Complementary roles of cholecystokinin- and parvalbumin-expressing GABAergic neurons in hippocampal network oscillations.
about
Autism-associated neuroligin-3 mutations commonly disrupt tonic endocannabinoid signalingNeurophysiological and computational principles of cortical rhythms in cognitionGABA neurons and the mechanisms of network oscillations: implications for understanding cortical dysfunction in schizophreniaChandelier Cells in Functional and Dysfunctional Neural CircuitsThe Diversity of Cortical Inhibitory SynapsesFunctional characteristics of parvalbumin- and cholecystokinin-expressing basket cellsFollowing the genes: a framework for animal modeling of psychiatric disordersTargeting brain serotonin synthesis: insights into neurodevelopmental disorders with long-term outcomes related to negative emotionality, aggression and antisocial behaviourInterneuron cell types are fit to functionLoss of Either Rac1 or Rac3 GTPase Differentially Affects the Behavior of Mutant Mice and the Development of Functional GABAergic NetworksDeterminants of different deep and superficial CA1 pyramidal cell dynamics during sharp-wave ripples.Hippocampal sharp wave-ripple: A cognitive biomarker for episodic memory and planningHippocampal-prefrontal circuit and disrupted functional connectivity in psychiatric and neurodegenerative disordersParvalbumin and neuropeptide Y expressing hippocampal GABA-ergic inhibitory interneuron numbers decline in a model of Gulf War illnessThe brain dynamics of linguistic computationEvaluation of gene, protein and neurotrophin expression in the brain of mice exposed to space environment for 91 daysBrain expression and song regulation of the cholecystokinin gene in the zebra finch (Taeniopygia guttata).Network mechanisms of theta related neuronal activity in hippocampal CA1 pyramidal neuronsNeuronal diversity and temporal dynamics: the unity of hippocampal circuit operationsPyramidal cell selective ablation of N-methyl-D-aspartate receptor 1 causes increase in cellular and network excitability.Asynchronous transmitter release from cholecystokinin-containing inhibitory interneurons is widespread and target-cell independent.Development of cannabinoid 1 receptor protein and messenger RNA in monkey dorsolateral prefrontal cortex.Presynaptic kainate receptor activation preserves asynchronous GABA release despite the reduction in synchronous release from hippocampal cholecystokinin interneuronsBehavior-dependent specialization of identified hippocampal interneurons.Recruitment of oriens-lacunosum-moleculare interneurons during hippocampal ripples.Augmented Inhibition from Cannabinoid-Sensitive Interneurons Diminishes CA1 Output after Traumatic Brain Injury.Encoding of spatio-temporal input characteristics by a CA1 pyramidal neuron model.Cannabis and cognitive dysfunction: parallels with endophenotypes of schizophrenia?Quantitative ultrastructural differences between local and medial septal GABAergic axon terminals in the rat hippocampus.An approach for reliably investigating hippocampal sharp wave-ripples in vitroEndogenous cannabinoid signaling at inhibitory interneurons.Cell type-specific long-term plasticity at glutamatergic synapses onto hippocampal interneurons expressing either parvalbumin or CB1 cannabinoid receptor.Molecular and electrophysiological characterization of GFP-expressing CA1 interneurons in GAD65-GFP mice.Ginseng Rb fraction protects glia, neurons and cognitive function in a rat model of neurodegenerationM3 muscarinic acetylcholine receptor expression confers differential cholinergic modulation to neurochemically distinct hippocampal basket cell subtypesDistinct endocannabinoid control of GABA release at perisomatic and dendritic synapses in the hippocampus.Differential susceptibility of interneurons expressing neuropeptide Y or parvalbumin in the aged hippocampus to acute seizure activity.Distinct synaptic properties of perisomatic inhibitory cell types and their different modulation by cholinergic receptor activation in the CA3 region of the mouse hippocampusBiocytin-labelling and its impact on late 20th century studies of cortical circuitrySelective populations of hippocampal interneurons express ErbB4 and their number and distribution is altered in ErbB4 knockout mice.
P2860
Q24621853-40F9A700-0E13-48DA-AC13-04FD9B1AC36EQ24630528-FD746D80-07A0-44DF-8C97-3F02CC223D78Q24642711-6827667A-5E81-484F-8160-88E7CAD4483EQ26747552-60CB99D5-9CC9-4609-9324-A2D5EDB9149EQ26747555-48206BF3-DF3B-40E3-89C4-4D790D9A9A35Q26823073-710E2378-265A-4E50-915F-D791737A4E35Q26830603-61572A31-F39B-4454-85B3-E3E254DCEA84Q26865831-7B6C614A-F68F-4605-B049-C3FBA1597899Q27021885-ACFAA3A9-21B6-49FE-8077-A191A69E24C9Q27302773-802ED828-0216-41AF-8510-669DEE76C28BQ27312078-A59E16B4-2AEE-419D-81F1-A0CA4A0D8FD3Q28083958-4E4B3A7F-72BF-4275-93D9-4856E4493769Q28084481-BFE5B55A-E964-45D9-946D-143C15474C21Q28385632-A95DF4A5-C693-400E-983D-204B004E08F5Q28606491-317A07BB-D13B-4538-8C7A-D7DA612B6557Q28727345-895C4FEF-446E-40BC-AD5B-A7BB02074484Q28741144-BD10A59C-EF29-4F45-ACA4-AA285760E271Q28749683-FC75CC89-7F32-4034-9D0B-9A574A655FC3Q29620030-55F340C3-DC12-45AB-89B2-B3B66A99E6DFQ30388341-28A74B45-3E34-469C-A644-CEA8CA1502D8Q30490991-34591F2A-79D2-4232-977D-39BD796AE65AQ30494037-00498BD1-56C7-4257-8230-A52A7F11635DQ30496566-655674A1-E319-411A-9FC0-62C9ECBE5398Q30524682-C98AFB5D-FDBA-4C9C-A4E3-7AD822EF9465Q30537750-61B2456E-953B-4D86-B9D0-3169A9F21747Q30609922-5E3CB7B2-C71A-42BE-8575-D99A40BAB7EFQ30993496-0C69E5D9-2CD5-4F71-B6CF-599FC6AF8364Q31095554-C9D1E019-47C7-4C42-813B-5FD81478490AQ33301407-182D4AF4-B190-46E0-B3BE-7042B3089B29Q33501182-FCD5D8CC-7D49-4620-A1A5-53044DB15EF4Q33624983-D0C074BE-4B50-4261-9D50-0A8C8A02E06FQ33635394-F861C4B4-2655-4708-A0AA-DD1DCA4DE7C0Q33786743-DEB14194-F205-459E-BC26-F27180BB8CFCQ33817511-36B04168-F7DA-4B40-87DC-0B7370043F62Q33904869-A0DB52EF-4E85-4AD2-9E24-DC6EEF0F4ACEQ33996513-FCDAFC6D-B612-4FD2-803D-466D338DCFDEQ34019077-D52B818A-3512-4F28-9934-DC18292D61EDQ34044829-216EAE92-B82F-4B56-994A-E87A9C5560C3Q34173729-15EEBEBB-7898-491A-B1C0-19A7CE6EDB6EQ34217453-6593FF75-649E-415C-AF0C-C1D8F6FA81B4
P2860
Complementary roles of cholecystokinin- and parvalbumin-expressing GABAergic neurons in hippocampal network oscillations.
description
2005 nî lūn-bûn
@nan
2005 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Complementary roles of cholecy ...... pocampal network oscillations.
@ast
Complementary roles of cholecy ...... pocampal network oscillations.
@en
Complementary roles of cholecy ...... pocampal network oscillations.
@nl
type
label
Complementary roles of cholecy ...... pocampal network oscillations.
@ast
Complementary roles of cholecy ...... pocampal network oscillations.
@en
Complementary roles of cholecy ...... pocampal network oscillations.
@nl
prefLabel
Complementary roles of cholecy ...... pocampal network oscillations.
@ast
Complementary roles of cholecy ...... pocampal network oscillations.
@en
Complementary roles of cholecy ...... pocampal network oscillations.
@nl
P2093
P1476
Complementary roles of cholecy ...... ppocampal network oscillations
@en
P2093
Joseph O'Neill
Jozsef Csicsvari
Laszlo F Marton
Masahiko Watanabe
Pablo Fuentealba
Peter Somogyi
Takeshi Kaneko
Thomas Klausberger
Wai Yee Suen
P304
P356
10.1523/JNEUROSCI.3269-05.2005
P407
P577
2005-10-01T00:00:00Z