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Constraints on the deformation of the vibrissa within the follicle
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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/(sici)1096-9861(19971229)389:4<545::aid-cne1>3.0.co;2-0openalex-snapshot
Different distributions of the sensory and autonomic innervation among the microvasculature of the rat mystacial pad
inferredcites →https://doi.org/10.1002/(sici)1096-9861(19990906)411:4<550::aid-cne2>3.0.co;2-gopenalex-snapshot
Structure and innervation of the vibrissal follicle-sinus complex in the Australian water rat,Hydromys chrysogaster
inferredcites →https://doi.org/10.1002/(sici)1097-4687(199807)237:1<33::aid-jmor3>3.0.co;2-popenalex-snapshot
Ovarian growth and folliculogenesis in breeding and nonbreeding females of a social rodent, the Zambian common mole-rat,Cryptomys sp.
inferredcites →https://doi.org/10.1002/9780470510858openalex-snapshot
A First Course in Finite Elements
inferredcites →https://doi.org/10.1002/9780470510858.oth1openalex-snapshot
A First Course in Finite Elements
inferredcites →https://doi.org/10.1002/ar.1091760406openalex-snapshot
Innervation of the vibrissae of the California sea lion, Zalophus californianus
inferredcites →https://doi.org/10.1002/ar.21156openalex-snapshot
Muscle Architecture in the Mystacial Pad of the Rat
inferredcites →https://doi.org/10.1002/ar.23061openalex-snapshot
Are Vibrissae Viable Sensory Structures for Prey Capture in Northern Elephant Seals, M irounga angustirostris?
inferredcites →https://doi.org/10.1002/ar.23989openalex-snapshot
Good Vibrations: The Evolution of Whisking in Small Mammals
inferredcites →https://doi.org/10.1002/ar.a.20273openalex-snapshot
Microstructure and innervation of the mystacial vibrissal follicle‐sinus complex in bearded seals, Erignathus barbatus (Pinnipedia: Phocidae)
inferredcites →https://doi.org/10.1002/cne.10277openalex-snapshot
Similarities and differences in the innervation of mystacial vibrissal follicle–sinus complexes in the rat and cat: A confocal microscopic study
inferredcites →https://doi.org/10.1002/cne.10824openalex-snapshot
Somatosensory organization and behavior in naked mole‐rats: II. Peripheral structures, innervation, and selective lack of neuropeptides associated with thermoregulation and pain
inferredcites →https://doi.org/10.1002/cne.21446openalex-snapshot
Adaptations in the structure and innervation of follicle‐sinus complexes to an aquatic environment as seen in the Florida manatee ( Trichechus manatus latirostris )
inferredcites →https://doi.org/10.1002/cne.902520203openalex-snapshot
A comparative light microscopic analysis of the sensory innervation of the mystacial pad. I. Innervation of vibrissal follicle‐sinus complexes
inferredcites →https://doi.org/10.1002/cne.902520205openalex-snapshot
A comparative light microscopic analysis of the sensory innervation of the mystacial pad. II. The common fur between the vibrissae
inferredcites →https://doi.org/10.1007/bf00335250openalex-snapshot
On the histology and histochemistry of the snout and vibrissae of the common shrew (Sorex araneus L.)
inferredcites →https://doi.org/10.1007/bf02213989openalex-snapshot
The role of vibrissae in behavior: A status review
inferredcites →https://doi.org/10.1007/s10914-019-09467-8openalex-snapshot
The Evolution of the Maxillary Canal in Probainognathia (Cynodontia, Synapsida): Reassessment of the Homology of the Infraorbital Foramen in Mammalian Ancestors
inferredcites →https://doi.org/10.1007/s12078-008-9012-6openalex-snapshot
Merkel Cells in Somatosensation
inferredcites →https://doi.org/10.1016/0166-4328(89)90011-9openalex-snapshot
Rats can learn a roughness discrimination using only their vibrissal system
inferredcites →https://doi.org/10.1016/b978-0-12-065301-0.50019-4openalex-snapshot
Somatosensory Development
inferredcites →https://doi.org/10.1016/j.conb.2006.06.009openalex-snapshot
Active sensation: insights from the rodent vibrissa sensorimotor system
inferredcites →https://doi.org/10.1016/j.cub.2019.12.068openalex-snapshot
The Cellular and Mechanical Basis for Response Characteristics of Identified Primary Afferents in the Rat Vibrissal System
inferredcites →https://doi.org/10.1016/j.jbiomech.2011.08.027openalex-snapshot
Variation in Young's modulus along the length of a rat vibrissa
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.2007.12.024openalex-snapshot
Embodied Information Processing: Vibrissa Mechanics and Texture Features Shape Micromotions in Actively Sensing Rats
inferredcites →https://doi.org/10.1016/j.neuron.2017.03.045openalex-snapshot
Active Touch and Self-Motion Encoding by Merkel Cell-Associated Afferents
inferredcites →https://doi.org/10.1037/h0093009openalex-snapshot
A study of the sensory control in the rat.
inferredcites →https://doi.org/10.1038/443525aopenalex-snapshot
Robotic whiskers used to sense features
inferredcites →https://doi.org/10.1038/nature14905openalex-snapshot
A Cretaceous eutriconodont and integument evolution in early mammals
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/nn.3378openalex-snapshot
Pre-neuronal morphological processing of object location by individual whiskers
inferredcites →https://doi.org/10.1038/nn.4221openalex-snapshot
On-going computation of whisking phase by mechanoreceptors
inferredcites →https://doi.org/10.1038/s41598-019-42492-4openalex-snapshot
The Piezo2 ion channel is mechanically activated by low-threshold positive pressure
inferredcites →https://doi.org/10.1038/srep25604openalex-snapshot
Palaeoneurological clues to the evolution of defining mammalian soft tissue traits
inferredcites →https://doi.org/10.1086/283249openalex-snapshot
The Evolution of Endothermy in the Phylogeny of Mammals
inferredcites →https://doi.org/10.1109/jsen.2011.2114341openalex-snapshot
Characterization of Statical Properties of Rat's Whisker System
inferredcites →https://doi.org/10.1111/j.1469-7998.1977.tb04162.xopenalex-snapshot
Functional structure of the carpal and ventral vibrissae of the squirrel (Sciurus vulgaris)
inferredcites →https://doi.org/10.1111/j.1469-7998.1989.tb05008.xopenalex-snapshot
Diving in darkness: whiskers as sense organs of the ringed seal (Phoca hispida saimensis)
inferredcites →https://doi.org/10.1111/srt.12171openalex-snapshot
Measurement of the uniaxial mechanical properties of rat skin using different stress–strain definitions
inferredcites →https://doi.org/10.1113/jphysiol.1969.sp008721openalex-snapshot
The structure and function of a slowly adapting touch corpuscle in hairy skin
inferredcites →https://doi.org/10.1113/jphysiol.1973.sp010388openalex-snapshot
Functional characteristics of mechanoreceptors in sinus hair follicles of the cat
inferredcites →https://doi.org/10.1126/sciadv.1600716openalex-snapshot
Whiskers aid anemotaxis in rats
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.1203117openalex-snapshot
Fossil Evidence on Origin of the Mammalian Brain
inferredcites →https://doi.org/10.1137/1.9780898718003openalex-snapshot
Iterative Methods for Sparse Linear Systems
inferredcites →https://doi.org/10.1152/ajplegacy.1947.151.2.612openalex-snapshot
MECHANICS OF HUMAN ISOLATED VOLUNTARY MUSCLE
inferredcites →https://doi.org/10.1152/jn.00179.2015openalex-snapshot
Deflection of a vibrissa leads to a gradient of strain across mechanoreceptors in a mystacial follicle
inferredcites →https://doi.org/10.1152/jn.00372.2011openalex-snapshot
Mechanical signals at the base of a rat vibrissa: the effect of intrinsic vibrissa curvature and implications for tactile exploration
inferredcites →https://doi.org/10.1152/jn.00571.2005openalex-snapshot
Responses of Trigeminal Ganglion Neurons to the Radial Distance of Contact During Active Vibrissal Touch
inferredcites →https://doi.org/10.1152/jn.00707.2006openalex-snapshot
Biomechanical Models for Radial Distance Determination by the Rat Vibrissal System
inferredcites →https://doi.org/10.1152/jn.90783.2008openalex-snapshot
Active Touch Sensing in the Rat: Anticipatory and Regulatory Control of Whisker Movements During Surface Exploration
inferredcites →https://doi.org/10.1159/000047257openalex-snapshot
Microanatomy of Facial Vibrissae in the Florida Manatee: The Basis for Specialized Sensory Function and Oripulation
inferredcites →https://doi.org/10.1159/000264662openalex-snapshot
Aquatic Environment and Differentiation of Vibrissae: Comparison of Sinus Hair Systems of Ringed Seal, Otter and Pole Cat
inferredcites →https://doi.org/10.1159/000381415openalex-snapshot
Elaboration and Innervation of the Vibrissal System in the Rock Hyrax (Procavia capensis)
inferredcites →https://doi.org/10.1163/156853964x00030openalex-snapshot
Analysis of Sniffing of the Albino Rat 1)
inferredcites →https://doi.org/10.1371/journal.pbio.0050305openalex-snapshot
Neuronal Activity in Rat Barrel Cortex Underlying Texture Discrimination
inferredcites →https://doi.org/10.1371/journal.pbio.0060215openalex-snapshot
Texture Coding in the Rat Whisker System: Slip-Stick Versus Differential Resonance
inferredcites →https://doi.org/10.1371/journal.pcbi.1001120openalex-snapshot
The Morphology of the Rat Vibrissal Array: A Model for Quantifying Spatiotemporal Patterns of Whisker-Object Contact
inferredcites →https://doi.org/10.1371/journal.pone.0044272openalex-snapshot
Fast Feedback in Active Sensing: Touch-Induced Changes to Whisker-Object Interaction
inferredcites →https://doi.org/10.1523/jneurosci.10-08-02638.1990openalex-snapshot
Biometric analyses of vibrissal tactile discrimination in the rat
inferredcites →https://doi.org/10.1523/jneurosci.1707-12.2014openalex-snapshot
Modeling Forces and Moments at the Base of a Rat Vibrissa during Noncontact Whisking and Whisking against an Object
inferredcites →https://doi.org/10.1523/jneurosci.21-14-05374.2001openalex-snapshot
Whisker Deafferentation and Rodent Whisking Patterns: Behavioral Evidence for a Central Pattern Generator
inferredcites →https://doi.org/10.1523/jneurosci.3762-09.2010openalex-snapshot
Vibrissa-Based Object Localization in Head-Fixed Mice
inferredcites →https://doi.org/10.1523/jneurosci.3942-12.2013openalex-snapshot
Runx1 Controls Terminal Morphology and Mechanosensitivity of VGLUT3-expressing C-Mechanoreceptors
inferredcites →https://doi.org/10.1523/jneurosci.6695-10.2011openalex-snapshot
A Unifying Framework Underlying Mechanotransduction in the Somatosensory System
inferredcites →https://doi.org/10.2307/2007640openalex-snapshot
Computer Solution of Large Sparse Positive Definite Systems.
inferredcites →https://doi.org/10.3109/08990229509063138openalex-snapshot
Task- and Subject-Related Differences in Sensorimotor Behavior during Active Touch
inferredcites →https://doi.org/10.3389/fnana.2014.00121openalex-snapshot
Innervation patterns of sea otter (Enhydra lutris) mystacial follicle-sinus complexes
inferredcites →https://doi.org/10.5962/bhl.title.147207openalex-snapshot
A study of sensory control in the rat,
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.jcz.2023.09.004zenodo-depositor-declared
Architecture of vibrissae in eight rodent species of Ctenohystrica (Rodentia): A comparative SEM study
inferred← citeshttps://doi.org/10.1002/ar.25305openalex-snapshot
Functional anatomy of mystacial active sensing in rats
inferred← citeshttps://doi.org/10.1002/ar.25604openalex-snapshot
Synapsids and sensitivity: Broad survey of tetrapod trigeminal canal morphology supports an evolutionary trend of increasing facial tactile specialization in the mammal lineage
inferred← citeshttps://doi.org/10.1002/ar.70051openalex-snapshot
An elastic segment of the whisker shaft enables coding of the whisking phase via whisker torsion in rats and mice
inferred← citeshttps://doi.org/10.1007/s11259-024-10342-yopenalex-snapshot
Supplemental vibrissal extensions as an alternative to improve the tactile sensitivity of blind dogs – a preliminary approach investigation
inferred← citeshttps://doi.org/10.1016/j.conb.2021.01.008openalex-snapshot
Body language signals for rodent social communication
inferred← citeshttps://doi.org/10.1016/j.cub.2025.12.021openalex-snapshot
Active sensing: How the rat moves its whiskers
inferred← citeshttps://doi.org/10.1016/j.cub.2025.12.041openalex-snapshot
Biomechanical simplification of the motor control of whisking
inferred← citeshttps://doi.org/10.1038/s41378-023-00560-wopenalex-snapshot
A nanonewton-scale biomimetic mechanosensor
inferred← citeshttps://doi.org/10.1038/s41467-025-67672-xopenalex-snapshot
Vibrissae-inspired vision-based magnetic-actuated whisker
inferred← citeshttps://doi.org/10.1073/pnas.2020194118openalex-snapshot
Continuous, multidimensional coding of 3D complex tactile stimuli by primary sensory neurons of the vibrissal system
inferred← citeshttps://doi.org/10.1080/15502287.2025.2606699openalex-snapshot
Sphar -whisker: Analysis of a bio-inspired design for the follicle sinus complex
inferred← citeshttps://doi.org/10.1109/lra.2022.3191172openalex-snapshot
Bioinspired, Multifunctional, Active Whisker Sensors for Tactile Sensing of Mobile Robots
inferred← citeshttps://doi.org/10.1364/prj.599931openalex-snapshot
Bionic fiber whisker for vector force sensing
inferred← citeshttps://doi.org/10.1371/journal.pone.0269210openalex-snapshot
On the intrinsic curvature of animal whiskers
inferred← citeshttps://doi.org/10.70675/779d5bbaz5470z4faczb771z288a715634b1openalex-snapshot
Optimisation du retour sensoriel cortical dans le cadre d'une interface cerveau machine en boucle fermée
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