cytokinesis-block micronucleus cytome assay
inferredcites →https://doi.org/10.1038/s41586-018-0534-zopenalex-snapshot
Nuclear envelope assembly defects link mitotic errors to chromothripsis
inferredcites →https://doi.org/10.1038/s41598-017-05875-zopenalex-snapshot
CDKL5 localizes at the centrosome and midbody and is required for faithful cell division
inferredcites →https://doi.org/10.1038/sj.onc.1201254openalex-snapshot
Ultraviolet light-induced G2 phase cell cycle checkpoint blocks cdc25-dependent progression into mitosis
inferredcites →https://doi.org/10.1038/sj.onc.1202648openalex-snapshot
Identification of three distinct regions of allelic deletions on the short arm of chromosome 8 in hepatocellular carcinoma
inferredcites →https://doi.org/10.1038/srep30325openalex-snapshot
In silico synchronization reveals regulators of nuclear ruptures in lamin A/C deficient model cells
inferredcites →https://doi.org/10.1073/pnas.0603779103openalex-snapshot
H2AX phosphorylation within the G 1 phase after UV irradiation depends on nucleotide excision repair and not DNA double-strand breaks
inferredcites →https://doi.org/10.1073/pnas.1005938107openalex-snapshot
Human ESCRT-III and VPS4 proteins are required for centrosome and spindle maintenance
inferredcites →https://doi.org/10.1073/pnas.1613916114openalex-snapshot
LEM2 recruits CHMP7 for ESCRT-mediated nuclear envelope closure in fission yeast and human cells
inferredcites →https://doi.org/10.1073/pnas.1705499114openalex-snapshot
cGAS is essential for cellular senescence
inferredcites →https://doi.org/10.1074/jbc.c100569200openalex-snapshot
Histone H2AX Is Phosphorylated in an ATR-dependent Manner in Response to Replicational Stress
inferredcites →https://doi.org/10.1083/jcb.144.1.11openalex-snapshot
Sequestration of Mammalian Rad51-Recombination Protein into Micronuclei
inferredcites →https://doi.org/10.1083/jcb.201708069openalex-snapshot
DNA damage-induced immune response: Micronuclei provide key platform
inferredcites →https://doi.org/10.1083/jcb.201711161openalex-snapshot
Nuclear rupture at sites of high curvature compromises retention of DNA repair factors
inferredcites →https://doi.org/10.1091/mbc.e15-05-0318openalex-snapshot
Replication stress in early S phase generates apparent micronuclei and chromosome rearrangement in fission yeast
inferredcites →https://doi.org/10.1093/hmg/ddr344openalex-snapshot
Repetitive disruptions of the nuclear envelope invoke temporary loss of cellular compartmentalization in laminopathies
inferredcites →https://doi.org/10.1093/hmg/ddx283openalex-snapshot
Absence of RNase H2 triggers generation of immunogenic micronuclei removed by autophagy
inferredcites →https://doi.org/10.1093/mutage/18.3.221openalex-snapshot
What do human micronuclei contain?
inferredcites →https://doi.org/10.1093/mutage/geq052openalex-snapshot
Molecular mechanisms of micronucleus, nucleoplasmic bridge and nuclear bud formation in mammalian and human cells
inferredcites →https://doi.org/10.1093/mutage/geq053openalex-snapshot
Molecular mechanisms of the origin of micronuclei from extrachromosomal elements
inferredcites →https://doi.org/10.1101/049312openalex-snapshot
LEM2 recruits CHMP7 for ESCRT-mediated nuclear envelope closure in fission yeast and human cells
inferredcites →https://doi.org/10.1101/cshperspect.a016766openalex-snapshot
Molecular Mechanisms of the Membrane Sculpting ESCRT Pathway
inferredcites →https://doi.org/10.1126/science.1217180openalex-snapshot
ESCRT-III Governs the Aurora B–Mediated Abscission Checkpoint Through CHMP4C
inferredcites →https://doi.org/10.1126/science.1219580openalex-snapshot
Recurrent Hemizygous Deletions in Cancers May Optimize Proliferative Potential
inferredcites →https://doi.org/10.1126/science.aad7297openalex-snapshot
Nuclear envelope rupture and repair during cancer cell migration
inferredcites →https://doi.org/10.1126/science.aad7611openalex-snapshot
ESCRT III repairs nuclear envelope ruptures during cell migration to limit DNA damage and cell death
inferredcites →https://doi.org/10.1155/2014/974393openalex-snapshot
Association of CHMP4B and Autophagy with Micronuclei: Implications for Cataract Formation
inferredcites →https://doi.org/10.1371/journal.pone.0018618openalex-snapshot
Replication Stress Induces Micronuclei Comprising of Aggregated DNA Double-Strand Breaks
inferredcites →https://doi.org/10.1371/journal.pone.0027233openalex-snapshot
Generation of Micronuclei during Interphase by Coupling between Cytoplasmic Membrane Blebbing and Nuclear Budding
inferredcites →https://doi.org/10.18632/oncotarget.23666openalex-snapshot
CDK1 and PLK1 coordinate the disassembly and reassembly of the nuclear envelope in vertebrate mitosis
inferredcites →https://doi.org/10.3390/genes6020267openalex-snapshot
Replication Stress in Mammalian Cells and Its Consequences for Mitosis
inferredcites →https://doi.org/10.3892/etm.2014.2123openalex-snapshot
Genomic alterations on 8p21-p23 are the most frequent genetic events in stage I squamous cell carcinoma of the lung
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.