Pages that link to "Q24314276"
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The following pages link to SCN4B-encoded sodium channel beta4 subunit in congenital long-QT syndrome (Q24314276):
Displaying 50 items.
- atrial fibrillation (Q815819) (← links)
- Sodium voltage-gated channel alpha subunit 5 (Q3459294) (← links)
- Sodium voltage-gated channel beta subunit 4 (Q7389191) (← links)
- Loss-of-function mutation of the SCN3B-encoded sodium channel {beta}3 subunit associated with a case of idiopathic ventricular fibrillation (Q24293547) (← links)
- Sudden infant death syndrome-associated mutations in the sodium channel beta subunits (Q24302400) (← links)
- Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex (Q24308697) (← links)
- Crystallographic insights into sodium-channel modulation by the β4 subunit (Q24310927) (← links)
- Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation (Q24322712) (← links)
- GPD1L links redox state to cardiac excitability by PKC-dependent phosphorylation of the sodium channel SCN5A (Q24323030) (← links)
- Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test (Q24607414) (← links)
- Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome (Q24634068) (← links)
- Scn3b knockout mice exhibit abnormal ventricular electrophysiological properties (Q24651316) (← links)
- Genetics of channelopathies associated with sudden cardiac death (Q26777170) (← links)
- Genetics of inherited primary arrhythmia disorders (Q26783570) (← links)
- Voltage-gated sodium channels and cancer: is excitability their primary role? (Q26797387) (← links)
- The role of late I Na in development of cardiac arrhythmias (Q26823149) (← links)
- Long-QT syndrome: from genetics to management (Q26823298) (← links)
- Channelopathies from mutations in the cardiac sodium channel protein complex (Q26824051) (← links)
- Molecular and genetic basis of sudden cardiac death (Q26825973) (← links)
- Ion Channels in the Heart (Q26829681) (← links)
- The role of the SCN5A-encoded channelopathy in irritable bowel syndrome and other gastrointestinal disorders (Q28081627) (← links)
- Sodium channel β subunits: emerging targets in channelopathies (Q28082122) (← links)
- Identification of a Kir3.4 mutation in congenital long QT syndrome (Q28114943) (← links)
- Cardiac sodium channel Na(v)1.5 and interacting proteins: Physiology and pathophysiology (Q28258096) (← links)
- The genetic basis of long QT and short QT syndromes: a mutation update (Q28262724) (← links)
- A novel and lethal de novo LQT-3 mutation in a newborn with distinct molecular pharmacology and therapeutic response (Q28471659) (← links)
- α1-Syntrophin Variant Identified in Drug-Induced Long QT Syndrome Increases Late Sodium Current (Q28551060) (← links)
- Functional protein expression of multiple sodium channel alpha- and beta-subunit isoforms in neonatal cardiomyocytes (Q28584225) (← links)
- Scn3b knockout mice exhibit abnormal sino-atrial and cardiac conduction properties (Q28587466) (← links)
- Control of transient, resurgent, and persistent current by open-channel block by Na channel beta4 in cultured cerebellar granule neurons (Q28592952) (← links)
- Congenital Long QT Syndrome: An Update and Present Perspective in Saudi Arabia (Q28661099) (← links)
- Genome analysis and signature discovery for diving and sensory properties of the endangered Chinese alligator (Q28681251) (← links)
- The importance of serine 161 in the sodium channel beta3 subunit for modulation of Na(V)1.2 gating (Q30430912) (← links)
- Sudden cardiac death prediction and prevention: report from a National Heart, Lung, and Blood Institute and Heart Rhythm Society Workshop (Q30433543) (← links)
- Clinical and genetic analysis of long QT syndrome in children from six families in Saudi Arabia: are they different? (Q33157079) (← links)
- QTc: how long is too long? (Q33157779) (← links)
- The prevalence and diagnostic/prognostic utility of sinus arrhythmia in the evaluation of congenital long QT syndrome (Q33159036) (← links)
- Prevalence and Spectrum of Large Deletions or Duplications in the Major Long QT Syndrome-Susceptibility Genes and Implications for Long QT Syndrome Genetic Testing (Q33159274) (← links)
- Overlapping LQT1 and LQT2 phenotype in a patient with long QT syndrome associated with loss-of-function variations in KCNQ1 and KCNH2 (Q33159536) (← links)
- Holter monitoring in the evaluation of congenital long QT syndrome (Q33159955) (← links)
- Subclinical cardiomyopathy and long QT syndrome: an echocardiographic observation (Q33161936) (← links)
- Long QT syndrome in South Africa: the results of comprehensive genetic screening (Q33163516) (← links)
- Genetics of long QT syndrome. (Q33164422) (← links)
- Deleterious protein-altering mutations in the SCN10A voltage-gated sodium channel gene are associated with prolonged QT. (Q33168530) (← links)
- Molecular cloning and analysis of zebrafish voltage-gated sodium channel beta subunit genes: implications for the evolution of electrical signaling in vertebrates (Q33290470) (← links)
- Microsatellites and SNPs linkage analysis in a Sardinian genetic isolate confirms several essential hypertension loci previously identified in different populations (Q33498133) (← links)
- A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype (Q33572315) (← links)
- A common single nucleotide polymorphism can exacerbate long-QT type 2 syndrome leading to sudden infant death. (Q33804950) (← links)
- Cardiac sodium channelopathies (Q33906972) (← links)
- Systems approach to understanding electromechanical activity in the human heart: a national heart, lung, and blood institute workshop summary. (Q34013724) (← links)