Very early-onset lone atrial fibrillation patients have a high prevalence of rare variants in genes previously associated with atrial fibrillation
Background Atrial fibrillation (AF) is the most common cardiac arrhythmia. Currently, 14
genes important for ion channel function, intercellular signaling, and homeostatic control …
genes important for ion channel function, intercellular signaling, and homeostatic control …
Response to Sodium Channel blocking Antiseizure medications and coding polymorphisms of Sodium Channel genes in Taiwanese epilepsy patients
CH Lin, CJ Ho, YT Lu, MH Tsai - BMC neurology, 2021 - Springer
Abstract Background Many antiseizure medications (ASMs) control seizures by blocking
voltage-dependent sodium channels. Polymorphisms of sodium channel genes may affect …
voltage-dependent sodium channels. Polymorphisms of sodium channel genes may affect …
Laboratory methods for investigating nuclear and cytoplasmic genomes and transcriptome
XQ Li - Somatic Genome Manipulation: Advances, Methods …, 2015 - Springer
A cell usually has several categories of DNA. For example, the widely used Agrobacterium
tumefaciens system used for plant genetic transformation has a large plasmid called a tumor …
tumefaciens system used for plant genetic transformation has a large plasmid called a tumor …
Reduced Penetrance and Variable Expression of Dilated Cardiomyopathy Associated With Biallelic Truncating Variants of NRAP Gene
AM Alqhtani - 2024 - search.proquest.com
Background. Dilated Cardiomyopathy (DCM) is a prevalent form of cardiomyopathy found in
children, characterized by ventricular dilation, systolic dysfunction, and heart failure. Despite …
children, characterized by ventricular dilation, systolic dysfunction, and heart failure. Despite …
Integrative analyses identify potential key genes and pathways in Keshan disease using whole-exome sequencing
J Huang, C Zheng, R Luo, M Liu, Q Gu, J Li, X Wu… - medRxiv, 2021 - medrxiv.org
Keshan disease (KD), an endemic heart disease with multifocal necrosis and replacement
fibrosis of the myocardium, is still a nightmare situation for human health. However …
fibrosis of the myocardium, is still a nightmare situation for human health. However …
[PDF][PDF] Study to establish genetic association of cardiac conduction defect in Indian patients undergoing pacemaker implantation
S GARDE, P BHATTACHARYYA, M IDRIS… - 2022 - academia.edu
Background: The aim was to study the genetic association of cardiac conduction defects
(CCDs) by evaluating single nucleotide polymorphism (SNP) in genes of SCN1B and …
(CCDs) by evaluating single nucleotide polymorphism (SNP) in genes of SCN1B and …