Associated Papers
SERPINA1 and More? A Putative Genetic Contributor to Pulmonary Dysfunction in Alpha-1 Antitrypsin Deficiency.
Jezela-Stanek A et al.
Journal of Clinical Medicine, 2023
NOS3 and CTH gene mutations as new molecular markers for detection of lung adenocarcinoma.
Abdullah Ramadhan I et al.
Peerj, 2023
38107574 (PubMed )
Supplement: peerj-11-16209-s004.xls › Cosmic
Interplay of physical activity and genetic variants of the endothelial lipase on cardiovascular disease risk factors.
Salazar-Tortosa DF et al.
Pediatric Research, 2022
Case report: Two unique nonsense mutations in HTRA1-related cerebral small vessel disease in a Chinese population and literature review.
Chen W et al.
Frontiers in Neurology, 2022
36619910 (PubMed )
Supplement: Data_Sheet_6.ZIP › case2-C › 3.________ › CA2275B________.____Exonic_Variants.xlsx › sheet1
[Pathogenetic significance of C774T single nucleotide polymorphism of the endothelial NO synthase gene in the development of metabolic syndrome].
Fattakhov NS et al.
Biomeditsinskaia Khimiia, 2016
Screening of the NOS3 gene identifies the variants 894G/T, 1998C/G and 2479G/A to be associated with acute onset ischemic stroke in young Asian Indians.
Akhter MS et al.
Journal of the Neurological Sciences, 2014
Endothelial nitric oxide synthase gene polymorphism (G894T) and diabetes mellitus (type II) among South Indians.
Angeline T et al.
Oxidative Medicine and Cellular Longevity, 2011
The T-786C and C774T endothelial nitric oxide synthase gene polymorphisms independently affect the onset pattern of severe diabetic retinopathy.
Taverna MJ et al.
Nitric Oxide : Biology and Chemistry, 2005
Endothelial nitric oxide synthase as a potential susceptibility gene in the pathogenesis of emphysema in alpha1-antitrypsin deficiency.
Novoradovsky A et al.
American Journal of Respiratory Cell and Molecular Biology, 1999
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