Cargando…

Identification of BMP10 as a Novel Gene Contributing to Dilated Cardiomyopathy

Dilated cardiomyopathy (DCM), characterized by left ventricular or biventricular enlargement with systolic dysfunction, is the most common type of cardiac muscle disease. It is a major cause of congestive heart failure and the most frequent indication for heart transplantation. Aggregating evidence...

Descripción completa

Detalles Bibliográficos
Autores principales:	Gu, Jia-Ning, Yang, Chen-Xi, Ding, Yuan-Yuan, Qiao, Qi, Di, Ruo-Min, Sun, Yu-Min, Wang, Jun, Yang, Ling, Xu, Ying-Jia, Yang, Yi-Qing
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2023
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9857772/ https://www.ncbi.nlm.nih.gov/pubmed/36673052 http://dx.doi.org/10.3390/diagnostics13020242

Ejemplares similares

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

Identification and Validation of Dilated Cardiomyopathy-Related Genes via Bioinformatics Analysis
por: Wang, Li-Jun, et al.
Publicado: (2022)

Effects of stem cell therapy on dilated cardiomyopathy
por: Jiao, Rong, et al.
Publicado: (2014)

Plasma Metabolomic Profiles Differentiate Patients With Dilated Cardiomyopathy and Ischemic Cardiomyopathy
por: Zhao, Junhan, et al.
Publicado: (2020)

the contribution of south Africans to the subject of dilated cardiomyopathy
por: Watkins, David A, et al.
Publicado: (2009)

Reevaluating the Genetic Contribution of Monogenic Dilated Cardiomyopathy
por: Mazzarotto, Francesco, et al.
Publicado: (2020)

KLF15 Loss-of-Function Mutation Underlying Atrial Fibrillation as well as Ventricular Arrhythmias and Cardiomyopathy
por: Li, Ning, et al.
Publicado: (2021)

Identification of the distinctive role of DPT in dilated cardiomyopathy: a study based on bulk and single-cell transcriptomic analysis
por: Lu, Yang, et al.
Publicado: (2021)

Identification and Functional Prediction of Long Non-Coding RNAs in Dilated Cardiomyopathy by Bioinformatics Analysis
por: Chen, Yu-Xiao, et al.
Publicado: (2021)

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

Identification of key immune-related genes in dilated cardiomyopathy using bioinformatics analysis
por: Li, Feng, et al.
Publicado: (2023)

Identification of Heparan Sulfate in Dilated Cardiomyopathy by Integrated Bioinformatics Analysis
por: Song, Wenyu, et al.
Publicado: (2022)

Identification of Signature Genes of Dilated Cardiomyopathy Using Integrated Bioinformatics Analysis
por: Wu, Zhimin, et al.
Publicado: (2023)

Dilated cardiomyopathy
por: Schultheiss, Heinz-Peter, et al.
Publicado: (2019)

Nonspecific intraventricular conduction delay predicts the prognosis of dilated cardiomyopathy
por: Yuan, Yong, et al.
Publicado: (2023)

NLRP3 inflammasome-mediated pyroptosis contributes to the pathogenesis of non-ischemic dilated cardiomyopathy
por: Zeng, Cheng, et al.
Publicado: (2020)

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

Identification of a novel variant in N-cadherin associated with dilated cardiomyopathy
por: Chen, Yuanying, et al.
Publicado: (2022)

Cardiac Proteome Profiling in Ischemic and Dilated Cardiomyopathy Mouse Models
por: Lu, Danbo, et al.
Publicado: (2019)

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

Publisher Correction: Identification of key immune-related genes in dilated cardiomyopathy using bioinformatics analysis
por: Li, Feng, et al.
Publicado: (2023)

A Kaposi’s sarcoma-associated herpes virus-encoded microRNA contributes to dilated cardiomyopathy
por: Zhao, Yanru, et al.
Publicado: (2023)

Clinical outcome of cardiac resynchronization therapy in dilated-phase hypertrophic cardiomyopathy
por: Gu, Min, et al.
Publicado: (2017)

Dilated cardiomyopathies and non-compaction cardiomyopathy
por: Hänselmann, A., et al.
Publicado: (2020)

Endothelial-to-mesenchymal transition in human idiopathic dilated cardiomyopathy
por: Xie, Yeqing, et al.
Publicado: (2018)

Dilated cardiomyopathy and aldosteronoma: a causal link?
por: Zhang, Jiyu, et al.
Publicado: (2019)

Retrospective study of dilated cardiomyopathy in dogs
por: Freid, Kimberly J., et al.
Publicado: (2020)

Circulating microRNA signature for the diagnosis of childhood dilated cardiomyopathy
por: Jiao, Meng, et al.
Publicado: (2018)

The Role of Leucine-Rich Repeat Containing Protein 10 (LRRC10) in Dilated Cardiomyopathy
por: Brody, Matthew J., et al.
Publicado: (2016)

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

Dilated cardiomyopathy in childhood
por: Franklin, OM, et al.
Publicado: (2000)

Immunoadsorption in dilated cardiomyopathy
por: Wakabayashi, Y, et al.
Publicado: (2009)

Apoptosis in Dilated Cardiomyopathy
por: Hong, Bum Kee, et al.
Publicado: (2000)

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

Identification and Verification of Feature Biomarkers Associated With Immune Cells in Dilated Cardiomyopathy by Bioinformatics Analysis
por: Zhu, Tingfang, et al.
Publicado: (2022)

Speckle tracking echocardiography in hypokinetic non‐dilated cardiomyopathy: comparison with dilated cardiomyopathy
por: Mombeini, Hoda, et al.
Publicado: (2020)

The Potential of Metabolism-Related Gene OGDHL as a Biomarker for Myocardial Remodeling in Dilated Cardiomyopathy
por: Tang, Yaohan, et al.
Publicado: (2022)

Identification of micro-RNA networks in end-stage heart failure because of dilated cardiomyopathy
por: Zhu, Xiaoming, et al.
Publicado: (2013)

Peripartum cardiomyopathy and dilated cardiomyopathy: different at heart
por: Bollen, Ilse A. E., et al.
Publicado: (2015)

Nomogram predicting death and heart transplantation before appropriate ICD shock in dilated cardiomyopathy
por: Deng, Yu, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_r2du0eg0ppisb6rlcv3bcaekhe