Forskolin-induced LTP in the CA1 hippocampal region is NMDA receptor dependent.
about
Light modulation of cellular cAMP by a small bacterial photoactivated adenylyl cyclase, bPAC, of the soil bacterium BeggiatoaFacilitation of AMPA receptor synaptic delivery as a molecular mechanism for cognitive enhancementSpreading depression sends microglia on Lévy flightsImpaired spatial learning and memory after sevoflurane-nitrous oxide anesthesia in aged rats is associated with down-regulated cAMP/CREB signalingSynaptically released matrix metalloproteinase activity in control of structural plasticity and the cell surface distribution of GluA1-AMPA receptorsSurface dynamics of GluN2B-NMDA receptors controls plasticity of maturing glutamate synapsesSynaptic activity prompts gamma-secretase-mediated cleavage of EphA4 and dendritic spine formationEndocytosis of synaptic ADAM10 in neuronal plasticity and Alzheimer's diseaseOligodendrocyte precursor cells modulate the neuronal network by activity-dependent ectodomain cleavage of glial NG2.Amyloid beta from axons and dendrites reduces local spine number and plasticity.STIM2 regulates PKA-dependent phosphorylation and trafficking of AMPARsMatrix metalloproteinase-9 is required for hippocampal late-phase long-term potentiation and memory.A new semisynthetic derivative of sauroine induces LTP in hippocampal slices and improves learning performance in the Morris Water Maze.CD44: a novel synaptic cell adhesion molecule regulating structural and functional plasticity of dendritic spines.Disrupted neuronal maturation in Angelman syndrome-derived induced pluripotent stem cells.Severe learning deficits of IRSp53 mutant mice are caused by altered NMDA receptor dependent signal transduction.Characterization of the time course of changes of the evoked electrical activity in a model of a chemically-induced neuronal plasticityPhosphodiesterase type 4 inhibition does not restore ocular dominance plasticity in a ferret model of fetal alcohol spectrum disorders.Experience-dependent plasticity in hypocretin/orexin neurones: re-setting arousal threshold.Growth arrest and forced differentiation of human primary glioblastoma multiforme by a novel small molecule.TNF-α and Microglial Hormetic Involvement in Neurological Health & MigraineSynaptic potentiation facilitates memory-like attractor dynamics in cultured in vitro hippocampal networks.Matrix metalloproteinases regulate the formation of dendritic spine head protrusions during chemically induced long-term potentiation.Neuroligin 1 is dynamically exchanged at postsynaptic sites.Seasonal variation of long-term potentiation at a central synapse in the medicinal leech.Soluble oligomers of amyloid-β peptide disrupt membrane trafficking of α-amino-3-hydroxy-5-methylisoxazole-4-propionic acid receptor contributing to early synapse dysfunction.LTP-triggered cholesterol redistribution activates Cdc42 and drives AMPA receptor synaptic deliverySignalling pathways underlying structural plasticity of dendritic spines.LIMK1 regulates long-term memory and synaptic plasticity via the transcriptional factor CREB.PKMζ, but not PKCλ, is rapidly synthesized and degraded at the neuronal synapse.Real-time imaging of discrete exocytic events mediating surface delivery of AMPA receptors.Long-Term Dynamical Constraints on Pharmacologically Evoked Potentiation Imply Activity Conservation within In Vitro Hippocampal NetworksPSD-95 is required for activity-driven synapse stabilizationFetal alcohol spectrum disorders and abnormal neuronal plasticity.Inositol 1,4,5-trisphosphate 3-kinase A is a novel microtubule-associated protein: PKA-dependent phosphoregulation of microtubule binding affinityAge-dependent requirement of AKAP150-anchored PKA and GluR2-lacking AMPA receptors in LTP.Prolonged wakefulness induces experience-dependent synaptic plasticity in mouse hypocretin/orexin neurons.miR-34a regulates cell proliferation, morphology and function of newborn neurons resulting in improved behavioural outcomesCalcium-Permeable AMPA Receptors Mediate the Induction of the Protein Kinase A-Dependent Component of Long-Term Potentiation in the Hippocampus.Rescue of Cyclic AMP Mediated Long Term Potentiation Impairment in the Hippocampus of Mecp2 Knockout (Mecp2(-/y) ) Mice by Rolipram
P2860
Q24598672-FCD0F002-5775-4326-A812-7BB2806F683FQ27320088-84B935AB-28D7-41F3-A3CA-DE34E532A832Q27345332-91731880-ABE3-4F4B-BE12-01E153137207Q28535169-F9F2D924-0094-4F87-95E5-6C9F45F7C81FQ28539061-884956E4-BBDC-447E-BE5B-B8708B8CD8D8Q28581987-DC71402B-23C4-4993-9F2E-7D9B193A5876Q28583254-F427B534-FB36-4152-BA1E-9FD780722DF6Q29048183-4F0A2B36-7479-4803-9B4B-A14E67FE2F90Q30425863-7359969B-73C8-4CB0-BBF0-74566948185CQ30511922-84C86447-983B-4CDC-8067-D3EACCF4A011Q30627178-6EFE4BE3-A606-437C-97AF-01BBBA410E66Q30650111-5D869C1E-05F6-4F9B-AD48-EA590DF51F18Q30786706-94E7DAB7-EFB1-48B0-8A4A-18DF71B62002Q30831991-999B85A2-0BA0-44F2-8DBE-BE51B239F10AQ30847511-755A5D01-7C42-43C4-A741-0BC60C7B5B6BQ33361898-47123BBB-3ECF-4A48-AC52-FC97BC98767EQ33403392-4BC87AD6-9B39-41F4-B6A0-39CF18A4D827Q33800535-5EA917BB-BE45-4EEF-AB70-E4B7DBBCB87AQ33814658-5704C0D4-0155-4F84-A400-9DDEB9F846D4Q33840263-CB8173B1-3436-47A8-BAD4-522CDD849A18Q34341918-F0E5DEA7-2A15-4C7D-BAFD-2A4CAA3974CDQ34633945-F5D0ABB4-6D94-40CA-8524-53AC46E22D9BQ34733795-065A932C-2135-4F83-8821-3A9CFE125509Q35027081-F5CF82AE-5B03-40F6-852B-AE88510729EBQ35102411-55B72EA2-46F4-4619-9502-5371881DEF71Q35144851-AB33ECC5-84E2-4C60-86C1-FA22F46F463EQ35184462-1B826BC3-A651-48B4-8100-141B1E1DFC51Q35195400-7E1855D3-86F7-49C1-BC9B-9701F1FA6F05Q35214701-1FA5AB22-E811-437A-918A-3891E146AC58Q35625729-131B8A66-C27C-4BF4-997F-EE0D9ED0A5C4Q35645097-C1BFE5B4-4C76-4A50-A52A-CE5A4BB08F03Q35662514-1612DAF0-6534-4627-A10B-29DF4B1B7B31Q35676844-C5B90C91-9DD5-4F30-BD65-EEA10155D0F2Q35915502-C7A564DD-EBBC-42AD-BA60-CB87B92FA83AQ35939950-B32422B2-90E2-46D1-B192-C74C608B8468Q36177209-84883032-C295-400C-B91D-3AE5587AE193Q36183647-85E636CA-AAC2-40D3-B912-A55A00C740E5Q36347201-A6754253-844C-486D-BE05-F194C427FA96Q36456724-6D87D2AB-A2D7-43D2-A66E-101C7601EEE0Q36534804-0B34F028-CB6D-406E-946E-ECA438B5E223
P2860
Forskolin-induced LTP in the CA1 hippocampal region is NMDA receptor dependent.
description
2003 nî lūn-bûn
@nan
2003 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Forskolin-induced LTP in the CA1 hippocampal region is NMDA receptor dependent.
@ast
Forskolin-induced LTP in the CA1 hippocampal region is NMDA receptor dependent.
@en
Forskolin-induced LTP in the CA1 hippocampal region is NMDA receptor dependent.
@nl
type
label
Forskolin-induced LTP in the CA1 hippocampal region is NMDA receptor dependent.
@ast
Forskolin-induced LTP in the CA1 hippocampal region is NMDA receptor dependent.
@en
Forskolin-induced LTP in the CA1 hippocampal region is NMDA receptor dependent.
@nl
prefLabel
Forskolin-induced LTP in the CA1 hippocampal region is NMDA receptor dependent.
@ast
Forskolin-induced LTP in the CA1 hippocampal region is NMDA receptor dependent.
@en
Forskolin-induced LTP in the CA1 hippocampal region is NMDA receptor dependent.
@nl
P2093
P2860
P356
P1476
Forskolin-induced LTP in the CA1 hippocampal region is NMDA receptor dependent
@en
P2093
Brent Asrican
John Lisman
Lena Khibnik
Nikolai Otmakhov
Nonna Otmakhova
Shervin Riahi
P2860
P304
P356
10.1152/JN.00941.2003
P407
P577
2003-12-31T00:00:00Z