On the public citation graph
Piezo1 channel activates ADAM10 sheddase to regulate Notch1 and gene expression
0 signed · 52 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known work and none has been retracted — and get a dated CiteStamped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/10.1002/hep.28713openalex-snapshot
Endothelial notch signaling is essential to prevent hepatic vascular malformations in mice
inferredcites →https://doi.org/10.1016/j.bbrc.2018.02.058openalex-snapshot
Yoda1-induced phosphorylation of Akt and ERK1/2 does not require Piezo1 activation
inferredcites →https://doi.org/10.1016/j.brainres.2006.06.050openalex-snapshot
A novel membrane protein, encoded by the gene covering KIAA0233, is transcriptionally induced in senile plaque-associated astrocytes
inferredcites →https://doi.org/10.1016/j.celrep.2016.10.033openalex-snapshot
Piezo1 Channels Are Inherently Mechanosensitive
inferredcites →https://doi.org/10.1016/j.devcel.2015.05.004openalex-snapshot
Mechanical Allostery: Evidence for a Force Requirement in the Proteolytic Activation of Notch
inferredcites →https://doi.org/10.1016/j.tibs.2016.09.004openalex-snapshot
Touch, Tension, and Transduction – The Function and Regulation of Piezo Ion Channels
inferredcites →https://doi.org/10.1021/acs.biochem.5b01102openalex-snapshot
A-Disintegrin-And-Metalloproteinase (ADAM) 10 Activity on Resting and Activated Platelets
inferredcites →https://doi.org/10.1038/nature13701openalex-snapshot
Piezo1 integration of vascular architecture with physiological force
inferredcites →https://doi.org/10.1038/nature25744openalex-snapshot
Mechanical regulation of stem-cell differentiation by the stretch-activated Piezo channel
inferredcites →https://doi.org/10.1038/nrm.2017.92openalex-snapshot
Piezos thrive under pressure: mechanically activated ion channels in health and disease
inferredcites →https://doi.org/10.1038/s41467-017-00429-3openalex-snapshot
Piezo1 channels sense whole body physical activity to reset cardiovascular homeostasis and enhance performance
inferredcites →https://doi.org/10.1038/s41467-017-01741-8openalex-snapshot
NOTCH1 is a mechanosensor in adult arteries
inferredcites →https://doi.org/10.1038/s41467-017-01742-7openalex-snapshot
Shear-induced Notch-Cx37-p27 axis arrests endothelial cell cycle to enable arterial specification
inferredcites →https://doi.org/10.1038/s41467-018-03570-9openalex-snapshot
A lever-like transduction pathway for long-distance chemical- and mechano-gating of the mechanosensitive Piezo1 channel
inferredcites →https://doi.org/10.1038/s41467-018-04194-9openalex-snapshot
Piezo1 is a mechanically activated ion channel and mediates pressure induced pancreatitis
inferredcites →https://doi.org/10.1038/s41467-018-04405-3openalex-snapshot
Probing the gating mechanism of the mechanosensitive channel Piezo1 with the small molecule Yoda1
inferredcites →https://doi.org/10.1038/s41467-018-04436-wopenalex-snapshot
Cell surface flip-flop of phosphatidylserine is critical for PIEZO1-mediated myotube formation
inferredcites →https://doi.org/10.1038/s41598-018-32572-2openalex-snapshot
Enantiomeric Aβ peptides inhibit the fluid shear stress response of PIEZO1
inferredcites →https://doi.org/10.1073/pnas.0500918102openalex-snapshot
ADAM10 mediates E-cadherin shedding and regulates epithelial cell-cell adhesion, migration, and β-catenin translocation
inferredcites →https://doi.org/10.1073/pnas.1409233111openalex-snapshot
Piezo1, a mechanically activated ion channel, is required for vascular development in mice
inferredcites →https://doi.org/10.1073/pnas.1414298111openalex-snapshot
Synergy between Piezo1 and Piezo2 channels confers high-strain mechanosensitivity to articular cartilage
inferredcites →https://doi.org/10.1073/pnas.1817070115openalex-snapshot
Mechanically activated ion channel PIEZO1 is required for lymphatic valve formation
inferredcites →https://doi.org/10.1073/pnas.1902165116openalex-snapshot
Endothelial cell Piezo1 mediates pressure-induced lung vascular hyperpermeability via disruption of adherens junctions
inferredcites →https://doi.org/10.1074/jbc.m110.176065openalex-snapshot
Feed-forward Signaling by Membrane-bound Ligand Receptor Circuit
inferredcites →https://doi.org/10.1074/jbc.m114.603753openalex-snapshot
The Cytoplasmic Domain of A Disintegrin and Metalloproteinase 10 (ADAM10) Regulates Its Constitutive Activity but Is Dispensable for Stimulated ADAM10-dependent Shedding
inferredcites →https://doi.org/10.1074/jbc.m116.766196openalex-snapshot
Evidence for shear-mediated Ca2+ entry through mechanosensitive cation channels in human platelets and a megakaryocytic cell line
inferredcites →https://doi.org/10.1074/jbc.ra118.005364openalex-snapshot
Proteolytic shedding of the prion protein via activation of metallopeptidase ADAM10 reduces cellular binding and toxicity of amyloid-β oligomers
inferredcites →https://doi.org/10.1083/jcb.200310024openalex-snapshot
Cell–matrix interaction via CD44 is independently regulated by different metalloproteinases activated in response to extracellular Ca2+ influx and PKC activation
inferredcites →https://doi.org/10.1084/jem.20180483openalex-snapshot
Piezo1 and Gq/G11 promote endothelial inflammation depending on flow pattern and integrin activation
inferredcites →https://doi.org/10.1096/fj.01-0007fjeopenalex-snapshot
Regulation of the α‐secretase ADAM10 by its prodomain and proprotein convertases
inferredcites →https://doi.org/10.1111/bph.14188openalex-snapshot
Yoda1 analogue ( D ooku1) which antagonizes Y oda1‐evoked activation of P iezo1 and aortic relaxation
inferredcites →https://doi.org/10.1126/science.1193270openalex-snapshot
Piezo1 and Piezo2 Are Essential Components of Distinct Mechanically Activated Cation Channels
inferredcites →https://doi.org/10.1152/physrev.00005.2017openalex-snapshot
Notch Signaling in Development, Tissue Homeostasis, and Disease
inferredcites →https://doi.org/10.1152/physrev.00029.2017openalex-snapshot
Intriguing Roles for Endothelial ADAM10/Notch Signaling in the Development of Organ-Specific Vascular Beds
inferredcites →https://doi.org/10.1161/circresaha.107.169805openalex-snapshot
ADAM10 Regulates Endothelial Permeability and T-Cell Transmigration by Proteolysis of Vascular Endothelial Cadherin
inferredcites →https://doi.org/10.1172/jci123825openalex-snapshot
Shear stress–induced endothelial adrenomedullin signaling regulates vascular tone and blood pressure
inferredcites →https://doi.org/10.1172/jci83496openalex-snapshot
4-Dimensional light-sheet microscopy to elucidate shear stress modulation of cardiac trabeculation
inferredcites →https://doi.org/10.1172/jci87343openalex-snapshot
Endothelial cation channel PIEZO1 controls blood pressure by mediating flow-induced ATP release
inferredcites →https://doi.org/10.1172/jci89549openalex-snapshot
4-Dimensional light-sheet microscopy to elucidate shear stress modulation of cardiac trabeculation
inferredcites →https://doi.org/10.1371/journal.pone.0122622openalex-snapshot
Notch1 Is Pan-Endothelial at the Onset of Flow and Regulated by Flow
inferredcites →https://doi.org/10.2174/1386207053258488openalex-snapshot
Metalloproteinase Inhibitors for the Disintegrin-Like Metalloproteinases ADAM10 and ADAM17 that Differentially Block Constitutive and Phorbol Ester-Inducible Shedding of Cell Surface Molecules
inferredcites →https://doi.org/10.2174/156802608783334015openalex-snapshot
Therapeutic Potential of γ -Secretase Inhibitors and Modulators
inferredcites →https://doi.org/10.3389/fnagi.2018.00332openalex-snapshot
Infection Augments Expression of Mechanosensing Piezo1 Channels in Amyloid Plaque-Reactive Astrocytes
inferredcites →https://doi.org/10.4049/jimmunol.1701118openalex-snapshot
Cutting Edge: Piezo1 Mechanosensors Optimize Human T Cell Activation
inferredcites →https://doi.org/10.7554/elife.07369openalex-snapshot
Chemical activation of the mechanotransduction channel Piezo1
inferredcites →https://doi.org/10.7554/elife.07370openalex-snapshot
Piezo1 links mechanical forces to red blood cell volume
inferredcites →https://doi.org/10.7554/elife.12088openalex-snapshot
Mechanical sensitivity of Piezo1 ion channels can be tuned by cellular membrane tension
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/dvdy.401openalex-snapshot
Emerging role of Piezo ion channels in cardiovascular development
inferred← citeshttps://doi.org/10.1007/s00441-020-03191-zopenalex-snapshot
The role of Piezo proteins and cellular mechanosensing in tuning the fate of transplanted stem cells
inferred← citeshttps://doi.org/10.1161/atvbaha.119.313348openalex-snapshot
Force Sensing by Piezo Channels in Cardiovascular Health and Disease
inferred← citeshttps://doi.org/10.3390/ijms26146598openalex-snapshot
Piezo-Type Mechanosensitive Ion Channel Component 1 (PIEZO1) as a Potential Prognostic Marker in Renal Clear Cell Carcinoma
inferred← citeshttps://doi.org/10.70675/14ada4ccz1a5ez4d6ez8aa4z6d2bde3d1f5bopenalex-snapshot
Antioxidant pretreatments of mesenchymal stem cells against oxidative stress and respiration deficiency : The investigation of cellular and molecular mechanisms
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.