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The cell biology of touch
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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/ar.a.10029openalex-snapshot
Friedrich Sigmund Merkel and his “Merkel cell”, morphology, development, and physiology: Review and new results
inferredcites →https://doi.org/10.1002/cne.21517openalex-snapshot
Central and peripheral anatomy of slowly adapting type I low‐threshold mechanoreceptors innervating trunk skin of neonatal mice
inferredcites →https://doi.org/10.1002/cne.21862openalex-snapshot
Visualizing mechanosensory endings of TrkC‐expressing neurons in HS3ST‐2‐hPLAP mice
inferredcites →https://doi.org/10.1002/cne.901630207openalex-snapshot
Dopaminergic neurons in the nematode Caenorhabditis elegans
inferredcites →https://doi.org/10.1002/dvdy.21531openalex-snapshot
Identification of genes involved in the ciliary trafficking of C. elegans PKD‐2
inferredcites →https://doi.org/10.1002/j.1460-2075.1992.tb05357.xopenalex-snapshot
The mec‐7 beta‐tubulin gene of Caenorhabditis elegans is expressed primarily in the touch receptor neurons.
inferredcites →https://doi.org/10.1002/syn.20236openalex-snapshot
Metabotropic glutamate receptor antagonists selectively enhance responses of slowly adapting type I mechanoreceptors
inferredcites →https://doi.org/10.1007/bf01181555openalex-snapshot
Merkel cells are not the mechanosensory transducers in the touch dome of the rat
inferredcites →https://doi.org/10.1007/bf02933819openalex-snapshot
Tastzellen und Tastkörperchen bei den Hausthieren und beim Menschen
inferredcites →https://doi.org/10.1007/s002329900068openalex-snapshot
Multiple Mechanosensitive Ion Channels from Escherichia coli, Activated at Different Thresholds of Applied Pressure
inferredcites →https://doi.org/10.1007/s00359-009-0482-zopenalex-snapshot
Nociceptors: a phylogenetic view
inferredcites →https://doi.org/10.1007/s00424-005-1438-yopenalex-snapshot
TRPV channels as thermosensory receptors in epithelial cells
inferredcites →https://doi.org/10.1007/s00424-007-0263-xopenalex-snapshot
Mechanotransduction and auditory transduction in Drosophila
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/10.1016/0012-1606(86)90314-3openalex-snapshot
Mutant sensory cilia in the nematode Caenorhabditis elegans
inferredcites →https://doi.org/10.1016/0304-3940(96)12906-2openalex-snapshot
Chloroquine specifically impairs Merkel cell mechanoreceptor function in isolated rat sinus hairs
inferredcites →https://doi.org/10.1016/0304-3959(85)90169-1openalex-snapshot
Sensory receptor mechanisms
inferredcites →https://doi.org/10.1016/0306-4522(88)90175-3openalex-snapshot
Merkel cells and the mechanosensitivity of normal and regenerating nerves in Xenopus skin
inferredcites →https://doi.org/10.1016/0896-6273(91)90343-xopenalex-snapshot
Tip-link integrity and mechanical transduction in vertebrate hair cells
inferredcites →https://doi.org/10.1016/0896-6273(94)90437-5openalex-snapshot
Genetic dissection of mechanosensory transduction: Mechanoreception-defective mutations of drosophila
inferredcites →https://doi.org/10.1016/0896-6273(95)90242-2openalex-snapshot
Sensory regulation of male mating behavior in caenorhabditis elegans
inferredcites →https://doi.org/10.1016/j.cub.2004.10.030openalex-snapshot
MEC-2 Is Recruited to the Putative Mechanosensory Complex in C. elegans Touch Receptor Neurons through Its Stomatin-like Domain
inferredcites →https://doi.org/10.1016/j.cub.2007.11.029openalex-snapshot
Nociceptive Neurons Protect Drosophila Larvae from Parasitoid Wasps
inferredcites →https://doi.org/10.1016/j.cub.2009.06.036openalex-snapshot
The Multipurpose 15-Protofilament Microtubules in C. elegans Have Specific Roles in Mechanosensation
inferredcites →https://doi.org/10.1016/j.cub.2009.12.057openalex-snapshot
Pickpocket Is a DEG/ENaC Protein Required for Mechanical Nociception in Drosophila Larvae
inferredcites →https://doi.org/10.1016/j.neuron.2003.08.015openalex-snapshot
In Vivo Imaging of C. elegans Mechanosensory Neurons Demonstrates a Specific Role for the MEC-4 Channel in the Process of Gentle Touch Sensation
inferredcites →https://doi.org/10.1016/j.neuron.2004.11.010openalex-snapshot
Extracellular Proteins Organize the Mechanosensory Channel Complex in C. elegans Touch Receptor Neurons
inferredcites →https://doi.org/10.1016/j.neuron.2004.12.015openalex-snapshot
Topographically Distinct Epidermal Nociceptive Circuits Revealed by Axonal Tracers Targeted to Mrgprd
inferredcites →https://doi.org/10.1016/j.neuron.2007.04.027openalex-snapshot
A Hierarchical NGF Signaling Cascade Controls Ret-Dependent and Ret-Independent Events during Development of Nonpeptidergic DRG Neurons
inferredcites →https://doi.org/10.1016/j.neuron.2009.11.003openalex-snapshot
Molecular Identification of Rapidly Adapting Mechanoreceptors and Their Developmental Dependence on Ret Signaling
inferredcites →https://doi.org/10.1016/j.neuron.2009.12.004openalex-snapshot
Low-Threshold Mechanoreceptor Subtypes Selectively Express MafA and Are Specified by Ret Signaling
inferredcites →https://doi.org/10.1016/j.neuron.2010.06.032openalex-snapshot
C. elegans TRP Family Protein TRP-4 Is a Pore-Forming Subunit of a Native Mechanotransduction Channel
inferredcites →https://doi.org/10.1016/j.neuron.2010.07.004openalex-snapshot
The Role of the TRP Channel NompC in Drosophila Larval and Adult Locomotion
inferredcites →https://doi.org/10.1016/j.neuroscience.2005.03.018openalex-snapshot
Are unconventional NMDA receptors involved in slowly adapting type I mechanoreceptor responses?
inferredcites →https://doi.org/10.1016/j.neuroscience.2009.07.015openalex-snapshot
Non-competitive metabotropic glutamate 1 receptor antagonists block activity of slowly adapting type I mechanoreceptor units in the rat sinus hair follicle
inferredcites →https://doi.org/10.1016/j.pain.2004.08.015openalex-snapshot
Nociceptor-specific gene deletion using heterozygous NaV1.8-Cre recombinase mice
inferredcites →https://doi.org/10.1016/j.ydbio.2009.09.032openalex-snapshot
Mammalian Merkel cells are descended from the epidermal lineage
inferredcites →https://doi.org/10.1016/j.ydbio.2010.05.502openalex-snapshot
Time-lapse imaging and cell-specific expression profiling reveal dynamic branching and molecular determinants of a multi-dendritic nociceptor in C. elegans
inferredcites →https://doi.org/10.1016/s0006-3495(79)85267-4openalex-snapshot
Response latency of vertebrate hair cells
inferredcites →https://doi.org/10.1016/s0092-8674(00)00143-4openalex-snapshot
Vanilloid Receptor–Related Osmotically Activated Channel (VR-OAC), a Candidate Vertebrate Osmoreceptor
inferredcites →https://doi.org/10.1016/s0092-8674(03)00272-1openalex-snapshot
painless, a Drosophila Gene Essential for Nociception
inferredcites →https://doi.org/10.1016/s0190-9622(03)02785-3openalex-snapshot
Infantile granular parakeratosis: Recognition of two clinical patterns
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/s0896-6273(00)80035-5openalex-snapshot
Extracellular Proteins Needed for C. elegans Mechanosensation
inferredcites →https://doi.org/10.1016/s0896-6273(00)80047-1openalex-snapshot
Specific Subtypes of Cutaneous Mechanoreceptors Require Neurotrophin-3 Following Peripheral Target Innervation
inferredcites →https://doi.org/10.1016/s0896-6273(00)81199-xopenalex-snapshot
C. elegans Locomotory Rate Is Modulated by the Environment through a Dopaminergic Pathway and by Experience through a Serotonergic Pathway
inferredcites →https://doi.org/10.1016/s0896-6273(01)00215-xopenalex-snapshot
nompA Encodes a PNS-Specific, ZP Domain Protein Required to Connect Mechanosensory Dendrites to Sensory Structures
inferredcites →https://doi.org/10.1016/s0896-6273(01)00547-5openalex-snapshot
The DRASIC Cation Channel Contributes to the Detection of Cutaneous Touch and Acid Stimuli in Mice
inferredcites →https://doi.org/10.1016/s0896-6273(02)00757-2openalex-snapshot
Combinatorial Expression of TRPV Channel Proteins Defines Their Sensory Functions and Subcellular Localization in C. elegans Neurons
inferredcites →https://doi.org/10.1016/s0959-4388(00)00234-8openalex-snapshot
The roles and functions of cutaneous mechanoreceptors
inferredcites →https://doi.org/10.1016/s0960-9822(01)00423-7openalex-snapshot
The Caenorhabditis elegans autosomal dominant polycystic kidney disease gene homologs lov-1 and pkd-2 act in the same pathway
inferredcites →https://doi.org/10.1016/s1567-133x(03)00089-9openalex-snapshot
Math1-driven GFP expression in the developing nervous system of transgenic mice
inferredcites →https://doi.org/10.1038/35039512openalex-snapshot
The mammalian sodium channel BNC1 is required for normal touch sensation
inferredcites →https://doi.org/10.1038/367470a0openalex-snapshot
A transmembrane domain of the putative channel subunit MEC-4 influences mechanotransduction and neurodegeneration in C. elegans
inferredcites →https://doi.org/10.1038/4151039aopenalex-snapshot
MEC-2 regulates C. elegans DEG/ENaC channels needed for mechanosensation
inferredcites →https://doi.org/10.1038/43913openalex-snapshot
A polycystic kidney-disease gene homologue required for male mating behaviour 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/emboj.2009.57openalex-snapshot
The mechano‐activated K+ channels TRAAK and TREK‐1 control both warm and cold perception
inferredcites →https://doi.org/10.1038/nature00891openalex-snapshot
Identification of genes expressed in C. elegans touch receptor neurons
inferredcites →https://doi.org/10.1038/nature01205openalex-snapshot
The mechanosensory protein MEC-6 is a subunit of the C. elegans touch-cell degenerin channel
inferredcites →https://doi.org/10.1038/nature01733openalex-snapshot
A TRPV family ion channel required for hearing in Drosophila
inferredcites →https://doi.org/10.1038/nature03896openalex-snapshot
A possible unifying principle for mechanosensation
inferredcites →https://doi.org/10.1038/nature04538openalex-snapshot
A C. elegans stretch receptor neuron revealed by a mechanosensitive TRP channel homologue
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/nature05413openalex-snapshot
An SCN9A channelopathy causes congenital inability to experience pain
inferredcites →https://doi.org/10.1038/nature05662openalex-snapshot
Mechanisms of sensory transduction in the skin
inferredcites →https://doi.org/10.1038/nature06163openalex-snapshot
Structure of acid-sensing ion channel 1 at 1.9 Å resolution and low pH
inferredcites →https://doi.org/10.1038/nature08505openalex-snapshot
Injury-induced mechanical hypersensitivity requires C-low threshold mechanoreceptors
inferredcites →https://doi.org/10.1038/nmeth.1463openalex-snapshot
Enhanced neuronal RNAi in C. elegans using SID-1
inferredcites →https://doi.org/10.1038/nn.2312openalex-snapshot
Coding of pleasant touch by unmyelinated afferents in humans
inferredcites →https://doi.org/10.1038/nn.2581openalex-snapshot
Specific roles for DEG/ENaC and TRP channels in touch and thermosensation in C. elegans nociceptors
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/nn1886openalex-snapshot
Caenorhabditis elegans TRPA-1 functions in mechanosensation
inferredcites →https://doi.org/10.1038/nn1937openalex-snapshot
Molecular genetic visualization of a rare subset of unmyelinated sensory neurons that may detect gentle touch
inferredcites →https://doi.org/10.1038/nn896openalex-snapshot
Unmyelinated tactile afferents signal touch and project to insular cortex
inferredcites →https://doi.org/10.1046/j.1460-9568.1999.00822.xopenalex-snapshot
Postnatal loss of Merkel cells, but not of slowly adapting mechanoreceptors in mice lacking the neurotrophin receptor p75
inferredcites →https://doi.org/10.1073/pnas.0404915101openalex-snapshot
Nociceptor-specific gene deletion reveals a major role for Na v 1.7 (PN1) in acute and inflammatory pain
inferredcites →https://doi.org/10.1073/pnas.0406308101openalex-snapshot
Molecular profiling reveals synaptic release machinery in Merkel cells
inferredcites →https://doi.org/10.1073/pnas.0502403102openalex-snapshot
Xenopus TRPN1 (NOMPC) localizes to microtubule-based cilia in epithelial cells, including inner-ear hair cells
inferredcites →https://doi.org/10.1073/pnas.0607465103openalex-snapshot
Podocin and MEC-2 bind cholesterol to regulate the activity of associated ion channels
inferredcites →https://doi.org/10.1073/pnas.0901507106openalex-snapshot
Distinct subsets of unmyelinated primary sensory fibers mediate behavioral responses to noxious thermal and mechanical stimuli
inferredcites →https://doi.org/10.1073/pnas.1735416100openalex-snapshot
Abnormal osmotic regulation in trpv4 -/- mice
inferredcites →https://doi.org/10.1073/pnas.86.8.2918openalex-snapshot
Voltage dependence of adaptation and active bundle movement in bullfrog saccular hair cells.
inferredcites →https://doi.org/10.1073/pnas.90.6.2227openalex-snapshot
A dual mechanosensory and chemosensory neuron in Caenorhabditis elegans.
inferredcites →https://doi.org/10.1073/pnas.93.13.6577openalex-snapshot
Genetic interactions affecting touch sensitivity in Caenorhabditis elegans.
inferredcites →https://doi.org/10.1073/pnas.94.26.14837openalex-snapshot
A genetic screen for mutations that disrupt an auditory response in Drosophila melanogaster
inferredcites →https://doi.org/10.1080/08990220701838996openalex-snapshot
Fingerprint lines may not directly affect SA-I mechanoreceptor response
inferredcites →https://doi.org/10.1083/jcb.129.2.535openalex-snapshot
Molecular cloning of chick beta-tectorin, an extracellular matrix molecule of the inner ear.
inferredcites →https://doi.org/10.1083/jcb.140.1.143openalex-snapshot
Ripped Pocket and Pickpocket, Novel Drosophila DEG/ENaC Subunits Expressed in Early Development and in Mechanosensory Neurons
inferredcites →https://doi.org/10.1083/jcb.200907080openalex-snapshot
Epidermal progenitors give rise to Merkel cells during embryonic development and adult homeostasis
inferredcites →https://doi.org/10.1083/jcb.82.1.278openalex-snapshot
Organization of neuronal microtubules in the nematode Caenorhabditis elegans.
inferredcites →https://doi.org/10.1083/jcb.93.1.15openalex-snapshot
Structural and functional diversity in the neuronal microtubules of Caenorhabditis elegans.
inferredcites →https://doi.org/10.1085/jgp.200709910openalex-snapshot
MEC-2 and MEC-6 in the Caenorhabditis elegans Sensory Mechanotransduction Complex: Auxiliary Subunits that Enable Channel Activity
inferredcites →https://doi.org/10.1093/hmg/11.10.1215openalex-snapshot
Studies of mechanosensation using the fly
inferredcites →https://doi.org/10.1096/fj.05-5424revopenalex-snapshot
Cellular mechanotransduction: putting all the pieces together again
inferredcites →https://doi.org/10.1097/00000478-198912000-00004openalex-snapshot
An Immunohistochemical Study
inferredcites →https://doi.org/10.1097/00001756-200102120-00032openalex-snapshot
Evidence for glutamate receptor mediated transmission at mechanoreceptors in the skin
inferredcites →https://doi.org/10.1101/gad.1758709openalex-snapshot
Genetic and cell biological analysis of integrin outside-in signaling
inferredcites →https://doi.org/10.1101/gad.3.12a.1823openalex-snapshot
The mec-3 gene of Caenorhabditis elegans requires its own product for maintained expression and is expressed in three neuronal cell types.
inferredcites →https://doi.org/10.1101/gad.3.6.870openalex-snapshot
mec-7 is a beta-tubulin gene required for the production of 15-protofilament microtubules in Caenorhabditis elegans.
inferredcites →https://doi.org/10.1111/j.1469-7580.2004.00266.xopenalex-snapshot
Merkel cells, a new localization of prepro‐orexin and orexin receptors
inferredcites →https://doi.org/10.1111/j.1469-7610.2007.01730.xopenalex-snapshot
Neurodevelopmental sequelae of postnatal maternal care in rodents: clinical and research implications of molecular insights
inferredcites →https://doi.org/10.1113/expphysiol.1972.sp002177openalex-snapshot
THE STRUCTURE AND FUNCTION OF THE SLOWLY ADAPTING TYPE II MECHANORECEPTOR IN HAIRY SKIN
inferredcites →https://doi.org/10.1113/jphysiol.1965.sp007598openalex-snapshot
Components of receptor adaptation in a Pacinian corpuscle
inferredcites →https://doi.org/10.1113/jphysiol.1994.sp020292openalex-snapshot
Selective phototoxic destruction of rat Merkel cells abolishes responses of slowly adapting type I mechanoreceptor units.
inferredcites →https://doi.org/10.1113/jphysiol.2003.058693openalex-snapshot
Acid‐sensing ion channels ASIC2 and ASIC3 do not contribute to mechanically activated currents in mammalian sensory neurones
inferredcites →https://doi.org/10.1113/jphysiol.2006.117648openalex-snapshot
Mechanosensitive currents in the neurites of cultured mouse sensory neurones
inferredcites →https://doi.org/10.1113/jphysiol.2009.182360openalex-snapshot
Kinetic properties of mechanically activated currents in spinal sensory neurons
inferredcites →https://doi.org/10.1126/science.1084370openalex-snapshot
NompC TRP Channel Required for Vertebrate Sensory Hair Cell Mechanotransduction
inferredcites →https://doi.org/10.1126/science.1166467openalex-snapshot
The Role of Fingerprints in the Coding of Tactile Information Probed with a Biomimetic Sensor
inferredcites →https://doi.org/10.1126/science.1172890openalex-snapshot
Merkel Cells Are Essential for Light-Touch Responses
inferredcites →https://doi.org/10.1126/science.1189095openalex-snapshot
The Fusogen EFF-1 Controls Sculpting of Mechanosensory Dendrites
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.2646709openalex-snapshot
Genetic Control of Differentiation of the Caenorhabditis elegans Touch Receptor Neurons
inferredcites →https://doi.org/10.1126/science.287.5461.2229openalex-snapshot
A Drosophila Mechanosensory Transduction Channel
inferredcites →https://doi.org/10.1146/annurev.neuro.29.051605.112917openalex-snapshot
The Micromachinery of Mechanotransduction in Hair Cells
inferredcites →https://doi.org/10.1146/annurev.physiol.68.040204.100715openalex-snapshot
TRP CHANNELS IN C. ELEGANS
inferredcites →https://doi.org/10.1152/jn.00810.2009openalex-snapshot
The Regularity of Sustained Firing Reveals Two Populations of Slowly Adapting Touch Receptors in Mouse Hairy Skin
inferredcites →https://doi.org/10.1152/jn.00860.2007openalex-snapshot
Stomatin and Sensory Neuron Mechanotransduction
inferredcites →https://doi.org/10.1177/002215549804601113openalex-snapshot
Identification of Merkel Cells by an Antibody to Villin
inferredcites →https://doi.org/10.1186/1471-213x-8-110openalex-snapshot
The C. elegansEMAP-like protein, ELP-1 is required for touch sensation and associates with microtubules and adhesion complexes
inferredcites →https://doi.org/10.1242/dev.123.1.399openalex-snapshot
Genes controlling and mediating locomotion behavior of the zebrafish embryo and larva
inferredcites →https://doi.org/10.1242/dev.128.6.883openalex-snapshot
Hemicentin, a conserved extracellular member of the immunoglobulin superfamily, organizes epithelial and other cell attachments into oriented line- shaped junctions
inferredcites →https://doi.org/10.1242/jcs.112.3.395openalex-snapshot
MEC-12, an α-tubulin required for touch sensitivity in C. elegans
inferredcites →https://doi.org/10.1371/journal.pone.0001750openalex-snapshot
Swelling-Activated Ca2+ Channels Trigger Ca2+ Signals in Merkel Cells
inferredcites →https://doi.org/10.1371/journal.pone.0007759openalex-snapshot
Rat Merkel Cells Are Mechanoreceptors and Osmoreceptors
inferredcites →https://doi.org/10.1371/journal.pone.0011012openalex-snapshot
Drosophila TRPN( = NOMPC) Channel Localizes to the Distal End of Mechanosensory Cilia
inferredcites →https://doi.org/10.1385/cbb:34:3:321openalex-snapshot
Mechanosensitive Channel of Thermoplasma, the Cell Wall-Less Archaea: Cloning and Molecular Characterization
inferredcites →https://doi.org/10.1503/cmaj.060146openalex-snapshot
Neuropathic pain: a practical guide for the clinician
inferredcites →https://doi.org/10.1523/jneurosci.0759-09.2009openalex-snapshot
α9 Integrin Promotes Neurite Outgrowth on Tenascin-C and Enhances Sensory Axon Regeneration
inferredcites →https://doi.org/10.1523/jneurosci.1279-04.2004openalex-snapshot
Espins Are Multifunctional Actin Cytoskeletal Regulatory Proteins in the Microvilli of Chemosensory and Mechanosensory Cells
inferredcites →https://doi.org/10.1523/jneurosci.13-11-04880.1993openalex-snapshot
Expression of beta 1 integrins in sensory neurons of the dorsal root ganglion and their functions in neurite outgrowth on two laminin isoforms
inferredcites →https://doi.org/10.1523/jneurosci.1405-07.2007openalex-snapshot
FMRFamide-Like Neuropeptides and Mechanosensory Touch Receptor Neurons Regulate Male Sexual Turning Behavior inCaenorhabditis elegans
inferredcites →https://doi.org/10.1523/jneurosci.1639-10.2010openalex-snapshot
touche Is Required for Touch-Evoked Generator Potentials within Vertebrate Sensory Neurons
inferredcites →https://doi.org/10.1523/jneurosci.1645-04.2004openalex-snapshot
Two Interdependent TRPV Channel Subunits, Inactive and Nanchung, Mediate Hearing in Drosophila
inferredcites →https://doi.org/10.1523/jneurosci.17-21-08259.1997openalex-snapshot
OSM-9, A Novel Protein with Structural Similarity to Channels, Is Required for Olfaction, Mechanosensation, and Olfactory Adaptation in Caenorhabditis elegans
inferredcites →https://doi.org/10.1523/jneurosci.18-17-07040.1998openalex-snapshot
Neurotrophin 4 Is Required for the Survival of a Subclass of Hair Follicle Receptors
inferredcites →https://doi.org/10.1523/jneurosci.18-22-09181.1998openalex-snapshot
Zebrafish Touch-Insensitive Mutants Reveal an Essential Role for the Developmental Regulation of Sodium Current
inferredcites →https://doi.org/10.1523/jneurosci.19-06-01952.1999openalex-snapshot
Distinct Signaling Pathways Mediate Touch and Osmosensory Responses in a Polymodal Sensory Neuron
inferredcites →https://doi.org/10.1523/jneurosci.21-17-06905.2001openalex-snapshot
Neural Coding Mechanisms Underlying Perceived Roughness of Finely Textured Surfaces
inferredcites →https://doi.org/10.1523/jneurosci.21-18-07236.2001openalex-snapshot
The Meissner Corpuscle Revised: A Multiafferented Mechanoreceptor with Nociceptor Immunochemical Properties
inferredcites →https://doi.org/10.1523/jneurosci.22-12-j0001.2002openalex-snapshot
Distinct Mechanosensitive Properties of Capsaicin-Sensitive and -Insensitive Sensory Neurons
inferredcites →https://doi.org/10.1523/jneurosci.3684-09.2009openalex-snapshot
Diminutive Digits Discern Delicate Details: Fingertip Size and the Sex Difference in Tactile Spatial Acuity
inferredcites →https://doi.org/10.1523/jneurosci.4179-07.2007openalex-snapshot
Nanoscale Organization of the MEC-4 DEG/ENaC Sensory Mechanotransduction Channel inCaenorhabditis elegansTouch Receptor Neurons
inferredcites →https://doi.org/10.1523/jneurosci.4666-09.2010openalex-snapshot
Physiological Basis of Tingling Paresthesia Evokedby Hydroxy-α-Sanshool
inferredcites →https://doi.org/10.1523/jneurosci.5380-08.2009openalex-snapshot
TRPA1 Modulates Mechanotransduction in Cutaneous Sensory Neurons
inferredcites →https://doi.org/10.1523/jneurosci.5974-08.2009openalex-snapshot
GABAergic/Glutamatergic–Glial/Neuronal Interaction Contributes to Rapid Adaptation in Pacinian Corpuscles
inferredcites →https://doi.org/10.1679/aohc.68.19openalex-snapshot
Receptors and transporter for serotonin in Merkel cell-nerve endings in the rat sinus hair follicle. An immunohistochemical study
inferredcites →https://doi.org/10.1679/aohc.68.383openalex-snapshot
Immunohistochemical reactions of receptors to met-enkephalin, VIP, substance P, and CGRP located on Merkel cells in the rat sinus hair follicle
inferredcites →https://doi.org/10.4161/psb.3.9.6487openalex-snapshot
AtMSL9 and AtMSL10: Sensors of plasma membrane tension in Arabidopsis roots
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9781118373903.ch13openalex-snapshot
Food Texture is Only Partly Rheology
inferred← citeshttps://doi.org/10.1002/9781118966174.ch1openalex-snapshot
Extracellular Matrix Structure and Stem Cell Mechanosensing
inferred← citeshttps://doi.org/10.1002/9781119723226.ch9.2openalex-snapshot
Applied Consumer Neuroscience and Behavioral Approaches for Innovation, Product Development, and Communications
inferred← citeshttps://doi.org/10.1002/aisy.201900017openalex-snapshot
Intelligent Liquid Integrated Functional Entity: A Basic Way to Innovate Future Advanced Biomimetic Soft Robotics
inferred← citeshttps://doi.org/10.1002/ar.22615openalex-snapshot
Immunohistochemical Detection of the Putative Mechanoproteins ASIC2 and TRPV4 in Avian Herbst Sensory Corpuscles
inferred← citeshttps://doi.org/10.1002/ar.22792openalex-snapshot
The Sensory Innervation of the Human Pharynx: Searching for Mechanoreceptors
inferred← citeshttps://doi.org/10.1002/ar.23522openalex-snapshot
Human Digital M eissner Corpuscles Display Immunoreactivity for the Multifunctional Ion Channels Trpc6 and Trpv4
inferred← citeshttps://doi.org/10.1002/cm.70145openalex-snapshot
Antagonistic Relationship Between Microtubule‐Stabilizing and Destabilizing Factors for the Maintenance of Axonal Microtubule Dynamics and Polarity in C. elegans Touch Neuron
inferred← citeshttps://doi.org/10.1002/jemt.22028openalex-snapshot
Mechanosensory neurons, cutaneous mechanoreceptors, and putative mechanoproteins
inferred← citeshttps://doi.org/10.1007/8415_2011_83openalex-snapshot
Mechanotransduction in the Nervous System
inferred← citeshttps://doi.org/10.1007/978-1-4939-6418-5_3openalex-snapshot
Cell Biology of Tactile Afferents
inferred← citeshttps://doi.org/10.1007/978-1-4939-9732-9_23openalex-snapshot
Live Morphometric Classification of Sensory Neurons in Larval Zebrafish
inferred← citeshttps://doi.org/10.1007/978-3-319-18705-1_7openalex-snapshot
TRP Channels and Mechanical Transduction
inferred← citeshttps://doi.org/10.1007/978-981-10-6526-2_1openalex-snapshot
Overview of Mechanosensory Transduction
inferred← citeshttps://doi.org/10.1007/978-981-10-6526-2_3openalex-snapshot
Mechanoreceptors in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1007/978-981-10-6526-2_4openalex-snapshot
Mechanotransduction in Drosophila Mechanoreceptors
inferred← citeshttps://doi.org/10.1007/978-981-16-4254-8_17openalex-snapshot
Mechanotransduction Ion Channels in Hearing and Touch
inferred← citeshttps://doi.org/10.1007/s00418-014-1278-yopenalex-snapshot
ASIC2 is present in human mechanosensory neurons of the dorsal root ganglia and in mechanoreceptors of the glabrous skin
inferred← citeshttps://doi.org/10.1007/s00424-014-1443-0openalex-snapshot
Reduced excitability of gp130-deficient nociceptors is associated with increased voltage-gated potassium currents and Kcna4 channel upregulation
inferred← citeshttps://doi.org/10.1007/s10803-019-03918-0openalex-snapshot
A Quantitative Sensory Testing Approach to Pain in Autism Spectrum Disorders
inferred← citeshttps://doi.org/10.1007/s40544-013-0015-1openalex-snapshot
Skin tribology: Science friction?
inferred← citeshttps://doi.org/10.1007/s40544-013-0016-0openalex-snapshot
Guest editorial: Special issue on bio-tribology
inferred← citeshttps://doi.org/10.1016/b978-0-12-387738-3.00026-3openalex-snapshot
Regulation of Ion Channel Localization and Activity Through Interactions with the Cytoskeleton
inferred← citeshttps://doi.org/10.1016/b978-0-12-387738-3.00036-6openalex-snapshot
Sensory Receptors and Mechanotransduction
inferred← citeshttps://doi.org/10.1016/b978-0-12-394305-7.00003-3openalex-snapshot
Ciliary and Flagellar Structure and Function—Their Regulations by Posttranslational Modifications of Axonemal Tubulin
inferred← citeshttps://doi.org/10.1016/b978-0-12-394624-9.00012-9openalex-snapshot
Mechanotransduction in C. elegans Morphogenesis and Tissue Function
inferred← citeshttps://doi.org/10.1016/b978-0-12-416022-4.00004-4openalex-snapshot
Epithelial Stem Cells in Adult Skin
inferred← citeshttps://doi.org/10.1016/b978-0-12-812832-9.00004-xopenalex-snapshot
The Nervous System
inferred← citeshttps://doi.org/10.1016/b978-0-12-823990-2.00016-7openalex-snapshot
Force-controlled robotic systems for mechanical stimulation of Drosophila larvae
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/j.aanat.2017.09.006openalex-snapshot
Molecular basis of dental sensitivity: The odontoblasts are multisensory cells and express multifunctional ion channels
inferred← citeshttps://doi.org/10.1016/j.actbio.2026.08.006openalex-snapshot
Convergent design principles for functional sensory innervation in bioprinted and engineered skin constructs
inferred← citeshttps://doi.org/10.1016/j.arr.2013.12.003openalex-snapshot
Effect of ageing on tactile transduction processes
inferred← citeshttps://doi.org/10.1016/j.bpj.2014.10.052openalex-snapshot
The Microtubule-Based Cytoskeleton Is a Component of a Mechanical Signaling Pathway in Fly Campaniform Receptors
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.2022.09.014openalex-snapshot
Electromechanical model for object roughness perception during finger sliding
inferred← citeshttps://doi.org/10.1016/j.brainres.2018.03.027openalex-snapshot
The now and then of gut-brain signaling
inferred← citeshttps://doi.org/10.1016/j.cej.2022.136028openalex-snapshot
Bioinspired hierarchical polydimethylsiloxane/polyaniline array for ultrasensitive pressure monitoring
inferred← citeshttps://doi.org/10.1016/j.celrep.2013.04.026openalex-snapshot
The Touch Dome Defines an Epidermal Niche Specialized for Mechanosensory Signaling
inferred← citeshttps://doi.org/10.1016/j.celrep.2013.08.051openalex-snapshot
The Organization of Submodality-Specific Touch Afferent Inputs in the Vibrissa Column
inferred← citeshttps://doi.org/10.1016/j.celrep.2013.09.013openalex-snapshot
TAFA4, a Chemokine-like Protein, Modulates Injury-Induced Mechanical and Chemical Pain Hypersensitivity in Mice
inferred← citeshttps://doi.org/10.1016/j.celrep.2015.01.022openalex-snapshot
Transcriptional Profiling of Cutaneous MRGPRD Free Nerve Endings and C-LTMRs
inferred← citeshttps://doi.org/10.1016/j.celrep.2018.02.068openalex-snapshot
TAFA4 Reverses Mechanical Allodynia through Activation of GABAergic Transmission and Microglial Process Retraction
inferred← citeshttps://doi.org/10.1016/j.celrep.2018.03.041openalex-snapshot
Brv1 Is Required for Drosophila Larvae to Sense Gentle Touch
inferred← citeshttps://doi.org/10.1016/j.celrep.2018.10.010openalex-snapshot
Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.116761openalex-snapshot
An ultrastructural map of a spinal sensorimotor circuit reveals the potential of astroglia modulation
inferred← citeshttps://doi.org/10.1016/j.compositesa.2024.108648openalex-snapshot
Polymer-based flexible piezoresistive pressure sensors based on various micro/nanostructures array
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.devcel.2024.04.005openalex-snapshot
Epithelial UNC-23 limits mechanical stress to maintain glia-neuron architecture in C. elegans
inferred← citeshttps://doi.org/10.1016/j.ibneur.2022.10.002openalex-snapshot
Effects of Potassium Channel Modulators on the Responses of Mammalian Slowly Adapting Mechanoreceptors
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2020.02.311openalex-snapshot
Assessing the potential of lignin nanoparticles as drug carrier: Synthesis, cytotoxicity and genotoxicity studies
inferred← citeshttps://doi.org/10.1016/j.jneumeth.2015.01.004openalex-snapshot
A novel vibrotactile system for stimulating the glabrous skin of awake freely behaving rats during operant conditioning
inferred← citeshttps://doi.org/10.1016/j.jpain.2015.08.014openalex-snapshot
Bedding Material Affects Mechanical Thresholds, Heat Thresholds, and Texture Preference
inferred← citeshttps://doi.org/10.1016/j.matlet.2021.130977openalex-snapshot
Low cost and highly sensitive flexible pressure sensor based on branched micro-structures
inferred← citeshttps://doi.org/10.1016/j.nanoen.2024.109799openalex-snapshot
Bioinspired composite fiber aerogel pressure sensor for machine-learning-assisted human activity and gesture recognition
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2015.12.009openalex-snapshot
Aδ-fiber low threshold mechanoreceptors innervating mammalian hairy skin: A review of their receptive, electrophysiological and cytochemical properties in relation to Aδ-fiber high threshold mechanoreceptors
inferred← citeshttps://doi.org/10.1016/j.neucli.2025.103135openalex-snapshot
Neurophysiology of pleasant touch: From peripheral mechanisms to clinical implications of caressing
inferred← citeshttps://doi.org/10.1016/j.neulet.2012.03.081openalex-snapshot
Immunohistochemical localization of acid-sensing ion channel 2 (ASIC2) in cutaneous Meissner and Pacinian corpuscles of Macaca fascicularis
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2025.121249openalex-snapshot
Cortical activations induced by electrical versus vibrotactile finger stimulation using EEG
inferred← citeshttps://doi.org/10.1016/j.neuron.2011.06.038openalex-snapshot
DEG/ENaC but Not TRP Channels Are the Major Mechanoelectrical Transduction Channels in a C. elegans Nociceptor
inferred← citeshttps://doi.org/10.1016/j.neuron.2026.05.017openalex-snapshot
A specialized population of hair afferents dedicated to transmitting mechanical itch
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2026.09.002openalex-snapshot
Biological mechanisms underlying avoidant/restrictive food intake disorder (ARFID)
inferred← citeshttps://doi.org/10.1016/j.nxcen.2026.100076openalex-snapshot
Sensory texturizing agents in cosmeceuticals: Navigating the skin-bioactive interface and recent advancements
inferred← citeshttps://doi.org/10.1016/j.psj.2026.106595openalex-snapshot
Different chick processing holding devices reveal welfare and stress effects via novel down-feather biomarkers
inferred← citeshttps://doi.org/10.1016/j.semcdb.2013.03.010openalex-snapshot
The role of Atonal transcription factors in the development of mechanosensitive cells
inferred← citeshttps://doi.org/10.1016/j.stem.2015.02.006openalex-snapshot
Basal Cell Carcinoma Preferentially Arises from Stem Cells within Hair Follicle and Mechanosensory Niches
inferred← citeshttps://doi.org/10.1016/j.tcb.2014.10.003openalex-snapshot
Merkel cells and neurons keep in touch
inferred← citeshttps://doi.org/10.1016/j.tins.2011.07.004openalex-snapshot
How does morphology relate to function in sensory arbors?
inferred← citeshttps://doi.org/10.1016/j.tins.2012.04.002openalex-snapshot
Sensing pressure with ion channels
inferred← citeshttps://doi.org/10.1016/j.ydbio.2013.08.004openalex-snapshot
Sox2 modulates the function of two distinct cell lineages in mouse skin
inferred← citeshttps://doi.org/10.1016/j.ydbio.2021.06.007openalex-snapshot
Microtubule organization of vertebrate sensory neurons in vivo
inferred← citeshttps://doi.org/10.1038/emboj.2012.203openalex-snapshot
A stomatin dimer modulates the activity of acid‐sensing ion channels
inferred← citeshttps://doi.org/10.1038/jid.2013.60openalex-snapshot
Three-Dimensional Morphology of Touch Domes in Human Hairy Skin by Correlative Light and Scanning Electron Microscopy
inferred← citeshttps://doi.org/10.1038/nature11685openalex-snapshot
Drosophila NOMPC is a mechanotransduction channel subunit for gentle-touch sensation
inferred← citeshttps://doi.org/10.1038/nrn2993openalex-snapshot
Molecular mechanisms of mechanotransduction in mammalian sensory neurons
inferred← citeshttps://doi.org/10.1038/s41467-018-04399-yopenalex-snapshot
FGF signalling controls the specification of hair placode-derived SOX9 positive progenitors to Merkel cells
inferred← citeshttps://doi.org/10.1038/s41467-018-07672-2openalex-snapshot
Bioinspired and bristled microparticles for ultrasensitive pressure and strain sensors
inferred← citeshttps://doi.org/10.1038/s41467-019-13956-yopenalex-snapshot
Astrocytes monitor cerebral perfusion and control systemic circulation to maintain brain blood flow
inferred← citeshttps://doi.org/10.1038/s41467-020-18895-7openalex-snapshot
A spinal neural circuitry for converting touch to itch sensation
inferred← citeshttps://doi.org/10.1038/s41556-023-01110-2openalex-snapshot
Co-option of epidermal cells enables touch sensing
inferred← citeshttps://doi.org/10.1039/9781782623885-00001openalex-snapshot
Mechanochemistry: Inspiration from Biology
inferred← citeshttps://doi.org/10.1039/9781788016155-00225openalex-snapshot
Design Structures for Optimal Sensory Performance
inferred← citeshttps://doi.org/10.1039/c5sm00770dopenalex-snapshot
An alternative theory to explain the effects of coalescing oil drops on mouthfeel
inferred← citeshttps://doi.org/10.1039/d3fd00035dopenalex-snapshot
Disentangling 1/ f noise from confined ion dynamics
inferred← citeshttps://doi.org/10.1042/bio03306018openalex-snapshot
In touch: The molecular basis of mechanosensory transduction
inferred← citeshttps://doi.org/10.1063/1.5144442openalex-snapshot
Hydrostatic pressure and interfacial tension induce mode instability in wave propagation along a liquid-filled microtubule
inferred← citeshttps://doi.org/10.1073/pnas.1514138112openalex-snapshot
Tissue mechanics govern the rapidly adapting and symmetrical response to touch
inferred← citeshttps://doi.org/10.1073/pnas.1901378116openalex-snapshot
Tiling and somatotopic alignment of mammalian low-threshold mechanoreceptors
inferred← citeshttps://doi.org/10.1080/01677063.2017.1395875openalex-snapshot
Novel genetic approaches to behavior in Drosophila
inferred← citeshttps://doi.org/10.1080/01677063.2020.1832091openalex-snapshot
Mechano-gated channels in C. elegans
inferred← citeshttps://doi.org/10.1083/jcb.201201041openalex-snapshot
Tracing epithelial stem cells during development, homeostasis, and repair
inferred← citeshttps://doi.org/10.1083/jcb.202004184openalex-snapshot
Katanin p60-like 1 sculpts the cytoskeleton in mechanosensory cilia
inferred← citeshttps://doi.org/10.1083/jcb.202005080openalex-snapshot
Wnt signaling establishes the microtubule polarity in neurons through regulation of Kinesin-13
inferred← citeshttps://doi.org/10.1083/jcb.202209116openalex-snapshot
DCX-EMAP is a core organizer for the ultrastructure of Drosophila mechanosensory organelles
inferred← citeshttps://doi.org/10.1085/jgp.201110637openalex-snapshot
Probing mammalian touch transduction
inferred← citeshttps://doi.org/10.1086/720097openalex-snapshot
Taste and Smell: A Unifying Chemosensory Theory
inferred← citeshttps://doi.org/10.1088/1361-6528/abe6c7openalex-snapshot
Nanomaterials and their applications on bio-inspired wearable electronics
inferred← citeshttps://doi.org/10.1089/ars.2013.5624openalex-snapshot
Mechanotransduction in the Endothelium: Role of Membrane Proteins and Reactive Oxygen Species in Sensing, Transduction, and Transmission of the Signal with Altered Blood Flow
inferred← citeshttps://doi.org/10.1097/j.pain.0000000000000711openalex-snapshot
Peripheral neuropathic changes in pachyonychia congenita
inferred← citeshttps://doi.org/10.1098/rsob.240036openalex-snapshot
Fly Fam161 is an essential centriole and cilium transition zone protein with unique and diverse cell type-specific localizations
inferred← citeshttps://doi.org/10.1098/rsos.182022openalex-snapshot
Ultrastructural evidence of a mechanosensory function of scale organs (sensilla) in sea snakes (Hydrophiinae)
inferred← citeshttps://doi.org/10.1098/rspb.2024.1524openalex-snapshot
Environmental complexity and regularity shape the evolution of cognition
inferred← citeshttps://doi.org/10.1101/2022.12.26.521704openalex-snapshot
Epithelia delimits glial apical polarity against mechanical shear to maintain glia-neuron - architecture
inferred← citeshttps://doi.org/10.1101/2025.03.05.641432openalex-snapshot
An ultrastructural map of a spinal sensorimotor circuit reveals the potential of astroglial modulation
inferred← citeshttps://doi.org/10.1101/2025.04.24.650367openalex-snapshot
The cytokinesis associated proteins CITK and ASPM-1 regulate neuronal microtubule dynamics and polarity in C. elegans
inferred← citeshttps://doi.org/10.1111/1744-7917.13459openalex-snapshot
NompC regulates locomotion and touch sensation in Bactrocera dorsalis
inferred← citeshttps://doi.org/10.1111/ahe.12969openalex-snapshot
Bovine Meissner‐like corpuscle and evolutionary ecology of mammalian somatosensory acuity
inferred← citeshttps://doi.org/10.1111/apa.13034openalex-snapshot
Imprinting, latchment and displacement: a mini review of early instinctual behaviour in newborn infants influencing breastfeeding success
inferred← citeshttps://doi.org/10.1111/azo.12475openalex-snapshot
Mechanosensory cells in annelid oligochaete Lumbricus terrestris (Linnaeus, 1758): A new insight on worm evolution
inferred← citeshttps://doi.org/10.1111/cpr.12677openalex-snapshot
The importance of the neuro‐immuno‐cutaneous system on human skin equivalent design
inferred← citeshttps://doi.org/10.1111/desc.13277openalex-snapshot
Anticipation across modalities in children and adults: Relating anticipatory alpha rhythm lateralization, reaction time, and executive function
inferred← citeshttps://doi.org/10.1111/exd.13901openalex-snapshot
Dissection of Merkel cell formation in hairy and glabrous skin reveals a common requirement for FGFR 2‐mediated signalling
inferred← citeshttps://doi.org/10.1111/exd.14415openalex-snapshot
Epigenetic regulation and signalling pathways in Merkel cell development
inferred← citeshttps://doi.org/10.1111/jcmm.12025openalex-snapshot
Neurosensory mechanotransduction through acid‐sensing ion channels
inferred← citeshttps://doi.org/10.1111/joa.12688openalex-snapshot
Merkel cells and Meissner's corpuscles in human digital skin display Piezo2 immunoreactivity
inferred← citeshttps://doi.org/10.1111/pce.14252openalex-snapshot
Mechanical stress acclimation in plants: Linking hormones and somatic memory to thigmomorphogenesis
inferred← citeshttps://doi.org/10.1113/jphysiol.2013.252106openalex-snapshot
A ‘toothache tree’ alkylamide inhibits Aδ mechanonociceptors to alleviate mechanical pain
inferred← citeshttps://doi.org/10.11154/pain.30.208openalex-snapshot
Molecular and cellular mechanisms underlying the tactile sensation
inferred← citeshttps://doi.org/10.1134/s2079086415040064openalex-snapshot
Genetic basis of skin sensitivity
inferred← citeshttps://doi.org/10.1146/annurev-cellbio-100913-013426openalex-snapshot
Feeling Force: Physical and Physiological Principles Enabling Sensory Mechanotransduction
inferred← citeshttps://doi.org/10.1159/000510890openalex-snapshot
Does Hyaluronidase Enhance Drug Penetration to Mechanoreceptors?
inferred← citeshttps://doi.org/10.1177/0278364912471865openalex-snapshot
Reaching in clutter with whole-arm tactile sensing
inferred← citeshttps://doi.org/10.1186/s13578-020-00522-zopenalex-snapshot
Structure, kinetic properties and biological function of mechanosensitive Piezo channels
inferred← citeshttps://doi.org/10.1242/dev.070847openalex-snapshot
Excitatory glutamate is essential for development and maintenance of the piloneural mechanoreceptor
inferred← citeshttps://doi.org/10.1242/dev.112169openalex-snapshot
Embryonic maturation of epidermal Merkel cells is controlled by a redundant transcription factor network
inferred← citeshttps://doi.org/10.1242/jcs.092353openalex-snapshot
Molecular force transduction by ion channels – diversity and unifying principles
inferred← citeshttps://doi.org/10.1242/jeb.060533openalex-snapshot
Associative learning between odorants and mechanosensory punishment in larval Drosophila
inferred← citeshttps://doi.org/10.1364/boe.7.002877openalex-snapshot
Investigation of mechanosensation in C elegans using light field calcium imaging
inferred← citeshttps://doi.org/10.1371/journal.pgen.1006151openalex-snapshot
Polycomb-Mediated Repression and Sonic Hedgehog Signaling Interact to Regulate Merkel Cell Specification during Skin Development
inferred← citeshttps://doi.org/10.1371/journal.pgen.1012106openalex-snapshot
Worm orthologues of cytokinesis-associated proteins CIT and ASPM regulate neuronal microtubule dynamics and polarity in C. elegans
inferred← citeshttps://doi.org/10.1371/journal.pone.0055001openalex-snapshot
The Star-Nosed Mole Reveals Clues to the Molecular Basis of Mammalian Touch
inferred← citeshttps://doi.org/10.1371/journal.pone.0084949openalex-snapshot
Water-Induced Finger Wrinkles Do Not Affect Touch Acuity or Dexterity in Handling Wet Objects
inferred← citeshttps://doi.org/10.1523/jneurosci.0522-13.2013openalex-snapshot
piezo2bRegulates Vertebrate Light Touch Response
inferred← citeshttps://doi.org/10.1523/jneurosci.1249-20.2020openalex-snapshot
Mechanosensory Signaling in Astrocytes
inferred← citeshttps://doi.org/10.1523/jneurosci.3942-12.2013openalex-snapshot
Runx1 Controls Terminal Morphology and Mechanosensitivity of VGLUT3-expressing C-Mechanoreceptors
inferred← citeshttps://doi.org/10.15252/emmm.202013347openalex-snapshot
Targeting the epigenetic addiction of Merkel cell carcinoma
inferred← citeshttps://doi.org/10.15760/honors.276openalex-snapshot
Defining Protein Interactions: Ankle Link Proteins of Stereocilia in Hair Cells
inferred← citeshttps://doi.org/10.17638/00016013openalex-snapshot
Vibrotactile perception of musical pitch
inferred← citeshttps://doi.org/10.21769/bioprotoc.4940openalex-snapshot
Resolving the in situ Three-Dimensional Structure of Fly Mechanosensory Organelles Using Serial Section Electron Tomography
inferred← citeshttps://doi.org/10.25772/a75b-6175openalex-snapshot
AVATAR, CYBORG, ICEVORG: SIMULACRA'S SCION
inferred← citeshttps://doi.org/10.26686/wgtn.17134067openalex-snapshot
Investigating the antinociceptive effects of N-docosahexaenoyl ethanolamine and novel kappa opioid receptor agonists
inferred← citeshttps://doi.org/10.3389/978-2-88963-463-7openalex-snapshot
From Stimulus to Behavioral Decision-Making
inferred← citeshttps://doi.org/10.3389/fbioe.2020.00289openalex-snapshot
Editorial: Mechanobiology: Emerging Tools and Methods
inferred← citeshttps://doi.org/10.3389/feduc.2020.582808openalex-snapshot
Tactile Hypersensitivity and “Overwhelming Subjectivity” in the Touch Experience of People With Congenital Deafblindness: Implications for a Touch-Based Pedagogy
inferred← citeshttps://doi.org/10.3389/fnbeh.2018.00239openalex-snapshot
Gentle Handling Attenuates Innate Defensive Responses to Visual Threats
inferred← citeshttps://doi.org/10.3389/fncel.2018.00130openalex-snapshot
Cell Mechanotransduction With Piconewton Forces Applied by Optical Tweezers
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/10.3389/fncir.2013.00047openalex-snapshot
Developmental and architectural principles of the lateral-line neural map
inferred← citeshttps://doi.org/10.3389/fnint.2011.00053openalex-snapshot
Anatomical Pathways Involved in Generating and Sensing Rhythmic Whisker Movements
inferred← citeshttps://doi.org/10.3389/fphys.2022.1093303openalex-snapshot
Photoablation at single cell resolution and its application in the Drosophila epidermis and peripheral nervous system
inferred← citeshttps://doi.org/10.3390/cells8070701openalex-snapshot
The Centrosome and the Primary Cilium: The Yin and Yang of a Hybrid Organelle
inferred← citeshttps://doi.org/10.3390/ijms20092266openalex-snapshot
Ion Channels Involved in Tooth Pain
inferred← citeshttps://doi.org/10.3390/ijms21176221openalex-snapshot
Peripheral Mechanobiology of Touch—Studies on Vertebrate Cutaneous Sensory Corpuscles
inferred← citeshttps://doi.org/10.3390/ijms24087637openalex-snapshot
SOX2-Sensing: Insights into the Role of SOX2 in the Generation of Sensory Cell Types in Vertebrates
inferred← citeshttps://doi.org/10.3390/reports2010004openalex-snapshot
Early Treatment with Growth Hormone (GH) and Rehabilitation Recovers Hearing in a Child with Cerebral Palsy
inferred← citeshttps://doi.org/10.3727/096368912x659925openalex-snapshot
In Search of the Pivot Point of Mechanotransduction: Mechanosensing of Stem Cells
inferred← citeshttps://doi.org/10.3791/54050openalex-snapshot
Cutaneous Surgical Denervation: A Method for Testing the Requirement for Nerves in Mouse Models of Skin Disease
inferred← citeshttps://doi.org/10.4161/fly.19249openalex-snapshot
Genetics and neurobiology of aggression in Drosophila
inferred← citeshttps://doi.org/10.5772/60883openalex-snapshot
Mechanical Sensing of Living Systems — From Statics to Dynamics
inferred← citeshttps://doi.org/10.5772/intechopen.91815openalex-snapshot
The Glial Cell of Human Cutaneous Sensory Corpuscles: Origin, Characterization, and Putative Roles
inferred← citeshttps://doi.org/10.5954/icarob.2019.os9-2openalex-snapshot
Tactileology; Haptic Informatics by using Tactile bit, T-bit
inferred← citeshttps://doi.org/10.64898/2026.09.27.754691openalex-snapshot
Cell type-resolved connectomic reconstruction of the spinal dorsal horn reveals sensory neuron synaptic organization and modality-specific inhibition
inferred← citeshttps://doi.org/10.70675/86d94a9az1f3ez4f45z9cdfzcbbb2714378dopenalex-snapshot
Développement par génie tissulaire d’un modèle de peau humaine innervée, vascularisée et immunocompétente pour l’étude des réactions inflammatoires cutanées
inferred← citeshttps://doi.org/10.70675/9d0090d2z02f1z4886z88dfz3be1509aaa7copenalex-snapshot
Rôle et régulation des co-transporteurs cation-chlorure NKCC1 et KCC3 dans les neurones sensitifs
inferred← citeshttps://doi.org/10.70675/b00291fezcae2z498az82e5zaf11f0672b45openalex-snapshot
Impact des activités synaptiques endogènes sur l'excitabilité cellulaire et le traitement sensoriel cortical : apports de l'état isoélectrique
inferred← citeshttps://doi.org/10.70675/ba020e0dzb058z4c55za932za8b2a533f153openalex-snapshot
Etude de l'implication des cellules de Merkel dans l'initiation du prurit mécanique
inferred← citeshttps://doi.org/10.70675/beb67c76z2e25z44feza3b2z59afcf689a5bopenalex-snapshot
Distributions et fonctions du canal Calcique Cav3.2 dans les voies somatosensorielles
inferred← citeshttps://doi.org/10.70675/d2187cf3z47a0z4420z8005zb0c6f6b4e73fopenalex-snapshot
Integration of sensory feedback in a closed-loop cortical brain-machine interface requires somatotopy
inferred← citeshttps://doi.org/10.70675/f2fa3de4z968bz4505zbb2ez213c572cc0b7openalex-snapshot
Sensibilité des cellules de Merkel humaines au froid : vers un rôle des complexes de Merkel dans la sensibilité thermique cutanée ?
inferred← citeshttps://doi.org/10.7554/elife.01901openalex-snapshot
The structure and organization of lanceolate mechanosensory complexes at mouse hair follicles
inferred← citeshttps://doi.org/10.7554/elife.12959openalex-snapshot
Neuronal processing of noxious thermal stimuli mediated by dendritic Ca2+ influx in Drosophila somatosensory neurons
inferred← citeshttps://doi.org/10.7554/elife.38883openalex-snapshot
Hair follicle epidermal stem cells define a niche for tactile sensation
inferred← citeshttps://doi.org/10.7554/elife.43226openalex-snapshot
Somatosensory neurons integrate the geometry of skin deformation and mechanotransduction channels to shape touch sensing
inferred← citeshttps://doi.org/10.7554/elife.76574openalex-snapshot
Drosophila mechanical nociceptors preferentially sense localized poking
inferred← citeshttps://doi.org/10.7907/wz8y-zm04openalex-snapshot
The Genomics of Stress-Induced Life Cycle Decisions in Nematodes
inferred← citeshttps://doi.org/10.7916/d83f4wq4openalex-snapshot
Modulation of touch sensitivity in Caenorhabditis elegans
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