Cargando…

Non-diabetic end-stage renal disease in Saudis associated with polymorphism of MYH9 gene but not UMOD gene

The prevalence of risk factors of chronic kidney disease in Saudi Arabia has augmented an already serious public health problem, therefore, determination of genetic variants associated with the risk of the disease presents potential screening tools that help reducing the incidence rates and promote...

Descripción completa

Detalles Bibliográficos
Autores principales:	Adam, Khalid Mohamed, Mohammed, Ali Mahmoud, Elamin, Abubakr Ali
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer Health 2020
Materias:	3500
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7220318/ https://www.ncbi.nlm.nih.gov/pubmed/32011449 http://dx.doi.org/10.1097/MD.0000000000018722

Ejemplares similares

UMOD as a susceptibility gene for end-stage renal disease
por: Reznichenko, Anna, et al.
Publicado: (2012)

Correlation of GLUT9 Polymorphisms With Gout Risk
por: Meng, Qingxi, et al.
Publicado: (2015)

NOTCH3 Gene Polymorphism is Associated With the Prognosis of Gliomas in Chinese Patients
por: Shen, Zhipeng, et al.
Publicado: (2015)

PEAR1 gene polymorphism in a Chinese pedigree with pulmonary thromboembolism
por: Fu, Yingyun, et al.
Publicado: (2016)

Association of epidermal growth factor receptor (EGFR) gene polymorphisms with endometriosis
por: Wang, Yu-Mei, et al.
Publicado: (2019)

The association of CDKN2BAS gene polymorphisms and intracranial aneurysm: A meta-analysis
por: Yu, Ting, et al.
Publicado: (2020)

Correlation of TGF-β signaling pathway gene polymorphisms with unexplained recurrent spontaneous abortion
por: Xue, Huiqin, et al.
Publicado: (2023)

Association between BACE1 gene polymorphisms and focal seizures in a Chinese Han population
por: Yang, Guangsheng, et al.
Publicado: (2018)

The relationship between gestational diabetes mellitus and interleukin 1beta gene polymorphisms in southwest of China
por: Liu, Ting, et al.
Publicado: (2020)

Association between polymorphisms in the XRCC1 gene and male infertility risk: A meta-analysis
por: Liu, Zhengsheng, et al.
Publicado: (2020)

Association between HIF-1α gene polymorphisms and lung cancer: A meta-analysis
por: Xu, Shuguang, et al.
Publicado: (2020)

Association between interleukin-6 gene polymorphisms and febrile seizure risk: A meta-analysis
por: Chen, Qingling, et al.
Publicado: (2019)

The effects of NLRP3 and MAVS gene polymorphisms on the risk of asthma: A case–control study
por: Xulong, Cai, et al.
Publicado: (2022)

A single nucleotide polymorphism in the UMOD promoter is associated with end stage renal disease
por: Chen, Tingyu, et al.
Publicado: (2016)

Family history and renin-angiotensin system gene polymorphisms in Chinese patients with type 2 diabetes mellitus
por: Pan, Yan-Hong, et al.
Publicado: (2017)

Association of CYP2J2 gene polymorphisms with ischemic stroke and stroke subtypes in Chinese population
por: Wang, Si-Yang, et al.
Publicado: (2017)

Association between common polymorphisms in ERCC gene and glioma risk: A meta-analysis of 15 studies
por: Qian, Tengda, et al.
Publicado: (2017)

Association of vitamin D receptor gene polymorphism with the risk of sepsis: A systematic review and meta-analysis
por: Li, Qian, et al.
Publicado: (2023)

Polymorphism in the IL4R gene and clinical features are associated with glioma prognosis: Analyses of case-cohort studies
por: Jin, Tian bo, et al.
Publicado: (2016)

Association between Unc-51-like autophagy activating kinase 2 gene polymorphisms and schizophrenia in the Korean population
por: Kang, Won Sub, et al.
Publicado: (2022)

Association between PAX7 and NTN1 gene polymorphisms and nonsyndromic orofacial clefts in a northern Chinese population
por: Guo, Qiang, et al.
Publicado: (2017)

Effects of paraoxonase 1 gene polymorphisms on heart diseases: Systematic review and meta-analysis of 64 case-control studies
por: Hernández-Díaz, Yazmín, et al.
Publicado: (2016)

Association study of single nucleotide polymorphism in tryptophan hydroxylase 1 gene with adolescent idiopathic scoliosis: A meta-analysis
por: Li, Junyu, et al.
Publicado: (2021)

Association of aspartic acid repeat polymorphism in the asporin gene with osteoarthritis of knee, hip, and hand: A PRISMA-compliant meta-analysis
por: Zhu, Xiaoyue, et al.
Publicado: (2018)

Correlation between SHBG gene polymorphism and male infertility in Han population of Henan province of China: A STROBE-compliant article
por: Cui, Yuan-rong, et al.
Publicado: (2017)

PRISMA-combined Myeloperoxidase -463G/A gene polymorphism and coronary artery disease: A meta-analysis of 4744 subjects
por: Li, Yan-Yan, et al.
Publicado: (2017)

Angiotensin Converting Enzyme Gene Insertion/Deletion Polymorphism and Vesicoureteral Reflux in Children: A Meta-Analysis of 14 Case–Control Studies
por: Ai, Jin-Wei, et al.
Publicado: (2015)

Gene polymorphisms (rs324957, rs324981) in NPSR1 are associated with increased risk of primary insomnia: A cross-sectional study
por: Xie, Yuping, et al.
Publicado: (2020)

Prenatal detection of terminal 9p24.3 microduplication encompassing DOCK8 gene: A variant of likely benign
por: Yue, Fagui, et al.
Publicado: (2021)

Value of Chromosome 9p21 Polymorphism for Prediction of Cardiovascular Mortality in Han Chinese Without Coronary Lesions: An Observational Study
por: Lee, I-Te, et al.
Publicado: (2015)

Impact of V-ets Erythroblastosis Virus E26 Oncogene Homolog 1 Gene Polymorphisms Upon Susceptibility to Autoimmune Diseases: A Meta-Analysis
por: Zhou, Ye, et al.
Publicado: (2015)

The association of single nucleotide polymorphism rs189037C>T in ATM gene with coronary artery disease in Chinese Han populations: A case control study
por: Ding, Xiang, et al.
Publicado: (2018)

Association between genetic polymorphism of telomere-associated gene ACYP2 and the risk of HAPE among the Chinese Han population: A Case–control study
por: Zhu, Linhao, et al.
Publicado: (2017)

Association Between SLCO1B1 Gene T521C Polymorphism and Statin-Related Myopathy Risk: A Meta-Analysis of Case–Control Studies
por: Hou, Qingtao, et al.
Publicado: (2015)

Association between the rs2106261 polymorphism in the zinc finger homeobox 3 gene and risk of atrial fibrillation: Evidence from a PRISMA-compliant meta-analysis
por: Wei, Yue, et al.
Publicado: (2021)

Significant associations between 5-hydroxytryptaminetransporter-linked promoter region polymorphisms of the serotonin transporter (solute carrier family 6 member 4) gene and Thai patients with autism spectrum disorder
por: Wongpaiboonwattana, Wikrom, et al.
Publicado: (2020)

CYP2C19, PON1, and ABCB1 gene polymorphisms in Han and Uygur populations with coronary artery disease in Northwestern Xinjiang, China, From 2014 Through 2019
por: Wang, Tingting, et al.
Publicado: (2020)

Identification of new genes of pleomorphic adenoma
por: Choi, Jeong-Seok, et al.
Publicado: (2019)

Constructing gene network for type 1 narcolepsy based on genome-wide association study and differential gene expression analysis (STROBE)
por: Ouyang, Hui, et al.
Publicado: (2020)

Network and pathway-based analyses of genes associated with osteoporosis
por: Gu, Huijie, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_d3g8esikbs7qk2q2kcpeke36uq