Cargando…

Single-Nucleotide Polymorphisms in the 3' Untranslated Region of CORIN Associated With Cardiovascular Diseases in a Chinese Han Population: A Case–Control Study

Background: Corin is a transmembrane serine protease that activates pro-forms of atrial and brain natriuretic peptides. Numerous studies have indicated that corin played an important role in cardiovascular diseases (CVDs). However, there have been few studies about the correlation between single-nuc...

Descripción completa

Detalles Bibliográficos
Autores principales:	Zhao, Yichang, Yuan, Xiaoyang, Zhong, Yang, Zhang, Yutao, Zhang, Shushan, Li, Sisi, Zhao, Yuanyuan, Zheng, Wenjun, Liu, Jinqiu, Xia, Yunlong, Yang, Yanzong, Liu, Ying, Chen, Feifei
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2021
Materias:	Cardiovascular Medicine
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8365884/ https://www.ncbi.nlm.nih.gov/pubmed/34409072 http://dx.doi.org/10.3389/fcvm.2021.625072

Ejemplares similares

Associations between potentially functional CORIN SNPs and serum corin levels in the Chinese Han population
por: Zhang, Huan, et al.
Publicado: (2019)

Corin deficiency impairs cardiac function in mouse models of heart failure
por: Niu, Yayan, et al.
Publicado: (2023)

Falling corin and ANP activity levels accelerate development of heart failure and cardiac fibrosis
por: Gladysheva, Inna P., et al.
Publicado: (2023)

The genetic variation rs12143842 in NOS1AP increases idiopathic ventricular tachycardia risk in Chinese Han populations
por: Zhang, Ronfeng, et al.
Publicado: (2017)

Atrioventricular Node Slow‐Pathway Ablation Reduces Atrial Fibrillation Inducibility: A Neuronal Mechanism
por: Yin, Xiaomeng, et al.
Publicado: (2016)

Highly Significant Association between Two Common Single Nucleotide Polymorphisms in CORIN Gene and Preeclampsia in Caucasian Women
por: Stepanian, Alain, et al.
Publicado: (2014)

Identification of dispensable nucleotide sequence in 3′ untranslated region of porcine reproductive and respiratory syndrome virus
por: Sun, Zhi, et al.
Publicado: (2010)

SNP rs3825214 in TBX5 Is Associated with Lone Atrial Fibrillation in Chinese Han Population
por: Zang, Xiaobiao, et al.
Publicado: (2013)

Common Variants in the TBX5 Gene Associated with Atrial Fibrillation in a Chinese Han Population
por: Zhang, Rongfeng, et al.
Publicado: (2016)

Renal Corin Is Essential for Normal Blood Pressure and Sodium Homeostasis
por: Zhou, Tiantian, et al.
Publicado: (2022)

The protease corin regulates electrolyte homeostasis in eccrine sweat glands
por: He, Meiling, et al.
Publicado: (2021)

Corin Deficiency Diminishes Intestinal Sodium Excretion in Mice
por: Gu, Xiabing, et al.
Publicado: (2023)

Corin Deficiency Alters Adipose Tissue Phenotype and Impairs Thermogenesis in Mice
por: Zhang, Xianrui, et al.
Publicado: (2022)

An Interactive Association of Advanced Glycation End-Product Receptor Gene Four Common Polymorphisms with Coronary Artery Disease in Northeastern Han Chinese
por: Yu, Xiaohong, et al.
Publicado: (2013)

Functional Characterization of a Single Nucleotide Polymorphism in the 3' Untranslated Region of Sheep DLX3 Gene
por: Rong, Enguang, et al.
Publicado: (2015)

E/E′ Is a New Independent Predictor of Recovered Ejection Fraction in Patients With Systolic Heart Failure Undergoing Ablation for Atrial Fibrillation
por: Yang, Minghui, et al.
Publicado: (2022)

Serum corin is associated with the risk of chronic heart failure
por: Yu, Zongliang, et al.
Publicado: (2017)

Corin—The Early Marker of Preeclampsia in Pregestational Diabetes Mellitus
por: Boroń, Daniel, et al.
Publicado: (2022)

Recombinant Soluble Corin Improves Cardiac Function in Mouse Models of Heart Failure
por: Niu, Yayan, et al.
Publicado: (2021)

Corin: A Key Mediator in Sodium Homeostasis, Vascular Remodeling, and Heart Failure
por: Zhang, Xianrui, et al.
Publicado: (2022)

Associations of corin genetic polymorphisms with salt sensitivity, blood pressure changes, and hypertension incidence in Chinese adults
por: Zou, Ting, et al.
Publicado: (2021)

Brazilian Experience with Zennith – Corin System Total Ankle Replacement
por: Baumfeld, Daniel, et al.
Publicado: (2020)

Identification of a nucleotide in 5′ untranslated region contributing to virus replication and virulence of Coxsackievirus A16
por: Li, Zhaolong, et al.
Publicado: (2016)

Association of Dectin-1 and DC-SIGN gene single nucleotide polymorphisms with fungal keratitis in the northern Han Chinese population
por: Qu, Xiaoli, et al.
Publicado: (2015)

Possible association of single nucleotide polymorphisms in the 3' untranslated region of HOXB9 with acetabular overcoverage
por: Sekimoto, T., et al.
Publicado: (2015)

Association between serum soluble corin and hyperglycaemia: a cross-sectional study among Chinese adults
por: Liu, Yan, et al.
Publicado: (2015)

A Corin Variant Identified in Hypertensive Patients That Alters Cytoplasmic Tail and Reduces Cell Surface Expression and Activity
por: Zhang, Yue, et al.
Publicado: (2014)

A Single-Nucleotide Polymorphism in 3′-Untranslated Region of Endothelin-1 Reduces Risk of Dementia After Ischemic Stroke
por: Ma, Wanwan, et al.
Publicado: (2016)

A Prediction Model for Rapid Identification of Ischemic Stroke: Application of Serum Soluble Corin
por: Lu, Ying, et al.
Publicado: (2022)

Increased nucleotide polymorphic changes in the 5′-untranslated region of δ-catenin (CTNND2) gene in prostate cancer
por: Wang, Tao, et al.
Publicado: (2008)

MMP-8 single-nucleotide polymorphisms are related to ankylosing spondylitis in Chinese Han population
por: Meng, Chenyang, et al.
Publicado: (2018)

Impaired sodium excretion and salt-sensitive hypertension in corin-deficient mice
por: Wang, Wei, et al.
Publicado: (2012)

Mitochondrial DNA Variation Correlated With the High Altitude Intolerance in Chinese Young Han Males
por: Li, Zongbin, et al.
Publicado: (2022)

Association of Single Nucleotide Polymorphisms of IL23R and IL17 with Ulcerative Colitis Risk in a Chinese Han Population
por: Yu, Pengli, et al.
Publicado: (2012)

Protein S Deficiency and the Risk of Venous Thromboembolism in the Han Chinese Population
por: Wu, Yingying, et al.
Publicado: (2022)

Association of Single Nucleotide Polymorphisms in TCF2 with Type 2 Diabetes Susceptibility in a Han Chinese Population
por: Zhang, Xuelong, et al.
Publicado: (2012)

C677T Gene Polymorphism of MTHFR Is a Risk Factor for Impaired Renal Function in Pregnant Women With Preeclampsia in the Chinese Han Population
por: Yun, Lin, et al.
Publicado: (2022)

The Early Stage of the Atrial Electroanatomic Remodeling as Substrates for Atrial Fibrillation in Hypertensive Patients
por: Yin, Xiaomeng, et al.
Publicado: (2014)

Frequency Gradient Within Coronary Sinus Predicts the Long‐Term Outcome of Persistent Atrial Fibrillation Catheter Ablation
por: Yin, Xiaomeng, et al.
Publicado: (2017)

A Common Variant at the 3'untranslated Region of the CCL7 Gene (rs17735770) Is Associated With Decreased Susceptibility to Coronary Heart Disease
por: Medina-Gil, José María, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_gp38s4jid3kk7v6bdeoef6jsc7