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Heidi Kiil Blomhoff

Researcher at University of Oslo

Publications -  104
Citations -  9949

Heidi Kiil Blomhoff is an academic researcher from University of Oslo. The author has contributed to research in topics: Apoptosis & Retinoic acid. The author has an hindex of 40, co-authored 103 publications receiving 9285 citations.

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Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

Daniel J. Klionsky, +2522 more
- 21 Jan 2016 - 
TL;DR: In this paper, the authors present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macro-autophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
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Overview of retinoid metabolism and function

TL;DR: Substantial progress has been made in the understanding of retinoid metabolism and function, and central aspects of vitamin A absorption, enzymatic oxidation of all-trans retinol to all-Trans retinal and all- trans retinoic acid, and esterification ofall-trans Retinol have been clarified.
Journal Article

TGF-beta 1 and cyclic AMP promote apoptosis in resting human B lymphocytes.

TL;DR: It is concluded that apoptosis is a regulated phenomenon in resting human B cells, and TGF-beta and cAMP may inhibit B cell responses not only by blocking cell cycle progression in activated cells, but also by inducing apoptosis in resting cells.
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Vitamin A is a key regulator for cell growth, cytokine production, and differentiation in normal B cells.

TL;DR: It is demonstrated that retinol-retinl-binding protein and chylomicron remnant retinyl esters in concentrations normally found in human plasma inhibit growth of normal human B lymphocytes, implying that vitamin A present in human Plasma is a normal modulator of B cell function.
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Novel isozymes of cAMP-dependent protein kinase exist in human cells due to formation of RI alpha-RI beta heterodimeric complexes.

TL;DR: RI alpha-RI beta heterodimers complexed with the catalytic subunit represent a novel isozyme of cAKI (RI alpha RI beta C2), which enhances the possibilities for diversification of cAMP-mediated effects.