The fractal heart—embracing mathematics in the cardiology clinic

G Captur, AL Karperien, AD Hughes… - Nature Reviews …, 2017 - nature.com
For clinicians grappling with quantifying the complex spatial and temporal patterns of
cardiac structure and function (such as myocardial trabeculae, coronary microvascular …

MYH7 in cardiomyopathy and skeletal muscle myopathy

Y Gao, L Peng, C Zhao - Molecular and Cellular Biochemistry, 2024 - Springer
Myosin heavy chain gene 7 (MYH7), a sarcomeric gene encoding the myosin heavy chain
(myosin-7), has attracted considerable interest as a result of its fundamental functions in …

Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy

I Mademont-Soler, J Mates, R Yotti, MA Espinosa… - PLoS …, 2017 - journals.plos.org
Introduction Hypertrophic cardiomyopathy (HCM) is the most prevalent inherited heart
disease. Next-generation sequencing (NGS) is the preferred genetic test, but the diagnostic …

Application of long-read nanopore sequencing to the search for mutations in hypertrophic cardiomyopathy

RR Salakhov, MV Golubenko… - International Journal of …, 2022 - mdpi.com
Increasing evidence suggests that both coding and non-coding regions of sarcomeric
protein genes can contribute to hypertrophic cardiomyopathy (HCM). Here, we introduce an …

Mutation analysis of the main hypertrophic cardiomyopathy genes using multiplex amplification and semiconductor next-generation sequencing

J Gómez, JR Reguero, C Morís, M Martín… - Circulation …, 2014 - jstage.jst.go.jp
Background: Mutations in at least 30 genes have been linked to hypertrophic
cardiomyopathy (HCM). Due to the large size of the main HCM genes, Sanger sequencing is …

Genetic variation at the long noncoding RNA H19 gene is associated with the risk of hypertrophic cardiomyopathy

J Gómez, R Lorca, JR Reguero, M Martín, C Morís… - …, 2018 - Taylor & Francis
Aim: The long noncoding RNA H19 and its host micro RNA miR-675 have been found
deregulated in cardiac hypertrophy and heart failure tissues. Our aim was to investigate …

Identification of a variant hotspot in" MYBPC3" and of a novel" CSRP3" autosomal recessive alteration in a cohort of Polish patients with hypertrophic cardiomyopathy

M Lipari, E Wypasek, M Karpinski… - … = Polish Archives of …, 2020 - ruj.uj.edu.pl
ABSTRACT INTRODUCTION Hypertrophic cardiomyopathy (HCM) is a heart disorder
caused by autosomal dominant alterations affecting both sarcomeric genes and other …

Sudden cardiac death and copy number variants: what do we know after 10 years of genetic analysis?

J Mates, I Mademont-Soler… - Forensic Science …, 2020 - Elsevier
Over the last ten years, analysis of copy number variants has increasingly been applied to
the study of arrhythmogenic pathologies associated with sudden death, mainly due to …

[HTML][HTML] Фенотипическая вариабельность гипертрофической кардиомиопатии у носителей патогенного варианта p. Arg870His гена MYH7

АН Кучер, НР Валиахметов, РР Салахов… - Бюллетень …, 2022 - cyberleninka.ru
Обзор посвящен анализу вариабельности клинических проявлений неоднократно
зарегистрированного у пациентов с гипертрофической кардиомиопатией (ГКМП) …

MicroRNAs in cardiovascular diseases

H Li, J Zhan, C Chen, D Wang - Medical Review, 2022 - degruyter.com
Cardiovascular diseases (CVDs) are the leading causes of death and disability worldwide,
despite the wide diversity of molecular targets identified and the development of therapeutic …