A sodium channel pore mutation causing Brugada syndrome - Wikidata - wikimedia - TriplyDB

A sodium channel pore mutation causing Brugada syndrome

A sodium channel pore mutation causing Brugada syndrome

http://www.wikidata.org/entity/Q35605502

about

Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias Cardiac Na+ current regulation by pyridine nucleotides Physiological and Pathophysiological Insights of Nav1.4 and Nav1.5 Comparison Cloning and expression of the two new variants of Nav1.5/SCN5A in rat brain The ataxia3 mutation in the N-terminal cytoplasmic domain of sodium channel Na(v)1.6 disrupts intracellular trafficking An atypical case of Brugada syndrome.Risk stratification and treatment of brugada syndrome.Cardiac sodium channelopathies.Emerging concepts in the pharmacogenomics of arrhythmias: ion channel trafficking.Human heart failure is associated with abnormal C-terminal splicing variants in the cardiac sodium channel The genetic component of Brugada syndrome Genetic biomarkers in Brugada syndrome.Cardiac sodium channels and inherited electrophysiological disorders: an update on the pharmacotherapy.A novel strategy using cardiac sodium channel polymorphic fragments to rescue trafficking-deficient SCN5A mutations Therapeutic Strategies Targeting Inherited Cardiomyopathies.A stop codon mutation in SCN9A causes lack of pain sensation.Atrial arrhythmogenicity in aged Scn5a+/DeltaKPQ mice modeling long QT type 3 syndrome and its relationship to Na+ channel expression and cardiac conduction.Effects of SO2 derivatives on sodium currents in acutely isolated rat hippocampal lead-exposed neurons.SCN5A gene mutations and the risk of ventricular fibrillation and syncope in Brugada syndrome patients: A meta-analysis

P2860

Q24298971-03B010A2-664B-4AD0-900D-782EE79D5D0F Q24315557-58FB53B2-37C1-4802-999C-2BE32B4FDB30 Q26772794-C064FE9C-0972-4BF5-A22C-E6EDF6A7A792 Q28581127-F49200A9-A6DD-40D9-9BBF-82BEF6C400E5 Q30487520-799DC26D-FCF4-438E-BE82-1421A4ED4CFE Q33160580-590BA669-7360-44E9-8930-437B013E6684 Q33164381-399D4245-03CC-4003-A9CA-2B83B22EE781 Q33906972-B46FCD0C-07CB-4A95-A045-BA5602058EE1 Q34066888-FB3798B0-673F-4295-8D5A-41124E99A5BC Q35169656-D7D4893E-F1C2-4106-A837-4B1E45210162 Q37011109-6141B1BC-73D2-4BCF-A031-5936AC2F1370 Q38125767-1FFE5C40-3338-4ED7-9D26-40A5BC9D4C21 Q38225937-545DE449-5B5D-42C4-877B-8EF15B7AF9A7 Q38769313-2259AE0D-7B10-4089-9FEC-D9D66C716F49 Q39404059-B9393CE1-504F-4A23-94CE-2A4C760BD9A6 Q40114322-DB636466-5172-457B-9D60-D5562757AAF4 Q41896872-E468A3C4-5540-4B43-8D9C-D259079764E7 Q48952345-49134F38-4AB3-4C65-8B10-ABB84A29836C Q57495982-9D4FCA4D-FA9C-4F3D-B74C-E8583D09FF63

P2860

A sodium channel pore mutation causing Brugada syndrome

http://www.wikidata.org/entity/Q35605502

description

2006 nî lūn-bûn

@nan

2006年の論文

@ja

2006年論文

@yue

2006年論文

@zh-hant

2006年論文

@zh-hk

2006年論文

@zh-mo

2006年論文

@zh-tw

2006年论文

@wuu

2006年论文

@zh

2006年论文

@zh-cn

name

A sodium channel pore mutation causing Brugada syndrome

@ast

A sodium channel pore mutation causing Brugada syndrome

@en

type

label

A sodium channel pore mutation causing Brugada syndrome

@ast

A sodium channel pore mutation causing Brugada syndrome

@en

prefLabel

A sodium channel pore mutation causing Brugada syndrome

@ast

A sodium channel pore mutation causing Brugada syndrome

@en

P1433

Q35605502-6B3CBF14-EE88-4282-8F9C-3FC0F178B335

P1476

Q35605502-9B3EFEFE-F0A8-49CA-A93C-BE5905986E2B

P2093

Q35605502-00233FC0-913F-48AC-9BA6-7A9DB257455B

Q35605502-00372E73-812D-4E00-B1A6-675A59D142FC

Q35605502-0AF6493D-ECEE-4656-89F4-CDE3FFDE42AB

Q35605502-183D22D3-1986-474F-B144-47FC1DE64C58

Q35605502-53A57D87-5924-4450-8314-CA6C833C4EB0

Q35605502-7C575FC0-70BC-4C22-A48E-6675B7E594BC

Q35605502-8CB39E91-7ECA-4FF9-8C65-6F0B601D8D85

Q35605502-A9AD7E1C-1D69-4A5C-A80F-5639FFD91726

Q35605502-AD747322-36A6-4D9F-B904-26BCF62A791B

P2860

Q35605502-020B6EC7-0F2A-47B5-93B5-499C528E085C

Q35605502-02196D57-EE0D-48EB-9019-5C44541C04C5

Q35605502-061D9770-AAD8-425C-98A9-52A52C2FC238

Q35605502-0BE00647-043D-4E29-B0DE-B5FE1E0337F8

Q35605502-0D4822BF-8916-4939-991A-F93302E66925

Q35605502-118C2D69-99CD-46BF-A701-47A2D3BBE8D3

Q35605502-1AC6DABD-D940-4AE4-8CD4-B0BE25FE2D48

Q35605502-1D947629-544A-4E3D-B2EB-C1A7FA9A633A

Q35605502-24CE8EEE-4014-4790-B139-4F630CA963DC

Q35605502-2AB3AF5F-FB12-48D0-8D76-8C49D86574F6

P304

Q35605502-B7313792-825E-4534-AC07-778742D9F66A

P31

Q35605502-4366DB50-10AC-416A-BB91-2C254BD927B6

P356

Q35605502-024EC65F-935A-431A-AAD8-72D7F6420A7B

P433

Q35605502-C5049FA2-6E95-4F2F-A9F3-5BCED6F57C67

P478

Q35605502-22C52051-94D1-4C3E-AFF3-107CD3F70A84

P577

Q35605502-42B09CF4-BD17-487D-9EFF-E86B95E04410

P5875

Q35605502-8B7ECD7A-F0A4-4096-B267-C432FA8CC021

P698

Q35605502-6F802FB8-F8B3-4EDB-934C-B3F58AA0A896

P932

Q35605502-494CAF9D-34DF-4E08-8ABF-4E79FB230713

P356

J.HRTHM.2006.09.031

P1433

P1476

A sodium channel pore mutation causing Brugada syndrome

@en

P2093

Arnold E Pfahnl

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

Barry London

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

Cari Kornblit

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

Lijuan L Shang

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

Prakash C Viswanathan

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

Raul Weiss

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

Samuel C Dudley

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

Shamarendra Sanyal

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

Vladimir Shusterman

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

P2860

A ubiquitous splice variant and a common polymorphism affect heterologous expression of recombinant human SCN5A heart sodium channels

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

Ultra-slow inactivation in mu1 Na+ channels is produced by a structural rearrangement of the outer vestibule

Pause induced early afterdepolarizations in the long QT syndrome: a simulation study.

Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families.

Double SCN5A mutation underlying asymptomatic Brugada syndrome.

The long QT syndrome: therapeutic implications of a genetic diagnosis.

Cardiac histological substrate in patients with clinical phenotype of Brugada syndrome.

Ionic mechanisms responsible for the electrocardiographic phenotype of the Brugada syndrome are temperature dependent.

Long-term follow-up of individuals with the electrocardiographic pattern of right bundle-branch block and ST-segment elevation in precordial leads V1 to V3.

P304

46-53

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

P31

scholarly article

P356

10.1016/J.HRTHM.2006.09.031

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

P433

1

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

P478

4

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

P577

2006-09-28T00:00:00Z

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

P5875

6601831

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

P698

17198989

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

P932

1779366

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