Novel mutations in the KCND3-encoded Kv4.3 K+ channel associated with autopsy-negative sudden unexplained death
about
Electrophysiological Mechanisms of Brugada Syndrome: Insights from Pre-clinical and Clinical StudiesAllitridi inhibits multiple cardiac potassium channels expressed in HEK 293 cellsProperties and molecular determinants of the natural flavone acacetin for blocking hKv4.3 channelsMaturing human pluripotent stem cell-derived cardiomyocytes in human engineered cardiac tissuesAbnormal repolarization as the basis for late potentials and fractionated electrograms recorded from epicardium in experimental models of Brugada syndrome.The potential role of Kv4.3 K+ channel in heart hypertrophy.First de novo KCND3 mutation causes severe Kv4.3 channel dysfunction leading to early onset cerebellar ataxia, intellectual disability, oral apraxia and epilepsyCardiac ion channelopathies and the sudden infant death syndromeAuxiliary KChIP4a suppresses A-type K+ current through endoplasmic reticulum (ER) retention and promoting closed-state inactivation of Kv4 channelsCellular and ionic mechanisms underlying the effects of cilostazol, milrinone, and isoproterenol to suppress arrhythmogenesis in an experimental model of early repolarization syndrome.Genetic testing in heritable cardiac arrhythmia syndromes: differentiating pathogenic mutations from background genetic noise.Cellular mechanisms underlying the effects of milrinone and cilostazol to suppress arrhythmogenesis associated with Brugada syndrome.Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram.Potassium channels: structures, diseases, and modulators.Modeling of the Binding of Peptide Blockers to Voltage-Gated Potassium Channels: Approaches and Evidence.KCNE4 and KCNE5: K(+) channel regulation and cardiac arrhythmogenesis.KCNA4 deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability.Pore size matters for potassium channel conductance.Sudden cardiac death in the young: how can disease recognition and prevention in family members be improved?A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation.Infant sudden death: Mutations responsible for impaired Nav1.5 channel trafficking and function.A novel KCND3 mutation associated with early-onset lone atrial fibrillation.Sudden infant death syndrome and inherited cardiac conditions.Novel Features and Abnormal Pattern of Cerebral Glucose Metabolism in Spinocerebellar Ataxia 19.
P2860
Q28073629-1A2DB88A-FD91-416F-A0A3-28CA87CC5CC9Q28484383-7E94D06D-6B16-47A2-95F0-2EC466CBC430Q28488517-32EA4137-C491-4D54-8EF6-87D691259F52Q28550738-E1739173-4084-4471-B570-4EE75B9A9759Q33625055-A60BEF4E-FEB9-49C3-B0F0-3F2F9FB0A6F4Q34373955-0BECA247-1BF0-4D17-89B1-5AAB819B3973Q35696704-DC461439-A9D3-4445-9936-8EF142391567Q36486478-9E5EE667-D7DF-472B-9CF3-67F04A8C96DEQ36873562-E50FBFEA-CDF5-47EE-AB00-573D0BA1DE17Q36932457-C4D3007D-205D-4DEB-B88F-C409E750CF0BQ36994901-DEC1E01B-B395-4F83-A3B7-0B0DA933CB20Q37302824-67712790-DE5A-4E1B-A42E-8F11F5941945Q37336109-E9704284-19AF-414C-AF08-7DAE7B8DF00FQ38151974-6BD07AA3-2A6B-4D4B-A4C8-39452EC292DDQ38903019-2188D4AA-B836-4DAB-AC11-530C9399203CQ38916407-FE0B18D3-EE36-4421-AA82-7AF5C52B6232Q40599284-0B51A86A-7166-499A-8D7E-58C95630B08CQ41189128-5FBCE25D-FF38-459A-AE43-B72BB2F66646Q44701011-408AF56A-32F7-43A5-A72D-A6B8257E5A38Q46648374-F34B8563-3AAE-4523-9FA6-360783D20656Q47746225-5C55E890-A431-412A-997A-004C54AE33A8Q49203273-7F01C9BA-B5F6-477A-BEE5-0C5F8F152CFDQ50208657-DCF53763-F4F9-4025-A808-ACF9485F5433Q52661472-FD173747-B9DE-43B3-A98A-6FF8C0C3DFF9
P2860
Novel mutations in the KCND3-encoded Kv4.3 K+ channel associated with autopsy-negative sudden unexplained death
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh
2012年學術文章
@zh-hant
name
Novel mutations in the KCND3-e ...... ative sudden unexplained death
@ast
Novel mutations in the KCND3-e ...... ative sudden unexplained death
@en
type
label
Novel mutations in the KCND3-e ...... ative sudden unexplained death
@ast
Novel mutations in the KCND3-e ...... ative sudden unexplained death
@en
prefLabel
Novel mutations in the KCND3-e ...... ative sudden unexplained death
@ast
Novel mutations in the KCND3-e ...... ative sudden unexplained death
@en
P2093
P2860
P356
P1433
P1476
Novel mutations in the KCND3-e ...... ative sudden unexplained death
@en
P2093
Chad J Kritzberger
David J Tester
John R Giudicessi
Michael J Ackerman
Vladislav V Nesterenko
P2860
P304
P356
10.1002/HUMU.22058
P577
2012-03-27T00:00:00Z