about
TNF-α promotes extracellular vesicle release in mouse astrocytes through glutaminaseGlutathione induces GABA release through P2X7R activation on Müller glia.Loss of μ opioid receptor signaling in nociceptors, but not microglia, abrogates morphine tolerance without disrupting analgesia.The malleable brain: plasticity of neural circuits and behavior - a review from students to students.Comparative biology of pain: What invertebrates can tell us about how nociception works.P2X receptor-channels in chronic pain pathways.Toll-like receptors and their role in persistent pain.Therapies and mechanisms of opioid withdrawal.Inflammation-associated regulation of RGS in astrocytes and putative implication in neuropathic pain.Cellular and molecular mechanisms driving neuropathic pain: recent advancements and challenges.From Mechanism to Cure: Renewing the Goal to Eliminate the Disease of Pain.Microglial modulation of neuronal activity in the healthy brain.Spinal CCL2 Promotes Central Sensitization, Long-Term Potentiation, and Inflammatory Pain via CCR2: Further Insights into Molecular, Synaptic, and Cellular Mechanisms.Physiology of Astroglia.Glial Activation, A Common Mechanism Underlying Spinal Synaptic Plasticity?Genetic variation in P2RX7 and pain tolerance.Neuroinflammation and Central Sensitization in Chronic and Widespread Pain.Lung-injury depresses glutamatergic synaptic transmission in the nucleus tractus solitarii via discrete age-dependent mechanisms in neonatal rats.Central sensitization and pain hypersensitivity: Some critical considerations
P2860
Q33587183-853CE8F7-A864-46C9-BE4E-D78C2D70243AQ34551884-9411DA71-9AC0-4D48-9046-28F44256140CQ37629809-1E64D64F-B347-46EA-8A47-D84CF38A9D66Q38668955-7E70AE0D-C945-463B-969E-C83A921FD6B8Q39067553-09F03EAB-F680-43B8-AFA3-0F9AAC18C95CQ39448037-D17B6C8D-A8E0-440F-8582-BCD3F3CB1278Q43075865-F03F843E-3E7E-4CF9-A5DE-C67E926C3DF1Q44350678-2C2D5D6F-1744-4641-BF58-895E336F7EBAQ46199286-7A5942A4-709F-4686-B341-A2F45DA4FF27Q47246872-C19DBA70-1B40-429A-880F-7493DC927F32Q47566382-0E6CC231-5891-4AC5-9ED9-7CD06724AB38Q47899668-C26004D9-20E9-4914-BD05-E47A88180068Q48278436-064AE7BA-FE83-42ED-91D4-DBAAF7D497A3Q49917383-71A13CF5-15A4-4FC3-AEE1-42A4DDD65E8BQ50260575-6C8A2644-4A0D-4231-A9B3-3899342DADF6Q51767986-7A9B1D01-DAB6-487D-8F10-52045A0E6EE6Q52692785-DE620E79-C2E3-42E4-8FF1-5F37E656E367Q54244939-BF257A2E-0AF6-4CD5-9F0E-112B96168BDFQ58778509-0A66D5D4-F48D-43EB-8A2B-3D478A283F6D
P2860
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh-hant
name
Gliogenic LTP spreads widely in nociceptive pathways.
@en
Gliogenic LTP spreads widely in nociceptive pathways.
@nl
type
label
Gliogenic LTP spreads widely in nociceptive pathways.
@en
Gliogenic LTP spreads widely in nociceptive pathways.
@nl
prefLabel
Gliogenic LTP spreads widely in nociceptive pathways.
@en
Gliogenic LTP spreads widely in nociceptive pathways.
@nl
P2093
P2860
P356
P1433
P1476
Gliogenic LTP spreads widely in nociceptive pathways.
@en
P2093
H L Teuchmann
M T Kronschläger
R Drdla-Schutting
S D Honsek
P2860
P304
P356
10.1126/SCIENCE.AAH5715
P407
P577
2016-11-10T00:00:00Z