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Piezo1, a mechanically activated ion channel, is required for vascular development in mice

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What this work says

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

inferredcites →https://doi.org/10.1002/gene.10152openalex-snapshot

What cardiovascular defect does my prenatal mouse mutant have, and why?

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Digital particle image velocimetry

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The mechano-gated K2P channel TREK-1

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The mechanosensitive nature of TRPV channels

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Fluid Dynamics of Heart Development

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Mechanotransduction by Hair Cells: Models, Molecules, and Mechanisms

inferredcites →https://doi.org/10.1016/j.cell.2014.02.026openalex-snapshot

Merkel Cells Transduce and Encode Tactile Stimuli to Drive Aβ-Afferent Impulses

inferredcites →https://doi.org/10.1016/j.conb.2009.07.008openalex-snapshot

Mammalian somatosensory mechanotransduction

inferredcites →https://doi.org/10.1016/j.devcel.2005.12.006openalex-snapshot

Mechanisms of Mechanotransduction

inferredcites →https://doi.org/10.1016/j.neuron.2012.04.023openalex-snapshot

How We Feel: Ion Channel Partnerships that Detect Mechanical Inputs and Give Rise to Touch and Pain Perception

inferredcites →https://doi.org/10.1016/j.tins.2012.04.002openalex-snapshot

Sensing pressure with ion channels

inferredcites →https://doi.org/10.1016/s0006-3495(79)85267-4openalex-snapshot

Response latency of vertebrate hair cells

inferredcites →https://doi.org/10.1038/35065539openalex-snapshot

Defining brain wiring patterns and mechanisms through gene trapping in mice

inferredcites →https://doi.org/10.1038/embor.2013.170openalex-snapshot

Piezo1‐dependent stretch‐activated channels are inhibited by Polycystin‐2 in renal tubular epithelial cells

inferredcites →https://doi.org/10.1038/nature01282openalex-snapshot

Intracardiac fluid forces are an essential epigenetic factor for embryonic cardiogenesis

inferredcites →https://doi.org/10.1038/nature03952openalex-snapshot

A mechanosensory complex that mediates the endothelial cell response to fluid shear stress

inferredcites →https://doi.org/10.1038/nature06254openalex-snapshot

Haemodynamics determined by a genetic programme govern asymmetric development of the aortic arch

inferredcites →https://doi.org/10.1038/nature10316openalex-snapshot

Dynamic molecular processes mediate cellular mechanotransduction

inferredcites →https://doi.org/10.1038/nature10801openalex-snapshot

The role of Drosophila Piezo in mechanical nociception

inferredcites →https://doi.org/10.1038/nature10812openalex-snapshot

Piezo proteins are pore-forming subunits of mechanically activated channels

inferredcites →https://doi.org/10.1038/nature11685openalex-snapshot

Drosophila NOMPC is a mechanotransduction channel subunit for gentle-touch sensation

inferredcites →https://doi.org/10.1038/nature13250openalex-snapshot

Epidermal Merkel cells are mechanosensory cells that tune mammalian touch receptors

inferredcites →https://doi.org/10.1038/nature13251openalex-snapshot

Piezo2 is required for Merkel-cell mechanotransduction

inferredcites →https://doi.org/10.1038/ncomms2899openalex-snapshot

Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels

inferredcites →https://doi.org/10.1038/nm1338openalex-snapshot

Impaired flow-dependent control of vascular tone and remodeling in P2X4-deficient mice

inferredcites →https://doi.org/10.1038/nn1362openalex-snapshot

The MEC-4 DEG/ENaC channel of Caenorhabditis elegans touch receptor neurons transduces mechanical signals

inferredcites →https://doi.org/10.1038/nrm2595openalex-snapshot

Neurosensory mechanotransduction

inferredcites →https://doi.org/10.1038/nrm2596openalex-snapshot

Mechanotransduction in vascular physiology and atherogenesis

inferredcites →https://doi.org/10.1038/nrm2597openalex-snapshot

Mechanotransduction gone awry

inferredcites →https://doi.org/10.1038/nrn2993openalex-snapshot

Molecular mechanisms of mechanotransduction in mammalian sensory neurons

inferredcites →https://doi.org/10.1073/pnas.0407474101openalex-snapshot

The role of the glycocalyx in reorganization of the actin cytoskeleton under fluid shear stress: A “bumper-car” model

inferredcites →https://doi.org/10.1073/pnas.1221400110openalex-snapshot

Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal Arthrogryposis

inferredcites →https://doi.org/10.1093/emboj/17.15.4283openalex-snapshot

A mammalian two pore domain mechano‐gated S‐like K+ channel

inferredcites →https://doi.org/10.1097/moh.0b013e3282fa7445openalex-snapshot

Rho signaling and mechanical control of vascular development

inferredcites →https://doi.org/10.1097/moh.0b013e32835f6870openalex-snapshot

Disorders of red cell volume regulation

inferredcites →https://doi.org/10.1111/j.1549-8719.2010.00025.xopenalex-snapshot

The Effects of Hemodynamic Force on Embryonic Development

inferredcites →https://doi.org/10.1113/jphysiol.1984.sp015317openalex-snapshot

Stretch‐activated single ion channel currents in tissue‐cultured embryonic chick skeletal muscle.

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/10.1126/science.287.5461.2229openalex-snapshot

A Drosophila Mechanosensory Transduction Channel

inferredcites →https://doi.org/10.1146/annurev.biophys.37.032807.125836openalex-snapshot

Eukaryotic Mechanosensitive Channels

inferredcites →https://doi.org/10.1152/ajpheart.01047.2006openalex-snapshot

Mechanotransduction and endothelial cell homeostasis: the wisdom of the cell

inferredcites →https://doi.org/10.1152/physrev.1995.75.3.519openalex-snapshot

Flow-mediated endothelial mechanotransduction

inferredcites →https://doi.org/10.1159/000356667openalex-snapshot

Calcium's Role in Mechanotransduction during Muscle Development

inferredcites →https://doi.org/10.1161/circresaha.108.192765openalex-snapshot

Ciliary Polycystin-2 Is a Mechanosensitive Calcium Channel Involved in Nitric Oxide Signaling Cascades

inferredcites →https://doi.org/10.1182/blood-2002-08-2531openalex-snapshot

Circulation is established in a stepwise pattern in the mammalian embryo

inferredcites →https://doi.org/10.1242/dev.00831openalex-snapshot

Embryonic atrial function is essential for mouse embryogenesis, cardiac morphogenesis and angiogenesis

inferredcites →https://doi.org/10.1242/dev.00929openalex-snapshot

Flow regulates arterial-venous differentiation in the chick embryo yolk sac

inferredcites →https://doi.org/10.1242/dev.02883openalex-snapshot

Vascular remodeling of the mouse yolk sac requires hemodynamic force

inferredcites →https://doi.org/10.1371/journal.pone.0002853openalex-snapshot

Three-Dimensional Analysis of Vascular Development in the Mouse Embryo

inferredcites →https://doi.org/10.1371/journal.pone.0024338openalex-snapshot

JNK2 Promotes Endothelial Cell Alignment under Flow

inferredcites →https://doi.org/10.1523/jneurosci.0522-13.2013openalex-snapshot

piezo2bRegulates Vertebrate Light Touch Response

inferredcites →https://doi.org/10.2144/000112034openalex-snapshot

Clearing and Photography of Whole Mount X-Gal Stained Mouse Embryos

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Force versus Response: Methods for Activating and Characterizing Mechanosensitive Ion Channels and GPCRs

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Mechanically Defined Microenvironment Promotes Stabilization of Microvasculature, Which Correlates with the Enrichment of a Novel Piezo‐1+ Population of Circulating CD11b+/CD115+ Monocytes

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High Shear Stress‐Induced Endothelial Piezo1 Downregulation Promotes Intracranial Aneurysm Formation via the PDGF ‐ BB / PDGFRβ Paracrine Signaling Pathway

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Generation of Piezo1‐CreER transgenic mice for visualization and lineage tracing of mechanical force responsive cells in vivo

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Piezo channels contribute to the regulation of myelination in Schwann cells

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Novel insights for the role of nitric oxide in placental vascular function during and beyond pregnancy

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Biphasic effect of mechanical stress on lymphocyte activation

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Piezo1 controls cell volume and migration by modulating swelling‐activated chloride current through Ca 2+ influx

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Signaling mechanisms in red blood cells: A view through the protein phosphorylation and deformability

inferred← citeshttps://doi.org/10.1002/jcp.31001openalex-snapshot

Regulation of PIEZO1 channels by lipids and the structural components of extracellular matrix/cell cytoskeleton

inferred← citeshttps://doi.org/10.1002/jcp.70036openalex-snapshot

Piezo1 Is Related to the Enamel Matrix Formation in Mouse Tooth Germ Development

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Engineering Piezo1‐Mediated Calcium Signalling for Enhanced Extracellular Vesicle Biogenesis and Cargo Loading

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PIEZO1 is the most common monogenic etiology of non‐immune hydrops fetalis detected by prenatal exome sequencing

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The Physical Factors Involved in Cancer Progression

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TRP Channels and Mechanical Transduction

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Adhesion GPCRs as a Putative Class of Metabotropic Mechanosensors

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Genetic Association in Lower Limb Swelling

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Piezo Channels: Roles in Craniofacial Development and Dentistry

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The Role of Stem Cells in Exercise-Enhanced Organogenesis and Regeneration

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The Role of Stem Cells in Exercise-Enhanced Organogenesis and Regeneration

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Blood flow mechanics in cardiovascular development

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Shear stress mediates exocytosis of functional TRPV4 channels in endothelial cells

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High-content method for mechanosignaling studies using IsoStretcher technology and quantitative Ca2+ imaging applied to Piezo1 in cardiac HL-1 cells

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PIEZO1 targeting in macrophages boosts phagocytic activity and foam cell apoptosis in atherosclerosis

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Piezo1 disrupts blood–brain barrier via CaMKII/Nrf2 in ischemic stroke

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Talin1 modulates the Piezo1–YAP axis to regulate endothelial cell inflammation and atherosclerosis

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Fontan Hepatic Fibrosis and Pulmonary Vascular Development

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Developmental function of Piezo1 in mouse submandibular gland morphogenesis

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Piezo1-dependent regulation of urinary osmolarity

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It takes more than two to tango: mechanosignaling of the endothelial surface

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Nobel somatosensations and pain

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Piezo1, the new actor in cell volume regulation

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Expression patterns of Piezo1 in the developing mouse forebrain

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The function of Piezo1 in colon cancer metastasis and its potential regulatory mechanism

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Mechanobiological response of osteocyte PIEZO1 to induced piezoelectricity of bone matrix

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Different transcriptional profiling between senescent and non-senescent human coronary artery endothelial cells (HCAECs) by Omeprazole and Lansoprazole treatment

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Piezo1-Induced Nasal Epithelial Barrier Dysfunction in Allergic Rhinitis

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PIEZO1: a mechanosensitive ion channel in the pathogenesis and pharmacotherapy of diabetic neuropathy

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The extracellular matrix Piezo1 feedback loop drives renal fibrosis through compartment-specific mechanotransduction

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Alteration of Essential Cell Function by Ultrasound-Targeted Microbubble Cavitation

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Biomechanical signal communication in vascular smooth muscle cells

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Computational studies of Piezo1 yield insights into key lipid–protein interactions, channel activation, and agonist binding

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Biological sensing of fluid flow—lessons from PIEZO1

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Piezo protein determines stem cell fate by transmitting mechanical signals

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Role of mechanically-sensitive cation channels Piezo1 and TRPV4 in trabecular meshwork cell mechanotransduction

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PIEZO Channels in Metabolism and Metabolic Diseases: Research Advances and Therapeutic Strategies

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Fluid Mechanics as a Driver of Tissue-Scale Mechanical Signaling in Organogenesis

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Mechanoregulation in Hematopoiesis and Hematologic Disorders

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Molecular Circuit Discovery for Mechanobiology of Cardiovascular Disease

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Piezo1 mediates oscillatory shear stress-induced endothelial-to-mesenchymal transition through the AP-1 and KLF2 regulatory pathways in mitral regurgitation

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Mechanosensory Transduction: Focus on Ion Channels ☆

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Genetic Disorders of the Lymphatic System

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Biomechanical regulation of endothelial function in atherosclerosis

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Molecular mechanisms of the vascular responses to hemodynamic forces

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Extracellular matrix–dependent mechanosensing and mechanotransduction

inferred← citeshttps://doi.org/10.1016/b978-0-323-95262-0.00014-0openalex-snapshot

Liver fibrosis

inferred← citeshttps://doi.org/10.1016/b978-0-323-99742-3.00016-3openalex-snapshot

Magnetic nanomaterials for minimally invasive neuromodulation

inferred← citeshttps://doi.org/10.1016/bs.acr.2022.01.001openalex-snapshot

Molecular sensors for detection of tumor-stroma crosstalk

inferred← citeshttps://doi.org/10.1016/bs.ctdb.2018.12.009openalex-snapshot

Fluid forces shape the embryonic heart: Insights from zebrafish

inferred← citeshttps://doi.org/10.1016/bs.ctdb.2022.02.013openalex-snapshot

Plumbing our organs: Lessons from vascular development to instruct lab generated tissues

inferred← citeshttps://doi.org/10.1016/bs.ctdb.2024.02.001openalex-snapshot

Vascular development, remodeling and maturation

inferred← citeshttps://doi.org/10.1016/bs.ctm.2016.10.001openalex-snapshot

The Structural Basis for Sensing by the Piezo1 Protein

inferred← citeshttps://doi.org/10.1016/bs.ctm.2016.10.002openalex-snapshot

Regulation of Piezo Channels by Cellular Signaling Pathways

inferred← citeshttps://doi.org/10.1016/bs.ctm.2016.11.001openalex-snapshot

Piezo1 Channels in Vascular Development and the Sensing of Shear Stress

inferred← citeshttps://doi.org/10.1016/bs.ctm.2016.11.003openalex-snapshot

Mechanosensitive Piezo Channels in the Gastrointestinal Tract

inferred← citeshttps://doi.org/10.1016/bs.ctm.2016.11.004openalex-snapshot

The Kinetics and the Permeation Properties of Piezo Channels

inferred← citeshttps://doi.org/10.1016/bs.ctm.2016.11.005openalex-snapshot

A Microfluidic Approach for Studying Piezo Channels

inferred← citeshttps://doi.org/10.1016/bs.ctm.2016.11.006openalex-snapshot

In Touch With the Mechanosensitive Piezo Channels

inferred← citeshttps://doi.org/10.1016/bs.ctm.2016.11.007openalex-snapshot

A Tour de Force

inferred← citeshttps://doi.org/10.1016/bs.ctm.2017.01.001openalex-snapshot

Genetic Diseases of PIEZO1 and PIEZO2 Dysfunction

inferred← citeshttps://doi.org/10.1016/bs.ctm.2020.01.005openalex-snapshot

Ion channels in capillary endothelium

inferred← citeshttps://doi.org/10.1016/bs.ctm.2020.02.002openalex-snapshot

Endothelial inwardly-rectifying K+ channels as a key component of shear stress-induced mechanotransduction

inferred← citeshttps://doi.org/10.1016/bs.ctm.2021.07.001openalex-snapshot

Cardiovascular mechanosensitive ion channels—Translating physical forces into physiological responses

inferred← citeshttps://doi.org/10.1016/bs.mie.2020.12.024openalex-snapshot

Stretch and poke stimulation for characterizing mechanically activated ion channels

inferred← citeshttps://doi.org/10.1016/j.actbio.2024.12.034openalex-snapshot

PIEZO1-mediated mechanotransduction regulates collagen synthesis on nanostructured 2D and 3D models of fibrosis

inferred← citeshttps://doi.org/10.1016/j.ajpath.2024.10.007openalex-snapshot

The mRNA Stability of PIEZO1, Regulated by Methyltransferase-Like 3 via N6-Methylation of Adenosine Modification in a YT521-B Homology Domain Family 2–Dependent Manner, Facilitates the Progression of Diabetic Retinopathy

inferred← citeshttps://doi.org/10.1016/j.archoralbio.2024.105963openalex-snapshot

The role of the Piezo1 channel in osteoblasts under cyclic stretching: A study on osteogenic and osteoclast factors

inferred← citeshttps://doi.org/10.1016/j.atherosclerosis.2016.03.007openalex-snapshot

Vascular endothelium – Gatekeeper of vessel health

inferred← citeshttps://doi.org/10.1016/j.atherosclerosis.2025.120553openalex-snapshot

Mechanisms of matrix stiffness affecting calcific aortic valve disease by regulating Piezo1

inferred← citeshttps://doi.org/10.1016/j.avsg.2018.04.030openalex-snapshot

Mechanisms Underlying Atheroma Induction: The Roles of Mechanotransduction, Vascular Wall Cells, and Blood Cells

inferred← citeshttps://doi.org/10.1016/j.bbamcr.2015.11.014openalex-snapshot

Hemodynamics driven cardiac valve morphogenesis

inferred← citeshttps://doi.org/10.1016/j.bbamcr.2016.03.004openalex-snapshot

Interplay between cardiac function and heart development

inferred← citeshttps://doi.org/10.1016/j.bbamcr.2019.02.016openalex-snapshot

An element for development: Calcium signaling in mammalian reproduction and development

inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.02.058openalex-snapshot

Yoda1-induced phosphorylation of Akt and ERK1/2 does not require Piezo1 activation

inferred← citeshttps://doi.org/10.1016/j.bbrc.2019.08.078openalex-snapshot

Activation of Piezo1 mechanosensitive ion channel in HEK293T cells by 30 MHz vertically deployed surface acoustic waves

inferred← citeshttps://doi.org/10.1016/j.bbrc.2022.11.060openalex-snapshot

Piezo1 in endothelial cells is involved in vitamin D-induced vascular calcification

inferred← citeshttps://doi.org/10.1016/j.bbrc.2024.151135openalex-snapshot

PIEZO1-mediated calcium influx transiently alters nuclear mechanical properties via actin remodeling in chondrocytes

inferred← citeshttps://doi.org/10.1016/j.bcmd.2020.102413openalex-snapshot

Heterogeneous phenotype of Hereditary Xerocytosis in association with PIEZO1 variants

inferred← citeshttps://doi.org/10.1016/j.bcmd.2021.102619openalex-snapshot

Trpv1 and Trpa1 are not essential for Psickle-like activity in red cells of the SAD mouse model of sickle cell disease

inferred← citeshttps://doi.org/10.1016/j.bcp.2018.10.023openalex-snapshot

Fluid shear stress sensing in vascular homeostasis and remodeling: Towards the development of innovative pharmacological approaches to treat vascular dysfunction

inferred← citeshttps://doi.org/10.1016/j.bcp.2019.08.013openalex-snapshot

Using Yoda-1 to mimic laminar flow in vitro: A tool to simplify drug testing

inferred← citeshttps://doi.org/10.1016/j.bcp.2022.115290openalex-snapshot

Endothelial mechanosensing: A forgotten target to treat vascular remodeling in hypertension?

inferred← citeshttps://doi.org/10.1016/j.bioadv.2023.213516openalex-snapshot

Mechanical activation of lung epithelial cells through the ion channel Piezo1 activates the metalloproteinases ADAM10 and ADAM17 and promotes growth factor and adhesion molecule release

inferred← citeshttps://doi.org/10.1016/j.biomaterials.2018.05.058openalex-snapshot

Extracellular fluid viscosity enhances liver cancer cell mechanosensing and migration

inferred← citeshttps://doi.org/10.1016/j.biomaterials.2019.01.010openalex-snapshot

Role of nuclear mechanosensitivity in determining cellular responses to forces and biomaterials

inferred← citeshttps://doi.org/10.1016/j.biomaterials.2020.120283openalex-snapshot

Bile canaliculi contract autonomously by releasing calcium into hepatocytes via mechanosensitive calcium channel

inferred← citeshttps://doi.org/10.1016/j.biopha.2021.111692openalex-snapshot

Piezo-type mechanosensitive ion channel component 1 (Piezo1) in human cancer

inferred← citeshttps://doi.org/10.1016/j.biopha.2022.114151openalex-snapshot

Endothelial GLUTs and vascular biology

inferred← citeshttps://doi.org/10.1016/j.biopha.2022.114198openalex-snapshot

Effects of shear stress on vascular endothelial functions in atherosclerosis and potential therapeutic approaches

inferred← citeshttps://doi.org/10.1016/j.biopha.2023.115343openalex-snapshot

Barasertib impedes chondrocyte senescence and alleviates osteoarthritis by mitigating the destabilization of heterochromatin induced by AURKB

inferred← citeshttps://doi.org/10.1016/j.biopha.2024.116545openalex-snapshot

Mechanical stress induced mitochondrial dysfunction in cardiovascular diseases: Novel mechanisms and therapeutic targets

inferred← citeshttps://doi.org/10.1016/j.bone.2020.115247openalex-snapshot

Identification of PIEZO1 polymorphisms for human bone mineral density

inferred← citeshttps://doi.org/10.1016/j.bpj.2016.12.009openalex-snapshot

Signatures of Mechanosensitive Gating

inferred← citeshttps://doi.org/10.1016/j.bpj.2017.10.035openalex-snapshot

Mechanical Transduction and the Dark Energy of Biology

inferred← citeshttps://doi.org/10.1016/j.bpj.2018.11.2049openalex-snapshot

Myosin-II Mediated Traction Forces Evoke Localized Piezo1 Ca2+ Flickers

inferred← citeshttps://doi.org/10.1016/j.bpj.2020.07.043openalex-snapshot

Piezo1 Forms Specific, Functionally Important Interactions with Phosphoinositides and Cholesterol

inferred← citeshttps://doi.org/10.1016/j.bpj.2020.11.2274openalex-snapshot

Mechanical Activation of MscL Revealed by a Locally Distributed Tension Molecular Dynamics Approach

inferred← citeshttps://doi.org/10.1016/j.bpj.2021.02.003openalex-snapshot

Modeling of full-length Piezo1 suggests importance of the proximal N-terminus for dome structure

inferred← citeshttps://doi.org/10.1016/j.bpj.2021.02.006openalex-snapshot

Molecular dynamics simulations of Piezo1 channel opening by increases in membrane tension

inferred← citeshttps://doi.org/10.1016/j.bpj.2024.12.025openalex-snapshot

Amyloid beta Aβ1-40 activates Piezo1 channels in brain capillary endothelial cells

inferred← citeshttps://doi.org/10.1016/j.bpj.2025.01.010openalex-snapshot

Single-particle tracking reveals heterogeneous PIEZO1 diffusion

inferred← citeshttps://doi.org/10.1016/j.bpj.2025.03.021openalex-snapshot

Flow-sensitive ion channels in vascular endothelial cells: Mechanisms of activation and roles in mechanotransduction

inferred← citeshttps://doi.org/10.1016/j.burns.2026.108078openalex-snapshot

Piezo1/2 in fibrosis: Cell-type-specific roles, organ-specific pathogenesis, and therapeutic implications

inferred← citeshttps://doi.org/10.1016/j.cdev.2021.203683openalex-snapshot

Mechanosensitive ion channels in cell migration

inferred← citeshttps://doi.org/10.1016/j.cdev.2021.203730openalex-snapshot

Reprint of: Mechanosensitive ion channels in cell migration

inferred← citeshttps://doi.org/10.1016/j.cdev.2021.203735openalex-snapshot

From remodeling to quiescence: The transformation of the vascular network

inferred← citeshttps://doi.org/10.1016/j.ceb.2017.10.003openalex-snapshot

Mechanical cell competition

inferred← citeshttps://doi.org/10.1016/j.ceb.2018.05.007openalex-snapshot

The mechanobiology of zebrafish cardiac valve leaflet formation

inferred← citeshttps://doi.org/10.1016/j.ceb.2023.102216openalex-snapshot

Mechanosensitive GPCRs and ion channels in shear stress sensing

inferred← citeshttps://doi.org/10.1016/j.ceca.2019.03.007openalex-snapshot

Mechanosensitive ion channels push cancer progression

inferred← citeshttps://doi.org/10.1016/j.ceca.2021.102367openalex-snapshot

Piezo1 impairs hepatocellular tumor growth via deregulation of the MAPK-mediated YAP signaling pathway

inferred← citeshttps://doi.org/10.1016/j.ceca.2021.102431openalex-snapshot

Mechanosensitive Piezo1 in endothelial cells promotes angiogenesis to support bone fracture repair

inferred← citeshttps://doi.org/10.1016/j.ceca.2022.102571openalex-snapshot

Mechanosensitive Piezo1 channel in rat epididymal epithelial cells promotes transepithelial K+ secretion

inferred← citeshttps://doi.org/10.1016/j.cej.2023.142521openalex-snapshot

Viscosity-triggered near-infrared fluorescence nanoprobe for in vivo non-invasive diagnosis of cancer

inferred← citeshttps://doi.org/10.1016/j.cej.2025.163315openalex-snapshot

Mechanotransduction-driven immunointegration at soft-hard tissue interfaces facilitates aged bone regeneration

inferred← citeshttps://doi.org/10.1016/j.cell.2018.02.047openalex-snapshot

Common PIEZO1 Allele in African Populations Causes RBC Dehydration and Attenuates Plasmodium Infection

inferred← citeshttps://doi.org/10.1016/j.cell.2018.03.076openalex-snapshot

GPR68 Senses Flow and Is Essential for Vascular Physiology

inferred← citeshttps://doi.org/10.1016/j.cell.2019.08.049openalex-snapshot

Mammalian Mechanoelectrical Transduction: Structure and Function of Force-Gated Ion Channels

inferred← citeshttps://doi.org/10.1016/j.cell.2020.01.033openalex-snapshot

TACAN Is an Ion Channel Involved in Sensing Mechanical Pain

inferred← citeshttps://doi.org/10.1016/j.cell.2020.06.022openalex-snapshot

RNA Sensing by Gut Piezo1 Is Essential for Systemic Serotonin Synthesis

inferred← citeshttps://doi.org/10.1016/j.cell.2021.01.024openalex-snapshot

A role of PIEZO1 in iron metabolism in mice and humans

inferred← citeshttps://doi.org/10.1016/j.cell.2024.04.010openalex-snapshot

Perivascular neurons instruct 3D vascular lattice formation via neurovascular contact

inferred← citeshttps://doi.org/10.1016/j.cell.2025.02.031openalex-snapshot

Enteric neuronal Piezo1 maintains mechanical and immunological homeostasis by sensing force

inferred← citeshttps://doi.org/10.1016/j.celrep.2015.09.072openalex-snapshot

Piezo1 in Smooth Muscle Cells Is Involved in Hypertension-Dependent Arterial Remodeling

inferred← citeshttps://doi.org/10.1016/j.celrep.2017.05.079openalex-snapshot

Transduction of Repetitive Mechanical Stimuli by Piezo1 and Piezo2 Ion Channels

inferred← citeshttps://doi.org/10.1016/j.celrep.2017.10.120openalex-snapshot

Inactivation of Mechanically Activated Piezo1 Ion Channels Is Determined by the C-Terminal Extracellular Domain and the Inner Pore Helix

inferred← citeshttps://doi.org/10.1016/j.celrep.2020.108225openalex-snapshot

Sphingomyelinase Disables Inactivation in Endogenous PIEZO1 Channels

inferred← citeshttps://doi.org/10.1016/j.celrep.2021.109914openalex-snapshot

Patch-seq of mouse DRG neurons reveals candidate genes for specific mechanosensory functions

inferred← citeshttps://doi.org/10.1016/j.celrep.2022.110342openalex-snapshot

Tethering Piezo channels to the actin cytoskeleton for mechanogating via the cadherin-β-catenin mechanotransduction complex

inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112837openalex-snapshot

Force-induced motions of the PIEZO1 blade probed with fluorimetry

inferred← citeshttps://doi.org/10.1016/j.celrep.2023.113128openalex-snapshot

Pannexin-1 opening in neuronal edema causes cell death but also leads to protection via increased microglia contacts

inferred← citeshttps://doi.org/10.1016/j.celrep.2023.113652openalex-snapshot

Piezo1-dependent regulation of pericyte proliferation by blood flow during brain vascular development

inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114014openalex-snapshot

TMC7 functions as a suppressor of Piezo2 in primary sensory neurons blunting peripheral mechanotransduction

inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114334openalex-snapshot

Tentonin 3 is a pore-forming subunit of a slow inactivation mechanosensitive channel

inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114398openalex-snapshot

Piezo regulates epithelial topology and promotes precision in organ size control

inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115405openalex-snapshot

PIEZO1-dependent mode switch of neuronal migration in heterogeneous microenvironments in the developing brain

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