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Diastrophic Dysplasia Sulfate Transporter (SLC26A2) Is Expressed in the Adrenal Cortex and Regulates Aldosterone Secretion
Spyroglou, Ariadni
, Bozoglu, Tarik, Rawal, Rajesh, De Leonardis, Fabio, Sterner, Christina, Boulkroun, Sheerazed
, Benecke, Arndt G., Monti, Luca, Zennaro, Maria-Christina
, Petersen, Ann-Kristin, Döring, Angela, Rossi, Antonio, Bidlingmaier, Martin, Warth, Richard
, Gieger, Christian
, Reincke, Martin and Beuschlein, Felix
(2014)
Diastrophic Dysplasia Sulfate Transporter (SLC26A2) Is Expressed in the Adrenal Cortex and Regulates Aldosterone Secretion.
Hypertension 63 (5), pp. 1102-1109.
Date of publication of this fulltext: 19 Dec 2024 08:10
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| Item type | Article | ||||
| Journal or Publication Title | Hypertension | ||||
| Publisher: | LIPPINCOTT WILLIAMS & WILKINS | ||||
|---|---|---|---|---|---|
| Place of Publication: | PHILADELPHIA | ||||
| Volume: | 63 | ||||
| Number of Issue or Book Chapter: | 5 | ||||
| Page Range: | pp. 1102-1109 | ||||
| Date | 2014 | ||||
| Institutions | Biology, Preclinical Medicine > Institut für Physiologie | ||||
| Identification Number |
| ||||
| Keywords | ASSOCIATION ANALYSES IDENTIFY; GENOME-WIDE ASSOCIATION; BLOOD-PRESSURE; SOMATIC MUTATIONS; CHANNEL MUTATIONS; KCNJ5 MUTATIONS; CA2+ CHANNELS; RENIN RATIO; HYPERTENSION; ADENOMAS; aldosterone to renin ratio; calcium signaling; genome-wide association study; knockout mice; primary hyperaldosteronism; solute carrier family 26 (sulfate transporter); member 2 protein; human | ||||
| Dewey Decimal Classification | 500 Science > 570 Life sciences | ||||
| Status | Published | ||||
| Refereed | Yes, this version has been refereed | ||||
| Created at the University of Regensburg | Yes | ||||
| Item ID | 61510 |
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