about
A genome-wide Drosophila screen for heat nociception identifies α2δ3 as an evolutionarily conserved pain gene.Knockout of the ASIC2 channel in mice does not impair cutaneous mechanosensation, visceral mechanonociception and hearingAblation of Sphingosine 1-Phosphate Receptor Subtype 3 Impairs Hippocampal Neuron Excitability In vitro and Spatial Working Memory In vivoCapsaicin, protons and heat: new excitement about nociceptors.Deletion of interleukin-6 signal transducer gp130 in small sensory neurons attenuates mechanonociception and down-regulates TRPA1 expression.Peripheral nerve regeneration and NGF-dependent neurite outgrowth of adult sensory neurons converge on STAT3 phosphorylation downstream of neuropoietic cytokine receptor gp130.Construction of a global pain systems network highlights phospholipid signaling as a regulator of heat nociception.Activated platelets release sphingosine 1-phosphate and induce hypersensitivity to noxious heat stimuli in vivo.Recent findings on how proinflammatory cytokines cause pain: peripheral mechanisms in inflammatory and neuropathic hyperalgesia.Interleukin-6-dependent influence of nociceptive sensory neurons on antigen-induced arthritis.Cannabinoids mediate analgesia largely via peripheral type 1 cannabinoid receptors in nociceptors.microRNAs in nociceptive circuits as predictors of future clinical applications.Therapeutic targeting of the ceramide-to-sphingosine 1-phosphate pathway in pain.Genetic evidence for an essential role of neuronally expressed IL-6 signal transducer gp130 in the induction and maintenance of experimentally induced mechanical hypersensitivity in vivo and in vitro.Stimulated prostaglandin E2 release from rat skin, in vitro.Changes in Ionic Conductance Signature of Nociceptive Neurons Underlying Fabry Disease Phenotype.Sphingosine 1-phosphate to p38 signaling via S1P1 receptor and Gαi/o evokes augmentation of capsaicin-induced ionic currents in mouse sensory neurons.Role of Rac and Cdc42 in lysophosphatidic acid-mediated cyclo-oxygenase-2 gene expression.Inflammatory mediators release calcitonin gene-related peptide from dorsal root ganglion neurons of the rat.Involvement of the proinflammatory cytokines tumor necrosis factor-alpha, IL-1 beta, and IL-6 but not IL-8 in the development of heat hyperalgesia: effects on heat-evoked calcitonin gene-related peptide release from rat skin.Gα(q/11) signaling tonically modulates nociceptor function and contributes to activity-dependent sensitization.Sphingosine-1-Phosphate and the S1P3 Receptor Initiate Neuronal Retraction via RhoA/ROCK Associated with CRMP2 Phosphorylation.Inhibitor kappaB Kinase beta deficiency in primary nociceptive neurons increases TRP channel sensitivity.Infection by human varicella-zoster virus confers norepinephrine sensitivity to sensory neurons from rat dorsal root ganglia.Pro- and anti-inflammatory actions of ricinoleic acid: similarities and differences with capsaicin.The nociceptor sensitization by bradykinin does not depend on sympathetic neurons.PKA/AKAP/VR-1 module: A common link of Gs-mediated signaling to thermal hyperalgesia.Varicella-zoster virus isolates, but not the vaccine strain OKA, induce sensitivity to alpha-1 and beta-1 adrenergic stimulation of sensory neurones in culture.The inflammatory mediators serotonin, prostaglandin E2 and bradykinin evoke calcium influx in rat sensory neurons.Fast Ca2+-induced potentiation of heat-activated ionic currents requires cAMP/PKA signaling and functional AKAP anchoring.Differences in calcium signalling in rat peripheral sensory neurons.Sphingosine-1-phosphate-induced nociceptor excitation and ongoing pain behavior in mice and humans is largely mediated by S1P3 receptor.Endogenous tumor necrosis factor alpha (TNFalpha) requires TNF receptor type 2 to generate heat hyperalgesia in a mouse cancer model.Social interaction and cocaine conditioning in mice increase spontaneous spike frequency in the nucleus accumbens or septal nuclei as revealed by multielectrode array recordings.Inflammatory mediators at acidic pH activate capsaicin receptors in cultured sensory neurons from newborn rats.Signatures of Altered Gene Expression in Dorsal Root Ganglia of a Fabry Disease Mouse Model.Methylene blue induces ongoing activity in rat cutaneous primary afferents and depolarization of DRG neurons via a photosensitive mechanism.Identification of voltage-gated K(+) channel beta 2 (Kvβ2) subunit as a novel interaction partner of the pain transducer Transient Receptor Potential Vanilloid 1 channel (TRPV1).Identification of Chloride Channels CLCN3 and CLCN5 Mediating the Excitatory Cl- Currents Activated by Sphingosine-1-Phosphate in Sensory Neurons.Reduced excitability of gp130-deficient nociceptors is associated with increased voltage-gated potassium currents and Kcna4 channel upregulation.
P50
Q24620790-08B8F40F-1AD0-4A93-A01E-67D5BA49C5C1Q28587926-DE718AEC-9F51-47A3-B0C0-65477DD66C90Q30827729-7BA62E78-6729-4075-803B-5F8CB3FAC648Q33594435-C24ADC0C-EF6C-47BF-8893-422BA971B5A4Q33935966-F4E36A17-6813-47B3-8830-EE1C26DC2D63Q34233497-0880965B-240D-400D-A2DB-75F5407D33BBQ34510177-CDC71209-E038-442B-B770-10232F59DB1EQ35522175-D96BF2F6-71EB-4CAD-B6C4-F36EA4BB604AQ35769711-BF630C49-16D2-4886-A42B-7B3AC1E2449BQ36304006-5C311994-D5B4-45FB-B542-907B0BE32050Q36447081-4961ACAB-5F7E-4AE5-A844-2CA6F632C685Q37233099-B2D38C1C-72A7-4278-83D5-9D267FE3CDD6Q38073981-AAAB7CD0-6EB5-4FCC-BD39-E876C9E2DDB9Q38765969-6B227680-E316-4526-B76B-36FAFCD302D0Q40855359-D282B33C-A067-4CDA-8E4E-3624FE1271F3Q41013852-354F9560-8AE7-4C73-85FD-393D4D170BB7Q41980318-6760791F-51CD-47B4-84DA-E022FDD8F419Q42157725-3B7C2D24-5447-41F5-9D8E-54B5F29DC931Q42489327-C6575305-AA46-4FC6-8132-737292459DEAQ42491715-52E729CF-74EF-481B-9A84-168AFA2DF4F6Q42497106-530E2C43-B1BB-4EBB-A2A3-2EE2E0D5306FQ42700486-E9A8F9D3-D2D7-4DA0-AC13-90BDE567EAA6Q43261415-B045D2F8-BCAC-43E7-BFA5-9E432F3A789BQ43568384-3C2ED74C-154A-41CA-B51A-8FDF66C0E0DFQ43727321-64CD7B62-FB88-44A8-B21B-3C740C688549Q43785000-F0DE5BE6-E224-45F6-B989-7D1805A85E99Q44012278-2A7CA50D-F5FB-4A8A-A917-DB3A8C975721Q44356021-E5FB500F-94AA-4CD3-AACC-A6D510F27E3BQ44390700-09B65158-0297-42AA-A79D-EEE751D08D83Q44436412-3D3BF14C-D85E-4C28-8608-466681DE0667Q44708400-C75C2366-C47B-4D8D-82CD-D8CB0E6BED8EQ46119380-C729E92E-1C29-4A0D-88E6-5373AF52241AQ46607378-D7352153-8552-4849-9DEF-0F5377AABD79Q47761962-6C2419FF-0EA9-40BF-9562-D020CD0F0242Q48490075-47D1753F-1D87-4695-B853-BB9300C6BB8DQ49296211-D1F0ED2C-E9F5-4A01-B992-98F21D69CDCFQ50526273-F23CD0A6-7066-4446-A1B0-49BA9B0980A9Q51751879-1CA96BC1-FB66-4CD4-84EB-07DA0EC71EDEQ52686040-6FF325FD-51D3-4D54-A5CB-B4C0EC5BB790Q53070307-1C53219A-8242-4B38-A2B0-D90FD820ED81
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Michaela Kress
@ast
Michaela Kress
@en
Michaela Kress
@es
Michaela Kress
@nl
type
label
Michaela Kress
@ast
Michaela Kress
@en
Michaela Kress
@es
Michaela Kress
@nl
prefLabel
Michaela Kress
@ast
Michaela Kress
@en
Michaela Kress
@es
Michaela Kress
@nl
P106
P31
P496
0000-0002-8921-7470