👤 Orazio J Slivano

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Amr R Salem, Jaser Doja, Chunyu Ge +17 more · 2026 · bioRxiv : the preprint server for biology · added 2026-04-24
Atherosclerosis is the primary underlying cause of coronary artery disease (CAD). Several distinct Under atherogenic conditions, Under proatherogenic conditions,
no PDF DOI: 10.64898/2026.02.15.705944
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Shun Matsumura, Catherine D'Addiaro, Orazio J Slivano +5 more · 2022 · Vascular pharmacology · Elsevier · added 2026-04-24
Epidemiological studies suggest that individuals in the Mediterranean region with deficiency of glucose-6-phosphate dehydrogenase (G6PD) are less susceptible to cardiovascular diseases. However, our k Show more
Epidemiological studies suggest that individuals in the Mediterranean region with deficiency of glucose-6-phosphate dehydrogenase (G6PD) are less susceptible to cardiovascular diseases. However, our knowledge regarding the effects of G6PD deficiency on pathogenesis of vascular diseases caused by factors, like angiotensin II (Ang-II), which stimulate synthesis of inflammatory cytokines and vascular inflammation, is lacking. Furthermore, to-date the effect of G6PD deficiency on vascular health has been controversial and difficult to experimentally prove due to a lack of good animal model. To determine the effect of Ang-II-induced hypertension (HTN) and stiffness in a rat model of the Mediterranean G6PD (G6PD Our findings revealed that infusion of Ang-II (490 ng/kg/min) elicited less HTN and medial hypertrophy of carotid artery in G6PD The G6PD Show less
📄 PDF DOI: 10.1016/j.vph.2022.107002
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Danny Halim, Michael P Wilson, Daniel Oliver +22 more · 2017 · Proceedings of the National Academy of Sciences of the United States of America · National Academy of Sciences · added 2026-04-24
Megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS) is a congenital visceral myopathy characterized by severe dilation of the urinary bladder and defective intestinal motility. The genet Show more
Megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS) is a congenital visceral myopathy characterized by severe dilation of the urinary bladder and defective intestinal motility. The genetic basis of MMIHS has been ascribed to spontaneous and autosomal dominant mutations in actin gamma 2 ( Show less
no PDF DOI: 10.1073/pnas.1620507114
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