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169 related items for PubMed ID: 30050647
1. The Effect of Chronic NO Synthase Inhibition on the Vasoactive and Structural Properties of Thoracic Aorta, NO Synthase Activity, and Oxidative Stress Biomarkers in Young SHR. Berenyiova A, Dovinova I, Kvandova M, Kristek F, Jansen E, Majzunova M, Cacanyiova S. Oxid Med Cell Longev; 2018; 2018():2502843. PubMed ID: 30050647 [Abstract] [Full Text] [Related]
2. The adaptive role of nitric oxide and hydrogen sulphide in vasoactive responses of thoracic aorta is triggered already in young spontaneously hypertensive rats. Cacanyiova S, Berenyiova A, Kristek F, Drobna M, Ondrias K, Grman M. J Physiol Pharmacol; 2016 Aug; 67(4):501-512. PubMed ID: 27779471 [Abstract] [Full Text] [Related]
16. Genetic variants on rat chromosome 8 exhibit profound effects on hypertension severity and survival during nitric oxide inhibition in spontaneously hypertensive rats. Schulz A, Schütten-Faber S, Schulte L, Unland J, Kossmehl P, Kreutz R. Am J Hypertens; 2014 Mar 28; 27(3):294-8. PubMed ID: 24363279 [Abstract] [Full Text] [Related]
18. Luteolin reduces high glucose-mediated impairment of endothelium-dependent relaxation in rat aorta by reducing oxidative stress. Qian LB, Wang HP, Chen Y, Chen FX, Ma YY, Bruce IC, Xia Q. Pharmacol Res; 2010 Apr 28; 61(4):281-7. PubMed ID: 19892019 [Abstract] [Full Text] [Related]
19. Cerebrovascular effects of nitric oxide manipulation in spontaneously hypertensive rats. Fouyas IP, Kelly PA, Ritchie IM, Whittle IR. Br J Pharmacol; 1997 May 28; 121(1):49-56. PubMed ID: 9146886 [Abstract] [Full Text] [Related]