Heterochromatin-Driven Nuclear Softening Protects the Genome against Mechanical Stress-Induced Damage is a research paper published in Cell (2020). On theSindex it has a DataRank of 0.966. It has been cited 626 times.
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Base Score Contribution
0.966
From this paper's citation signal
Citation Network Contribution
0
Citation network not refreshed for this result
This paper's DataRank is currently driven only by its base citation score. Citation network data was not refreshed for this result.
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Grant: T32 EB003392
Deutsche Forschungsgemeinschaft
Grant: unidentified
unidentified
National Science Foundation
Grant: 1300476
Alpha II-Spectrin: Mechanical Spring and Structural Scaffold for the Nucleoskeleton
Deutsche Forschungsgemeinschaft
Grant: 73111208/SFB 829
Molecular Mechanisms regulating Skin Homeostasis
European Commission
Grant: 748004
Molecular mechanisms of the mechanical interaction between the cell nucleus and the actin cytoskeleton
European Commission
Grant: 770877
Mechanisms of stem cell population dynamics and reprogramming
Deutsche Forschungsgemeinschaft
Grant: 255103767/SPP 1782
Epithelial intercellular junctions as dynamic hubs to integrate forces, signals and cell behaviour
European Research Council
Human Frontier Science Program
Academy of Finland
Helsinki Institute of Life Science, Helsingin Yliopisto
National Institutes of Health
National Science Foundation
Jenny ja Antti Wihurin Rahasto
European Molecular Biology Organization
Deutsche Forschungsgemeinschaft
Max-Planck-Gesellschaft
FWCI
33.14
Citation Percentile
1.0%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Additional file 1 of Deformation of the nucleus by TGFβ1 via the remodeling of nuclear envelope and histone isoforms
Additional file 1 of Deformation of the nucleus by TGFβ1 via the remodeling of nuclear envelope and histone isoforms
Additional file 1 of Activation of goblet cell Piezo1 alleviates mucus barrier damage in mice exposed to WAS by inhibiting H3K9me3 modification
Additional file 1 of Activation of goblet cell Piezo1 alleviates mucus barrier damage in mice exposed to WAS by inhibiting H3K9me3 modification