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Similarities and differences in the innervation of mystacial vibrissal follicle–sinus complexes in the rat and cat: A confocal microscopic study
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1096-9861(19970825)385:2<149::aid-cne1>3.0.co;2-1openalex-snapshot
Comprehensive immunofluorescence and lectin binding analysis of vibrissal follicle sinus complex innervation in the mystacial pad of the rat
inferredcites →https://doi.org/10.1002/(sici)1096-9861(19970825)385:2<185::aid-cne2>3.0.co;2-yopenalex-snapshot
Comprehensive immunofluorescence and lectin binding analysis of intervibrissal fur innervation in the mystacial pad of the rat
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(19980817)398:1<98::aid-cne6>3.0.co;2-4openalex-snapshot
Merkel complexes of human digital skin: Three-dimensional imaging with confocal laser microscopy and double immunofluorescence
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/10.1002/1096-9861(20001016)426:2<259::aid-cne7>3.0.co;2-nopenalex-snapshot
Three-dimensional microanatomy of longitudinal lanceolate endings in rat vibrissae
inferredcites →https://doi.org/10.1002/ar.1091150202openalex-snapshot
The tactile hair follicles in the mouse
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.1091980410openalex-snapshot
The sensory innervation of primate eyelid
inferredcites →https://doi.org/10.1002/ar.1092230114openalex-snapshot
The ultrastructure of ruffini endings in the periodontal ligament of rat incisors with special reference to the terminal schwann cells (K‐cells)
inferredcites →https://doi.org/10.1002/cne.1365openalex-snapshot
Three‐dimensional mapping of brain neuropils in the cockroach, Diploptera punctata
inferredcites →https://doi.org/10.1002/cne.900230101openalex-snapshot
The tactile hair of the white rat
inferredcites →https://doi.org/10.1002/cne.901260305openalex-snapshot
The ultrastructure and innervation of rat vibrissae
inferredcites →https://doi.org/10.1002/cne.901660205openalex-snapshot
Receptive fields of barrels in the somatosensory neocortex of the rat
inferredcites →https://doi.org/10.1002/cne.901920403openalex-snapshot
Sensory nerve endings in rhesus monkey sinus hairs
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/10.1002/cne.902530110openalex-snapshot
Mystacial vibrissae representation within the trigeminal sensory nuclei of the cat
inferredcites →https://doi.org/10.1002/cne.903090102openalex-snapshot
Central projections of primary sensory neurons innervating different parts of the vibrissae follicles and intervibrissal skin on the mystacial pad of the rat
inferredcites →https://doi.org/10.1002/cne.903280206openalex-snapshot
Sensory innervation in the inner conical body of the vibrissal follicle‐sinus complex of the rat
inferredcites →https://doi.org/10.1002/cne.903330302openalex-snapshot
Sequential differentiation of sensory innervation in the mystacial pad of the ferret
inferredcites →https://doi.org/10.1002/cne.903370303openalex-snapshot
The innervation of the mystacial pad of the rat as revealed by PGP 9.5 immunofluorescence
inferredcites →https://doi.org/10.1002/cne.903510402openalex-snapshot
Innervation of the hard palate in the rat studied by anterograde transport of horseradish peroxidase conjugates
inferredcites →https://doi.org/10.1002/cne.903570402openalex-snapshot
Innervation of nonmystacial vibrissae in the adult rat
inferredcites →https://doi.org/10.1002/cne.903620409openalex-snapshot
Postnatal development of periodontal ruffini endings in rat incisors: An immunoelectron microscopic study using protein gene product 9.5 (PGP 9.5) antibody
inferredcites →https://doi.org/10.1002/jmor.1051530211openalex-snapshot
Structure of the sinus hair follicle in the big‐clawed shrew, Sorex unguiculatus
inferredcites →https://doi.org/10.1006/dbio.1997.8658openalex-snapshot
Differential Dependency of Cutaneous Mechanoreceptors on Neurotrophins, trk Receptors, and P75 LNGFR
inferredcites →https://doi.org/10.1007/978-3-642-45465-3openalex-snapshot
The Mechanoreceptors of the Mammalian Skin Ultrastructure and Morphological Classification
inferredcites →https://doi.org/10.1007/bf00239590openalex-snapshot
The innervation of the mystacial pad in the adult rat studied by anterograde transport of HRP conjugates
inferredcites →https://doi.org/10.1007/bf00407165openalex-snapshot
�ber die Feinstruktur der Rezeptoren an Sinushaaren
inferredcites →https://doi.org/10.1007/s002210050226openalex-snapshot
Alterations in mystacial pad innervation in the aged rat
inferredcites →https://doi.org/10.1016/0006-8993(69)90061-4openalex-snapshot
Coding of somatic sensory input by vibrissae neurons in the rat's trigeminal ganglion
inferredcites →https://doi.org/10.1016/0006-8993(78)90631-5openalex-snapshot
The pilo-ruffini complex: A non-sinus hair and associated slowly-adapting mechanoreceptor in primate facial skin
inferredcites →https://doi.org/10.1016/s0079-6123(08)63021-6openalex-snapshot
Chapter 28 Morphological features of thin sensory afferent fibers: a new interpretation of ‘nociceptor’ function
inferredcites →https://doi.org/10.1016/s0166-2236(99)01452-6openalex-snapshot
Dynamics of neuronal processing in rat somatosensory cortex
inferredcites →https://doi.org/10.1016/s0166-4328(97)83328-1openalex-snapshot
Functional architecture of the mystacial vibrissae
inferredcites →https://doi.org/10.1046/j.1460-9568.2000.00149.xopenalex-snapshot
Regulation of NGF‐family ligands and receptors in adulthood and senescence: correlation to degenerative and regenerative changes in cutaneous innervation
inferredcites →https://doi.org/10.1071/zo9740263openalex-snapshot
Innervation of vibrissa follicles in the marsupial Trichosurus vulpecula
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/science.2530630openalex-snapshot
The Neuron-Specific Protein PGP 9.5 Is a Ubiquitin Carboxyl-Terminal Hydrolase
inferredcites →https://doi.org/10.1126/science.7280690openalex-snapshot
Merkel Cell Receptors: Structure and Transducer Function
inferredcites →https://doi.org/10.1152/jn.1975.38.3.650openalex-snapshot
Afferent fibers from mystacial vibrissae of cats and seals
inferredcites →https://doi.org/10.1159/000155325openalex-snapshot
Vibrissae Structure in the Rhesus Monkey
inferredcites →https://doi.org/10.1163/156854289x00336openalex-snapshot
Touch Organs in the Hairy and Glabrous Skin of Some Mammals (an Ultrastructural Comparison)
inferredcites →https://doi.org/10.1523/jneurosci.20-16-06241.2000openalex-snapshot
Physiological and Anatomical Organization of Multiwhisker Response Interactions in the Barrel Cortex of Rats
inferredcites →https://doi.org/10.1523/jneurosci.20-19-07455.2000openalex-snapshot
Parallel Streams for the Relay of Vibrissal Information through Thalamic Barreloids
inferredcites →https://doi.org/10.2535/ofaj1936.67.5_365openalex-snapshot
Fine Structure of the Sinus Hair (Pillus labialis maxillaris) and its Microvascular Architecture in the Cat
inferredcites →https://doi.org/10.3109/07367228309144540openalex-snapshot
Quantitative Studies of Stimulus Coding in First-Order Vibrissa Afferents of Rats. 1. Receptive Field Properties and Threshold Distributions
inferredcites →https://doi.org/10.3109/07367228309144543openalex-snapshot
Quantitative Studies of Stimulus Coding in First-Order Vibrissa Afferents of Rats. 2. Adaptation and Coding of Stimulus Parameters
inferredcites →https://doi.org/10.3109/08990229009144697openalex-snapshot
Responses of Rat Trigeminal Ganglion Neurons to Movements of Vibrissae in Different Directions
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ASICs mediate fast excitatory synaptic transmission for tactile discrimination
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Peri-head distance coding in the mouse brainstem
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Non-competitive metabotropic glutamate 1 receptor antagonists block activity of slowly adapting type I mechanoreceptor units in the rat sinus hair follicle
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La médecine régénératrice : les cellules souches, les interactions cellulaires et matricielles dans la reconstruction cutanée et cornéenne par génie tissulaire
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Whisker sensory system – From receptor to decision
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2012.11.002openalex-snapshot
Barrel cortex function
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2021.102008openalex-snapshot
Of mice and monkeys: Somatosensory processing in two prominent animal models
inferred← citeshttps://doi.org/10.1016/j.tins.2008.10.002openalex-snapshot
Orthogonal coding of object location
inferred← citeshttps://doi.org/10.1016/j.zool.2020.125773openalex-snapshot
MORPHOLOGICAL DIVERSITY OF FACIAL VIBRISSAE IN Chaetophractus vellerosus (MAMMALIA, XENARTHRA, DASYPODIDAE) AND DIFFERENTIAL MECHANOPERCEPTION
inferred← citeshttps://doi.org/10.1016/s0896-6273(03)00671-8openalex-snapshot
Encoding of Vibrissal Active Touch
inferred← citeshttps://doi.org/10.1016/s1672-6529(16)60304-9openalex-snapshot
Analysis of the vibrissa parametric resonance causing a signal amplification during whisking behaviour
inferred← citeshttps://doi.org/10.1017/9781108676526openalex-snapshot
Evolution, Ecology and Conservation of Lorises and Pottos
inferred← citeshttps://doi.org/10.1017/9781108676526.003openalex-snapshot
Evolution, Morphology and the Fossil Record
inferred← citeshttps://doi.org/10.1017/9781108676526.005openalex-snapshot
What We Know (and Don’t Know) About the Fossil Records of Lorisids
inferred← citeshttps://doi.org/10.1017/9781108676526.007openalex-snapshot
Molecular Advances in Lorisid Taxonomy and Phylogeny
inferred← citeshttps://doi.org/10.1017/9781108676526.008openalex-snapshot
The Toothcomb ofKaranisia clarki
inferred← citeshttps://doi.org/10.1017/9781108676526.009openalex-snapshot
The Soft-Tissue Anatomy of the Highly Derived Hand ofPerodicticusRelative to the More GeneralisedNycticebus
inferred← citeshttps://doi.org/10.1017/9781108676526.010openalex-snapshot
MakingScentsof Olfactory Sensitivity in Lorises and Pottos
inferred← citeshttps://doi.org/10.1017/9781108676526.011openalex-snapshot
Allometric and Phylogenetic Diversity in Lorisiform Orbit Orientation
inferred← citeshttps://doi.org/10.1017/9781108676526.012openalex-snapshot
The Evolution of Social Organisation in Lorisiformes
inferred← citeshttps://doi.org/10.1017/9781108676526.013openalex-snapshot
Biomechanics of Loris Locomotion
inferred← citeshttps://doi.org/10.1017/9781108676526.014openalex-snapshot
What Role Did Gum-Feeding Play in the Evolution of the Lorises?
inferred← citeshttps://doi.org/10.1017/9781108676526.015openalex-snapshot
Ecology and Captive Management
inferred← citeshttps://doi.org/10.1017/9781108676526.018openalex-snapshot
Thermoregulation in Lorises
inferred← citeshttps://doi.org/10.1017/9781108676526.019openalex-snapshot
Home Range, Activity Budgets and Habitat Use in the Bengal Slow Loris (Nycticebus bengalensis) in Bangladesh
inferred← citeshttps://doi.org/10.1017/9781108676526.020openalex-snapshot
Behaviour of Pottos and Angwantibos
inferred← citeshttps://doi.org/10.1017/9781108676526.021openalex-snapshot
Positional Behaviour and Substrate Preference of Slow Lorises, with a Case Study ofNycticebus bengalensisin Northeast India
inferred← citeshttps://doi.org/10.1017/9781108676526.022openalex-snapshot
Sexual Differences in Feeding and Foraging of Released Philippine Slow Loris (Nycticebus menagensis)
inferred← citeshttps://doi.org/10.1017/9781108676526.023openalex-snapshot
Ranging Patterns of the Pygmy Slow Loris (Nycticebus pygmaeus) in a Mixed Deciduous Forest in Eastern Cambodia
inferred← citeshttps://doi.org/10.1017/9781108676526.024openalex-snapshot
Utilising Current and Historical Zoo Records to Provide an Insight into the Captive Biology of the Rarely Kept Species Pottos and Angwantibos
inferred← citeshttps://doi.org/10.1017/9781108676526.025openalex-snapshot
Mother–Infant Behaviours in Greater Slow Loris (Nycticebus coucang) Dyads Consisting of Mothers Pregnant at Confiscation and Their Sanctuary-Born Infants
inferred← citeshttps://doi.org/10.1017/9781108676526.026openalex-snapshot
Husbandry and Reproductive Management Recommendations for Captive Lorises and Pottos (Nycticebus,LorisandPerodicticus)
inferred← citeshttps://doi.org/10.1017/9781108676526.027openalex-snapshot
Research, Trade and Conservation
inferred← citeshttps://doi.org/10.1017/9781108676526.028openalex-snapshot
Trapping, Collaring and Monitoring the Lorisinae of Asia (Loris,Nycticebus) and Perodicticinae (Arctocebus,Perodicticus) of Africa
inferred← citeshttps://doi.org/10.1017/9781108676526.029openalex-snapshot
Evaluation of Field Techniques Used to Assess Populations of Pottos and Lorises
inferred← citeshttps://doi.org/10.1017/9781108676526.030openalex-snapshot
Occupancy Modelling as a Method to Study Slender Loris Density
inferred← citeshttps://doi.org/10.1017/9781108676526.031openalex-snapshot
Using Accelerometers to Measure Nocturnal Primate Behaviour
inferred← citeshttps://doi.org/10.1017/9781108676526.032openalex-snapshot
Distribution and Conservation Status of Slow Lorises in Indo-China
inferred← citeshttps://doi.org/10.1017/9781108676526.033openalex-snapshot
Wildlife Trade Research Methods
inferred← citeshttps://doi.org/10.1017/9781108676526.034openalex-snapshot
Online Imagery and Loris Conservation
inferred← citeshttps://doi.org/10.1017/9781108676526.035openalex-snapshot
Slow Lorises (Nycticebusspp.) as Photo Props on Instagram
inferred← citeshttps://doi.org/10.1017/9781108676526.036openalex-snapshot
Integrating Science and Puppetry to Inspire Teenagers in Rural Asia to Value Slow Lorises
inferred← citeshttps://doi.org/10.1017/9781108676526.037openalex-snapshot
Developing a Rescue and Rehabilitation Centre as a Reaction to the Extensive Illegal Wildlife Trade in Slow Lorises
inferred← citeshttps://doi.org/10.1017/cbo9780511994838.004openalex-snapshot
Biomimetic robots as scientific models: a view from the whisker tip
inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00291openalex-snapshot
Nature-Inspired Structural Materials for Flexible Electronic Devices
inferred← citeshttps://doi.org/10.1038/nn.3378openalex-snapshot
Pre-neuronal morphological processing of object location by individual whiskers
inferred← citeshttps://doi.org/10.1038/nn.3720openalex-snapshot
Spatiotemporal receptive fields of barrel cortex revealed by reverse correlation of synaptic input
inferred← citeshttps://doi.org/10.1038/nn.4221openalex-snapshot
On-going computation of whisking phase by mechanoreceptors
inferred← citeshttps://doi.org/10.1038/s41378-023-00560-wopenalex-snapshot
A nanonewton-scale biomimetic mechanosensor
inferred← citeshttps://doi.org/10.1038/s41467-024-55468-4openalex-snapshot
Three-dimensional architecture and linearized mapping of vibrissa follicle afferents
inferred← citeshttps://doi.org/10.1038/s41467-025-67514-wopenalex-snapshot
Club-like receptors respond to light touch but not to whisking
inferred← citeshttps://doi.org/10.1038/s41598-018-22628-8openalex-snapshot
Fetal extracellular matrix nerve wraps locally improve peripheral nerve remodeling after complete transection and direct repair in rat
inferred← citeshttps://doi.org/10.1038/s41598-019-40688-2openalex-snapshot
Optogenetic study of the response interaction among multi-afferent inputs in the barrel cortex of rats
inferred← citeshttps://doi.org/10.1038/s41598-021-92770-3openalex-snapshot
Conveyance of texture signals along a rat whisker
inferred← citeshttps://doi.org/10.1038/s41598-023-40675-8openalex-snapshot
Pre-neuronal processing of haptic sensory cues via dispersive high-frequency vibrational modes
inferred← citeshttps://doi.org/10.1038/s42003-023-04945-5openalex-snapshot
The functional anatomy of elephant trunk whiskers
inferred← citeshttps://doi.org/10.1038/s42003-025-08336-wopenalex-snapshot
Follicle architecture and innervation of functionally distinct rat vibrissae
inferred← citeshttps://doi.org/10.1071/am25023openalex-snapshot
The marsupial nasal system: a review of its structure, function, and evolutionary significance, with a focus on wombats
inferred← citeshttps://doi.org/10.1071/am25025openalex-snapshot
Whisker morphology and distribution in wombats: a comparative anatomical study
inferred← citeshttps://doi.org/10.1073/pnas.1301430110openalex-snapshot
Responses of hair follicle–associated structures to loss of planar cell polarity signaling
inferred← citeshttps://doi.org/10.1073/pnas.1610176113openalex-snapshot
Merkel disc is a serotonergic synapse in the epidermis for transmitting tactile signals in mammals
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/10.1080/08990220310001622951openalex-snapshot
Whisker plucking alters responses of rat trigeminal ganglion neurons
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/10.1088/1748-3182/2/4/s03openalex-snapshot
Using hardware models to quantify sensory data acquisition across the rat vibrissal array
inferred← citeshttps://doi.org/10.1088/1757-899x/1261/1/012013openalex-snapshot
Mechanical Sensing in Embodied Agents
inferred← citeshttps://doi.org/10.1093/acrefore/9780190264086.013.226openalex-snapshot
Sensing the Environment With Whiskers
inferred← citeshttps://doi.org/10.1093/cercor/bhw280openalex-snapshot
Layer-Specific Refinement of Sensory Coding in Developing Mouse Barrel Cortex
inferred← citeshttps://doi.org/10.1093/cercor/bhy038openalex-snapshot
Gap Junctions Interconnect Different Subtypes of Parvalbumin-Positive Interneurons in Barrels and Septa with Connectivity Unique to Each Subtype
inferred← citeshttps://doi.org/10.1098/rspb.2004.2882openalex-snapshot
Empirically inspired simulated electro-mechanical model of the rat mystacial follicle-sinus complex
inferred← citeshttps://doi.org/10.1098/rstb.2011.0155openalex-snapshot
Flow sensing by pinniped whiskers
inferred← citeshttps://doi.org/10.1098/rstb.2011.0164openalex-snapshot
Biomimetic vibrissal sensing for robots
inferred← citeshttps://doi.org/10.1098/rstb.2011.0166openalex-snapshot
Radial distance determination in the rat vibrissal system and the effects of Weber's law
inferred← citeshttps://doi.org/10.1101/024364openalex-snapshot
Prediction of Primary Somatosensory Neuron Activity During Active Tactile Exploration
inferred← citeshttps://doi.org/10.1101/2020.03.09.983387openalex-snapshot
Three-dimensional contact point determination and contour reconstruction during active whisking behavior of the awake rat
inferred← citeshttps://doi.org/10.1109/biorob.2018.8487886openalex-snapshot
Contact-Resistive Sensing of Touch and Airflow Using A Rat Whisker
inferred← citeshttps://doi.org/10.1109/fleps.2019.8792255openalex-snapshot
3D Recognition of Obstacles Using A Vibrissa-like Tactile Sensor
inferred← citeshttps://doi.org/10.1109/fpl.2008.4629930openalex-snapshot
Towards an “early neural circuit simulator”: A FPGA implementation of processing in the rat whisker system
inferred← citeshttps://doi.org/10.1109/icra57147.2024.10610850openalex-snapshot
A Biomorphic Whisker Sensor for Aerial Tactile Applications
inferred← citeshttps://doi.org/10.1109/icsens.2013.6688235openalex-snapshot
Contact sensing in a bio-inspired whisker driven by electroactive polymer artificial muscles
inferred← citeshttps://doi.org/10.1109/lra.2021.3062816openalex-snapshot
WhiskSight: A Reconfigurable, Vision-Based, Optical Whisker Sensing Array for Simultaneous Contact, Airflow, and Inertia Stimulus Detection
inferred← citeshttps://doi.org/10.1111/1749-4877.70064openalex-snapshot
Sensory Biology of the Franciscana ( Pontoporia blainvillei , Pontoporiidae, Cetartiodactyla): Ontogenetic Modifications of Vibrissae and Vibrissal Crypts
inferred← citeshttps://doi.org/10.1111/j.1439-0264.2004.00558.xopenalex-snapshot
The Scanning Electron and Light Microscopic Structure of Bovine Tactile Hair
inferred← citeshttps://doi.org/10.1111/j.1748-1716.2008.01925.xopenalex-snapshot
Genetic manipulation, whole‐cell recordings and functional imaging of the sensorimotor cortex of behaving mice
inferred← citeshttps://doi.org/10.1111/j.1749-6632.2011.06007.xopenalex-snapshot
A night in the life of a rat: vibrissal mechanics and tactile exploration
inferred← citeshttps://doi.org/10.1111/jnc.16135openalex-snapshot
Tactile sensory processing deficits in genetic mouse models of autism spectrum disorder
inferred← citeshttps://doi.org/10.1111/joa.13188openalex-snapshot
Anatomy of avian rictal bristles in Caprimulgiformes reveals reduced tactile function in open‐habitat, partially diurnal foraging species
inferred← citeshttps://doi.org/10.1111/joa.13345openalex-snapshot
The follicle‐sinus complex of the bottlenose dolphin (Tursiops truncatus). Functional anatomy and possible evolutional significance of its somato‐sensory innervation
inferred← citeshttps://doi.org/10.1111/joa.13655openalex-snapshot
Anatomy of bristles on the nares and rictus of western barn owls (Tyto alba)
inferred← citeshttps://doi.org/10.1126/sciadv.adt3068openalex-snapshot
Self-powered artificial vibrissal system with anemotaxis behavior
inferred← citeshttps://doi.org/10.1146/annurev-neuro-072116-031437openalex-snapshot
Lessons from Worm Dendritic Patterning
inferred← citeshttps://doi.org/10.1152/jn.00011.2015openalex-snapshot
Tactile signals transmitted by the vibrissa during active whisking behavior
inferred← citeshttps://doi.org/10.1152/jn.00054.2016openalex-snapshot
Variations in vibrissal geometry across the rat mystacial pad: base diameter, medulla, and taper
inferred← citeshttps://doi.org/10.1152/jn.00116.2019openalex-snapshot
Sensorimotor integration in the whisker somatosensory brain stem trigeminal loop
inferred← citeshttps://doi.org/10.1152/jn.00157.2005openalex-snapshot
Relationship Between Physiological Response Type (RA and SA) and Vibrissal Receptive Field of Neurons Within the Rat Trigeminal Ganglion
inferred← citeshttps://doi.org/10.1152/jn.00179.2015openalex-snapshot
Deflection of a vibrissa leads to a gradient of strain across mechanoreceptors in a mystacial follicle
inferred← citeshttps://doi.org/10.1152/jn.00333.2018openalex-snapshot
Layer 4 barrel cortex neurons retain their response properties during whisker replacement
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1152/jn.00419.2003openalex-snapshot
Protracted Development of Responses to Whisker Deflection in Rat Trigeminal Ganglion Neurons
inferred← citeshttps://doi.org/10.1152/jn.00571.2005openalex-snapshot
Responses of Trigeminal Ganglion Neurons to the Radial Distance of Contact During Active Vibrissal Touch
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