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Functional characteristics of mechanoreceptors in sinus hair follicles of the cat
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/archneur.1964.00460240025003openalex-snapshot
Somatotopic Organization of Trigeminal-Ganglion Neurones
inferredcites →https://doi.org/10.1002/aja.1001060206openalex-snapshot
Sensory hair follicles in mammalian skin: The tylotrich follicle
inferredcites →https://doi.org/10.1002/cne.901300406openalex-snapshot
Somatotopic organization in the spinal trigeminal nucleus, the dorsal column nuclei and related structures in the rat
inferredcites →https://doi.org/10.1002/cne.901360106openalex-snapshot
The fine morphology of the sensory receptor organs in the auricle of the rat
inferredcites →https://doi.org/10.1007/bf00234457openalex-snapshot
The sense of flutter-vibration evoked by stimulation of the hairy skin of primates: Comparison of human sensory capacity with the responses of mechanoreceptive afferents innervating the hairy skin of monkeys
inferredcites →https://doi.org/10.1007/bf00407165openalex-snapshot
�ber die Feinstruktur der Rezeptoren an Sinushaaren
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/10.1016/0014-4886(62)90030-4openalex-snapshot
A morphological and somatotopic analysis of single unit activity in the trigeminal sensory complex of the cat
inferredcites →https://doi.org/10.1016/0020-708x(60)90141-1openalex-snapshot
A method for curve-fitting by exponential functions
inferredcites →https://doi.org/10.1016/s0006-8993(71)80004-5openalex-snapshot
Microelectrode delineation of fine grain somatotopic organization of SmI cerebral neocortex in albino rat
inferredcites →https://doi.org/10.1083/jcb.3.3.331openalex-snapshot
ELECTRON MICROSCOPY OF THE PACINIAN CORPUSCLE
inferredcites →https://doi.org/10.1093/oxfordjournals.jmicro.a049523openalex-snapshot
The Fine Structure of the Palisade-type Sensory Endings in Relation to Hair Follicles *
inferredcites →https://doi.org/10.1111/j.1748-1716.1969.tb04584.xopenalex-snapshot
Structure and Function of the Tactile Hair Receptors on the Cat's Foreleg
inferredcites →https://doi.org/10.1111/j.1748-1716.1969.tb04585.xopenalex-snapshot
Hair Discs and Pacinian Corpuscles Functionally Associated with the Carpal Tactile Hairs in the Cat
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.1926.sp002273openalex-snapshot
The impulses produced by sensory nerve endings
inferredcites →https://doi.org/10.1113/jphysiol.1940.sp003841openalex-snapshot
Discharges from the sensory organs of the cat's vibrissae and the modification in their activity by ions
inferredcites →https://doi.org/10.1113/jphysiol.1950.sp004479openalex-snapshot
Depolarization of sensory terminals and the initiation of impulses in the muscle spindle
inferredcites →https://doi.org/10.1113/jphysiol.1960.sp006521openalex-snapshot
An analysis of fibre diameter and receptor characteristics of myelinated cutaneous afferent fibres in cat
inferredcites →https://doi.org/10.1113/jphysiol.1961.sp006784openalex-snapshot
The functional characteristics of single cells in the caudal part of the spinal nucleus of the trigeminal nerve of the cat
inferredcites →https://doi.org/10.1113/jphysiol.1967.sp008390openalex-snapshot
A quantitative study of cutaneous receptors and afferent fibres in the cat and rabbit
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.1971.sp009308openalex-snapshot
Two classes of slowly adapting mechanoreceptor fibres in reptile cutaneous nerve
inferredcites →https://doi.org/10.1113/jphysiol.1971.sp009377openalex-snapshot
Stimulus—response relationships in first‐order sensory fibres from cat vibrissae
inferredcites →https://doi.org/10.1113/jphysiol.1973.sp010099openalex-snapshot
The responses of cells in the rat thalamus to mechanical movements of the whiskers
inferredcites →https://doi.org/10.1126/science.147.3661.1043openalex-snapshot
Tylotrich (Hair) Follicle: Association with a Slowly Adapting Tactile Receptor in the Cat
inferredcites →https://doi.org/10.1152/jn.1961.24.6.621openalex-snapshot
SOME CHARACTERISTICS OF TRANSMISSION THROUGH SPINAL TRIGEMINAL NUCLEUS OF RAT
inferredcites →https://doi.org/10.1152/jn.1968.31.6.833openalex-snapshot
Receptor types in cat hairy skin supplied by myelinated fibers.
inferredcites →https://doi.org/10.3109/13813456009083545openalex-snapshot
Peripheral and Cortical Responses to Mechanical Stimulation of the Cat's Vibrissae
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/(sici)1096-9861(19961118)375:3<481::aid-cne10>3.0.co;2-popenalex-snapshot
Peripheral and central predictors of whisker afferent morphology in the rat brainstem
inferred← citeshttps://doi.org/10.1002/(sici)1096-9861(19970505)381:2<219::aid-cne8>3.0.co;2-6openalex-snapshot
Long-term effects of neonatal axoplasmic transport attenuation on the organization of the rat's trigeminal system
inferred← citeshttps://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
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1002/(sici)1097-4687(199707)233:1<53::aid-jmor5>3.0.co;2-popenalex-snapshot
Adaptive differentiations of the skin of the head in a subterranean rodent, Spalax ehrenbergi
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1002/ar.1091980410openalex-snapshot
The sensory innervation of primate eyelid
inferred← citeshttps://doi.org/10.1002/ar.1092140217openalex-snapshot
The sensory innervation of the rat rhinarium
inferred← citeshttps://doi.org/10.1002/ar.20742openalex-snapshot
The Relationship Between the Infraorbital Foramen, Infraorbital Nerve, and Maxillary Mechanoreception: Implications for Interpreting the Paleoecology of Fossil Mammals Based on Infraorbital Foramen Size
inferred← citeshttps://doi.org/10.1002/ar.23061openalex-snapshot
Are Vibrissae Viable Sensory Structures for Prey Capture in Northern Elephant Seals, M irounga angustirostris?
inferred← citeshttps://doi.org/10.1002/ar.23163openalex-snapshot
Sensory Hairs in the Bowhead Whale, B alaena mysticetus (Cetacea, Mammalia)
inferred← citeshttps://doi.org/10.1002/ar.a.10029openalex-snapshot
Friedrich Sigmund Merkel and his “Merkel cell”, morphology, development, and physiology: Review and new results
inferred← citeshttps://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)
inferred← citeshttps://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
inferred← citeshttps://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
inferred← citeshttps://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 )
inferred← citeshttps://doi.org/10.1002/cne.901640107openalex-snapshot
Comparative anatomical studies of the Sml face cortex with special reference to the occurrence of “barrels” in layer IV
inferred← citeshttps://doi.org/10.1002/cne.901920403openalex-snapshot
Sensory nerve endings in rhesus monkey sinus hairs
inferred← citeshttps://doi.org/10.1002/cne.902400106openalex-snapshot
Morphology of terminations of small and large myelinated trigeminal primary afferent fibers in the cat
inferred← citeshttps://doi.org/10.1002/cne.902430209openalex-snapshot
Structure‐function relationships in rat brainstem subnucleus interpolaris. I. Vibrissa primary afferents
inferred← citeshttps://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
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1002/cne.902640407openalex-snapshot
Morphological characteristics of low‐threshold primary afferents in the trigeminal subnuclei interpolaris and caudalis (the medullary dorsal horn) of the golden hamster
inferred← citeshttps://doi.org/10.1002/cne.903220209openalex-snapshot
Dual innervation of the rat vibrissa: Responses of trigeminal ganglion cells projecting through deep or superficial nerves
inferred← citeshttps://doi.org/10.1002/cne.903280206openalex-snapshot
Sensory innervation in the inner conical body of the vibrissal follicle‐sinus complex of the rat
inferred← citeshttps://doi.org/10.1002/cne.903370303openalex-snapshot
The innervation of the mystacial pad of the rat as revealed by PGP 9.5 immunofluorescence
inferred← citeshttps://doi.org/10.1002/cne.903370304openalex-snapshot
Structure, vascularization, and innervation of the mystacial pad of the rat as revealed by the lectin griffonia simplicifolia
inferred← citeshttps://doi.org/10.1002/cne.903570402openalex-snapshot
Innervation of nonmystacial vibrissae in the adult rat
inferred← citeshttps://doi.org/10.1002/cphy.cp010317openalex-snapshot
The Sense of Touch: Performance and Peripheral Neural Processes
inferred← citeshttps://doi.org/10.1002/j.2040-4603.1984.tb00889.xopenalex-snapshot
The Sense of Touch: Performance and Peripheral Neural Processes
inferred← citeshttps://doi.org/10.1002/jmor.20363openalex-snapshot
A complex sensory organ in the nose skin of the prosimian primate L emur catta
inferred← citeshttps://doi.org/10.1007/978-1-4613-0579-8_2openalex-snapshot
Sensory Innervation of the Hairless and Hairy Skin in Mammals including Humans
inferred← citeshttps://doi.org/10.1007/978-1-4615-0035-3_7openalex-snapshot
Functional Organization of Dorsal Horn Interneurons
inferred← citeshttps://doi.org/10.1007/978-1-4615-0037-7_7openalex-snapshot
Functional Organization of Dorsal Horn Interneurons
inferred← citeshttps://doi.org/10.1007/978-1-4757-9616-2_1openalex-snapshot
Comparative Aspects of Barrel Structure and Development
inferred← citeshttps://doi.org/10.1007/978-3-642-68421-0_4openalex-snapshot
Organe der Koordination und der Umweltbeziehungen
inferred← citeshttps://doi.org/10.1007/978-3-642-73797-8_10openalex-snapshot
Structure, Function and Control: Afferent Nerve Endings in the Skin
inferred← citeshttps://doi.org/10.1007/978-3-642-74612-3_7openalex-snapshot
Specific Nerve Endings in Vellus Hair, Guard Hair, and Sinus Hair
inferred← citeshttps://doi.org/10.1007/978-3-642-76690-9_8openalex-snapshot
Comparative Physiology of Cutaneous Mechanoreceptors
inferred← citeshttps://doi.org/10.1007/978-3-642-81055-8_78openalex-snapshot
Thalamo-Cortical Response Transformation in the Cortical Whisker Projection Area of the Cat
inferred← citeshttps://doi.org/10.1007/978-3-642-81650-5_8openalex-snapshot
Cytochemistry of Merkel Cell-neurite Complex in Mouse Sinus Hair Follicles
inferred← citeshttps://doi.org/10.1007/978-3-662-10358-6_16openalex-snapshot
Merkel Cells Are Postmitotic Cells of Neural Crest Origin
inferred← citeshttps://doi.org/10.1007/978-3-663-01719-6_12openalex-snapshot
Cutaneous Mechanoreceptors in Simple and in Complex Sensory Structures
inferred← citeshttps://doi.org/10.1007/bf00191851openalex-snapshot
Tactile size discrimination by a California sea lion (Zalophus californianus) using its mystacial vibrissae
inferred← citeshttps://doi.org/10.1007/bf00227259openalex-snapshot
Cytoplasmic Ca2+ concentrations in intact Merkel cells of an isolated, functioning rat sinus hair preparation
inferred← citeshttps://doi.org/10.1007/bf00229133openalex-snapshot
Selective phototoxic destruction of quinacrine-loaded Merkel cells is neither selective nor complete
inferred← citeshttps://doi.org/10.1007/bf00231542openalex-snapshot
The peripheral morphological basis of tactile sensibility in the beak of geese
inferred← citeshttps://doi.org/10.1007/bf00235004openalex-snapshot
A comparison of primary afferent and cortical neurone activity coding sinus hair movements in the cat
inferred← citeshttps://doi.org/10.1007/bf00236470openalex-snapshot
Neurones in the spinal trigeminal nucleus of the cat responding to movement of the vibrissae
inferred← citeshttps://doi.org/10.1007/bf00237533openalex-snapshot
Spatio-temporal patterns of pre- and postsynaptic inhibition induced by primary afferent activation in the trigeminal sensory nucleus in cats
inferred← citeshttps://doi.org/10.1007/bf00238833openalex-snapshot
The vibrissal pad as a source of sensory information for the oculomotor system of the cat
inferred← citeshttps://doi.org/10.1007/bf00583397openalex-snapshot
A new combination of methods for the localization, identification, and three-dimensional reconstruction of the sensory endings of articular afferents characterized by electrophysiology
inferred← citeshttps://doi.org/10.1007/bf00624349openalex-snapshot
The physiological basis of tactile sensibility in the beak of geese
inferred← citeshttps://doi.org/10.1007/bf00799450openalex-snapshot
Afferent impulses from skin receptors in response to a jet of air
inferred← citeshttps://doi.org/10.1007/bf01062836openalex-snapshot
Responses of neurons in the vibrissae projection area of the cat somatosensory cortex to afferent activation
inferred← citeshttps://doi.org/10.1007/bf01063355openalex-snapshot
EPSPs of masseter motoneurons evoked by stimulation of low-threshold infraorbital nerve afferents in cat
inferred← citeshttps://doi.org/10.1007/bf01063521openalex-snapshot
EPSPs of masseter motoneurons evoked by stimulation of low-threshold infraorbital nerve afferents in cat
inferred← citeshttps://doi.org/10.1007/bf01065301openalex-snapshot
Somatosensory cortical unit responses to stimulation of the vibrissae in cats
inferred← citeshttps://doi.org/10.1007/bf01071721openalex-snapshot
Action potentials of masseter motoneurons evoked by stimulation of low-threshold infraorbital nerve afferents in cats
inferred← citeshttps://doi.org/10.1007/bf01181555openalex-snapshot
Merkel cells are not the mechanosensory transducers in the touch dome of the rat
inferred← citeshttps://doi.org/10.1007/bf01208608openalex-snapshot
Evidence against transmitter function of met-enkephalin and chemosynaptic impulse generation in ?Merkel cell? mechanoreceptors
inferred← citeshttps://doi.org/10.1007/bf01839339openalex-snapshot
Afferent activity in the superior spermatic nerve of lambs — The effects of application of rubber castration rings
inferred← citeshttps://doi.org/10.1007/bf02213989openalex-snapshot
The role of vibrissae in behavior: A status review
inferred← citeshttps://doi.org/10.1007/s00221-003-1623-1openalex-snapshot
Temporal shaping of phasic neuronal responses by GABA- and non-GABA-mediated mechanisms in the somatosensory thalamus of the rat
inferred← citeshttps://doi.org/10.1007/s002210050226openalex-snapshot
Alterations in mystacial pad innervation in the aged rat
inferred← citeshttps://doi.org/10.1007/s00359-012-0778-2openalex-snapshot
Hydrodynamic perception in true seals (Phocidae) and eared seals (Otariidae)
inferred← citeshttps://doi.org/10.1007/s00359-020-01408-8openalex-snapshot
Pinnipeds orient and control their whiskers: a study on Pacific walrus, California sea lion and Harbor seal
inferred← citeshttps://doi.org/10.1007/s00422-007-0208-7openalex-snapshot
Spike-timing in primary sensory neurons: a model of somatosensory transduction in the rat
inferred← citeshttps://doi.org/10.1007/s00441-003-0816-zopenalex-snapshot
Innervation of the maxillary vibrissae in mice as revealed by anterograde and retrograde tract tracing
inferred← citeshttps://doi.org/10.1007/s004410050031openalex-snapshot
Epithelial Na + channels and stomatin are expressed in rat trigeminal mechanosensory neurons
inferred← citeshttps://doi.org/10.1007/s11515-013-1271-1openalex-snapshot
The anatomy, function, and development of mammalian Aβ low-threshold mechanoreceptors
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/0006-8993(79)90694-2openalex-snapshot
The organization of projections to selected points of somatosensory cortex from the cat ventrobasal complex
inferred← citeshttps://doi.org/10.1016/0006-8993(79)90801-1openalex-snapshot
Tactile neurons of the superior colliculus of the cat: Input and physiological properties
inferred← citeshttps://doi.org/10.1016/0006-8993(84)91165-xopenalex-snapshot
Axon arbors of functionally distinct whisker afferents are similar in medullary dorsal horn
inferred← citeshttps://doi.org/10.1016/0006-8993(88)90572-0openalex-snapshot
An electron microscopic analysis of the morphology and connectivity of individual HRP-labeled slowly adapting vibrissa primary afferents in the adult rat
inferred← citeshttps://doi.org/10.1016/0006-8993(94)91227-0openalex-snapshot
Amino acids modify thalamo-cortical response transformation expressed by neurons of the ventrobasal complex
inferred← citeshttps://doi.org/10.1016/0013-4694(79)90111-1openalex-snapshot
Projections on the cortical somatic I barrel subfield from ipsilateral vibrissae in adult rodents
inferred← citeshttps://doi.org/10.1016/0014-4886(75)90022-9openalex-snapshot
Physiological properties of neurons in the principal sensory trigeminal nucleus of the cat
inferred← citeshttps://doi.org/10.1016/0022-202x(93)90505-copenalex-snapshot
Sensory innervation of the hairy skin (light-and electronmicroscopic study)
inferred← citeshttps://doi.org/10.1016/0165-0173(83)90021-8openalex-snapshot
The sensory innervation of primate facial skin. I. Hairy skin
inferred← citeshttps://doi.org/10.1016/0301-0082(78)90019-9openalex-snapshot
The anatomy and physiology of the somatic sensory cortical regions
inferred← citeshttps://doi.org/10.1016/0301-0082(92)90013-5openalex-snapshot
Plasticity of the barrel cortex neurons
inferred← citeshttps://doi.org/10.1016/0301-0082(96)00018-4openalex-snapshot
The Merkel cell as a possible mechanoreceptor cell
inferred← citeshttps://doi.org/10.1016/0304-3940(76)90053-7openalex-snapshot
Responses evoked in mouse and rat SI cortex by vibrissa stimulation
inferred← citeshttps://doi.org/10.1016/0304-3940(77)90036-2openalex-snapshot
Functional maturation of rat trigeminal nerve
inferred← citeshttps://doi.org/10.1016/0304-3940(96)12813-5openalex-snapshot
An isolated rat vibrissal preparation with stable responses of slowly adapting mechanoreceptors
inferred← citeshttps://doi.org/10.1016/0304-3940(96)12906-2openalex-snapshot
Chloroquine specifically impairs Merkel cell mechanoreceptor function in isolated rat sinus hairs
inferred← citeshttps://doi.org/10.1016/0306-4522(93)90327-copenalex-snapshot
Morphological and electrophysiological peculiarities of sensory bush-like receptors of the frog urinary bladder
inferred← citeshttps://doi.org/10.1016/b978-0-08-028892-5.50017-7openalex-snapshot
ORAL MECHANORECEPTORS
inferred← citeshttps://doi.org/10.1016/b978-0-12-065301-0.50019-4openalex-snapshot
Somatosensory Development
inferred← citeshttps://doi.org/10.1016/b978-0-12-374236-0.10031-8openalex-snapshot
Trigeminal Sensory System
inferred← citeshttps://doi.org/10.1016/b978-0-12-805408-6.00340-7openalex-snapshot
Cutaneous Mechanisms of Tactile Perception: Morphological and Chemical Organization of the Innervation to the Skin
inferred← citeshttps://doi.org/10.1016/b978-0-12-805408-6.00361-4openalex-snapshot
Specialized Somatosensory Systems
inferred← citeshttps://doi.org/10.1016/b978-012370880-9.00340-6openalex-snapshot
Cutaneous Mechanisms of Tactile Perception: Morphological and Chemical Organization of the Innervation to the Skin
inferred← citeshttps://doi.org/10.1016/b978-012370880-9.00361-3openalex-snapshot
Specialized Somatosensory Systems
inferred← citeshttps://doi.org/10.1016/b978-012547638-6/50027-4openalex-snapshot
Trigeminal Sensory System
inferred← citeshttps://doi.org/10.1016/j.brainresbull.2014.01.007openalex-snapshot
Involvement of trigeminal mesencephalic nucleus in kinetic encoding of whisker movements
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.ibneur.2022.07.002openalex-snapshot
Effects of camphor and related compounds on slowly adapting mechanoreceptors in the rat sinus hair follicle
inferred← citeshttps://doi.org/10.1016/j.ibneur.2022.09.008openalex-snapshot
Reducing Merkel cell activity in the whisker follicle disrupts cortical encoding of whisker movement amplitude and velocity
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.jneumeth.2008.03.004openalex-snapshot
A two-dimensional force sensor in the millinewton range for measuring vibrissal contacts
inferred← citeshttps://doi.org/10.1016/j.neulet.2019.134321openalex-snapshot
Functional properties of mechanoreceptors in mouse whisker hair follicles determined by the pressure-clamped single-fiber recording technique
inferred← citeshttps://doi.org/10.1016/j.neuron.2019.08.042openalex-snapshot
TREK-1 and TRAAK Are Principal K+ Channels at the Nodes of Ranvier for Rapid Action Potential Conduction on Mammalian Myelinated Afferent Nerves
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2007.06.018openalex-snapshot
A pharmacological study of slowly adapting mechanoreceptors responsive to cold thermal stimulation
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.pbb.2008.09.011openalex-snapshot
Activation of mu, delta or kappa opioid receptors by DAMGO, DPDPE, U-50488 or U-69593 respectively causes antinociception in the formalin test in the naked mole-rat (Heterocephalus glaber)
inferred← citeshttps://doi.org/10.1016/j.robot.2006.08.001openalex-snapshot
Biomimetic whiskers for shape recognition
inferred← citeshttps://doi.org/10.1016/s0024-3205(00)00465-3openalex-snapshot
Expressions of putative neurotransmitters and neuronal growth related genes in merkel cell-neurite complexes of the rats
inferred← citeshttps://doi.org/10.1016/s0034-5288(18)30754-9openalex-snapshot
The afferent innervation of the face of sheep and goats
inferred← citeshttps://doi.org/10.1016/s0079-6123(08)64334-4openalex-snapshot
Is the Physiology of Cutaneous Receptors Determined by Morphology?
inferred← citeshttps://doi.org/10.1016/s0079-6123(08)64353-8openalex-snapshot
The Mechanoreceptors of the Sinus Hair Organ on the Cat's Foreleg
inferred← citeshttps://doi.org/10.1016/s0896-6273(03)00671-8openalex-snapshot
Encoding of Vibrissal Active Touch
inferred← citeshttps://doi.org/10.1021/acs.nanolett.5c00818openalex-snapshot
Bioinspired 3D-Nanoprinted Optical Sensilla for Bidirectional Respiratory Monitoring
inferred← citeshttps://doi.org/10.1023/b:neur.0000044196.45602.92openalex-snapshot
Merkel cells, corpuscular nerve endings and free nerve endings in the mouse palatine mucosa express three subtypes of vesicular glutamate transporters
inferred← citeshttps://doi.org/10.1037//0033-2909.84.3.477openalex-snapshot
Behavioral and neural approaches to the function of the mystacial vibrissae.
inferred← citeshttps://doi.org/10.1039/c9tc05392aopenalex-snapshot
Biomimetics for high-performance flexible tactile sensors and advanced artificial sensory systems
inferred← citeshttps://doi.org/10.1073/pnas.1018740108openalex-snapshot
Bat wing sensors support flight control
inferred← citeshttps://doi.org/10.1080/08990220050020580openalex-snapshot
Coding of deflection velocity and amplitude by whisker primary afferent neurons: implications for higher level processing
inferred← citeshttps://doi.org/10.1080/08990220802467612openalex-snapshot
Response properties of mouse trigeminal ganglion neurons
inferred← citeshttps://doi.org/10.1080/10236248309378593openalex-snapshot
The response of horseshoe crab lateral spine mechanoreceptors to slow ramp stimuli
inferred← citeshttps://doi.org/10.1088/1361-6528/abe6c7openalex-snapshot
Nanomaterials and their applications on bio-inspired wearable electronics
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.001.0001openalex-snapshot
The Head-Neck Sensory Motor System
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.002.0003openalex-snapshot
Copyright Page
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.002.0004openalex-snapshot
Contributors
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.002.0006openalex-snapshot
Investigations Relating to the Head-Neck Movement System Around the Time of the French Revolution (1789)
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0001openalex-snapshot
The Upright Head in Hominid Evolution
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0002openalex-snapshot
Why Develop a Neck?
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0003openalex-snapshot
Evolution of the Dorsal Muscles of the Spine in Light of Their Adaptation to Gravity Effects
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0004openalex-snapshot
Modeling of the Craniofacial Architecture during Ontogenesis and Phylogenesis
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0005openalex-snapshot
Stabilizing Head/Eye Movements in the BlowflyCalliphora erythrocephala
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0006openalex-snapshot
The Head-Neck System of the BlowflyCalliphora:1. Anatomic Organization of Neck Muscles, Motoneurons, and Multimodal and Visual Inputs
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0007openalex-snapshot
The Head-Neck System of the BlowflyCalliphora:2. Functional Organization and Comparisons with the Sphinx MothManduca sexta
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0008openalex-snapshot
The Absence of a True Head-Neck in Decapod Crustaceans: Consequences for Orientation and Equilibration
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0009openalex-snapshot
Neural Processes between Visual Sign Stimuli and Head Movements in Toads
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0010openalex-snapshot
Control of Gaze in Salamanders
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0011openalex-snapshot
Reflex Contributions to the Control of Head Movement in the Lizard
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0012openalex-snapshot
Optocollic Reflexes and Neck Flexion—Related Activity of Flight Control Muscles in the Airflow-Stimulated Pigeon
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0013openalex-snapshot
Comparison of Head Movement Strategies among Mammals
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0014openalex-snapshot
Development of the Vertebral Joints (C3 through T2) in Man
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0015openalex-snapshot
Head Position and Posture in Newborn Infants
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0016openalex-snapshot
Head-Trunk Coordination and Locomotor Equilibrium in 3-to 8-Year-Old Children
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0017openalex-snapshot
Skeletal Geometry in Vertebrates and Its Relation to the Vestibular End Organs
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0018openalex-snapshot
The Cervical Spine, from Anatomy and Physiology to Clinical Care
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0019openalex-snapshot
Heterogeneous Structure and Function among Intervertebral Muscles
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0020openalex-snapshot
Relationship between Force and Cross-Sectional Area of Postcervical Muscles in Man: Influence of Variations in the Morphology of the Neck
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0021openalex-snapshot
Biomechanical Models of the Head-Neck System
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0022openalex-snapshot
Muscle Behavior May Solve Motor Coordination Problems
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0023openalex-snapshot
Multidimensional Geometry Intrinsic to Head Movements around Distributed Centers of Rotation: A Neurocomputer Paradigm
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0024openalex-snapshot
Somatosensory Pathways from the Neck
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0025openalex-snapshot
Physiologic Properties and Central Actions of Neck Muscle Spindles
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0026openalex-snapshot
Excitatory and Inhibitory Mechanisms Involved in the Dynamic Control of Posture during the Cervicospinal Reflexes
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0027openalex-snapshot
Suppression of Cervical Afferents Impairs Visual Cortical Cells Development
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0028openalex-snapshot
Eye and Neck Proprioceptive Messages Contribute to the Specification of Gaze Direction in Visually Oriented Activities
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0029openalex-snapshot
Influence of Neck Receptor Stimulation on Eye Rotation and on the Subjective Vertical: Experiments on the Tilt Table, under Water, and in Weightlessness
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0030openalex-snapshot
Cervico-ocular Reflexes with and without Simultaneous Vestibular Stimulation in Rabbits
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0031openalex-snapshot
Vestibular and Optokinetic Asymmetries in the Ocular and Cervical Reflexes
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0032openalex-snapshot
Cervicovestibular Interactions in Coriolis-Like Effects
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0033openalex-snapshot
Gravitational, Inertial, and Coriolis Force Influences on Nystagmus, Motion Sickness, and Perceived Head Trajectory
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0034openalex-snapshot
Head Position versus Head Motion in the Inhibition of Horizontal Postrotary Nystagmus
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0035openalex-snapshot
Intrinsic Properties of Neck Motoneurons
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0036openalex-snapshot
Organization of the Motor Nuclei Innervating Epaxial Muscles in the Neck and Back
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0037openalex-snapshot
Eye and Head Movements as Specialized Functions of Vestibular Circuits
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0038openalex-snapshot
Electrophysiology and Pharmacology of Two Types of Neurons in the Medial Vestibular Nucleus and Nucleus Gigantocellularis of the Guinea Pig In Vitro
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0039openalex-snapshot
Examination of the Descending Projections of the Vestibular Nuclei Using Anterograde Transport ofPhaseolus vulgarisLeukoagglutinin
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0040openalex-snapshot
Vestibular Nerve Inputs to Vestibulospinal and Vestibulo-ocular Neurons of the Squirrel Monkey
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0041openalex-snapshot
Spatial Innervation Patterns of Single Vestibulospinal Axons in Neck Motor Nuclei
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0042openalex-snapshot
Properties of Vestibulo-ocular and/or Vestibulocollic Neurons in the Cat
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0043openalex-snapshot
Eye Movement–Related Activity in the Vestibulo-ocular and Vestibulocollic Pathways in the Cat
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0044openalex-snapshot
Single Vestibular Unit Recordings in the Alert Cat during Active and Passive Head Movements
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0045openalex-snapshot
The Superior Colliculus and Head Movements in the Cat
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0046openalex-snapshot
Properties of Eye and Head Movements Evoked by Electrical Stimulation of the Monkey Superior Colliculus
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0047openalex-snapshot
Role of the Tectoreticulospinal System in the Coordination of Eye-Head Orienting Movements
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0048openalex-snapshot
Retrograde Axonal Transport of Fluorescent Tracers from Medullary Reticular Structures to the “Neck” and “Forelimb” Segments of the Cervical Spinal Cord
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0049openalex-snapshot
Reticulospinal Control of Head Movements in the Cat
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0050openalex-snapshot
Contribution of Reticulospinal Neurons to the Dynamic Control of Head Movements: Presumed Neck Bursters
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0051openalex-snapshot
Involvement of the Interstitial Nucleus of Cajal in the Midbrain Reticular Formation in the Position-Related, Tonic Component of Vertical Eye Movement and Head Posture
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0052openalex-snapshot
Control of Vertical Head Movement via Forel's Field H
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0053openalex-snapshot
Role of the Lateral Mesencephalic Reticular Formation in the Control of Head Movements
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0054openalex-snapshot
Brain Stem Control of Coordinated Eye-Head Gaze Shifts
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0055openalex-snapshot
Electromyographic Activity of Neck Muscles in Relation to the Initiation of Head Turning Induced by Stimulation of the Caudate Nucleus in the Cat
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0056openalex-snapshot
From Interdepedent to Independent Control of Head and Trunk
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0057openalex-snapshot
Multidimensional Analysis of Head Stabilization—Progress and Prospects
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0058openalex-snapshot
Multiple Control Mechanisms Contribute to Functional Behaviors of the Head and Neck
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0059openalex-snapshot
Listing's Law for Gaze-Directing Head Movements
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0060openalex-snapshot
Sensitivity Analysis of a Human Head Movement Model
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0061openalex-snapshot
Non-linear Dynamics of Involuntary Head Movements
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0062openalex-snapshot
Active Head Movement Analysis of Vestibulo-ocular Reflex Dynamics
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0063openalex-snapshot
Eye-Head Main Sequence in Midsagittal Vertical Plane in Humans
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0064openalex-snapshot
Effect of Freeing the Head on Eye Movement Characteristics during Three-Dimensional Shifts of Gaze and Tracking
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195068207.003.0065openalex-snapshot
Coordination of Head and Eyes during the Performance of Natural (and Unnatural) Visual Tasks
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