دانلود مقالات ISI درباره Scn1B + ترجمه فارسی

Functional implications of a rare variant in the sodium channel β1B subunit (SCN1B) in a 5-month-old male sudden infant death syndrome case

Keywords: Cardiac channelopathy; Electrophysiological analysis; SCN1B; Sudden infant death syndrome; Whole-cell patch clamp; Whole-exome sequencing;

دانلود رایگان متن کامل مقاله ISI 4 صفحه سال انتشار : 2018 سفارش ترجمه

Lack of genotype-phenotype correlation in Brugada Syndrome and Sudden Arrhythmic Death Syndrome families with reported pathogenic SCN1B variants

Keywords: Brugada Syndrome; Genotype-phenotype correlation; Reclassification; SADS; SCN1B; Sudden cardiac death;

دانلود رایگان متن کامل مقاله ISI 7 صفحه سال انتشار : 2018 سفارش ترجمه

Association of a synonymous SCN1B variant affecting splicing efficiency with Benign Familial Infantile Epilepsy (BFIE)

Keywords: Benign Familial Infantile Epilepsy (BFIE); SCN1B; PRRT2; Splice variant; Minigene reporter assay; BIS; Benign Infantile Seizures; BFIC/BFIS; Benign Familial Infantile Convulsions/Seizures; BFIE; Benign Familial Infantile Epilepsy; WES; Whole Exome Sequenc

دانلود رایگان متن کامل مقاله ISI 10 صفحه سال انتشار : 2017 سفارش ترجمه

Do mutations in SCN1B cause Dravet syndrome?

Keywords: SCN1B; Dravet syndrome; Epileptic encephalopathy;

دانلود رایگان متن کامل مقاله ISI 4 صفحه سال انتشار : 2013 سفارش ترجمه

A putative disease-associated haplotype within the SCN1A gene in Dravet syndrome

Keywords: Febrile seizures; SCN1A; SCN1B; Dravet syndrome; SMEI; Haplotype;

دانلود رایگان متن کامل مقاله ISI 4 صفحه سال انتشار : 2011 سفارش ترجمه

Molecular basis of severe myoclonic epilepsy in infancy

Keywords: Severe myoclonic epilepsy in infancy; Sodium channel gene; SCN1A; SCN2A; SCN1B

دانلود رایگان متن کامل مقاله ISI 4 صفحه سال انتشار : 2009 سفارش ترجمه

Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?

Keywords: Dravet syndrome; SMEI; GEFS+; Febrile seizures; SCN1A; SCN1B; GABRG2

دانلود رایگان متن کامل مقاله ISI 7 صفحه سال انتشار : 2009 سفارش ترجمه

Gene expression profiling reveals the mechanism of action of anticonvulsant drug QYS

Keywords: Qingyangshenylycosides (QYS); Audiogenic seizure (AGS); Anticonvulsant drug; Gene expression; Scn1b; Metabolic enzyme;

دانلود رایگان متن کامل مقاله ISI 7 صفحه سال انتشار : 2005 سفارش ترجمه

Involvement of Scn1b and Kcna1 ion channels in audiogenic seizures and PTZ-induced epilepsy

Keywords: AGS; audiogenic seizure; GABAA; gamma-aminobutyric acid (GABA-A) receptor; IC; inferior colliculus; Kcna1; potassium voltage-gated channel, shaker-related subfamily, member 1; PTZ; pentylenetatrazol; QYS; Qingyangshenylycosides; Scn1b; sodium channel, vol

دانلود رایگان متن کامل مقاله ISI 9 صفحه سال انتشار : 2005 سفارش ترجمه