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Androgen-sensitive hypertension associated with soluble guanylate cyclase-α₁ deficiency is mediated by 20-HETE
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- Journal Article
- A1
- open access
Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing
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Identification of renin signaling as a blood pressure modifying mechanism in soluble guanylate cyclase alpha(1)-deficient mice
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- Journal Article
- A1
- open access
Genetic modifiers of hypertension in soluble guanylate cyclase α1-deficient mice
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Genetic mapping of a modifier locus affecting blood pressure in soluble guanylate cyclase alpha 1-deficient mice
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Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease