Cargando…

Lack of associations between polymorphisms in SOD2 (rs2758331), NOS3 (rs1808593), PPARδ (rs9794 and rs10865710) and the risk of osteoarthritis in a Chinese Han population: a case-control study

Detalles Bibliográficos
Autores principales:	Zhang, Le-Cheng, Hu, Yong, Sui, Cong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer Health 2019
Materias:	Correspondence
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6595880/ https://www.ncbi.nlm.nih.gov/pubmed/30839355 http://dx.doi.org/10.1097/CM9.0000000000000179

Ejemplares similares

Enhancer polymorphism rs10865710 associated with traumatic sepsis is a regulator of PPARG gene expression
por: Lu, Hongxiang, et al.
Publicado: (2019)

Lack of association between MMP13 (rs3819089), ADAM12 (rs3740199-rs1871054) and ADAMTS14 (rs4747096) genotypes and advanced-stage knee osteoarthritis
por: Haberal, Bahtiyar, et al.
Publicado: (2021)

Association of rs12487066, rs12044852, rs10735781, rs3135388, rs6897932, rs1321172, rs10492972, and rs9657904 Polymorphisms with Multiple Sclerosis in Iranian Population
por: Razavian, Takavar, et al.
Publicado: (2020)

TIMP-2 SNPs rs7342880 and rs4789936 are linked to risk of knee osteoarthritis in the Chinese Han Population
por: Xu, Pengcheng, et al.
Publicado: (2016)

Cytokine rs361525, rs1800750, rs1800629, rs1800896, rs1800872, rs1800795, rs1800470, and rs2430561 SNPs in relation with prognostic factors in acute myeloid leukemia
por: Bănescu, Claudia, et al.
Publicado: (2019)

SOD2 Gene Variants (rs4880 and rs5746136) and Their Association with Breast Cancer Risk
por: Gallegos-Arreola, Martha P., et al.
Publicado: (2022)

The association between peroxisome proliferator-activated receptor Δ rs3777744, rs3798343, and rs6922548 and coronary artery disease
por: Zhang, Jing, et al.
Publicado: (2019)

Association of NOS3 (rs 2070744) and SOD2Val16Ala (rs4880) gene polymorphisms with increased risk of ESRD among Egyptian patients
por: Elsaid, Afaf, et al.
Publicado: (2021)

Association Between rs12037447, rs146732504, rs151078858, rs55723436, and rs6094136 Polymorphisms and Kawasaki Disease in the Population of Polish Children
por: Buda, Piotr, et al.
Publicado: (2021)

The rs2619566, rs10260404, and rs79609816 Polymorphisms Are Associated With Sporadic Amyotrophic Lateral Sclerosis in Individuals of Han Ancestry From Mainland China
por: Zhang, Jie, et al.
Publicado: (2021)

Association of ESR1 (rs2234693 and rs9340799), CETP (rs708272), MTHFR (rs1801133 and rs2274976) and MS (rs185087) polymorphisms with Coronary Artery Disease (CAD)
por: Raina, Jyotdeep Kour, et al.
Publicado: (2020)

TIRAP Rs8177376, Rs611953, Rs3802814, and Rs8177374 Polymorphisms and Their Association with Cervical Cancer Phenotype and Prognosis
por: Bekampytė, Justina, et al.
Publicado: (2022)

Association between ABC family variants rs1800977, rs4149313, and rs1128503 and susceptibility to type 2 diabetes in a Chinese Han population
por: Yan, Ruicheng, et al.
Publicado: (2020)

PSMA6 (rs2277460, rs1048990), PSMC6 (rs2295826, rs2295827) and PSMA3 (rs2348071) genetic diversity in Latvians, Lithuanians and Taiwanese
por: Sjakste, Tatjana, et al.
Publicado: (2014)

Association between interleukin 6 polymorphisms (rs1800796, rs1800795, rs2069837, rs17147230, and rs1800797) and hepatocellular carcinoma susceptibility: a meta-analysis
por: Aleagha, Omid Emami, et al.
Publicado: (2020)

Molecular Analysis of rs2070744 and rs1799983 Polymorphisms of NOS3 Gene in Iranian Patients With Multiple Sclerosis
por: Heidari, Mohammad Mehdi, et al.
Publicado: (2017)

Genetic Variations of DAOA (rs947267 and rs3918342) and COMT Genes (rs165599 and rs4680) in Schizophrenia and Bipolar I Disorder
por: Ahmadi, Leila, et al.
Publicado: (2018)

Functional Analysis of the rs774872314, rs116171003, rs200231898 and rs201107751 Polymorphisms in the Human RORγT Gene Promoter Region
por: Ratajewski, Marcin, et al.
Publicado: (2017)

Association of the interaction between the rs9619311 and rs402007 polymorphisms and smoking with essential hypertension in Chinese Han population
por: Chen, Chao, et al.
Publicado: (2020)

Associations of rs823128, rs1572931, and rs823156 polymorphisms with reduced Parkinson’s disease risks
por: Bai, Ye, et al.
Publicado: (2017)

Lack of Association of the CD247 SNP rs2056626 with Systemic Sclerosis in Han Chinese
por: Wang, Jiucun, et al.
Publicado: (2014)

The Association between Five Genetic Variants in MicroRNAs (rs2910164, rs11614913, rs3746444, rs11134527, and rs531564) and Cervical Cancer Risk: A Meta-Analysis
por: Liu, Jia, et al.
Publicado: (2021)

The Correlation of Mouse Double Minute 4 (MDM4) Polymorphisms (rs4245739, rs1563828, rs11801299, rs10900598, and rs1380576) with Cancer Susceptibility: A Meta-Analysis
por: Chen, Jian, et al.
Publicado: (2022)

Association of rs944289, rs965513, and rs1443434 in TITF1/TITF2 with Risks of Papillary Thyroid Carcinoma and with Nodular Goiter in Northern Chinese Han Populations
por: Zhang, Xin, et al.
Publicado: (2020)

Rs420137, rs386360 and rs7763726 polymorphisms in fibronectin type III domain containing 1 are associated with susceptibility to coronary heart disease: Analysis in the Han population
por: He, Xiaodan, et al.
Publicado: (2022)

RAD51B (rs8017304 and rs2588809), TRIB1 (rs6987702, rs4351379, and rs4351376), COL8A1 (rs13095226), and COL10A1 (rs1064583) Gene Variants with Predisposition to Age-Related Macular Degeneration
por: Vilkeviciute, Alvita, et al.
Publicado: (2019)

The NOS3 G894T (rs1799983) and -786T/C (rs2070744) polymorphisms are associated with elite swimmer status
por: Zmijewski, Piotr, et al.
Publicado: (2018)

Evaluation of MC4R [RS17782313, RS17700633], AGRP [RS3412352] and POMC [RS1042571] polymorphisms with obesity in Northern India
por: Srivastava, Apurva, et al.
Publicado: (2014)

Risk association, linkage disequilibrium and haplotype analyses of FASN rs4246445, rs2229425, rs2228305 and rs2229422 polymorphisms in overweight and obesity
por: Chong, Eric Tzyy Jiann, et al.
Publicado: (2018)

Lack of Association between Missense Variants in GRHL3 (rs2486668 and rs545809) and Susceptibility to Non-Syndromic Orofacial Clefts in a Han Chinese Population
por: He, Miao, et al.
Publicado: (2016)

Haplotypes of HTRA1 rs1120638, TIMP3 rs9621532, VEGFA rs833068, CFI rs10033900, ERCC6 rs3793784, and KCTD10 rs56209061 Gene Polymorphisms in Age-Related Macular Degeneration
por: Liutkeviciene, Rasa, et al.
Publicado: (2019)

Deciphering the Role of the rs2651899, rs10166942, and rs11172113 Polymorphisms in Migraine: A Meta-Analysis
por: Siokas, Vasileios, et al.
Publicado: (2022)

The 5Rs dilemma of radiotherapy for non-malignant diseases: 5Rs to darken OR 5Rs to shine
por: Montero, Angel, et al.
Publicado: (2023)

AB200. Association of rs3129878 and rs498422in the HLA region with non-obstructive azoospermia in the Han Chinese population
por: Zou, Shasha, et al.
Publicado: (2014)

The Fc Receptor-Like 3 Polymorphisms (rs7528684, rs945635, rs3761959 and rs2282284) and The Risk of Neuromyelitis Optica in A Chinese Population
por: Lan, Wenjing, et al.
Publicado: (2015)

Polymorphisms FTO rs9939609, PPARG rs1801282 and ADIPOQ rs4632532 and rs182052 but not lifestyle are associated with obesity related-traits in Mexican children
por: Muñoz-Yáñez, C, et al.
Publicado: (2016)

Gene Polymorphisms in FAS (Rs3740286 and Rs4064) Are Involved in Endometriosis Development in Brazilian Women, but not those in CASP8 (rs13416436 and rs2037815)
por: Pissetti, Cristina Wide, et al.
Publicado: (2018)

RS and composites
por: Panico, Giuliano
Publicado: (2017)

Polymorphisms in Four Genes (KCNQ1 rs151290, KLF14 rs972283, GCKR rs780094 and MTNR1B rs10830963) and Their Correlation with Type 2 Diabetes Mellitus in Han Chinese in Henan Province, China
por: Gao, Kaiping, et al.
Publicado: (2016)

The Association of Polymorphisms in Genes Encoding Antioxidant Enzymes GPX1 (rs1050450), SOD2 (rs4880) and Transcriptional Factor Nrf2 (rs6721961) with the Risk and Development of Prostate Cancer
por: Djokic, Milica, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_7p74fek5r4n5dh8bsb3levtrf2