Enhanced learning after genetic overexpression of a brain growth protein
about
Structural plasticity of climbing fibers and the growth-associated protein GAP-43Impaired sprouting and axonal atrophy in cerebellar climbing fibres following in vivo silencing of the growth-associated protein GAP-43Long-Term Potentiation and MemoryGenes and signaling pathways involved in memory enhancement in mutant miceStructural Basis for the Interaction of Unstructured Neuron Specific Substrates Neuromodulin and Neurogranin with CalmodulinBoth cell-autonomous and cell non-autonomous functions of GAP-43 are required for normal patterning of the cerebellum in vivoNerve growth factor controls GAP-43 mRNA stability via the phosphoprotein ARPP-19Increase of the RNA-binding protein HuD and posttranscriptional up-regulation of the GAP-43 gene during spatial memoryExpression profiling and Ingenuity biological function analyses of interleukin-6- versus nerve growth factor-stimulated PC12 cellsBehavioral inhibition and impaired spatial learning and memory in hypothyroid mice lacking thyroid hormone receptor alphaGenetic enhancement of visual learning by activation of protein kinase C pathways in small groups of rat cortical neuronsDevelopmental and adult GAP-43 deficiency in mice dynamically alters hippocampal neurogenesis and mossy fiber volumeExperience-dependent plasticity and modulation of growth regulatory molecules at central synapses.Postsynaptic deregulation in GAP-43 heterozygous mouse barrel cortex.Posttranscriptional regulation of gene expression in learning by the neuronal ELAV-like mRNA-stabilizing proteins.Brain and spinal cord interaction: protective effects of exercise prior to spinal cord injuryVoluntary exercise increases axonal regeneration from sensory neuronsThe molecular and cellular biology of enhanced cognition.Opposite effects of acute ethanol exposure on GAP-43 and BDNF expression in the hippocampus versus the cerebellum of juvenile rats.Transgenic and knock-out mouse pups: the growing need for behavioral analysis.Exercise influences hippocampal plasticity by modulating brain-derived neurotrophic factor processing.Mammalian Target of Rapamycin (mTOR) Tagging Promotes Dendritic Branch Variability through the Capture of Ca2+/Calmodulin-dependent Protein Kinase II α (CaMKIIα) mRNAs by the RNA-binding Protein HuD.GAP-43 gene expression regulates information storage.Recurrent HERV-H-mediated 3q13.2-q13.31 deletions cause a syndrome of hypotonia and motor, language, and cognitive delays.Gene targeting of presynaptic proteins in synaptic plasticity and memory: across the great divide.Integrated analysis of genetic, behavioral, and biochemical data implicates neural stem cell-induced changes in immunity, neurotransmission and mitochondrial function in Dementia with Lewy Body mice.Cognitive outcome following brain injury and treatment with an inhibitor of Nogo-A in association with an attenuated downregulation of hippocampal growth-associated protein-43 expression.Altered neural connectivity in excitatory and inhibitory cortical circuits in autism.Molecular mechanisms, biological actions, and neuropharmacology of the growth-associated protein GAP-43.Alterations in mossy fiber physiology and GAP-43 expression and function in transgenic mice overexpressing HuDEmerging complexity of the HuD/ELAVl4 gene; implications for neuronal development, function, and dysfunctionHigh-order oligomers of intrinsically disordered brain proteins BASP1 and GAP-43 preserve the structural disorder.Overexpression of GAP-43 reveals unexpected properties of hippocampal mossy fibers.The protein kinase C phosphorylation site on GAP-43 differentially regulates information storage.Hippocampal Proteome of Rats Subjected to the Li-Pilocarpine Epilepsy Model and the Effect of Carisbamate Treatment.BDNF-exercise interactions in the recovery of symmetrical stepping after a cervical hemisection in rats.A high-fat diet induces lower expression of retinoid receptors and their target genes GAP-43/neuromodulin and RC3/neurogranin in the rat brain.PKC activation rescues LTP from NMDA receptor blockade.A point mutant of GAP-43 induces enhanced short-term and long-term hippocampal plasticity.Cholinergic dysfunctions and enhanced oxidative stress in the neurobehavioral toxicity of lambda-cyhalothrin in developing rats.
P2860
Q21129464-F6A8CA7B-9FE4-4FE5-A2E5-01529730ADBCQ21135348-E1DCDC43-85D2-42D3-8F85-781200DB3DE2Q22337020-559FEBE0-C393-4C8E-8363-10BB0BEBB64DQ27009274-4DD8D188-2B93-4B79-B50E-52EC06203EC7Q27676705-3509E59E-5DF2-4DC9-B859-1896770AA97EQ28293307-5F7586DC-C723-4DF2-862B-16F2BFFF4330Q28564744-B55C8017-6D03-40FE-BA44-11EFD7E5809EQ28578336-98E7FB60-8F35-4D86-B6C4-69E95A12D4E1Q28581575-F7017653-A7BF-49BE-AEB2-A2A3804100BFQ28588135-47D9F0F1-1AAC-436C-95C4-42E2DDDCD139Q30484492-D376E155-179C-490C-9AFC-200FAF4A534CQ33670572-301B6E5C-242A-4538-8519-0FAE6DD82989Q33815606-7E52D761-7771-448D-9A39-25CFD79984D4Q33902317-F9E16332-6BAB-4EC5-ADFF-94FBA3F192F4Q33944818-2F35036F-675F-4311-A3F4-B5AB92A9D845Q34182485-07374A00-16B8-49AA-AB2F-3BBE78B94D88Q34376201-20E1FA99-641C-4A53-AA98-3A1D6A1C6137Q34925043-DDCEAB91-95EF-4CE9-928B-B1815E55CD96Q35059020-B883579A-0F06-4928-A0BE-766FF293BFE7Q35186496-762801C1-CAF9-44B2-8EC9-6EC22A528337Q35576197-FEFC8371-166B-451C-A235-272C9D22CE13Q35783171-19A98955-DD0E-4AFE-BFEC-F69AE34E0C01Q35850597-2A009BDF-7E63-4A65-A6A0-202E78B2AE69Q36141110-1426F2D3-4D00-4B42-A60B-D32A0AF35C08Q36288486-3AE7FF0E-0963-4649-A55D-AF8F60B74609Q36304737-00899A2C-4EFA-42DC-9D1A-30729CADC8D2Q36631029-F003E0D4-2E42-49CA-B5F2-D88C8F629927Q37201156-F148F74F-9F25-4272-AAAC-42C3F715E5F1Q37226514-FADA008D-D138-4410-BADA-EE6AEE665434Q37398638-AC21D26D-C33C-4D4B-A093-DC7E1134A5DCQ38122142-C5024176-2EAD-43D2-8E0A-218D482898DEQ39966175-79E17C76-2C28-4F46-A4F4-04D9E342B106Q40698799-1441DBD3-3C92-42C3-811F-AD140B8039DDQ41145391-8C63D1A6-E4A3-410C-8AA6-6C26BE68A2EFQ42366877-CDFECB02-5B16-41A8-A503-9BEDCF09EA40Q42938474-AC465756-F2B9-4E25-A292-068E4AE852E5Q43183804-79993C7D-752F-4660-8A80-F3411C692D8CQ43602232-0EE28F3F-2E3E-42F5-8797-5A430EF636BEQ44051625-0341FB54-BFB0-455F-9BC8-258B4E920D6AQ44440602-3C4115CF-2442-40D8-8CAA-9221D803EC68
P2860
Enhanced learning after genetic overexpression of a brain growth protein
description
2000 nî lūn-bûn
@nan
2000 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Enhanced learning after genetic overexpression of a brain growth protein
@ast
Enhanced learning after genetic overexpression of a brain growth protein
@en
Enhanced learning after genetic overexpression of a brain growth protein
@nl
type
label
Enhanced learning after genetic overexpression of a brain growth protein
@ast
Enhanced learning after genetic overexpression of a brain growth protein
@en
Enhanced learning after genetic overexpression of a brain growth protein
@nl
prefLabel
Enhanced learning after genetic overexpression of a brain growth protein
@ast
Enhanced learning after genetic overexpression of a brain growth protein
@en
Enhanced learning after genetic overexpression of a brain growth protein
@nl
P2093
P2860
P356
P1476
Enhanced learning after genetic overexpression of a brain growth protein
@en
P2093
A Routtenberg
I Cantallops
P2860
P304
P356
10.1073/PNAS.97.13.7657
P407
P577
2000-06-20T00:00:00Z