Cargando…
Common rs5918 (PlA1/A2) polymorphism in the ITGB3 gene and risk of coronary artery disease
INTRODUCTION: The T to C transition at nucleotide 1565 of the human glycoprotein IIIa (ITGB3) gene represents a genetic polymorphism (PlA1/A2) that can influence both platelet activation and aggregation and that has been associated with many types of disease. Here, we present a newly designed multip...
Autores principales: | Khatami, Mehri, Heidari, Mohammad Mehdi, Soheilyfar, Sorour |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5421535/ https://www.ncbi.nlm.nih.gov/pubmed/28905013 http://dx.doi.org/10.5114/amsad.2016.59587 |
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) -
Apolipoprotein E Gene Polymorphism in Iranian Coronary Atherosclerosis Patients Candidate for Coronary Artery Bypass Graft
por: Heidari, Mohammad Mehdi, et al.
Publicado: (2013) -
Simultaneous Genotyping of the rs4762 and rs699 Polymorphisms in Angiotensinogen Gene and Correlation with Iranian CAD Patients with Novel Hexa-primer ARMS-PCR
por: KHATAMI, Mehri, et al.
Publicado: (2017) -
Investigating Association of rs5918 Human Platelets Antigen 1 and rs1800790 Fibrinogen β Chain as Critical Players with Recurrent Pregnancy Loss
por: Karami, Fatemeh, et al.
Publicado: (2018) -
Platelet Glycoprotein Receptor Ia-C807T and IIIa-PlA1/PlA2 Genetic Polymorphisms Are Associated With Enhanced Platelet Function in Women With Recurrent Miscarriages
por: Tsamadias, Vassilios, et al.
Publicado: (2023)