Cargando…

G894T endothelial nitric oxide synthase polymorphism and ischemic stroke in Morocco

Nitric oxide plays a major role in the regulation of cerebral blood flow and loss of its function leads to alteration of the vascular relaxation given its central role in the physiology of the vascular system. G894T eNOS polymorphism could have adverse effects on the expression and activity of endot...

Descripción completa

Detalles Bibliográficos
Autores principales:	Diakite, Brehima, Hamzi, Khalil, Slassi, Ilham, EL Yahyaoui, Mohammed, EL Alaoui, Moulay M.F., Habbal, Rachida, Sellama, Nadifi
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2014
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4287825/ https://www.ncbi.nlm.nih.gov/pubmed/25606419 http://dx.doi.org/10.1016/j.mgene.2014.04.003

Ejemplares similares

Association of G894T eNOS, 4G/5G PAI and T1131C APOA5 polymorphisms with susceptibility to myocardial infarction in Morocco
por: Hassani Idrissi, Hind, et al.
Publicado: (2016)

The polymorphism G894 T of endothelial nitric oxide synthase (eNOS) gene is associated with susceptibility to essential hypertension (EH) in Morocco
por: Nassereddine, Sanaa, et al.
Publicado: (2018)

Large scale meta-analysis of genetic studies in ischemic stroke: Five genes involving 152,297 individuals
por: Hamzi, Khalil, et al.
Publicado: (2013)

Duchenne and Becker Muscular Dystrophy: Contribution of a Molecular and Immunohistochemical Analysis in Diagnosis in Morocco
por: Bellayou, Hanane, et al.
Publicado: (2009)

Duchenne muscular dystrophy: Advances in molecular appraoch
por: Benitto, Afaf, et al.
Publicado: (2013)

Association of methylenetetrahydrofolate reductase gene (C677T) with the risk of hypertension in Morocco
por: Nassereddine, Sanaa, et al.
Publicado: (2015)

Large-scale meta-analysis of genetic studies in ischemic stroke: Five genes involving 152,797 individuals
por: Hamzi, Khalil, et al.
Publicado: (2011)

Screening of exon 11 of BRCA1 gene using the high resolution melting approach for diagnosis in Moroccan breast cancer patients
por: El Khachibi, Meryam, et al.
Publicado: (2015)

Impact of I/D polymorphism of angiotensin-converting enzyme (ACE) gene on myocardial infarction susceptibility among young Moroccan patients
por: Hmimech, Wiam, et al.
Publicado: (2017)

IL23R and ATG16L1 variants in Moroccan patients with inflammatory bowel disease
por: Serbati, Nadia, et al.
Publicado: (2014)

Toll-like receptor 4 Asp299Gly and Thr399Ile polymorphisms: New data and a meta-analysis
por: Senhaji, Nezha, et al.
Publicado: (2014)

A synergic effect between CYP2C19*2, CYP2C19*3 loss-of-function and CYP2C19*17 gain-of-function alleles is associated with Clopidogrel resistance among Moroccan Acute Coronary Syndromes patients
por: Hassani Idrissi, Hind, et al.
Publicado: (2018)

Does i-T744C P2Y12 Polymorphism Modulate Clopidogrel Response among Moroccan Acute Coronary Syndromes Patients?
por: Hassani Idrissi, Hind, et al.
Publicado: (2017)

Prader-Willi syndrome: Methylation study or fluorescence in situ hybridization first?
por: Hamzi, Khalil, et al.
Publicado: (2010)

Association of Nitric Oxide Levels and Endothelial Nitric Oxide Synthase G894T Polymorphism with Coronary Artery Disease in the Iranian Population
por: Mahmoodi, Khalil, et al.
Publicado: (2016)

The CHEK2 1100delC allelic variant is not present in familial and sporadic breast cancer cases from Moroccan population
por: Marouf, Chaymaa, et al.
Publicado: (2015)

Association between ABCB1 C3435T polymorphism and breast cancer risk: a Moroccan case-control study and meta-analysis
por: Tazzite, Amal, et al.
Publicado: (2016)

Effect of the novel Moroccan BRCA1 and BRCA2 frameshift mutations
por: Tazzite, Amal, et al.
Publicado: (2013)

The 894G>T variant in the endothelial nitric oxide synthase gene and spina bifida risk
por: van der Linden, Ivon J. M., et al.
Publicado: (2007)

A novel mutation in the ABCD1 gene of a Moroccan patient with X-linked adrenoleukodystrophy: case report
por: Karkar, Adnane, et al.
Publicado: (2015)

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

Association of the 894G>T polymorphism in the endothelial nitric oxide synthase gene with risk of acute myocardial infarction
por: Andrikopoulos, George K, et al.
Publicado: (2008)

Endothelial Nitric Oxide Synthase G894T Polymorphism Associates with Disease Severity in Puumala Hantavirus Infection
por: Koskela, Sirpa, et al.
Publicado: (2015)

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 (eNOS) 4a/b and G894T Polymorphisms and Susceptibility to Preeclampsia
por: Rahimi, Zohreh, et al.
Publicado: (2013)

The nitric oxide synthase 3 G894T polymorphism associated with Alzheimer’s disease risk: a meta-analysis
por: Liu, Shengyuan, et al.
Publicado: (2015)

Association of the endothelial nitric oxide synthase gene G894T polymorphism with the risk of diabetic nephropathy in Qassim region, Saudi Arabia—A pilot study
por: Mackawy, Amal Mohammed Husein, et al.
Publicado: (2014)

Endothelial Nitric Oxide Synthase Gene Polymorphism (G894T) and Diabetes Mellitus (Type II) among South Indians
por: Angeline, T., et al.
Publicado: (2011)

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 Glu 298 Asp (G894T) and Apolipoprotein E gene polymorphism as possible risk factors for coronary heart disease among Egyptians
por: Arafa, Sherif, et al.
Publicado: (2018)

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)

Evidence for zoonotic transmission of species A rotavirus from goat and cattle in nomadic herds in Morocco, 2012–2014
por: Alaoui Amine, Sanaâ, et al.
Publicado: (2020)

Endothelial Nitric Oxide Synthase Gene G894T Polymorphism and Myocardial Infarction: A Meta-Analysis of 34 Studies Involving 21068 Subjects
por: Luo, Jian-Quan, et al.
Publicado: (2014)

Prevalence of resistance to integrase strand-transfer inhibitors (INSTIs) among untreated HIV-1 infected patients in Morocco
por: Alaoui, Najwa, et al.
Publicado: (2018)

Prevalence of endothelial nitric oxide synthase (ENOS) gene G894T polymorphism and its association with hypertension: a population-based study with Brazilian women
por: Neto, Abel Barbosa Lira, et al.
Publicado: (2019)

TP53 R72P Polymorphism and Susceptibility to Human Papillomavirus Infection Among Women With Human Immunodeficiency Virus in Morocco: A Case-control Study
por: Lahsen, Ahd Oulad, et al.
Publicado: (2017)

Modifiable predictors of severe heart failure in Morocco: a descriptive study using routinely collected health data
por: Kone, Alpha, et al.
Publicado: (2019)

Distribution of alleles, genotypes and haplotypes of the CYP2B6 (rs3745274; rs2279343) and CYP3A4 (rs2740574) genes in the Malian population: Implication for pharmacogenetics
por: Kassogue, Yaya, et al.
Publicado: (2021)

Paediatric Osteoarticular Infections Caused by Staphylococcus aureus Producing Panton–Valentine Leucocidin in Morocco: Risk factors and Clinical Features
por: Moutaouakkil, Kaoutar, et al.
Publicado: (2022)

Tumor Necrosis Factor (TNF) –308G>A, Nitric Oxide Synthase 3 (NOS3) +894G>T Polymorphisms and Migraine Risk: A Meta-Analysis
por: Chen, Min, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_jer28l0k0u7j3pr7erlbif7epv