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Published in 2023 at "Current opinion in nephrology and hypertension"
DOI: 10.1097/mnh.0000000000000891
Abstract: PURPOSE OF REVIEW Mutations in the E3 ubiquitin ligase scaffold cullin 3 (CUL3) cause the disease familial hyperkalemic hypertension (FHHt) by hyperactivating the NaCl cotransporter (NCC). The effects of these mutations are complex and still…
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Keywords:
hypertension;
familial hyperkalemic;
hyperkalemic hypertension;
cul3 mutations ... See more keywords
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2
Published in 2023 at "Acta Physiologica"
DOI: 10.1111/apha.13948
Abstract: Cyclosporin A (CsA) is a widely used immunosuppressive drug that causes hypertension and hyperkalemia. Moreover, CsA‐induced stimulation of the thiazide‐sensitive NaCl cotransporter (NCC) in the kidney has been shown to be responsible for the development…
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Keywords:
hypertension;
hyperkalemic hypertension;
nacl cotransporter;
induced stimulation ... See more keywords
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Published in 2023 at "Hypertension"
DOI: 10.1161/hypertensionaha.123.20525
Abstract: The study of rare monogenic forms of hypertension has led to the elucidation of important physiological pathways controlling blood pressure. Mutations in several genes cause familial hyperkalemic hypertension (also known as Gordon syndrome or pseudohypoaldosteronism…
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Keywords:
familial hyperkalemic;
hyperkalemic hypertension;
blood pressure;
hypertension ... See more keywords
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0
Published in 2017 at "JCI insight"
DOI: 10.1172/jci.insight.96700
Abstract: Mutations in the ubiquitin ligase scaffold protein Cullin 3 (CUL3) cause the disease familial hyperkalemic hypertension (FHHt). In the kidney, mutant CUL3 (CUL3-Δ9) increases abundance of With-No-Lysine [K] Kinase 4 (WNK4), with excessive activation of…
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Keywords:
dominant effects;
hyperkalemic hypertension;
familial hyperkalemic;
cul3 ... See more keywords