scispace - formally typeset
D

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.

Papers
More filters
Journal ArticleDOI

Biodiversity and distribution of polar freshwater DNA viruses

TL;DR: The study uncovers some viral lineages with a bipolar distribution, suggesting a global dispersal capacity for viruses, and seemingly indicates that viruses do not follow the latitudinal diversity gradient known for macroorganisms.
Journal ArticleDOI

Patterns, processes and vulnerability of Southern Ocean benthos: a decadal leap in knowledge and understanding

TL;DR: This paper evaluates recent progress in Southern Ocean benthic research and identifies priorities for future research, including timely and accurate species identifications, application of standardized sampling and reporting procedures, as well as cooperation between disciplines and nations.
Journal ArticleDOI

Defective lysosomal arginine transport in juvenile Batten disease

TL;DR: It is reported that lysosomes isolated from juvenile Batten disease lymphoblasts are only defective for arginine transport, suggesting that the CLN3 defect in juvenile batten disease may affect how intracellular levels ofArginine are regulated or distributed throughout the cell.
Journal ArticleDOI

A clinical rating scale for Batten disease: reliable and relevant for clinical trials.

TL;DR: The Unified Batten Disease Rating Scale (UBDRS) is a reliable instrument that effectively tests for neurologic function in blind and demented patients and is useful for monitoring the diverse clinical findings seen in Batten disease.
Journal ArticleDOI

Pleiotropic action of aldosterone in epithelia mediated by transcription and post-transcription mechanisms

TL;DR: The aldosterone-induced increase in sodium reabsorption across tight epithelia can be divided schematically into two functional phases: an early regulatory phase starting after a lag period of 20 to 60 minutes, during which the pre-existing transport machinery is activated, and a late phase which can be viewed as an anabolic action leading to a further amplification/differentiation of the Na+ transport machinery.