Pages that link to "Q46656529"
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The following pages link to Liddle's syndrome caused by a novel missense mutation (P617L) of the epithelial sodium channel beta subunit (Q46656529):
Displaying 13 items.
- A Therapeutic Challenge: Liddle's Syndrome Managed with Amiloride during Pregnancy (Q34152668) (← links)
- Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndrome (Q34682504) (← links)
- Associations of epithelial sodium channel genes with blood pressure changes and hypertension incidence: the GenSalt study (Q34683716) (← links)
- Common variants in epithelial sodium channel genes contribute to salt sensitivity of blood pressure: The GenSalt study (Q35169020) (← links)
- ENaCs and ASICs as therapeutic targets (Q35900722) (← links)
- Hsp70 promotes epithelial sodium channel functional expression by increasing its association with coat complex II and its exit from endoplasmic reticulum. (Q36003749) (← links)
- Hsc70 negatively regulates epithelial sodium channel trafficking at multiple sites in epithelial cells (Q37234555) (← links)
- Interactions of genetic variants with physical activity are associated with blood pressure in Chinese: the GenSalt study (Q37247312) (← links)
- Liddle syndrome in a Serbian family and literature review of underlying mutations (Q37940326) (← links)
- Three Reportedly Unrelated Families With Liddle Syndrome Inherited From a Common Ancestor (Q49920783) (← links)
- Liddle Syndrome: Review of the Literature and Description of a New Case. (Q52657742) (← links)
- A clinical phenotype mimicking essential hypertension in a newly discovered family with Liddle's syndrome (Q83987131) (← links)
- Phenotype-genotype analysis in two Chinese families with Liddle syndrome (Q87185973) (← links)