Cargando…

Endothelial nitric oxide synthase gene T(−786)C and 27-bp repeat gene polymorphisms in retinopathy of prematurity

PURPOSE: Retinopathy of prematurity (ROP), which is associated with abnormal retinal vessel development, is the leading cause of visual loss in preterm infants. Endothelial nitric oxide synthase (eNOS) is believed to play a central role in both retinal angiogenesis and vasculogenesis. The aim of thi...

Descripción completa

Detalles Bibliográficos
Autores principales:	Rusai, Krisztina, Vannay, Adám, Szebeni, Beáta, Borgulya, Gábor, Fekete, Andrea, Vásárhelyi, Barna, Tulassay, Tivadar, Szabó, Attila J
Formato:	Texto
Lenguaje:	English
Publicado:	Molecular Vision 2008
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2263012/ https://www.ncbi.nlm.nih.gov/pubmed/18334945

Ejemplares similares

Endothelial Nitric Oxide Synthase Gene T-786C Polymorphism in Renal Transplant Recipients
por: Azarpira, N., et al.
Publicado: (2011)

High Salt Promotes Inflammatory and Fibrotic Response in Peritoneal Cells
por: Pap, Domonkos, et al.
Publicado: (2023)

Selective measurement of α smooth muscle actin: why β-actin can not be used as a housekeeping gene when tissue fibrosis occurs
por: Veres-Székely, Apor, et al.
Publicado: (2017)

The Role of −786T/C Polymorphism in the Endothelial Nitric Oxide Synthase Gene in Males with Clinical and Biochemical Features of the Metabolic Syndrome
por: Misiak, Blazej, et al.
Publicado: (2011)

Endothelial nitric oxide synthase gene (T786C and G894T) polymorphisms in Egyptian patients with type 2 diabetes
por: Moguib, Omneya, et al.
Publicado: (2017)

The Endothelial Nitric Oxide Synthase Gene T-786C Polymorphism Increases Myocardial Infarction Risk: A Meta-Analysis
por: Kong, Xiang-Zhen, et al.
Publicado: (2017)

Altered calcium influx of peripheral Th2 cells in pediatric Crohn's disease: infliximab may normalize activation patterns
por: Orbán, Csaba, et al.
Publicado: (2016)

High salt diet impairs dermal tissue remodeling in a mouse model of IMQ induced dermatitis
por: Pajtók, Csenge, et al.
Publicado: (2021)

T(−786)→C polymorphism of the endothelial nitric oxide synthase gene is associated with insulin resistance in patients with ischemic or non ischemic cardiomyopathy
por: Vecoli, Cecilia, et al.
Publicado: (2012)

Endothelial nitric oxide synthase gene polymorphisms -786T >C and 894G >T in coronary artery bypass graft surgery patients
por: Ragia, Georgia, et al.
Publicado: (2010)

Endothelial nitric oxide synthase (−786T>C) polymorphism and migraine susceptibility: A meta-analysis
por: Dong, Han, et al.
Publicado: (2018)

Association of endothelial nitric oxide synthase promoter region (T-786C) gene polymorphism with acute coronary syndrome and coronary heart disease
por: Çiftçi, Ç, et al.
Publicado: (2008)

Expression of lymphocyte activation markers of preterm neonates is associated with perinatal complications
por: Sava, Florentina, et al.
Publicado: (2016)

Assessment of the role of plasma nitric oxide levels, T-786C genetic polymorphism, and gene expression levels of endothelial nitric oxide synthase in the development of coronary artery disease
por: Mahmoodi, Khalil, et al.
Publicado: (2017)

Endothelial Nitric Oxide Gene T-786C Polymorphism and Subarachnoid Hemorrhage in Korean Population
por: Song, Min-Kyung, et al.
Publicado: (2006)

Investigation of the relationship between ischemic stroke and endothelial nitric oxide synthase gene polymorphisms [G894T, intron 4 VNTR and T786C]
por: ANLIAÇIK, Süleyman Ömer, et al.
Publicado: (2019)

Endothelial Nitric Oxide Synthase (−786T>C) and Endothelin-1 (5665G>T) Gene Polymorphisms as Vascular Dysfunction Risk Factors in Sickle Cell Anemia
por: Vilas-Boas, Wendell, et al.
Publicado: (2016)

Association of the Endothelial Nitric Oxide Synthase Gene T786C Polymorphism with In-Stent Restenosis in Chinese Han Patients with Coronary Artery Disease Treated with Drug-Eluting Stent
por: Zeng, Wen-ping, et al.
Publicado: (2017)

Gene polymorphism associated with endothelial nitric oxide synthase (4VNTR, G894T, C786T) and unexplained recurrent spontaneous abortion risk: A meta-analysis
por: Zhao, Xiaoxuan, et al.
Publicado: (2019)

Investigation of the relationship between endothelial nitric oxide synthase T786C polymorphism and PSA, PSA derivatives, and prostate cancer in the Turkish population
por: Balci, Senay, et al.
Publicado: (2023)

Cyclooxygenase-2 Modulates Glycosaminoglycan Production in the Skin During Salt Overload
por: Agócs, Róbert, et al.
Publicado: (2020)

Association between nitric oxide synthase T-786C genetic polymorphism and chronic kidney disease: Meta-analysis incorporating trial sequential analysis
por: Hsiao, Po-Jen, et al.
Publicado: (2021)

Endothelial Nitric Oxide Synthase T-786C Mutation, Prothrombin Gene Mutation (G-20210-A) and Protein S Deficiency Could Lead to Myocardial Infarction in a Very Young Male Adult
por: Klincheva, Milka, et al.
Publicado: (2016)

PARK7/DJ-1 as a Therapeutic Target in Gut-Brain Axis Diseases
por: Pap, Domonkos, et al.
Publicado: (2022)

Influence of Endothelial Nitric Oxide Synthase Gene Intron-4 27bp Repeat Polymorphism on Its Expression in Autoimmune Diseases
por: AlFadhli, Suad
Publicado: (2013)

Association of polymorphisms of renin angiotensin system and endothelial nitric oxide synthase genes with premature cardiovascular disease in an Iranian population
por: Poorzand, Hoorak, et al.
Publicado: (2023)

Aldosterone Antagonists in Monotherapy Are Protective against Streptozotocin-Induced Diabetic Nephropathy in Rats
por: Banki, Nora F., et al.
Publicado: (2012)

Characterization of IL-19, -20, and -24 in acute and chronic kidney diseases reveals a pro-fibrotic role of IL-24
por: Pap, Domonkos, et al.
Publicado: (2020)

Zonulin as a Potential Therapeutic Target in Microbiota-Gut-Brain Axis Disorders: Encouraging Results and Emerging Questions
por: Veres-Székely, Apor, et al.
Publicado: (2023)

The -786T>C promoter polymorphism of the NOS3 gene is associated with prostate cancer progression
por: Marangoni, Karina, et al.
Publicado: (2008)

Transient Agarose Spot (TAS) Assay: A New Method to Investigate Cell Migration
por: Veres-Székely, Apor, et al.
Publicado: (2022)

786-0 Renal cancer cell line-derived exosomes promote 786-0 cell migration and invasion in vitro
por: CHEN, GANG, et al.
Publicado: (2014)

An association between the endothelial nitric oxide synthase gene G894T polymorphism and premature coronary artery disease: a meta-analysis
por: Zhu, Boqian, et al.
Publicado: (2017)

Role of IL-24 in the mucosal remodeling of children with coeliac disease
por: Rokonay, Réka, et al.
Publicado: (2020)

Association of endothelial nitric oxide synthase gene variants with preeclampsia
por: Shaheen, Ghazala, et al.
Publicado: (2021)

Germline pathogenic variants in 786 neuroblastoma patients
por: Kim, Jung, et al.
Publicado: (2023)

Association of eNOS Gene Polymorphisms G894T and T-786C with Risk of Hepatorenal Syndrome
por: Seckin, Yuksel, et al.
Publicado: (2016)

PARK7 Diminishes Oxidative Stress-Induced Mucosal Damage in Celiac Disease
por: Veres-Székely, Apor, et al.
Publicado: (2020)

Interleukin-24 regulates mucosal remodeling in inflammatory bowel diseases
por: Ónody, Anna, et al.
Publicado: (2021)

Association between eNOS Gene Polymorphism (T786C and VNTR) and Sickle Cell Disease Patients in Ghana
por: Antwi-Boasiako, Charles, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_9p3hcl5sif3hm2r0gphanr9glu