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Enrichment induces structural changes and recovery from nonspatial memory deficits in CA1 NMDAR1-knockout mice
scientific journal article
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scholarly article
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PubMed
PubMed ID
10700255
retrieved
25 January 2017
title
Enrichment induces structural changes and recovery from nonspatial memory deficits in CA1 NMDAR1-knockout mice
(English)
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PubMed
PubMed ID
10700255
retrieved
25 January 2017
main subject
knockout mouse
0 references
Glutamate receptor, ionotropic, NMDA1 (zeta 1)
1 reference
stated in
GOA release 2020-03-11
author
Claire Rampon
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ORCID Public Data File 2021
author name string
C. Rampon
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1
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PubMed
PubMed ID
10700255
retrieved
25 January 2017
Y. P. Tang
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
10700255
retrieved
25 January 2017
J. Goodhouse
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3
1 reference
stated in
PubMed
PubMed ID
10700255
retrieved
25 January 2017
E. Shimizu
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4
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PubMed
PubMed ID
10700255
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25 January 2017
M. Kyin
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5
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PubMed
PubMed ID
10700255
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25 January 2017
J. Z. Tsien
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6
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PubMed
PubMed ID
10700255
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25 January 2017
language of work or name
English
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publication date
1 March 2000
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PubMed
PubMed ID
10700255
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25 January 2017
published in
Nature Neuroscience
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stated in
PubMed
PubMed ID
10700255
retrieved
25 January 2017
volume
3
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PubMed
PubMed ID
10700255
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25 January 2017
page(s)
238–244
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PubMed
PubMed ID
10700255
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25 January 2017
issue
3
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PubMed
PubMed ID
10700255
retrieved
25 January 2017
cites work
Loss of recent memory after bilateral hippocampal lesions
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Human amnesia and the medial temporal region: enduring memory impairment following a bilateral lesion limited to field CA1 of the hippocampus
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Crossref
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Memory and the hippocampus: a synthesis from findings with rats, monkeys, and humans
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The global record of memory in hippocampal neuronal activity.
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Genetic enhancement of learning and memory in mice
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Subregion- and cell type-restricted gene knockout in mouse brain
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The essential role of hippocampal CA1 NMDA receptor-dependent synaptic plasticity in spatial memory
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Impaired hippocampal representation of space in CA1-specific NMDAR1 knockout mice
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A structural basis for memory storage in mammals
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Crossref
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Structural changes accompanying memory storage
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An increase in dendritic spine density on hippocampal CA1 pyramidal cells following spatial learning in adult rats suggests the formation of new synapses
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Developmental mechanisms that generate precise patterns of neuronal connectivity
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Whisker-related neuronal patterns fail to develop in the trigeminal brainstem nuclei of NMDAR1 knockout mice
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Dendrites are more spiny on mature hippocampal neurons when synapses are inactivated.
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Stability in synapse number and size at 2 hr after long-term potentiation in hippocampal area CA1.
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Restricted and regulated overexpression reveals calcineurin as a key component in the transition from short-term to long-term memory.
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Spaced training induces normal long-term memory in CREB mutant mice.
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Selective damage to the hippocampal region blocks long-term retention of a natural and nonspatial stimulus-stimulus association
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Differential contribution of amygdala and hippocampus to cued and contextual fear conditioning
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Environmental complexity modulates growth of granule cell dendrites in developing but not adult hippocampus of rats
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A critical evaluation of methods for estimating the numerical density of synapses.
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Synaptic plasticity
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
Naturally occurring fluctuation in dendritic spine density on adult hippocampal pyramidal neurons.
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Crossref
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Ischemia-induced object-recognition deficits in rats are attenuated by hippocampal ablation before or soon after ischemia.
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Preoperative differential housing and dorsal hippocampal lesions in rats.
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Crossref
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Identifiers
DOI
10.1038/72945
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1978901
OpenCitations bibliographic resource ID
1978901
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1978901
PubMed ID
10700255
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1978901
ResearchGate publication ID
12615942
0 references
Springer Nature article ID
10.1038/72945
0 references
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