Cargando…

Association of aspartic acid repeat polymorphism in the asporin gene with osteoarthritis of knee, hip, and hand: A PRISMA-compliant meta-analysis

OBJECTIVE: Several human studies have been conducted to explore the association between aspirin (ASPN) D-repeat polymorphisms and OA susceptibility, but these provide inconsistent results. Our primary aim is to examine whether D-repeat polymorphisms are related to OA risk. METHODS: We conducted a me...

Descripción completa

Detalles Bibliográficos
Autores principales:	Zhu, Xiaoyue, Jiang, Liying, Lu, Yihua, Wang, Chunli, Zhou, Shuai, Wang, He, Tian, Tian
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer Health 2018
Materias:	3500
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5895348/ https://www.ncbi.nlm.nih.gov/pubmed/29561445 http://dx.doi.org/10.1097/MD.0000000000010200

Ejemplares similares

A PRISMA-compliant meta-analysis of MDR1 polymorphisms and idiopathic nephrotic syndrome: Susceptibility and steroid responsiveness
por: Han, Shi-Sheng, et al.
Publicado: (2017)

Association of IL-23R Polymorphisms (rs6682925, rs10889677, rs1884444) With Cancer Risk: A PRISMA-Compliant Meta-Analysis
por: Liu, Xing-Han, et al.
Publicado: (2015)

Diagnostic Value of SLC26A4 Mutation Status in Hereditary Hearing Loss With EVA: A PRISMA-Compliant Meta-Analysis
por: Lu, Ya-Jie, 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)

Association between interleukin 37 (rs3811047) polymorphism and multiple autoimmune diseases in a Chinese population: A PRISMA-compliant meta-analysis
por: Lin, Xiao-Yan, et al.
Publicado: (2018)

Genetic Variation in Metastasis-Associated in Colon Cancer-1 and the Risk of Breast Cancer Among the Chinese Han Population: A STROBE-Compliant Observational Study
por: Dai, Zhi-Jun, et al.
Publicado: (2016)

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)

Association between aspartic acid repeat polymorphism of the asporin gene and risk of knee osteoarthritis: A systematic review and meta-analysis
por: Sobhan, Mohammad Reza, et al.
Publicado: (2017)

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)

The relationship between RASSF1A promoter methylation and thyroid carcinoma: A meta-analysis of 14 articles and a bioinformatics of 2 databases (PRISMA)
por: Niu, Heng, et al.
Publicado: (2017)

Novel heterozygous mutations of SLC12A3 gene in a Chinese pedigree with Gitelman syndrome: A care-compliant case report
por: Bi, Ye, et al.
Publicado: (2023)

An updated meta-analysis of the asporin gene D-repeat in knee osteoarthritis: effects of gender and ethnicity
por: Liu, Ruoxi, et al.
Publicado: (2017)

Integrating multiple microarray datasets to explore the significance of ferroptosis regulators in the diagnosis and subtype classification of osteoarthritis
por: Huang, Yue, et al.
Publicado: (2023)

Antenatal screening and diagnosis of tuberous sclerosis complex by fetal echocardiography and targeted genomic sequencing
por: Gu, Xiaoyan, et al.
Publicado: (2018)

Functional polymorphisms in asporin and CILP together with joint loading predispose to hand osteoarthritis
por: Taipale, Mari, et al.
Publicado: (2017)

CD74, a novel predictor for bronchopulmonary dysplasia in preterm infants
por: Gao, Junyan, et al.
Publicado: (2020)

A novel HNF1B mutation p.R177Q in autosomal dominant tubulointerstitial kidney disease and maturity-onset diabetes of the young type 5: A pedigree-based case report
por: Tao, Tian, et al.
Publicado: (2020)

Aberrantly methylated-differentially expressed genes and related pathways in cholangiocarcinoma
por: Lin, Guan, et al.
Publicado: (2022)

Application of array-comparative genomic hybridization in tetralogy of Fallot
por: Liu, Lin, et al.
Publicado: (2016)

Progressive hemifacial atrophy in a Chinese patient: A case report
por: Li, Rongrong, et al.
Publicado: (2022)

The genotype and phenotype of chromosome 18p deletion syndrome: Case series
por: Jin, Qiujie, et al.
Publicado: (2021)

Prognostic evaluation of microRNA-210 in various carcinomas: Evidence from 19 studies
por: Liu, Yincheng, 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)

A novel AVPR2 missense mutation in an Asian family with inherited nephrogenic diabetes insipidus: A case report
por: Zhang, Min, et al.
Publicado: (2019)

PD-1 rs2227982 Polymorphism Is Associated With the Decreased Risk of Breast Cancer in Northwest Chinese Women: A Hospital-Based Observational Study
por: Ren, Hong-Tao, et al.
Publicado: (2016)

Association of Vitamin D Receptor Cdx-2 Polymorphism With Cancer Risk: A Meta-Analysis
por: Dai, Zhi-Ming, et al.
Publicado: (2015)

Prenatal diagnosis of chromosome 18 long arm deletion syndrome by high-throughput sequencing: Two case reports
por: Bai, Xuechun, et al.
Publicado: (2021)

Performance characterization of PCR-free whole genome sequencing for clinical diagnosis
por: Zhou, Guiju, et al.
Publicado: (2022)

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)

Identification of THSD7B and PRMT9 mutations as risk factors for familial lung adenocarcinoma: A case report
por: Zhang, Qianqian, et al.
Publicado: (2023)

Replication of association of the D-repeat polymorphism in asporin with osteoarthristis
por: Ikegawa, Shiro, et al.
Publicado: (2006)

Bohring-Opitz syndrome caused by a novel ASXL1 mutation (c.3762delT) in an IVF baby: A case report
por: Wang, Dongbo, et al.
Publicado: (2022)

Fibrodysplasia ossificans progressiva in a young adult with genetic mutation: Case report
por: Wang, Zhankui, et al.
Publicado: (2021)

CLPTM1L Genetic Polymorphisms and Interaction With Smoking and Alcohol Drinking in Lung Cancer Risk: A Case–Control Study in the Han Population From Northwest China
por: Xun, Xiaojie, et al.
Publicado: (2014)

OPG and RANKL polymorphisms are associated with alcohol-induced osteonecrosis of the femoral head in the north area of China population in men
por: Li, Yizhou, et al.
Publicado: (2016)

Association of ERBB4 genetic polymorphism with the risk and prognosis of non-small cell lung cancer in Chinese Han population: A population-based case–control study
por: Wang, Wan-ping, et al.
Publicado: (2021)

Nuclear Factor-Kappa B1 is Associated With Gastric Cancer in a Chinese Population
por: Hua, Tang, et al.
Publicado: (2014)

Exome sequencing identifies a de novo mutation of CTNNB1 gene in a patient mainly presented with retinal detachment, lens and vitreous opacities, microcephaly, and developmental delay: Case report and literature review
por: Li, Niu, et al.
Publicado: (2017)

A case report of congenital idiopathic hypogonadotropic hypogonadism caused by novel mutation of GNRHR gene
por: Wang, Liping, et al.
Publicado: (2021)

Association Between Genetic Polymorphisms in the Promoter Regions of Let-7 and Risk of Papillary Thyroid Carcinoma: A Case-Control Study
por: Wang, Yichao, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_86i1jbfouralqtvqf7q7kjkok1