Association between genetic variation of CACNA1H and childhood absence epilepsy - Wikidata - thesis-toulmin - TriplyDB

Association between genetic variation of CACNA1H and childhood absence epilepsy

Association between genetic variation of CACNA1H and childhood absence epilepsy

http://www.wikidata.org/entity/Q28191095

about

GABRB3 mutation, G32R, associated with childhood absence epilepsy alters α1β3γ2L γ-aminobutyric acid type A (GABAA) receptor expression and channel gating Linkage and association analysis of CACNG3 in childhood absence epilepsy Why is intelligence correlated with semen quality?: Biochemical pathways common to sperm and neuron function and their vulnerability to pleiotropic mutations The molecular basis for T-type Ca2+ channel inhibition by G protein beta2gamma2 subunits.Molecular targets for antiepileptic drug development Therapeutic Approaches to Genetic Ion Channelopathies and Perspectives in Drug Discovery Genetic neurological channelopathies: molecular genetics and clinical phenotypes.The Physiology, Pathology, and Pharmacology of Voltage-Gated Calcium Channels and Their Future Therapeutic Potential Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders Genetic epilepsy syndromes without structural brain abnormalities: clinical features and experimental models CaV3.2 calcium channels control NMDA receptor-mediated transmission: a new mechanism for absence epilepsy.Adult Deletion of SRF Increases Epileptogenesis and Decreases Activity-Induced Gene Expression.Quantitative magnetic resonance imaging traits as endophenotypes for genetic mapping in epilepsy Understanding Genotypes and Phenotypes in Epileptic Encephalopathies A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar Ataxia Gating effects of mutations in the Cav3.2 T-type calcium channel associated with childhood absence epilepsy The neurobiology of antiepileptic drugs Role of voltage-gated calcium channels in epilepsy.The voltage dependence of gating currents of the neuronal CA(v)3.3 channel is determined by the gating brake in the I-II loop Characterization of the gating brake in the I-II loop of CaV3 T-type calcium channels.Characterization of the gating brake in the I-II loop of Ca(v)3.2 T-type Ca(2+) channels I-II loop structural determinants in the gating and surface expression of low voltage-activated calcium channels.Ins and outs of T-channel structure function.Genetic enhancement of thalamocortical network activity by elevating alpha 1g-mediated low-voltage-activated calcium current induces pure absence epilepsy.Neurological channelopathies.Cav3.2 T-type calcium channel is required for the NFAT-dependent Sox9 expression in tracheal cartilage Neonatal seizures: an update on mechanisms and management Developmental factors in the pathogenesis of neonatal seizures Genetic testing in the epilepsies--report of the ILAE Genetics Commission Familial clustering of seizure types within the idiopathic generalized epilepsies.Antiseizure effects of TrkB kinase inhibition.Rebound burst firing in the reticular thalamus is not essential for pharmacological absence seizures in mice.Importance of mast cell Prss31/transmembrane tryptase/tryptase-γ in lung function and experimental chronic obstructive pulmonary disease and colitis Retrieval of context-associated memory is dependent on the Ca(v)3.2 T-type calcium channel.Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies A genetic interaction network model of a complex neurological disease.Genes associated with idiopathic epilepsies: a current overview.Genetics and function of neocortical GABAergic interneurons in neurodevelopmental disorders Behavior training reverses asymmetry in hippocampal transcriptome of the cav3.2 knockout mice.Cellular and network mechanisms of genetically-determined absence seizures.

P2860

Q24304333-8D12481B-B9EE-465C-9AAD-741410A1E197 Q24642036-9056C02D-1E22-491C-9A2E-47479018C0BC Q24642169-646F2D76-7ECE-4910-93E7-12902DAD8092 Q24676565-8D7EFC7D-62C2-4887-9F92-1BB8F445B602 Q24683346-87D78828-81E2-4B11-98D9-E120F9F4E3AD Q26744730-0786D4B4-ABF2-4C50-96F0-7D47DBC15A84 Q26777559-B4348A3E-3927-4652-9455-8806B88F34D0 Q26781422-B724D4B0-F2BA-47FC-851B-0A8DC5EBBB10 Q26783154-0DA4C168-A86E-40C2-BA69-D6864FAEB004 Q26861471-EAC3B085-A792-4269-9D86-EC3334A03150 Q27323026-6F761611-634B-4DAB-8D77-77D5B1DD4416 Q27345329-914041BC-4DD7-44C1-8515-3059B96B1370 Q28067109-D9AE85C3-A52F-44A2-944A-BAEB82713629 Q28080066-64D52848-AEE0-4393-A01D-814B9C75E771 Q28115409-D5337613-36E1-444E-AADF-328AE9E4EA54 Q28239380-C19511B8-1384-4BB3-A446-CBFAF527C8E5 Q28267900-51EC9A0B-CD2D-4ABE-A462-8C70EC7F8DE3 Q30427731-9E0611CB-7A3C-43DB-BC03-242450985F54 Q30427770-594B41CC-9AC2-42B6-B44C-D2FB432AFE00 Q30429903-5F3B996F-8E8A-4316-8E23-CA589450CA8C Q30439985-79419513-2DBE-48CD-B82B-A24EB135099B Q30441251-18BCB903-0B56-4C31-ACA0-CCBAF967ED9F Q30457231-12815EAF-B8C0-40F2-830F-3AD43C6D4FC4 Q30486665-721054B6-20F5-4747-9E76-552F2973AC78 Q30493341-0E720ED6-F7F5-4431-ACC4-42D7495BC67B Q30578389-778BC974-8096-4D7F-915B-24F0CFAC3693 Q33639690-8A72BF8F-8404-43F3-B634-F0DA6208036E Q33688474-C658B090-6CAA-4895-AA1D-9185C4CEEFCA Q33794130-1DFCA398-3BE6-4B68-89D3-3D1FF7D930E0 Q34019222-CB25C2F1-D334-4DD1-BD14-77143A4D4083 Q34021014-218B75A4-9727-46F1-82AA-997CF161ECE0 Q34060780-68F1FDDC-55D3-4AA1-A0D1-93FB924FF84F Q34073928-59EEDD62-9C38-48BE-A442-6EB3C0369B3F Q34123666-46D31304-54B5-4544-B9F1-B695009AC016 Q34307393-86636797-F8E4-402C-9CB6-C2F45E4C4DEC Q34559798-DD2A9B07-0362-42B3-871D-3ABF85E064A2 Q34605560-A33924AD-E071-46DE-AC0D-54AFA3E21D39 Q35173644-10493201-480A-49D9-B535-7FBA3B435284 Q35174776-1DF355CE-7E3B-4C2A-A01D-57C95F9159EB Q35199746-DF29BC90-97BA-4319-8FA5-A6980E393A0F

P2860

Association between genetic variation of CACNA1H and childhood absence epilepsy

http://www.wikidata.org/entity/Q28191095

description

2003 nî lūn-bûn

@nan

2003 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2003 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2003年の論文

@ja

2003年論文

@yue

2003年論文

@zh-hant

2003年論文

@zh-hk

2003年論文

@zh-mo

2003年論文

@zh-tw

2003年论文

@wuu

name

Association between genetic variation of CACNA1H and childhood absence epilepsy

@ast

Association between genetic variation of CACNA1H and childhood absence epilepsy

@en

Association between genetic variation of CACNA1H and childhood absence epilepsy

@nl

type

label

Association between genetic variation of CACNA1H and childhood absence epilepsy

@ast

Association between genetic variation of CACNA1H and childhood absence epilepsy

@en

Association between genetic variation of CACNA1H and childhood absence epilepsy

@nl

prefLabel

Association between genetic variation of CACNA1H and childhood absence epilepsy

@ast

Association between genetic variation of CACNA1H and childhood absence epilepsy

@en

Association between genetic variation of CACNA1H and childhood absence epilepsy

@nl

P1433

Q28191095-A4EC6B62-3703-4C38-B42D-3468BF8D816B

P1476

Q28191095-1367C9E4-B97E-4F00-81AB-D63DCAB17294

P2093

Q28191095-18DB010F-FBF0-4EFE-AC7F-F28773B75EAE

Q28191095-1A169F8D-F1B9-4941-BCB4-AFD6AA08AF44

Q28191095-1E042681-E12B-4130-9F08-2B60A7779CB3

Q28191095-3F2468EB-1285-46B5-B94D-984DF5E02F0E

Q28191095-5A89802C-1A5F-42B6-92AC-FA7718F34DC3

Q28191095-5EBF93B8-7A97-4333-BF3C-5B258C08CE06

Q28191095-7279F8DE-FBCF-4303-9AE2-F4D744784100

Q28191095-A6103314-F680-48BE-94D7-C3E4AAC891D4

Q28191095-BDC33B46-A052-4B02-AFED-7E6316279CC5

Q28191095-CBBADB36-9AA8-40CE-891B-4AD78E14C6DE

P304

Q28191095-04B8C845-451B-4199-9143-0C1697EED5CC

P31

Q28191095-16703769-DC7B-48A1-B828-7AAD71CF4EEA

P3181

Q28191095-B6AD7769-DF6E-45C6-AF15-2CF9DAF21763

P356

Q28191095-228D6267-DF6F-4555-BA2C-E519023D223A

P407

Q28191095-44028AFA-802A-410C-83C8-93A5289922DB

P433

Q28191095-82580A04-0FD4-4520-9FED-45C7D3F791FB

P478

Q28191095-E69F564E-DC4D-4C47-A04A-55ED1127E16F

P50

Q28191095-7CBB02E1-281D-4F02-897F-897917085099

Q28191095-EEE492E9-E5EF-45E7-BE6E-EA1B723582A9

P577

Q28191095-74A8ABA9-5DD0-4076-BD44-60DEDF65FD33

P698

Q28191095-C06FE433-6A73-453B-B372-0E1E04BAF6F7

P3181

P356

P1433

Annals of Neurology

P1476

Association between genetic variation of CACNA1H and childhood absence epilepsy

@en

P2093

Boqin Qiang

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

Hong Pan

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

Husheng Wu

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

Jianjun Lu

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

Keming Xu

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

Piu Chan

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

Wilson H Y Lo

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

Xiaoyan Liu

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

Xinhua Bao

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

Xiru Wu

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

P304

239-243

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

P31

scholarly article

P3181

1741064

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

P356

10.1002/ANA.10607

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

P407

P433

2

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

P478

54

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

P50

P577

2003-08-01T00:00:00Z

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

P698

12891677

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