Progressive dendritic HCN channelopathy during epileptogenesis in the rat pilocarpine model of epilepsy. - Wikidata - wikimedia - TriplyDB

Progressive dendritic HCN channelopathy during epileptogenesis in the rat pilocarpine model of epilepsy.

Progressive dendritic HCN channelopathy during epileptogenesis in the rat pilocarpine model of epilepsy.

http://www.wikidata.org/entity/Q34922351

about

HCN1 channel subunits are a molecular substrate for hypnotic actions of ketamine.Searching for new targets for treatment of pediatric epilepsy Cortical HCN channels: function, trafficking and plasticity Immediate Epileptogenesis after Kainate-Induced Status Epilepticus in C57BL/6J Mice: Evidence from Long Term Continuous Video-EEG Telemetry Homeostasis or channelopathy? Acquired cell type-specific ion channel changes in temporal lobe epilepsy and their antiepileptic potential Classic hippocampal sclerosis and hippocampal-onset epilepsy produced by a single “cryptic” episode of focal hippocampal excitation in awake rats Deletion of the hyperpolarization-activated cyclic nucleotide-gated channel auxiliary subunit TRIP8b impairs hippocampal Ih localization and function and promotes antidepressant behavior in mice.Homeostatic regulation of synaptic excitability: tonic GABA(A) receptor currents replace I(h) in cortical pyramidal neurons of HCN1 knock-out mice.Subunit-specific effects of isoflurane on neuronal Ih in HCN1 knockout mice.Mislocalization of h channel subunits underlies h channelopathy in temporal lobe epilepsy.Loss of dendritic HCN1 subunits enhances cortical excitability and epileptogenesis.Development of spontaneous recurrent seizures after kainate-induced status epilepticus.Neuron-restrictive silencer factor-mediated hyperpolarization-activated cyclic nucleotide gated channelopathy in experimental temporal lobe epilepsy Down-regulation of BK channel expression in the pilocarpine model of temporal lobe epilepsy.Sub region-specific modulation of synchronous neuronal burst firing after a kainic acid insult in organotypic hippocampal cultures.HCN Channel Modulation of Synaptic Integration in GABAergic Interneurons in Malformed Rat Neocortex.Downregulation of dendritic HCN channel gating in epilepsy is mediated by altered phosphorylation signaling.Dendritic ion channel trafficking and plasticity.5-HT7 receptors as modulators of neuronal excitability, synaptic transmission and plasticity: physiological role and possible implications in autism spectrum disorders.Regulation of axonal HCN1 trafficking in perforant path involves expression of specific TRIP8b isoforms.Chronic deficit in the expression of voltage-gated potassium channel Kv3.4 subunit in the hippocampus of pilocarpine-treated epileptic rats Calcium store depletion induces persistent perisomatic increases in the functional density of h channels in hippocampal pyramidal neurons.Altered intrinsic properties of neuronal subtypes in malformed epileptogenic cortex.Rapamycin reverses status epilepticus-induced memory deficits and dendritic damage.HCN channels in behavior and neurological disease: too hyper or not active enough?Initial loss but later excess of GABAergic synapses with dentate granule cells in a rat model of temporal lobe epilepsy.I(h)-mediated depolarization enhances the temporal precision of neuronal integration.Epileptogenesis after prolonged febrile seizures: mechanisms, biomarkers and therapeutic opportunities.Novel HCN2 mutation contributes to febrile seizures by shifting the channel's kinetics in a temperature-dependent manner The fast and slow ups and downs of HCN channel regulation.Differential modulation of repetitive firing and synchronous network activity in neocortical interneurons by inhibition of A-type K(+) channels and Ih.Rapid loss of dendritic HCN channel expression in hippocampal pyramidal neurons following status epilepticus Decreased hyperpolarization-activated currents in layer 5 pyramidal neurons enhances excitability in focal cortical dysplasia.Corticospinal-specific HCN expression in mouse motor cortex: I(h)-dependent synaptic integration as a candidate microcircuit mechanism involved in motor control HCN channelopathies: pathophysiology in genetic epilepsy and therapeutic implications Impaired dendritic expression and plasticity of h-channels in the fmr1(-/y) mouse model of fragile X syndrome.Augmented currents of an HCN2 variant in patients with febrile seizure syndromes Defining "epileptogenesis" and identifying "antiepileptogenic targets" in animal models of acquired temporal lobe epilepsy is not as simple as it might seem.The Role of HCN Channels on Membrane Excitability in the Nervous System Epigenetic mechanisms in stroke and epilepsy.

P2860

Q24653694-F377ABE0-AEBF-44DC-BCE6-734F90677A63 Q27014368-0C6E8EB5-208A-4BD4-9D69-5E108B6B3AC6 Q27027165-D13BD9FB-9A72-43CD-BB6A-57AE93FEAA02 Q27303313-852FEF32-58FE-441B-8ECE-651839C4AB50 Q28080655-FEFE59E2-7715-45DB-9A32-C0442370C4E8 Q29037057-6D947539-798D-4F29-BC76-BF22A3EEC0C1 Q30429700-99835461-D8D8-408F-9B23-4BD9FC22AC2B Q30435045-78DB1637-ABFC-4565-9808-4B8846B7622E Q30437516-A47FC857-6D8D-409A-A4C3-7E080A33B3FD Q30485454-2DB6E483-6874-4FF5-9146-1329C4D6C0A0 Q30490207-800C0B5A-B26B-47C8-B9A2-74AD60BDC61D Q30495304-4A54197A-8BA4-4027-AB57-7CE2DD12723E Q30504521-F30CA58F-EBFA-45C3-8620-C079B2A0B1A9 Q33320921-1618E914-18F3-4D5C-9AEB-3490172405FF Q33348173-B806ECB9-714A-4400-B223-C0CD4E1B6D78 Q33578800-32B687C9-AA83-47F8-AC05-C1CF456B02EF Q33897319-EFDA56A7-99A1-4600-82E5-1BFD7CF3DAD2 Q33987823-1EFEA62B-A243-4A61-A692-41601DA51FA9 Q34093279-D1007BA9-2EC1-4B79-B162-1390B37D76A5 Q34171697-6FF06576-C04D-4341-8671-C35B2C7EDC12 Q34459275-88E62DF0-C216-43D0-B64D-FAC290029140 Q34508404-DC247A48-6B3D-4F0B-89B5-0A9797BA6DDF Q34632262-82F9CCE8-3B8A-46C4-9D4A-68D0F8E3D321 Q34639033-B29F9624-C0ED-4DBA-BD67-9E820D3B57CD Q34777401-1AC3BF24-DC63-48D8-BA6E-871356B2D086 Q34992835-FF979970-AE00-4250-990C-FD52C0494BFB Q35017661-C783B01E-8D68-4436-A9C4-1DA682338F70 Q35028306-27B3D576-F0E8-4D4E-945F-4D21EE15C52B Q35063727-606482EB-9925-4E89-9A10-04C5F819F126 Q35147010-D80FBE26-9B02-4A73-B398-043E488CB6C7 Q35190244-45B6B94A-5C74-43E9-877B-1C8729B48C0A Q35530042-A049B0D2-319F-411A-ACCD-4588740FF253 Q35543912-5FEA02C9-7F79-45D1-8207-45BD6711F55E Q35543931-707F3612-1905-4E2C-BAA7-1E86D3C941D7 Q35657898-F7BD9870-7633-495E-9001-9B36F0260E90 Q35997685-3677D2B4-9165-43EC-A4BD-64BC63E86380 Q36057848-41BD7843-EA1D-4468-8492-640F687316EC Q36098745-CC466AA0-FF1D-4B0F-99CE-2CA51F30DC2F Q36183863-002BDC8D-951C-4D4D-8516-51677C0AC70D Q36465823-D6C7121B-AC81-4B39-8AC6-9D4FD0FDE065

P2860

Progressive dendritic HCN channelopathy during epileptogenesis in the rat pilocarpine model of epilepsy.

http://www.wikidata.org/entity/Q34922351

description

2007 nî lūn-bûn

@nan

2007 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2007年の論文

@ja

2007年論文

@yue

2007年論文

@zh-hant

2007年論文

@zh-hk

2007年論文

@zh-mo

2007年論文

@zh-tw

2007年论文

@wuu

name

Progressive dendritic HCN chan ...... pilocarpine model of epilepsy.

@ast

Progressive dendritic HCN chan ...... pilocarpine model of epilepsy.

@en

Progressive dendritic HCN chan ...... pilocarpine model of epilepsy.

@nl

type

label

Progressive dendritic HCN chan ...... pilocarpine model of epilepsy.

@ast

Progressive dendritic HCN chan ...... pilocarpine model of epilepsy.

@en

Progressive dendritic HCN chan ...... pilocarpine model of epilepsy.

@nl

prefLabel

Progressive dendritic HCN chan ...... pilocarpine model of epilepsy.

@ast

Progressive dendritic HCN chan ...... pilocarpine model of epilepsy.

@en

Progressive dendritic HCN chan ...... pilocarpine model of epilepsy.

@nl

P1433

Q34922351-534E8D33-6121-4E0B-B210-E36F4EB4DAAE

P1476

Q34922351-03CCC3EF-38D8-4566-AD67-895FA26A33CE

P2093

Q34922351-1DBC8A30-1EC2-4EC6-91B0-09E7A1F0106E

Q34922351-2DB0E8A5-216D-41DA-893F-72D99FB3507C

Q34922351-7C178FCF-D9BC-42C3-9BB7-2EFC746C07CA

Q34922351-A940BF6D-F2CF-4D6E-9D6B-BF6E45C49926

Q34922351-C42637A2-4C14-460C-95C9-CB7F8BCC2178

Q34922351-D4C931A3-C506-4AD9-AEDA-948A2A351DBD

Q34922351-DFF0738E-CC59-4C8E-8E97-75A8B4E7AC26

Q34922351-F2C40A56-39B0-44E1-8E0E-754FD1E84DD2

P2860

Q34922351-0A769B4D-8438-4476-A610-5DF6810428D0

Q34922351-1C67CF79-D802-475F-A223-C92B8B762545

Q34922351-1DDD412F-F202-4B20-83BA-98FAC65B0F4B

Q34922351-247ECF4C-A6D8-4020-A8BF-589A0B789E68

Q34922351-2A233883-08E5-4EDC-A345-C8E53762C3C7

Q34922351-2BD12018-BFCA-4A45-AC97-17D1A404B68A

Q34922351-2C0D66F0-1633-4C47-BB9D-9B7B1D851212

Q34922351-2CF9573F-A602-40CC-AFC6-D08AC88498E3

Q34922351-39F7FE2F-AFC3-47E7-BCC0-9283BA1E0040

Q34922351-3A38CA8A-380E-4906-8C99-333BB5FB9098

P304

Q34922351-C27652D2-2856-4DE6-B7C5-540EDFF9D608

P31

Q34922351-D3A7B9C1-2736-49BD-AD70-33A00D590C41

P356

Q34922351-FBA9ABED-D75B-46E0-885B-CE76370A21E6

P407

Q34922351-0C92AD27-EFD9-4150-B55F-FE64FBD642EE

P433

Q34922351-AFED1D30-41D6-4F72-84BF-0D269972D0C0

P478

Q34922351-A77819E6-42F3-48D2-AB16-A0DC7474D2C3

P577

Q34922351-B80C5FA7-0D5F-4659-89B2-7BF9311DE4CF

P698

Q34922351-F48DB312-FA8A-448F-899B-64D7F682B7E3

P932

Q34922351-F3998C7F-7667-4C51-8F38-2416DDD08952

P356

JNEUROSCI.3605-07.2007

P1433

Journal of Neuroscience

P1476

Progressive dendritic HCN chan ...... pilocarpine model of epilepsy.

@en

P2093

Aaron H Sheerin

http://www.w3.org/2001/XMLSchema#string

Anne E Anderson

http://www.w3.org/2001/XMLSchema#string

Joaquin N Lugo

http://www.w3.org/2001/XMLSchema#string

John W Miller

http://www.w3.org/2001/XMLSchema#string

Nicholas P Poolos

http://www.w3.org/2001/XMLSchema#string

Raimondo D'Ambrosio

http://www.w3.org/2001/XMLSchema#string

Sangwook Jung

http://www.w3.org/2001/XMLSchema#string

Terrance D Jones

http://www.w3.org/2001/XMLSchema#string

P2860

Modification of seizure activity by electrical stimulation. II. Motor seizure

Spontaneous recurrent seizures in rats: an experimental model of partial epilepsy

Input-specific immunolocalization of differentially phosphorylated Kv4.2 in the mouse brain

The HCN gene family: molecular basis of the hyperpolarization-activated pacemaker channels.

Temporal lobe epilepsy after experimental prolonged febrile seizures: prospective analysis

Anticonvulsant drugs: mechanisms of action.

Molecular signaling mechanisms underlying epileptogenesis.

Genetic mechanisms that underlie epilepsy.

Developmental febrile seizures modulate hippocampal gene expression of hyperpolarization-activated channels in an isoform- and cell-specific manner.

Homeostatic scaling of neuronal excitability by synaptic modulation of somatic hyperpolarization-activated Ih channels

P304

13012-13021

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1523/JNEUROSCI.3605-07.2007

http://www.w3.org/2001/XMLSchema#string

P407

P433

47

http://www.w3.org/2001/XMLSchema#string

P478

27

http://www.w3.org/2001/XMLSchema#string

P577

2007-11-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

18032674

http://www.w3.org/2001/XMLSchema#string

P932

3087381

http://www.w3.org/2001/XMLSchema#string