Associated Papers
Cardiovascular and metabolic characters of KCNJ5 somatic mutations in primary aldosteronism.
Chang YY et al.
Frontiers in Endocrinology, 2023
Genetic Dissection of Primary Aldosteronism in a Patient With MEN1 and Ipsilateral Adrenocortical Carcinoma and Adenoma.
Parisien-La Salle S et al.
The Journal of Clinical Endocrinology and Metabolism, 2022
Pathogenesis of Primary Aldosteronism: Impact on Clinical Outcome.
Santana LS et al.
Frontiers in Endocrinology, 2022
Novel Mutations Detection with Next-Generation Sequencing and Its Association with Clinical Outcome in Unilateral Primary Aldosteronism.
Wu CH et al.
Biomedicines, 2021
34572353 (PubMed )
Supplement: biomedicines-09-01167-s001.zip › biomedicines-1321403-supplementary.pdf
Approaches to Gene Mutation Analysis Using Formalin-Fixed Paraffin-Embedded Adrenal Tumor Tissue From Patients With Primary Aldosteronism.
Nanba K et al.
Frontiers in Endocrinology, 2021
Primary aldosteronism diagnostics: KCNJ5 mutations and hybrid steroid synthesis in aldosterone-producing adenomas.
Rege J et al.
Gland Surgery, 2020
Double adrenocortical adenomas harboring independent KCNJ5 and PRKACA somatic mutations.
Nanba K et al.
European Journal of Endocrinology, 2016
New roles for a key glycine and its neighboring residue in potassium channel gating.
Rosenhouse-Dantsker A et al.
Biophysical Journal, 2006
Potassium channel gating in the absence of the highly conserved glycine of the inner transmembrane helix.
Rosenhouse-Dantsker A et al.
Channels (austin, Tex.), 0
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