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searching for SCN5A 18 found (46 total)

alternate case: sCN5A

Lev's disease (2,738 words) [view diff] case mismatch in snippet view article find links to article

risk. A mouse model studied mice with a heterogenous mutation to their SCN5a gene, which impacts the formation of Na+ channels, leaving them with myocardial

Sudden unexpected death in epilepsy (3,405 words) [view diff] exact match in snippet view article find links to article

1 (LQT1), and epilepsy. Similarly, mutations in KCNH2 (linked to LQT2), SCN5A (LQT3), KCNJ2 (LQT7), and CACNA1C (LQT8) have been reported in cases of

SCN1B (1,000 words) [view diff] case mismatch in snippet view article find links to article

(2002). "The sodium channel beta-subunit SCN3b modulates the kinetics of SCN5a and is expressed heterogeneously in sheep heart". J. Physiol. 537 (Pt 3):

List of circulatory system conditions (476 words) [view diff] exact match in snippet view article find links to article

Brugada syndrome displaying a sudden unexpected death syndrome mutation in SCN5A". J. Cardiovasc. Electrophysiol. 15 (1): 64–9. doi:10.1046/j.1540-8167.2004

Sodium channel (5,625 words) [view diff] exact match in snippet view article find links to article

Nav1.1 through Nav1.9. The gene names are referred to as SCN1A through SCN5A, then SCN8A through SCN11A. The "tenth member", Nax, does not act in a voltage-gated

Ankyrin-3 (1,738 words) [view diff] exact match in snippet view article find links to article

firing. The ANK3 protein associates with the cardiac sodium channel Nav1.5 (SCN5A). Both proteins are highly expressed at ventricular intercalated disc and

Phrixotoxin (692 words) [view diff] exact match in snippet view article find links to article

sodium channel subtypes (Nav1.1/SCN1A, Nav1.2/SCN2A, Nav1.4/SCN4A, Nav1.5/SCN5A, and Nav1.8/SCN10A) (Bosmans 2006) harv error: no target: CITEREFBosmans2006

LmαTX5 (994 words) [view diff] exact match in snippet view article find links to article

sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2020-10-23. "SCN5A sodium voltage-gated channel alpha subunit 5 [Homo sapiens (human)] - Gene

Simple Mendelian genetics in humans (860 words) [view diff] exact match in snippet view article find links to article

syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)". Journal of Clinical Investigation. 112 (7): 1019–1028. doi:10.1172/JCI18062

Functional gastrointestinal disorder (4,513 words) [view diff] exact match in snippet view article find links to article

(TNF-SF15); intracellular cell signaling (G proteins); and ion channels (SCN5A). However, the expression of a FGID requires the influence of additional

KCNE1 (3,763 words) [view diff] exact match in snippet view article find links to article

2000). "Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2". Circulation. 102 (10): 1178–1185. doi:10.1161/01.cir

Salimuzzaman Siddiqui (2,330 words) [view diff] exact match in snippet view article find links to article

Parameters and Ajmaline Test in the Diagnosis of Brugada Syndrome Caused by SCN5A Mutations". Circulation. 110 (19): 3023–3027. doi:10.1161/01.CIR.0000144299

Molecular autopsy (1,912 words) [view diff] exact match in snippet view article find links to article

tested. The molecular autopsy focuses on four main genes: KCNQ1, KCNH2, SCN5A, and RYR2. Greater than 95% of the mutations found in the molecular autopsy

Masonic Medical Research Institute (1,703 words) [view diff] exact match in snippet view article find links to article

J, T and U waves. Between 1996 and 1998 MMRI published the first gene, SCN5A, to be linked to idiopathic ventricular fibrillation (IVF). The MMRI named

Cheetah (19,877 words) [view diff] exact match in snippet view article find links to article

Regulation of muscle contraction (Five genes: ADORA1, ADRA1B, CACNA1C, RGS2, SCN5A). Physiological stress response (Two genes: ADORA1, TAOK2). Negative regulation

CSRP3 (4,114 words) [view diff] exact match in snippet view article find links to article

Litt M (May 2008). "Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated

Developmental bioelectricity (17,264 words) [view diff] exact match in snippet view article find links to article

Hales, T. G; Stuart, J. M; Lee, N. H (2010). "Voltage-gated Na+ channel SCN5A is a key regulator of a gene transcriptional network that controls colon

Voltage-gated sodium channel (3,706 words) [view diff] exact match in snippet view article find links to article

Nav1.1 through Nav1.9. The gene names are referred to as SCN1A through SCN5A, then SCN8A through SCN11A. The "tenth member", Nax, does not act in a voltage-gated