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Elena E. Pohl

Researcher at University of Veterinary Medicine Vienna

Publications -  93
Citations -  4138

Elena E. Pohl is an academic researcher from University of Veterinary Medicine Vienna. The author has contributed to research in topics: Lipid bilayer & Chemistry. The author has an hindex of 30, co-authored 78 publications receiving 3626 citations. Previous affiliations of Elena E. Pohl include Humboldt University of Berlin & Charité.

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Comparative analysis of uncoupling protein 4 distribution in various tissues under physiological conditions and during development.

TL;DR: It is shown that UCP4 is present in fetal murine brain tissue as early as embryonic days 12-14 (E12-E14), which coincides with the beginning of neuronal differentiation.
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Permeation of phloretin across bilayer lipid membranes monitored by dipole potential and microelectrode measurements.

TL;DR: The transmembrane diffusion of phloretin across planar bilayer lipid membranes is studied under steady-state conditions and the membrane permeability is found to agree very well with the permeability deduced from the microelectrode measurements.
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The expression of UCP3 directly correlates to UCP1 abundance in brown adipose tissue

TL;DR: The results do not support the participation of UCP3 in thermogenesis in the absence of U CP1 in BAT, but clearly demonstrate the correlation in abundance between both proteins.
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Superresolution microscopy reveals spatial separation of UCP4 and F0F1-ATP synthase in neuronal mitochondria

TL;DR: The results suggest that the local separation of the proteins on the inner mitochondrial membrane makes it impossible for uncoupling protein 4 (UCP4) to uncouple phosphorylation from proton pumping, but UCP4 should be well able to shortcut excessive transmembrane proton gradients to thereby regulate reactive oxygen species production.
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Quantification of uncoupling protein 2 reveals its main expression in immune cells and selective up-regulation during T-cell proliferation.

TL;DR: Both the U CP2 expression pattern and the time course of up-regulation in stimulated T-cells imply UCP2’s involvement in the immune response, probably by controlling the metabolism during cell proliferation.