Pages that link to "Q51614266"

The following pages link to Assignment of the human heart tetrodotoxin-resistant voltage-gated Na channel alpha-subunit gene (SCN5A) to band 3p21. (Q51614266):

Displaying 34 items.

• SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome (Q24317024) (← links)
• The genetic basis of Brugada syndrome: a mutation update (Q28252115) (← links)
• The genetic basis of long QT and short QT syndromes: a mutation update (Q28262724) (← links)
• long QT syndrome 3 (Q32139750) (← links)
• Molecular biology and the prolonged QT syndromes (Q33146297) (← links)
• Molecular mechanism for an inherited cardiac arrhythmia (Q33173678) (← links)
• The Molecular Ggenetics of the Long QT Syndrome: Genes Causing Fainting and Sudden Death (Q33175543) (← links)
• Caveolae, ion channels and cardiac arrhythmias (Q33720799) (← links)
• Distinct local anesthetic affinities in Na channel subtypes (Q34017596) (← links)
• Molecular genetic basis of sudden cardiac death (Q34469735) (← links)
• A heterozygous deletion mutation in the cardiac sodium channel gene SCN5A with loss- and gain-of-function characteristics manifests as isolated conduction disease, without signs of Brugada or long QT syndrome (Q34808264) (← links)
• Cardiac Sodium Channel Diseases (Q35127761) (← links)
• Cardiac Safety Implications of hNav1.5 Blockade and a Framework for Pre-Clinical Evaluation. (Q35698299) (← links)
• Brugada and long QT-3 syndromes: two phenotypes of the sodium channel disease. (Q35831609) (← links)
• Computational biology in the study of cardiac ion channels and cell electrophysiology. (Q36015209) (← links)
• RBM25/LUC7L3 function in cardiac sodium channel splicing regulation of human heart failure. (Q36494631) (← links)
• Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy. (Q36615476) (← links)
• Characterization of human cardiac Na channel mutations in the congenital long QT syndrome (Q36689783) (← links)
• Pharmacological targeting of long QT mutant sodium channels (Q37365724) (← links)
• Phenotypical Manifestations of Mutations in the Genes Encoding Subunits of the Cardiac Sodium Channel (Q37860068) (← links)
• Long-term flecainide therapy in type 3 long QT syndrome (Q38878680) (← links)
• Differential modulation of late sodium current by protein kinase A in R1623Q mutant of LQT3. (Q39891244) (← links)
• SCN5A mutation (T1620M) causing Brugada syndrome exhibits different phenotypes when expressed in Xenopus oocytes and mammalian cells (Q40901536) (← links)
• Ion Channel Mutations and Diseases of Skeletal Muscle (Q41636125) (← links)
• Long QT syndrome: from channels to cardiac arrhythmias (Q41867575) (← links)
• SCN5A splicing variants and the possibility of predicting heart failure-associated arrhythmia. (Q41968270) (← links)
• Cardiac Arrhythmias Related to Sodium Channel Dysfunction. (Q47720327) (← links)
• A de novo missense mutation of human cardiac Na channel exhibiting novel molecular mechanisms of long QT syndrome (Q48944651) (← links)
• Phenotypic Characterization of a Novel Long-QT Syndrome Mutation (R1623Q) in the Cardiac Sodium Channel (Q48944880) (← links)
• Polymorphisms in the cardiac sodium channel promoter displaying variant in vitro expression activity (Q51792782) (← links)
• Polymorphism H558R in the human cardiac sodium channel SCN5A gene is associated with atrial fibrillation. (Q53964824) (← links)
• Replication of Associations with Electrocardio-graphic Traits in African Americans from Clinical and Epidemiologic Studies (Q57398487) (← links)
• Variants: Association With Cardiac Disorders (Q58578329) (← links)
• Long QT syndrome (Q73885519) (← links)