Cargando…

Association between the Polymorphisms rs2070744, 4b/a and rs1799983 of the NOS3 Gene with Chronic Kidney Disease of Uncertain or Non-Traditional Etiology in Mexican Patients

Background and Objectives: Chronic Kidney Disease of uncertain or non-traditional etiology (CKDnT) is a form of chronic kidney disease of undetermined etiology (CKDu) and is not associated with traditional risk factors. The aim of this study was to investigate the association of polymorphisms rs2070...

Descripción completa

Detalles Bibliográficos
Autores principales:	Marín-Medina, Alejandro, Gómez-Ramos, José Juan, Mendoza-Morales, Norberto, Figuera-Villanueva, Luis Eduardo
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2023
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10221284/ https://www.ncbi.nlm.nih.gov/pubmed/37241060 http://dx.doi.org/10.3390/medicina59050829

Ejemplares similares

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

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

Influence of NOS3 rs2070744 genotypes on hepatocellular carcinoma patients treated with lenvatinib
por: Azuma, Shintaro, et al.
Publicado: (2020)

Author Correction: Influence of NOS3 rs2070744 genotypes on hepatocellular carcinoma patients treated with lenvatinib
por: Azuma, Shintaro, et al.
Publicado: (2021)

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 of eNOS (G894T, rs1799983) and KCNJ11 (E23K, rs5219) gene polymorphism with coronary artery disease in North Indian population
por: Raza, Syed Tasleem, et al.
Publicado: (2021)

eNOS rs2070744 polymorphism might influence predisposition to hemorrhagic cerebral vascular diseases in East Asians: A meta‐analysis
por: Wang, Qiuling, et al.
Publicado: (2020)

Association between eNOS rs1799983 polymorphism and hypertension: a meta-analysis involving 14,185 cases and 13,407 controls
por: Shi, Jikang, et al.
Publicado: (2021)

Interaction between endothelial nitric oxide synthase rs1799983, cholesteryl ester-transfer protein rs708272 and angiopoietin-like protein 8 rs2278426 gene variants highly elevates the risk of type 2 diabetes mellitus and cardiovascular disease
por: El-Lebedy, Dalia
Publicado: (2018)

Association of the rs8720 and rs12587 KRAS Gene Variants with Colorectal Cancer in a Mexican Population and Their Analysis In Silico
por: Gallegos-Arreola, Martha Patricia, et al.
Publicado: (2023)

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)

High frequency of the risk allele of rs4132601 and rs11978267 from the IKZF1 gene in indigenous Mexican population
por: Gutiérrez‐Franco, Jorge, et al.
Publicado: (2021)

AURKA Gene Variants rs1047972, and rs8173 Are Associated With Breast Cancer
por: Maciel-Cruz, Eric Jonathan, et al.
Publicado: (2023)

Association Between rs3833912/rs16944 SNPs and Risk for Cerebral Palsy in Mexican Children
por: Torres-Merino, Sofia, et al.
Publicado: (2018)

ESR2 gene variants (rs1256049, rs4986938, and rs1256030) and their association with breast cancer risk
por: Gallegos-Arreola, Martha Patricia, et al.
Publicado: (2022)

Analysis of the APOB Gene and Apolipoprotein B Serum Levels in a Mexican Population with Acute Coronary Syndrome: Association with the Single Nucleotide Variants rs1469513, rs673548, rs676210, and rs1042034
por: Aceves-Ramírez, Maricela, et al.
Publicado: (2022)

Polymorphisms rs12998 and rs5780218 in KiSS1 Suppressor Metastasis Gene in Mexican Patients with Breast Cancer
por: Cruz Quevedo, Edhit Guadalupe, et al.
Publicado: (2015)

IL-21 (rs2055979 and rs2221903)/IL-21R (rs3093301) Polymorphism and High Levels of IL-21 Are Associated with Rheumatoid Arthritis in Mexican Patients
por: Carreño-Saavedra, Noemi Magdalena, et al.
Publicado: (2023)

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)

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
por: Zhang, Le-Cheng, et al.
Publicado: (2019)

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)

Association between the CTLA4 +49A/G (rs231775) and CT60 (rs3087243) gene variants with vitiligo: study on a Mexican population()
por: Salinas-Santander, Mauricio Andrés, et al.
Publicado: (2022)

Interaction between FTO rs9939609 and the Native American-origin ABCA1 rs9282541 affects BMI in the admixed Mexican population
por: Villalobos-Comparán, Marisela, et al.
Publicado: (2017)

Unravelling the Contribution of the rs7041 and rs4588 Polymorphisms of the GC Gene and Serum VDBP Levels for Developing Metabolic Syndrome in the Mexican Population
por: Hidalgo-Bravo, Alberto, et al.
Publicado: (2022)

The rs2682826 Polymorphism of the NOS1 Gene Is Associated with the Degree of Disability of Erectile Dysfunction
por: Perticarrara Ferezin, Leticia, et al.
Publicado: (2023)

Copy Number Variation and Frequency of rs179008 in TLR7 Gene Associated with Systemic Lupus Erythematosus in Two Mexican Populations
por: Pacheco, Guillermo Valencia, et al.
Publicado: (2022)

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)

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)

MON-092 Role of Genetic Variants of NNMT rs694539 and rs1941404, FTO rs1421085 and Irx3 rs3751723 Polymorphisms on Resting Energy Expenditure and BMI
por: Bañales Luna, Maciel, et al.
Publicado: (2019)

The ERBB2 gene polymorphisms rs2643194, rs2934971, and rs1058808 are associated with increased risk of gastric cancer
por: Vázquez-Ibarra, K.C., et al.
Publicado: (2019)

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

ADIPOQ rs2241766 SNP as protective marker against DIBC development in Mexican population
por: Macías-Gómez, Nelly Margarita, et al.
Publicado: (2019)

Association of MTHFR rs1801133 and homocysteine with Legg–Calvé–Perthes disease in Mexican patients
por: Buendía-Pazarán, José Guillermo, et al.
Publicado: (2022)

NOS3 (rs61722009) gene variants testing in prediction of COVID-19 pneumonia severity
por: Fishchuk, Liliia, et al.
Publicado: (2023)

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)

Role of PAX7 Gene rs766325 and rs4920520 Polymorphisms in the Etiology of Non-syndromic Cleft Lip and Palate: A Genetic Study
por: Khan, Mahamad Irfanulla, et al.
Publicado: (2022)

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)

Cannot write session to /tmp/vufind_sessions/sess_fd2222h09facsba06i013v6r98