Pages that link to "Q73343837"
Jump to navigation
Jump to search
The following pages link to Familial hyperkalemic hypertension: phenotypic analysis in a large family with the WNK1 deletion mutation (Q73343837):
Displaying 16 items.
- WNK3 positively regulates epithelial calcium channels TRPV5 and TRPV6 via a kinase-dependent pathway (Q24310130) (← links)
- Antagonistic regulation of ROMK by long and kidney-specific WNK1 isoforms (Q24537454) (← links)
- Multiple promoters in the WNK1 gene: one controls expression of a kidney-specific kinase-defective isoform (Q24633475) (← links)
- Role of with-no-lysine [K] kinases in the pathogenesis of Gordon's syndrome. (Q31039816) (← links)
- Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretion (Q33426861) (← links)
- WNK4 kinase stimulates caveola-mediated endocytosis of TRPV5 amplifying the dynamic range of regulation of the channel by protein kinase C (Q33673789) (← links)
- Mechanisms of WNK1 and WNK4 interaction in the regulation of thiazide-sensitive NaCl cotransport (Q33736529) (← links)
- WNK1 activates SGK1 to regulate the epithelial sodium channel. (Q33900653) (← links)
- WNK kinases and renal sodium transport in health and disease: an integrated view (Q34548846) (← links)
- The WNKs: atypical protein kinases with pleiotropic actions. (Q34560188) (← links)
- Overexpression of the sodium chloride cotransporter is not sufficient to cause familial hyperkalemic hypertension (Q35421933) (← links)
- Hereditary disorders of potassium homeostasis (Q35612242) (← links)
- Distal potassium handling based on flow modulation of maxi-K channel activity (Q37485817) (← links)
- The WNK kinase network regulating sodium, potassium, and blood pressure (Q37857562) (← links)
- Distal convoluted tubule. (Q52975643) (← links)
- The Molecular Genetics of Gordon Syndrome (Q91646718) (← links)