Cargando…

Genetic mutation of familial dilated cardiomyopathy based on next-generation semiconductor sequencing

Dilated cardiomyopathy (DCM) is a complex myocardial disease of multifactorial etiologies, including enlarged cardiac chambers and contractile dysfunction. It has been suggested that the inheritance of DCM-associated mutations predominates its onset. Therefore, the present study investigated the pat...

Descripción completa

Detalles Bibliográficos
Autores principales:	Lin, Xin-Fu, Luo, Jie-Wei, Liu, Gui, Zhu, Yao-Bin, Jin, Zhao, Lin, Xing
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	D.A. Spandidos 2018
Materias:	Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6172371/ https://www.ncbi.nlm.nih.gov/pubmed/30221713 http://dx.doi.org/10.3892/mmr.2018.9455

Ejemplares similares

Genetic Variants Are Not Rare in ICD Candidates with Dilated Cardiomyopathy: Time for Next-Generation Sequencing?
por: Sousa, Alexandra, et al.
Publicado: (2019)

Targeted next-generation sequencing of candidate genes reveals novel mutations in patients with dilated cardiomyopathy
por: ZHAO, YUE, et al.
Publicado: (2015)

Molecular analysis of inherited cardiomyopathy using next generation semiconductor sequencing technologies
por: Lu, Chaoxia, et al.
Publicado: (2018)

Genetic analysis using targeted next-generation sequencing of sporadic Chinese patients with idiopathic dilated cardiomyopathy
por: Li, Mingmin, et al.
Publicado: (2021)

Genetic Variations Leading to Familial Dilated Cardiomyopathy
por: Cho, Kae Won, et al.
Publicado: (2016)

Heterozygous desmin gene (DES) mutation contributes to familial dilated cardiomyopathy
por: Huang, Ying-shuo, et al.
Publicado: (2021)

Whole exome sequencing identifies a KCNJ12 mutation as a cause of familial dilated cardiomyopathy
por: Yuan, Hai-Xin, et al.
Publicado: (2017)

Next-generation sequencing identifies pathogenic and modifier mutations in a consanguineous Chinese family with hypertrophic cardiomyopathy
por: Zhang, Xinlin, et al.
Publicado: (2017)

Cardiomyopathy, familial dilated
por: Taylor, Matthew RG, et al.
Publicado: (2006)

Identification of MYLK3 mutations in familial dilated cardiomyopathy
por: Tobita, Takashige, et al.
Publicado: (2017)

Mutation in δ-Sg Gene in Familial Dilated Cardiomyopathy
por: Asadi, Marzieh, et al.
Publicado: (2017)

Potential genetic predisposition for anthracycline-associated cardiomyopathy in families with dilated cardiomyopathy
por: Wasielewski, Marijke, et al.
Publicado: (2014)

Identification of TAZ mutations in pediatric patients with cardiomyopathy by targeted next-generation sequencing in a Chinese cohort
por: Wang, Jian, et al.
Publicado: (2017)

Validation of a semiconductor next-generation sequencing assay for the clinical genetic screening of CFTR
por: Trujillano, Daniel, et al.
Publicado: (2015)

Genetic Spectrum of Idiopathic Restrictive Cardiomyopathy Uncovered by Next-Generation Sequencing
por: Kostareva, Anna, et al.
Publicado: (2016)

KLF13 Loss‐of‐Function Mutations Underlying Familial Dilated Cardiomyopathy
por: Guo, Yu‐Han, et al.
Publicado: (2022)

Genomic study of dilated cardiomyopathy in a group of Mexican patients using site‐directed next generation sequencing
por: Carnevale, Alessandra, et al.
Publicado: (2020)

Targeted Next-Generation Sequencing Reveals Hot Spots and Doubly Heterozygous Mutations in Chinese Patients with Familial Cardiomyopathy
por: Zhao, Yue, et al.
Publicado: (2015)

Whole-Genome Sequencing as a First-Line Genetic Test in Familial Dilated Cardiomyopathy
por: Minoche, Andre E., et al.
Publicado: (2018)

Whole Exome Sequencing Identifies a Troponin T Mutation Hot Spot in Familial Dilated Cardiomyopathy
por: Campbell, Nzali, et al.
Publicado: (2013)

The Mutations Associated with Dilated Cardiomyopathy
por: Parvari, Ruti, et al.
Publicado: (2012)

Shared Genetic Etiology of Primary Dilated Cardiomyopathy and Ischemic Dilated Cardiomyopathy
por: Sun, Yang, et al.
Publicado: (2021)

Rapid molecular genetic diagnosis of hypertrophic cardiomyopathy by semiconductor sequencing
por: Li, Zongzhe, et al.
Publicado: (2014)

Educational Case: Genetic Mutations and Multifactorial Inheritance: Dilated Cardiomyopathy
por: Suarez, Eric S., et al.
Publicado: (2017)

The Genetic Evaluation of Dilated Cardiomyopathy
por: Bui, Quan M., et al.
Publicado: (2023)

Genotype-Phenotype Correlation in Familial BAG3 Mutation Dilated Cardiomyopathy
por: Mėlinytė-Ankudavičė, Karolina, et al.
Publicado: (2022)

Whole exome sequencing identifies a novel EMD mutation in a Chinese family with dilated cardiomyopathy
por: Zhang, Mingqiu, et al.
Publicado: (2014)

Rare combination of dilated cardiomyopathy and ankylosing spondylitis in a family
por: Xing, Yun-Li, et al.
Publicado: (2018)

Targeted next-generation sequencing helps to decipher the genetic and phenotypic heterogeneity of hypertrophic cardiomyopathy
por: Cecconi, Massimiliano, et al.
Publicado: (2016)

Genetic diagnosis of familial hypercholesterolaemia by targeted next-generation sequencing
por: Maglio, C, et al.
Publicado: (2014)

Next Generation Sequencing and Bioinformatics Analysis of Family Genetic Inheritance
por: Kanzi, Aquillah M., et al.
Publicado: (2020)

Identification of a novel hypertrophic cardiomyopathy-associated mutation using targeted next-generation sequencing
por: Zhao, Yue, et al.
Publicado: (2017)

Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the MYBPC3 gene
por: Ehlermann, Philipp, et al.
Publicado: (2008)

Inherited dilated cardiomyopathy in a large Moroccan family caused by LMNA mutation
por: Adadi, Najlae, et al.
Publicado: (2018)

The mutation spectrum in familial versus sporadic congenital cataract based on next-generation sequencing
por: Fan, Fan, et al.
Publicado: (2020)

Genetics of Human and Canine Dilated Cardiomyopathy
por: Simpson, Siobhan, et al.
Publicado: (2015)

Next generation diagnostics on cardiomyopathy
por: Blouin, Jean-Louis, et al.
Publicado: (2014)

Next-generation sequencing for genetic testing of familial colorectal cancer syndromes
por: Simbolo, Michele, et al.
Publicado: (2015)

Mitochondrial DNA Variant Discovery and Evaluation in Human Cardiomyopathies through Next-Generation Sequencing
por: Zaragoza, Michael V., et al.
Publicado: (2010)

OBSCN Mutations Associated with Dilated Cardiomyopathy and Haploinsufficiency
por: Marston, Steven, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_3d69bng276r34vpt0eomnnfdp5