Cell Signaling Technology

PathScan® Di-Methyl-Histone H3 (Lys4) Sandwich ELISA Kit

#7124 · elisa · $66,129,740

100
Citing papers
13.4k
Combined citations
Supplier page Find this product

Research areas

Protein Degradation and Inhibitors18Ubiquitin and proteasome pathways17Cell death mechanisms and regulation9Histone Deacetylase Inhibitors Research7Peptidase Inhibition and Analysis7Autophagy in Disease and Therapy6Cancer, Hypoxia, and Metabolism5Cancer, Lipids, and Metabolism5

Papers citing this product

1
PD-L1 regulates the development, maintenance, and function of induced regulatory T cells
The Journal of Experimental Medicine·2009·2k cit.·DOI
2
Differential PROTAC substrate specificity dictated by orientation of recruited E3 ligase
Nature Communications·2019·516 cit.·DOI
3
SARS-CoV-2 infects cells after viral entry via clathrin-mediated endocytosis
Journal of Biological Chemistry·2021·503 cit.·DOI
4
Mapping the Degradable Kinome Provides a Resource for Expedited Degrader Development
Cell·2020·366 cit.·DOI
5
Iterative Design and Optimization of Initially Inactive Proteolysis Targeting Chimeras (PROTACs) Identify VZ185 as a Potent, Fast, and Selective von Hippel–Lindau (VHL) Based Dual Degrader Probe of BRD9 and BRD7
Journal of Medicinal Chemistry·2018·330 cit.·DOI
6
Antihelminth Compound Niclosamide Downregulates Wnt Signaling and Elicits Antitumor Responses in Tumors with Activating APC Mutations
Cancer Research·2011·265 cit.·DOI
7
Discovery of QCA570 as an Exceptionally Potent and Efficacious Proteolysis Targeting Chimera (PROTAC) Degrader of the Bromodomain and Extra-Terminal (BET) Proteins Capable of Inducing Complete and Durable Tumor Regression
Journal of Medicinal Chemistry·2018·261 cit.·DOI
8
Effective delivery of large genes to the retina by dual AAV vectors
EMBO Molecular Medicine·2013·258 cit.·DOI
9
Homo-PROTACs: bivalent small-molecule dimerizers of the VHL E3 ubiquitin ligase to induce self-degradation
Nature Communications·2017·238 cit.·DOI
10
Targeting the CoREST complex with dual histone deacetylase and demethylase inhibitors
Nature Communications·2018·231 cit.·DOI

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