Ligand-induced dynamic membrane changes and cell deletion conferred by vanilloid receptor 1 - Wikidata - wikimedia - TriplyDB

Ligand-induced dynamic membrane changes and cell deletion conferred by vanilloid receptor 1

Ligand-induced dynamic membrane changes and cell deletion conferred by vanilloid receptor 1

http://www.wikidata.org/entity/Q28140829

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Deletion of vanilloid receptor 1-expressing primary afferent neurons for pain control TRPV1: a target for next generation analgesics Endocannabinoids in the retina: from marijuana to neuroprotection Resiniferatoxin: The Evolution of the "Molecular Scalpel" for Chronic Pain Relief Integrating TRPV1 Receptor Function with Capsaicin Psychophysics Functionally important amino acid residues in the transient receptor potential vanilloid 1 (TRPV1) ion channel--an overview of the current mutational data CT-guided injection of a TRPV1 agonist around dorsal root ganglia decreases pain transmission in swine.Use of Capsaicin to Treat Pain: Mechanistic and Therapeutic Considerations Neuroprotective effect of erythropoietin against pressure ulcer in a mouse model of small fiber neuropathy Golgi inheritance in mammalian cells is mediated through endoplasmic reticulum export activities.Ablation of TrpV1 neurons reveals their selective role in thermal pain sensation.Anti-calmodulins and tricyclic adjuvants in pain therapy block the TRPV1 channel Human keratinocytes are vanilloid resistant Sex differences in mouse Transient Receptor Potential Cation Channel, Subfamily M, Member 8 expressing trigeminal ganglion neurons.Signaling in TRPV1-induced platelet activating factor (PAF) in human esophageal epithelial cells.Molecular Surgery Concept from Bench to Bedside: A Focus on TRPV1+ Pain-Sensing Neurons.Molecular signatures of mouse TRPV1-lineage neurons revealed by RNA-Seq transcriptome analysis.Targeting breast cancer cells by MRS1477, a positive allosteric modulator of TRPV1 channels.Prolonged analgesic response of cornea to topical resiniferatoxin, a potent TRPV1 agonist Cyclin-dependent kinase 5 activity regulates pain signaling.Characterization of functional TRPV1 channels in the sarcoplasmic reticulum of mouse skeletal muscle Subgroup-elimination transcriptomics identifies signaling proteins that define subclasses of TRPV1-positive neurons and a novel paracrine circuit.The vanilloid agonist resiniferatoxin for interventional-based pain control Disruption of the transient receptor potential vanilloid 1 can affect survival, bacterial clearance, and cytokine gene expression during murine sepsis.Intraganglionic signaling as a novel nasal-meningeal pathway for TRPA1-dependent trigeminovascular activation by inhaled environmental irritants.ATP: a mediator for HCl-induced TRPV1 activation in esophageal mucosa.Resistance to morphine analgesic tolerance in rats with deleted transient receptor potential vanilloid type 1-expressing sensory neurons.Vanilloids in pancreatic cancer: potential for chemotherapy and pain management.Apoptosis as a novel target for cancer chemoprevention.N-glycosylation determines ionic permeability and desensitization of the TRPV1 capsaicin receptor.Resiniferatoxin for Pain Treatment: An Interventional Approach to Personalized Pain Medicine.Perineural resiniferatoxin selectively inhibits inflammatory hyperalgesia Calcium-dependent and independent mechanisms of capsaicin receptor (TRPV1)-mediated cytokine production and cell death in human bronchial epithelial cells.TRPV1 antagonists elevate cell surface populations of receptor protein and exacerbate TRPV1-mediated toxicities in human lung epithelial cells Vanilloid-induced conduction analgesia: selective, dose-dependent, long-lasting, with a low level of potential neurotoxicity.Preservation of acute pain and efferent functions following intrathecal resiniferatoxin-induced analgesia in rats.TGF-β1 sensitizes TRPV1 through Cdk5 signaling in odontoblast-like cells.Emerging neuropeptide targets in inflammation: NPY and VIP Removing TRPV1-expressing primary afferent neurons potentiates the spinal analgesic effect of delta-opioid agonists on mechano-nociception.Structure-activity relationships of 1,4-dihydropyridines that act as enhancers of the vanilloid receptor 1 (TRPV1)

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Ligand-induced dynamic membrane changes and cell deletion conferred by vanilloid receptor 1

http://www.wikidata.org/entity/Q28140829

description

2001 nî lūn-bûn

@nan

2001 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2001 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2001年の論文

@ja

2001年論文

@yue

2001年論文

@zh-hant

2001年論文

@zh-hk

2001年論文

@zh-mo

2001年論文

@zh-tw

2001年论文

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name

Ligand-induced dynamic membran ...... ferred by vanilloid receptor 1

@ast

Ligand-induced dynamic membran ...... ferred by vanilloid receptor 1

@en

Ligand-induced dynamic membran ...... ferred by vanilloid receptor 1

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type

label

Ligand-induced dynamic membran ...... ferred by vanilloid receptor 1

@ast

Ligand-induced dynamic membran ...... ferred by vanilloid receptor 1

@en

Ligand-induced dynamic membran ...... ferred by vanilloid receptor 1

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prefLabel

Ligand-induced dynamic membran ...... ferred by vanilloid receptor 1

@ast

Ligand-induced dynamic membran ...... ferred by vanilloid receptor 1

@en

Ligand-induced dynamic membran ...... ferred by vanilloid receptor 1

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P2860

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P1433

Journal of Biological Chemistry

P1476

Ligand-induced dynamic membran ...... ferred by vanilloid receptor 1

@en

P2093

C Hough

http://www.w3.org/2001/XMLSchema#string

L Karai

http://www.w3.org/2001/XMLSchema#string

M J Iadarola

http://www.w3.org/2001/XMLSchema#string

P M Blumberg

http://www.w3.org/2001/XMLSchema#string

R D Fields

http://www.w3.org/2001/XMLSchema#string

R M Caudle

http://www.w3.org/2001/XMLSchema#string

T Szabo

http://www.w3.org/2001/XMLSchema#string

Z Olah

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P2860

The capsaicin receptor: a heat-activated ion channel in the pain pathway

Vanilloid receptor-1 is essential for inflammatory thermal hyperalgesia

Impaired nociception and pain sensation in mice lacking the capsaicin receptor

The cloned capsaicin receptor integrates multiple pain-producing stimuli

Neuronal calcium signaling

Controlling the urge for a Ca(2+) surge: all-or-none Ca(2+) release in neurons.

The stimulation of capsaicin-sensitive neurones in a vanilloid receptor-mediated fashion by pungent terpenoids possessing an unsaturated 1,4-dialdehyde moiety

Epidural capsaicin produces prolonged segmental analgesia in the rat.

Calcium-mediated neurotoxicity: relationship to specific channel types and role in ischemic damage.

Immunocytochemical localization of the vanilloid receptor 1 (VR1): relationship to neuropeptides, the P2X3 purinoceptor and IB4 binding sites.

P304

11021-30

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scholarly article

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3993641

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10.1074/JBC.M008392200

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P407

P433

14

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P478

276

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P577

2001-04-06T00:00:00Z

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P698

11124944

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