about
Suppression to visual, auditory, and gustatory stimuli habituates normally in rats with excitotoxic lesions of the perirhinal cortex.The group II metabotropic glutamate receptor agonist LY354740 and the D2 receptor antagonist haloperidol reduce locomotor hyperactivity but fail to rescue spatial working memory in GluA1 knockout mice.Altered balance of excitatory and inhibitory learning in a genetically modified mouse model of glutamatergic dysfunction relevant to schizophrenia.Malaise in the water maze: untangling the effects of LPS and IL-1beta on learning and memory.The effect of US signalling and the US-CS interval on backward conditioning in mice.Deletion of the GluA1 AMPA receptor subunit impairs recency-dependent object recognition memoryDeletion of the GluA1 AMPA receptor subunit alters the expression of short-term memory.Worsening cognitive impairment and neurodegenerative pathology progressively increase risk for deliriumCompetitive short-term and long-term memory processes in spatial habituation.Systemic inflammation induces acute working memory deficits in the primed brain: relevance for delirium.Do GluA1 knockout mice exhibit behavioral abnormalities relevant to the negative or cognitive symptoms of schizophrenia and schizoaffective disorder?Dissociations within short-term memory in GluA1 AMPA receptor subunit knockout mice.Hippocampal lesions can enhance discrimination learning despite normal sensitivity to interference from incidental information.Contexts control negative contrast and restrict the expression of flavor preference conditioning.The effect of the amount of blocking cue training on blocking of appetitive conditioning in mice.Structural learning and the hippocampus.Enhanced long-term and impaired short-term spatial memory in GluA1 AMPA receptor subunit knockout mice: evidence for a dual-process memory modelMemory-dependent effects on palatability in mice.Spatial working memory deficits in GluA1 AMPA receptor subunit knockout mice reflect impaired short-term habituation: evidence for Wagner's dual-process memory model.The role of habituation in hippocampus-dependent spatial working memory tasks: evidence from GluA1 AMPA receptor subunit knockout mice.What causes aberrant salience in schizophrenia? A role for impaired short-term habituation and the GRIA1 (GluA1) AMPA receptor subunit.GluA1 AMPAR subunit deletion reduces the hedonic response to sucrose but leaves satiety and conditioned responses intact.Dissecting spatial knowledge from spatial choice by hippocampal NMDA receptor deletion.Contribution of hippocampal and extra-hippocampal NR2B-containing NMDA receptors to performance on spatial learning tasks.NMDA receptor subunit NR2A is required for rapidly acquired spatial working memory but not incremental spatial reference memory.Supersmart mice: surprising or surprised? Theoretical comment on Singer, Boison, Möhler, Feldon, and Yee (2007).Hippocampal synaptic plasticity, spatial memory and anxiety.Neurotoxic lesions of the rat perirhinal and postrhinal cortices and their impact on biconditional visual discrimination tasks.Deletion of glutamate receptor-A (GluR-A) AMPA receptor subunits impairs one-trial spatial memory.The importance of the rat hippocampus for learning the structure of visual arrays.A double dissociation between the effects of sub-pyrogenic systemic inflammation and hippocampal lesions on learning.A biphasic reduction in a measure of palatability following sucrose consumption in mice.Age-dependent and -independent behavioral deficits in Tg2576 mice.Optogenetic induction of the schizophrenia-related endophenotype of ventral hippocampal hyperactivity causes rodent correlates of positive and cognitive symptomsThe NMDA receptor antagonist MK-801 fails to impair long-term recognition memory in mice when the state-dependency of memory is controlled
P50
Q30426106-51095A22-DB10-4401-9FCD-241007678DCAQ33578312-9AAADDB3-E6B2-437F-96D9-191B0D5EC0DAQ33686891-D8AF6D41-0A81-4F24-83F2-DB2400AAAC1AQ34147135-3FF3D6CA-4EE7-48E1-B3F8-234CABB7EB54Q34664177-6369B944-8F93-49E3-8051-39C468A0AF05Q34667158-D07024E2-B834-429B-B792-194E1090256EQ34667172-069F1EB4-13D3-4A53-9BEE-778C10172468Q34784435-D8A54541-5821-4148-B740-3F7A50184A89Q34898346-C6DC99D2-DFC7-4042-A3CC-2E2F778A8909Q35431528-82744EA4-3D39-4D76-9A85-8B214E10D99CQ35522856-423620A8-01B8-4DE7-B621-24CB89566283Q35631892-C99EEA90-49BB-49A1-ACA9-5463994C3AD9Q36424921-587F93FD-38C3-4938-AF0B-D073BE99FE3BQ36451225-7C2ECF3F-847D-4DAD-9CDB-ADD855266D29Q36485888-4E40DDD9-E5AB-470A-9707-6468A93255E2Q36863683-16EBB3F7-348F-4862-82E4-4F9D613E1904Q37246175-9CE32803-C14E-4322-BBDC-2D14C65B8CD0Q37409357-97E39767-8887-4F23-B1A9-8E32709A5642Q37720835-A731DF95-B708-471B-83FA-1B5A2FB9711EQ37815114-DB253573-0674-4638-A1DA-64ED4BD74686Q38249908-381A8560-8FD3-40B3-8F12-26192B2D6030Q41287252-D8FCD649-9634-4ACF-87E8-856ACECAD5DCQ41944017-A5AF9C0C-AC9E-4B89-A427-E25B2405EEBFQ46199208-D0D2D025-7588-4D77-8A00-AB0D36489AF0Q46667155-D225917D-F78B-46F1-8558-64F39D63949DQ46972941-FA568FA7-B4D6-457C-A21E-3D796738C4B1Q47914550-1ACEA3F3-14A1-47A7-A6EB-781C4AA1885FQ48375950-7B84F93B-4013-42B2-ABD4-FFC31D8AE6A4Q48395493-AFAC4B9D-7F9F-4987-AFF1-533D8805EEEFQ48412065-2BCDDB9C-01ED-431E-9D05-E7400262FA62Q48624163-6B1987C7-9A7E-4C42-8514-DFCC6909CD86Q49861234-6A098F7E-9F33-4D7B-8735-A4A77C57030BQ53391464-C2FE97EC-6819-44D9-A2C4-20FC6E8389CEQ58701316-A2AF4096-EB2B-4787-A7D4-381E3CE73AD5Q92562938-E2F29119-714C-4B1B-84D2-84B1AADD70CC
P50
description
hulumtues
@sq
researcher
@en
ricercatore
@it
wetenschapper
@nl
հետազոտող
@hy
name
David J Sanderson
@nl
David J Sanderson
@sl
David J. Sanderson
@en
David J. Sanderson
@es
David Sanderson
@de
type
label
David J Sanderson
@nl
David J Sanderson
@sl
David J. Sanderson
@en
David J. Sanderson
@es
David Sanderson
@de
prefLabel
David J Sanderson
@nl
David J Sanderson
@sl
David J. Sanderson
@en
David J. Sanderson
@es
David Sanderson
@de
P227
P1053
E-5285-2011
P21
P214
4083153596637951900005
P227
1165816865
P31
P3829
P496
0000-0002-3560-5507