Cargando…

ACTB Variants Confer the Genetic Susceptibility to Diabetic Kidney Disease in a Han Chinese Population

Beta-actin (ACTB) loss-of-function mutations result in a pleiotropic developmental disorder of kidney. The present study aims to explore whether the common variants at the ACTB gene contribute to diabetic kidney disease (DKD) susceptibility in patients with type 2 diabetes mellitus (T2DM). From the...

Descripción completa

Detalles Bibliográficos
Autores principales:	Li, Mengxia, Wu, Ming, Qin, Yu, Zhou, Jinyi, Su, Jian, Pan, Enchun, Zhang, Qin, Zhang, Ning, Sheng, Hongyan, Dong, Jiayi, Tong, Ye, Shen, Chong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2019
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6664243/ https://www.ncbi.nlm.nih.gov/pubmed/31396261 http://dx.doi.org/10.3389/fgene.2019.00663

Ejemplares similares

The ACTB Variants and Alcohol Drinking Confer Joint Effect to Ischemic Stroke in Chinese Han Population
por: Yang, Song, et al.
Publicado: (2020)

Identification of a De Novo Heterozygous Missense ACTB Variant in Baraitser–Winter Cerebrofrontofacial Syndrome
por: Nie, Kailai, et al.
Publicado: (2022)

Validation of Susceptibility Loci for Vitiligo Identified by GWAS in the Chinese Han Population
por: Cheng, Lu, et al.
Publicado: (2020)

A frameshift variant in the SIRPB1 gene confers susceptibility to Crohn’s disease in a Chinese population
por: Tang, Jian, et al.
Publicado: (2023)

ETS1 variants confer susceptibility to ankylosing spondylitis in Han Chinese
por: Shan, Shan, et al.
Publicado: (2014)

The cis-Regulatory Element of SNCA Intron 4 Modulates Susceptibility to Parkinson’s Disease in Han Chinese
por: Zhu, Shi-Guo, et al.
Publicado: (2020)

Association of SGK1 Polymorphisms With Susceptibility to Coronary Heart Disease in Chinese Han Patients With Comorbid Depression
por: Han, Wenxiu, et al.
Publicado: (2019)

Association of SLC11A1 Polymorphisms With Tuberculosis Susceptibility in the Chinese Han Population
por: Hu, Baoping, et al.
Publicado: (2022)

Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopenia
por: Latham, Sharissa L., et al.
Publicado: (2018)

Intercellular Adhesion Molecule-1 Gene Polymorphisms and Susceptibility to Cervical Cancer in the Northern Chinese Han Population
por: Feng, Yanan, et al.
Publicado: (2021)

Interaction of Wnt pathway related variants with type 2 diabetes in a Chinese Han population
por: Zhou, Jian-Bo, et al.
Publicado: (2015)

Genetic Variants in GAPDH Confer Susceptibility to Sporadic Parkinson’s Disease in a Chinese Han Population
por: Liu, Ling, et al.
Publicado: (2015)

Identification of DNAH17 Variants in Han-Chinese Patients With Left–Right Asymmetry Disorders
por: Yu, Xuehui, et al.
Publicado: (2022)

Diversity of clinical phenotypes in a cohort of Han Chinese patients with PAX6 variants
por: Huang, Lijuan, et al.
Publicado: (2023)

Common promoter variants of the NDUFV2 gene do not confer susceptibility to schizophrenia in Han Chinese
por: Zhang, Wen, et al.
Publicado: (2010)

Validations of Top and Novel Susceptibility Variants in All-Age Chinese Patients With Acute Lymphoblastic Leukemia
por: Liao, Fei, et al.
Publicado: (2020)

Genotype-phenotype pattern analysis of pathogenic PAX9 variants in Chinese Han families with non-syndromic oligodontia
por: Ren, Jiabao, et al.
Publicado: (2023)

Functional characterization of the chlorzoxazone 6-hydroxylation activity of human cytochrome P450 2E1 allelic variants in Han Chinese
por: Wang, Ting, et al.
Publicado: (2020)

Exome-Wide Association Study Reveals Several Susceptibility Genes and Pathways Associated With Acute Coronary Syndromes in Han Chinese
por: Zheng, Qiwen, et al.
Publicado: (2020)

Autoimmune Disease Associated CLEC16A Variants Convey Risk of Parkinson’s Disease in Han Chinese
por: Fan, Hui-Hui, et al.
Publicado: (2022)

ACTB Methylation in Blood as a Potential Marker for the Pre-clinical Detection of Stroke: A Prospective Nested Case-Control Study
por: Liu, Chunlan, et al.
Publicado: (2021)

The R93C Variant of PCSK9 Reduces the Risk of Premature MI in a Chinese Han Population
por: Yang, Lincheng, et al.
Publicado: (2022)

Candidate Gene Polymorphisms Influence the Susceptibility to Salt Sensitivity of Blood Pressure in a Han Chinese Population: Risk Factors as Mediators
por: Xie, Yunyi, et al.
Publicado: (2021)

Association between the g.296596G > A genetic variant of RELN gene and susceptibility to autism in a Chinese Han population
por: Fu, Xiaoyan, et al.
Publicado: (2013)

Association between RAGE variants and the susceptibility to atherosclerotic lesions in Chinese Han population
por: Zhang, Xiaolin, et al.
Publicado: (2019)

Pseudogenes as Weaknesses of ACTB (Actb) and GAPDH (Gapdh) Used as Reference Genes in Reverse Transcription and Polymerase Chain Reactions
por: Sun, Yuan, et al.
Publicado: (2012)

NLRP3 Influences Cognitive Function in Schizophrenia in Han Chinese
por: Liu, Ruimei, et al.
Publicado: (2021)

Association study of WNK1 genetic variants and essential hypertension risk in the Northern Han Chinese in Beijing
por: Liu, Kuo, et al.
Publicado: (2023)

Author Correction: Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopenia
por: Latham, Sharissa L., et al.
Publicado: (2018)

WTAP gene variants and susceptibility to ovarian endometriosis in a Chinese population
por: Wan, Zixian, et al.
Publicado: (2023)

Case Report: DNAAF4 Variants Cause Primary Ciliary Dyskinesia and Infertility in Two Han Chinese Families
por: Guo, Ting, et al.
Publicado: (2022)

Novel Compound Heterozygous Pathogenic Variants in SUOX Cause Isolated Sulfite Oxidase Deficiency in a Chinese Han Family
por: Zhao, Jiangang, et al.
Publicado: (2021)

Further delineation of putative ACTB loss‐of‐function variants: A 4‐patient series
por: Baumann, Matthias, et al.
Publicado: (2020)

Polymorphisms in ERAP1 and ERAP2 Genes Are Associated With Tuberculosis in the Han Chinese
por: Zhang, Shuqiong, et al.
Publicado: (2020)

Variants in the Toll-interacting protein gene are associated with susceptibility to sepsis in the Chinese Han population
por: Song, Zhenju, et al.
Publicado: (2011)

Association of the CACNA2D2 gene with schizophrenia in Chinese Han population
por: Fu, Yingli, et al.
Publicado: (2020)

Replication study of susceptibility variants associated with allergic rhinitis and allergy in Han Chinese
por: Gao, Yunbo, et al.
Publicado: (2020)

A Novel Nonsense Mutation of ABCA8 in a Han-Chinese Family With ASCVD Leads to the Reduction of HDL-c Levels
por: Wang, Chen-Yu, et al.
Publicado: (2020)

Polymorphisms of protamine genes contribute to male infertility susceptibility in the Chinese Han population
por: Jiang, Weijun, et al.
Publicado: (2017)

Functional Genetic Polymorphisms in the IL1RL1–IL18R1 Region Confer Risk for Ocular Behçet’s Disease in a Chinese Han Population
por: Tan, Xiao, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_o46cfpchd856khi4p0lml85fpn