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David A. Pearce

Researcher at Northumbria University

Publications -  405
Citations -  20297

David A. Pearce is an academic researcher from Northumbria University. The author has contributed to research in topics: Batten disease & CLN3. The author has an hindex of 72, co-authored 396 publications receiving 18416 citations. Previous affiliations of David A. Pearce include University of Zurich & University of York.

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Epithelial sodium channel regulated by aldosterone-induced protein sgk.

TL;DR: Sgk (serum and glucocorticoid-regulated kinase), a member of the serine-threonine kinase family, is identified as an aldosterone-induced regulator of ENaC activity, suggesting that sgk plays a central role in ald testosterone regulation of Na+ absorption and thus in the control of extracellular fluid volume, blood pressure, and sodium homeostasis.
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Mineralocorticoid and glucocorticoid receptor activities distinguished by nonreceptor factors at a composite response element

TL;DR: The distinct physiologic effects mediated by MR and GR may be determined by differential interactions of nonreceptor factors with specific receptor domains at composite response elements at plfG, a 25-base pair composite response element to which both the steroid receptors and transcription factor AP1 can bind.
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A multi-decade record of high-quality fCO2 data in version 3 of the Surface Ocean CO2 Atlas (SOCAT)

Dorothee C. E. Bakker, +103 more
TL;DR: This ESSD "living data" publication documents the methods and data sets used for the assembly of this new version of the SOCAT data collection and compares these with those used for earlier versions of the data collection.
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Aldosterone induces rapid apical translocation of ENaC in early portion of renal collecting system: possible role of SGK.

TL;DR: It is shown by real-time RT-PCR and immunofluorescence that an aldosterone injection in adrenalectomized rats induces alpha-ENaC subunit expression along the entire ASDN within 2 h, whereas beta- and gamma- ENaC are constitutively expressed.