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From stretch to deflection: the importance of context in the activation of mammalian, mechanically activated ion channels
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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/adma.201800927openalex-snapshot
A 3D Magnetic Hyaluronic Acid Hydrogel for Magnetomechanical Neuromodulation of Primary Dorsal Root Ganglion Neurons
inferredcites →https://doi.org/10.1007/8415_2010_20openalex-snapshot
Biomechanical Characterization of Single Chondrocytes
inferredcites →https://doi.org/10.1007/s00359-009-0482-zopenalex-snapshot
Nociceptors: a phylogenetic view
inferredcites →https://doi.org/10.1007/s00424-016-1811-zopenalex-snapshot
Piezo1-dependent regulation of urinary osmolarity
inferredcites →https://doi.org/10.1016/0012-1606(81)90459-0openalex-snapshot
Developmental genetics of the mechanosensory neurons of Caenorhabditis elegans
inferredcites →https://doi.org/10.1016/b978-0-12-812952-4.00004-0openalex-snapshot
Cartilage mechanobiology: How chondrocytes respond to mechanical load
inferredcites →https://doi.org/10.1016/b978-0-12-812952-4.00015-5openalex-snapshot
Mechanobiology of metastatic cancer
inferredcites →https://doi.org/10.1016/bs.ctm.2020.08.002openalex-snapshot
Cell membrane mechanics and mechanosensory transduction
inferredcites →https://doi.org/10.1016/c2016-0-04529-1openalex-snapshot
Mechanobiology in Health and Disease
inferredcites →https://doi.org/10.1016/j.bpj.2009.05.018openalex-snapshot
Biophysics and Structure of the Patch and the Gigaseal
inferredcites →https://doi.org/10.1016/j.bpj.2017.11.641openalex-snapshot
Cytoskeleton-Associated Proteins Modulate the Tension Sensitivity of Piezo1
inferredcites →https://doi.org/10.1016/j.cell.2020.01.033openalex-snapshot
TACAN Is an Ion Channel Involved in Sensing Mechanical Pain
inferredcites →https://doi.org/10.1016/j.cell.2021.01.024openalex-snapshot
A role of PIEZO1 in iron metabolism in mice and humans
inferredcites →https://doi.org/10.1016/j.celrep.2015.09.072openalex-snapshot
Piezo1 in Smooth Muscle Cells Is Involved in Hypertension-Dependent Arterial Remodeling
inferredcites →https://doi.org/10.1016/j.celrep.2016.04.035openalex-snapshot
Confinement Sensing and Signal Optimization via Piezo1/PKA and Myosin II Pathways
inferredcites →https://doi.org/10.1016/j.celrep.2016.10.033openalex-snapshot
Piezo1 Channels Are Inherently Mechanosensitive
inferredcites →https://doi.org/10.1016/j.celrep.2017.09.029openalex-snapshot
Omega-3 Fatty Acids Modulate TRPV4 Function through Plasma Membrane Remodeling
inferredcites →https://doi.org/10.1016/j.celrep.2018.03.094openalex-snapshot
TMEM150C/Tentonin3 Is a Regulator of Mechano-gated Ion Channels
inferredcites →https://doi.org/10.1016/j.celrep.2018.09.075openalex-snapshot
Microtubule Acetylation Is Required for Mechanosensation in Drosophila
inferredcites →https://doi.org/10.1016/j.celrep.2019.12.040openalex-snapshot
Inactivation Kinetics and Mechanical Gating of Piezo1 Ion Channels Depend on Subdomains within the Cap
inferredcites →https://doi.org/10.1016/j.celrep.2020.108225openalex-snapshot
Sphingomyelinase Disables Inactivation in Endogenous PIEZO1 Channels
inferredcites →https://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
inferredcites →https://doi.org/10.1016/j.cub.2013.03.065openalex-snapshot
A NOMPC-Dependent Membrane-Microtubule Connector Is a Candidate for the Gating Spring in Fly Mechanoreceptors
inferredcites →https://doi.org/10.1016/j.cub.2018.02.078openalex-snapshot
Structural Biology: Piezo Senses Tension through Curvature
inferredcites →https://doi.org/10.1016/j.isci.2019.10.037openalex-snapshot
The Mechanosensitive Ion Channel Piezo1 Significantly Mediates In Vitro Ultrasonic Stimulation of Neurons
inferredcites →https://doi.org/10.1016/j.neulet.2014.05.055openalex-snapshot
Piezo2 channel conductance and localization domains in Merkel cells of rat whisker hair follicles
inferredcites →https://doi.org/10.1016/j.neuron.2010.12.028openalex-snapshot
The Molecular and Cellular Identity of Peripheral Osmoreceptors
inferredcites →https://doi.org/10.1016/j.neuron.2016.05.029openalex-snapshot
Tentonin 3/TMEM150c Confers Distinct Mechanosensitive Currents in Dorsal-Root Ganglion Neurons with Proprioceptive Function
inferredcites →https://doi.org/10.1016/j.neuron.2017.03.039openalex-snapshot
Endogenous Piezo1 Can Confound Mechanically Activated Channel Identification and Characterization
inferredcites →https://doi.org/10.1016/j.neuron.2020.02.010openalex-snapshot
A Plug-and-Latch Mechanism for Gating the Mechanosensitive Piezo Channel
inferredcites →https://doi.org/10.1016/j.tibs.2021.01.008openalex-snapshot
Structural Designs and Mechanogating Mechanisms of the Mechanosensitive Piezo Channels
inferredcites →https://doi.org/10.1016/j.yjmcc.2021.05.002openalex-snapshot
Piezo1 and BKCa channels in human atrial fibroblasts: Interplay and remodelling in atrial fibrillation
inferredcites →https://doi.org/10.1016/s0006-3495(02)75169-2openalex-snapshot
Purification of the Small Mechanosensitive Channel of Escherichia coli (MscS): the Subunit Structure, Conduction, and Gating Characteristicsin Liposomes
inferredcites →https://doi.org/10.1016/s0304-3940(99)00665-5openalex-snapshot
Mechanical transduction by rat dorsal root ganglion neurons in vitro
inferredcites →https://doi.org/10.1016/s1063-5823(18)30023-1openalex-snapshot
Current Topics in Membranes
inferredcites →https://doi.org/10.1021/acs.jpclett.6b02027openalex-snapshot
Energy of Liposome Patch Adhesion to the Pipet Glass Determined by Confocal Fluorescence Microscopy
inferredcites →https://doi.org/10.1021/acs.nanolett.7b00177openalex-snapshot
Mechanical Stimulation of Piezo1 Receptors Depends on Extracellular Matrix Proteins and Directionality of Force
inferredcites →https://doi.org/10.1021/acsnano.9b07499openalex-snapshot
PIEZO1-Mediated Currents Are Modulated by Substrate Mechanics
inferredcites →https://doi.org/10.1021/bi0509649openalex-snapshot
Assessment of Potential Stimuli for Mechano-Dependent Gating of MscL: Effects of Pressure, Tension, and Lipid Headgroups
inferredcites →https://doi.org/10.1038/35036318openalex-snapshot
OTRPC4, a nonselective cation channel that confers sensitivity to extracellular osmolarity
inferredcites →https://doi.org/10.1038/368265a0openalex-snapshot
A large-conductance mechanosensitive channel in E. coli encoded by mscL alone
inferredcites →https://doi.org/10.1038/378292a0openalex-snapshot
A stomatin-like protein necessary for mechanosensation in C. elegans
inferredcites →https://doi.org/10.1038/emboj.2009.398openalex-snapshot
Evidence for a protein tether involved in somatic touch
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/nature03896openalex-snapshot
A possible unifying principle for mechanosensation
inferredcites →https://doi.org/10.1038/nature05394openalex-snapshot
A stomatin-domain protein essential for touch sensation in the mouse
inferredcites →https://doi.org/10.1038/nature10812openalex-snapshot
Piezo proteins are pore-forming subunits of mechanically activated channels
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/nature13980openalex-snapshot
Piezo2 is the major transducer of mechanical forces for touch sensation in mice
inferredcites →https://doi.org/10.1038/nature14013openalex-snapshot
Physical mechanism for gating and mechanosensitivity of the human TRAAK K+ channel
inferredcites →https://doi.org/10.1038/nature15247openalex-snapshot
Architecture of the mammalian mechanosensitive Piezo1 channel
inferredcites →https://doi.org/10.1038/nature25453openalex-snapshot
Structure of the mechanically activated ion channel Piezo1
inferredcites →https://doi.org/10.1038/nature25743openalex-snapshot
Structure and mechanogating mechanism of the Piezo1 channel
inferredcites →https://doi.org/10.1038/ncomms10366openalex-snapshot
Removal of the mechanoprotective influence of the cytoskeleton reveals PIEZO1 is gated by bilayer tension
inferredcites →https://doi.org/10.1038/ncomms12939openalex-snapshot
Localized force application reveals mechanically sensitive domains of Piezo1
inferredcites →https://doi.org/10.1038/ncomms4520openalex-snapshot
Tuning Piezo ion channels to detect molecular-scale movements relevant for fine touch
inferredcites →https://doi.org/10.1038/ncomms9512openalex-snapshot
Membrane stiffening by STOML3 facilitates mechanosensation in sensory neurons
inferredcites →https://doi.org/10.1038/nn.2873openalex-snapshot
Laminin-332 coordinates mechanotransduction and growth cone bifurcation in sensory neurons
inferredcites →https://doi.org/10.1038/nn.4162openalex-snapshot
Piezo2 is the principal mechanotransduction channel for proprioception
inferredcites →https://doi.org/10.1038/nn.4454openalex-snapshot
Small-molecule inhibition of STOML3 oligomerization reverses pathological mechanical hypersensitivity
inferredcites →https://doi.org/10.1038/nrm2592openalex-snapshot
Mechanotransduction in development: a growing role for contractility
inferredcites →https://doi.org/10.1038/nrm2596openalex-snapshot
Mechanotransduction in vascular physiology and atherogenesis
inferredcites →https://doi.org/10.1038/nrn2993openalex-snapshot
Molecular mechanisms of mechanotransduction in mammalian sensory neurons
inferredcites →https://doi.org/10.1038/s41467-017-01712-zopenalex-snapshot
A protein interaction mechanism for suppressing the mechanosensitive Piezo channels
inferredcites →https://doi.org/10.1038/s41467-018-03502-7openalex-snapshot
Voltage gating of mechanosensitive PIEZO channels
inferredcites →https://doi.org/10.1038/s41467-019-09055-7openalex-snapshot
Dietary fatty acids fine-tune Piezo1 mechanical response
inferredcites →https://doi.org/10.1038/s41467-020-16026-wopenalex-snapshot
Adipocyte Piezo1 mediates obesogenic adipogenesis through the FGF1/FGFR1 signaling pathway in mice
inferredcites →https://doi.org/10.1038/s41467-020-16816-2openalex-snapshot
A dietary fatty acid counteracts neuronal mechanical sensitization
inferredcites →https://doi.org/10.1038/s41586-019-1505-8openalex-snapshot
Structure and mechanogating of the mammalian tactile channel PIEZO2
inferredcites →https://doi.org/10.1038/s41594-018-0117-6openalex-snapshot
Structure of the mechanosensitive OSCA channels
inferredcites →https://doi.org/10.1038/s42003-019-0514-3openalex-snapshot
Myosin-II mediated traction forces evoke localized Piezo1-dependent Ca2+ flickers
inferredcites →https://doi.org/10.1038/s42003-020-01600-1openalex-snapshot
Crowding-induced opening of the mechanosensitive Piezo1 channel in silico
inferredcites →https://doi.org/10.1038/sj.emboj.7601116openalex-snapshot
TREK‐1, a K+ channel involved in polymodal pain perception
inferredcites →https://doi.org/10.1038/sj.embor.7400449openalex-snapshot
Cross‐talk between the mechano‐gated K2P channel TREK‐1 and the actin cytoskeleton
inferredcites →https://doi.org/10.1038/srep08364openalex-snapshot
Piezo1 forms mechanosensitive ion channels in the human MCF-7 breast cancer cell line
inferredcites →https://doi.org/10.1038/srep29053openalex-snapshot
Cartilage-Specific Knockout of the Mechanosensory Ion Channel TRPV4 Decreases Age-Related Osteoarthritis
inferredcites →https://doi.org/10.1073/pnas.0303329101openalex-snapshot
Cell swelling, heat, and chemical agonists use distinct pathways for the activation of the cation channel TRPV4
inferredcites →https://doi.org/10.1073/pnas.1013728107openalex-snapshot
The major α-tubulin K40 acetyltransferase αTAT1 promotes rapid ciliogenesis and efficient mechanosensation
inferredcites →https://doi.org/10.1073/pnas.1200051109openalex-snapshot
Differential effects of lipids and lyso-lipids on the mechanosensitivity of the mechanosensitive channels MscL and MscS
inferredcites →https://doi.org/10.1073/pnas.1319569111openalex-snapshot
TRPV4-mediated mechanotransduction regulates the metabolic response of chondrocytes to dynamic loading
inferredcites →https://doi.org/10.1073/pnas.1320768111openalex-snapshot
Mechanosensitivity is mediated directly by the lipid membrane in TRAAK and TREK1 K + channels
inferredcites →https://doi.org/10.1073/pnas.1409011111openalex-snapshot
Biophysical implications of lipid bilayer rheometry for mechanosensitive channels
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.1409802111openalex-snapshot
Stretch-activated ion channel Piezo1 directs lineage choice in human neural stem cells
inferredcites →https://doi.org/10.1073/pnas.1412740111openalex-snapshot
Stochastic nanoroughness modulates neuron–astrocyte interactions and function via mechanosensing cation channels
inferredcites →https://doi.org/10.1073/pnas.1708793114openalex-snapshot
Molecular basis of tactile specialization in the duck bill
inferredcites →https://doi.org/10.1073/pnas.2235619100openalex-snapshot
Mammalian TRPV4 (VR-OAC) directs behavioral responses to osmotic and mechanical stimuli in Caenorhabditis elegans
inferredcites →https://doi.org/10.1074/jbc.m113.478321openalex-snapshot
The Purified Mechanosensitive Channel TREK-1 Is Directly Sensitive to Membrane Tension
inferredcites →https://doi.org/10.1074/jbc.m113.528638openalex-snapshot
Functional Role for Piezo1 in Stretch-evoked Ca2+ Influx and ATP Release in Urothelial Cell Cultures
inferredcites →https://doi.org/10.1074/jbc.ra119.009167openalex-snapshot
Mechanically activated Piezo1 channels of cardiac fibroblasts stimulate p38 mitogen-activated protein kinase activity and interleukin-6 secretion
inferredcites →https://doi.org/10.1080/10255842.2012.705081openalex-snapshot
Cellular and biomolecular mechanics and mechanobiology
inferredcites →https://doi.org/10.1085/jgp.201912515openalex-snapshot
Disruption of membrane cholesterol organization impairs the activity of PIEZO1 channel clusters
inferredcites →https://doi.org/10.1093/emboj/20.8.1888openalex-snapshot
Structural and functional differences between two homologous mechanosensitive channels of Methanococcus jannaschii
inferredcites →https://doi.org/10.1101/2021.01.13.426495openalex-snapshot
“An intrinsically disordered intracellular domain of PIEZO2 is required for force-from-filament activation of the channel”
inferredcites →https://doi.org/10.1113/jp272718openalex-snapshot
Mechanosensitive ion channel Piezo2 is important for enterochromaffin cell response to mechanical forces
inferredcites →https://doi.org/10.1113/jp281011openalex-snapshot
Piezo1 channels mediate trabecular meshwork mechanotransduction and promote aqueous fluid outflow
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/10.1113/jphysiol.2006.117648openalex-snapshot
Mechanosensitive currents in the neurites of cultured mouse sensory neurones
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/scisignal.2005667openalex-snapshot
Activation of TRPV1 channels inhibits mechanosensitive Piezo channel activity by depleting membrane phosphoinositides
inferredcites →https://doi.org/10.1126/scitranslmed.aah4066openalex-snapshot
Inflammasome inhibition prevents α-synuclein pathology and dopaminergic neurodegeneration in mice
inferredcites →https://doi.org/10.1126/scitranslmed.aat9892openalex-snapshot
PIEZO2 mediates injury-induced tactile pain in mice and humans
inferredcites →https://doi.org/10.1126/scitranslmed.aat9897openalex-snapshot
The mechanosensitive ion channel Piezo2 mediates sensitivity to mechanical pain in mice
inferredcites →https://doi.org/10.1126/stke.2192004re4openalex-snapshot
Mechanosensitive Channels: Multiplicity of Families and Gating Paradigms
inferredcites →https://doi.org/10.1146/annurev-cellbio-100913-013426openalex-snapshot
Feeling Force: Physical and Physiological Principles Enabling Sensory Mechanotransduction
inferredcites →https://doi.org/10.1152/physrev.00016.2015openalex-snapshot
TRPV4: Molecular Conductor of a Diverse Orchestra
inferredcites →https://doi.org/10.1152/physrev.00041.2019openalex-snapshot
The Urothelium: Life in a Liquid Environment
inferredcites →https://doi.org/10.1172/jci31766openalex-snapshot
Deletion of the transient receptor potential cation channel TRPV4 impairs murine bladder voiding
inferredcites →https://doi.org/10.1182/blood.2019004174openalex-snapshot
RBCs prevent rapid PIEZO1 inactivation and expose slow deactivation as a mechanism of dehydrated hereditary stomatocytosis
inferredcites →https://doi.org/10.1242/jcs.238360openalex-snapshot
Mammalian TRP ion channels are insensitive to membrane stretch
inferredcites →https://doi.org/10.1515/hsz-2018-0328openalex-snapshot
Unforgettable force – crosstalk and memory of mechanosensitive structures
inferredcites →https://doi.org/10.1523/jneurosci.0247-20.2020openalex-snapshot
Piezo2 Mediates Low-Threshold Mechanically Evoked Pain in the Cornea
inferredcites →https://doi.org/10.3389/fbioe.2019.00047openalex-snapshot
Analysis of Mechanically Activated Ion Channels at the Cell-Substrate Interface: Combining Pillar Arrays and Whole-Cell Patch-Clamp
inferredcites →https://doi.org/10.3389/fbioe.2019.00162openalex-snapshot
Innovative Tools for Mechanobiology: Unraveling Outside-In and Inside-Out Mechanotransduction
inferredcites →https://doi.org/10.3389/fbioe.2020.608951openalex-snapshot
Modulating the Mechanical Activation of TRPV4 at the Cell-Substrate Interface
inferredcites →https://doi.org/10.4161/chan.21064openalex-snapshot
Gating the mechanical channel Piezo1
inferredcites →https://doi.org/10.7554/elife.01901openalex-snapshot
The structure and organization of lanceolate mechanosensory complexes at mouse hair follicles
inferredcites →https://doi.org/10.7554/elife.12088openalex-snapshot
Mechanical sensitivity of Piezo1 ion channels can be tuned by cellular membrane tension
inferredcites →https://doi.org/10.7554/elife.20813openalex-snapshot
Acetylated tubulin is essential for touch sensation in mice
inferredcites →https://doi.org/10.7554/elife.21074openalex-snapshot
Direct measurement of TRPV4 and PIEZO1 activity reveals multiple mechanotransduction pathways in chondrocytes
inferredcites →https://doi.org/10.7554/elife.33149openalex-snapshot
Piezo1 forms a slowly-inactivating mechanosensory channel in mouse embryonic stem cells
inferredcites →https://doi.org/10.7554/elife.33660openalex-snapshot
Structure-based membrane dome mechanism for Piezo mechanosensitivity
inferredcites →https://doi.org/10.7554/elife.41844openalex-snapshot
OSCA/TMEM63 are an evolutionarily conserved family of mechanically activated ion channels
inferredcites →https://doi.org/10.7554/elife.47454openalex-snapshot
The mechanosensitive Piezo1 channel is required for bone formation
inferredcites →https://doi.org/10.7554/elife.53308openalex-snapshot
TMEM87a/Elkin1, a component of a novel mechanoelectrical transduction pathway, modulates melanoma adhesion and migration
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4776522openalex-extracted
Morphomechanics: An Updated View
inferred← citeshttps://doi.org/10.1002/adbi.202400018openalex-snapshot
Generation of Anterior Segment of the Eye Cells from hiPSCs in Microfluidic Platforms
inferred← citeshttps://doi.org/10.1002/adhm.202402167openalex-snapshot
Force versus Response: Methods for Activating and Characterizing Mechanosensitive Ion Channels and GPCRs
inferred← citeshttps://doi.org/10.1002/advs.202413680openalex-snapshot
4D Biofabrication of Magnetically Augmented Callus Assembloid Implants Enables Rapid Endochondral Ossification via Activation of Mechanosensitive Pathways
inferred← citeshttps://doi.org/10.1002/advs.202416992openalex-snapshot
Mechanobiological Dynamics‐Inspired Mechanomodulatory Biomaterials
inferred← citeshttps://doi.org/10.1007/978-1-0716-2851-5_10openalex-snapshot
Analysing Mechanically Evoked Currents at Cell-Substrate Junctions
inferred← citeshttps://doi.org/10.1007/s40279-024-02043-yopenalex-snapshot
Discussing Conflicting Explanatory Approaches in Flexibility Training Under Consideration of Physiology: A Narrative Review
inferred← citeshttps://doi.org/10.1016/j.bioactmat.2024.11.035openalex-snapshot
In situ magnetic-field-assisted bioprinting process using magnetorheological bioink to obtain engineered muscle constructs
inferred← citeshttps://doi.org/10.1016/j.devcel.2022.08.012openalex-snapshot
T cell cytoskeletal forces shape synapse topography for targeted lysis via membrane curvature bias of perforin
inferred← citeshttps://doi.org/10.1016/j.isci.2022.103807openalex-snapshot
Mechanotransduction in hippocampal neurons operates under localized low picoNewton forces
inferred← citeshttps://doi.org/10.1016/j.jbc.2024.107133openalex-snapshot
High-throughput virtual search of small molecules for controlling the mechanical stability of human CD4
inferred← citeshttps://doi.org/10.1016/j.jpha.2026.101753openalex-snapshot
Mechanosensitive ion channels: Shedding light on their functions and mechanisms in digestive system diseases
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2023.108528openalex-snapshot
Novel approaches to target fibroblast mechanotransduction in fibroproliferative diseases
inferred← citeshttps://doi.org/10.1016/j.tibs.2024.05.004openalex-snapshot
Re-evaluating TRP channel mechanosensitivity
inferred← citeshttps://doi.org/10.1016/j.ultrasmedbio.2025.12.016openalex-snapshot
Preclinical Applications and Parameter Optimization of Low-Intensity Pulsed Ultrasound Therapy in Neurological Diseases: A Review
inferred← citeshttps://doi.org/10.1038/s41467-025-59150-1openalex-snapshot
Visualizing PIEZO1 localization and activity in hiPSC-derived single cells and organoids with HaloTag technology
inferred← citeshttps://doi.org/10.1038/s41526-025-00466-zopenalex-snapshot
The mechanosensitive channel ELKIN1 regulates cellular adaptations to simulated microgravity
inferred← citeshttps://doi.org/10.1038/s41563-024-02060-2openalex-snapshot
Stretch-induced endogenous electric fields drive directed collective cell migration in vivo
inferred← citeshttps://doi.org/10.1038/s41598-023-47090-zopenalex-snapshot
Single-neuron mechanical perturbation evokes calcium plateaus that excite and modulate the network
inferred← citeshttps://doi.org/10.1038/s44460-026-00068-6openalex-snapshot
Activating Piezo1 using DNA-based extracellular tethers
inferred← citeshttps://doi.org/10.1039/d5lc00419eopenalex-snapshot
Enhancing cancer therapy via acoustics: chemotherapy-enhanced tunable acoustofluidic permeabilization (ChemoTAP)
inferred← citeshttps://doi.org/10.1080/19336950.2024.2355123openalex-snapshot
The activation thresholds and inactivation kinetics of poking-evoked PIEZO1 and PIEZO2 currents are sensitive to subtle variations in mechanical stimulation parameters
inferred← citeshttps://doi.org/10.1085/jgp.202213084openalex-snapshot
Piezo1 regulates cholesterol biosynthesis to influence neural stem cell fate during brain development
inferred← citeshttps://doi.org/10.1101/2021.10.11.463916openalex-snapshot
Stretch-induced endogenous electric fields drive neural crest directed collective cell migration in vivo
inferred← citeshttps://doi.org/10.1101/2023.10.03.560740openalex-snapshot
Structure-guided mutagenesis of OSCAs reveals differential activation to mechanical stimuli
inferred← citeshttps://doi.org/10.1101/2025.11.06.687026openalex-snapshot
NF-κB-Dependent Transcriptional Regulation of Piezo1 Mediates Bacterial Clearance on Stiffened Lung Matrix
inferred← citeshttps://doi.org/10.1103/xc5f-xr7nopenalex-snapshot
Improved Anisotropic Network Models for Membrane Protein Dynamics and Mechanosensitive Ion Channels
inferred← citeshttps://doi.org/10.1126/sciadv.aeb1271openalex-snapshot
Compressive stress–driven Piezo1 activation and Rho-ROCK mechanotransduction promote tumor progression via epigenetic mechanical memory
inferred← citeshttps://doi.org/10.1134/s0022093023040269openalex-snapshot
Mechanosensory Structures in the Mechanotransduction System of Muscle Fibers
inferred← citeshttps://doi.org/10.1152/ajpregu.00327.2022openalex-snapshot
Neural discharge of muscle afferents and pressor response to mechanical stimulation are associated with muscle deformation velocity in rats
inferred← citeshttps://doi.org/10.1161/hypertensionaha.122.20109openalex-snapshot
Vascular Smooth Muscle TRPV4 (Transient Receptor Potential Vanilloid Family Member 4) Channels Regulate Vasoconstriction and Blood Pressure in Obesity
inferred← citeshttps://doi.org/10.1186/s12951-026-04105-xopenalex-snapshot
f-SPION-mediated magnetic stimulation induces reparative Schwann cell reprogramming via cytoskeletal dynamics - gated activation of Piezo1
inferred← citeshttps://doi.org/10.1186/s13578-022-00931-2openalex-snapshot
Activation of Piezo1 downregulates renin in juxtaglomerular cells and contributes to blood pressure homeostasis
inferred← citeshttps://doi.org/10.1242/jcs.264038openalex-snapshot
Evaluating the roles of ion channels in cellular force sensing
inferred← citeshttps://doi.org/10.1242/jcs.264456openalex-snapshot
Sensing of shear stress in vascular endothelial cells – from physiology to pathology
inferred← citeshttps://doi.org/10.20517/and.2025.02openalex-snapshot
Mechanosensitive apoptosis in Alzheimer’s disease
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4859720/v1openalex-snapshot
In situ magnetic-field-assisted bioprinting process using magnetorheological bioink to obtain engineered muscle constructs
inferred← citeshttps://doi.org/10.31857/s0869813923080083openalex-snapshot
Mechanosensory Structures in the Mechanotransduction System of Muscle Fibers
inferred← citeshttps://doi.org/10.3389/fcell.2022.886048openalex-snapshot
Force From Filaments: The Role of the Cytoskeleton and Extracellular Matrix in the Gating of Mechanosensitive Channels
inferred← citeshttps://doi.org/10.3389/fimmu.2022.816149openalex-snapshot
Piezo1 Channels as Force Sensors in Mechanical Force-Related Chronic Inflammation
inferred← citeshttps://doi.org/10.3389/fncel.2024.1367476openalex-snapshot
A helping hand: roles for accessory cells in the sense of touch across species
inferred← citeshttps://doi.org/10.3390/neurosci4040023openalex-snapshot
The Effects of Lithium on Proprioceptive Sensory Function and Nerve Conduction
inferred← citeshttps://doi.org/10.3892/mmr.2025.13565openalex-snapshot
Roles of Piezo1 in chronic inflammatory diseases and prospects for drug treatment (Review)
inferred← citeshttps://doi.org/10.5357/koubyou.91.2-3_93openalex-snapshot
Biological Roles of Mechanosensitive Ion Channels in Mesenchymal Stem Cells
inferred← citeshttps://doi.org/10.64898/2026.07.13.737685openalex-snapshot
Macrophage calcium signaling dynamics revealed using genetically-encoded sensors
inferred← citeshttps://doi.org/10.7554/elife.84179openalex-snapshot
Mechanotransduction events at the physiological site of touch detection
inferred← citeshttps://doi.org/10.7554/elife.93147openalex-snapshot
Structure-guided mutagenesis of OSCAs reveals differential activation to mechanical stimuli
inferred← citeshttps://doi.org/10.7554/elife.93147.1openalex-snapshot
Structure-guided mutagenesis of OSCAs reveals differential activation to mechanical stimuli
inferred← citeshttps://doi.org/10.7554/elife.93147.2openalex-snapshot
Structure-guided mutagenesis of OSCAs reveals differential activation to mechanical stimuli
inferred← citeshttps://doi.org/10.7554/elife.93147.3openalex-snapshot
Structure-guided mutagenesis of OSCAs reveals differential activation to mechanical stimuli
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