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René Rezsohazy

Researcher at Université catholique de Louvain

Publications -  53
Citations -  1630

René Rezsohazy is an academic researcher from Université catholique de Louvain. The author has contributed to research in topics: Hox gene & Transcription factor. The author has an hindex of 22, co-authored 51 publications receiving 1496 citations. Previous affiliations of René Rezsohazy include Catholic University of Leuven & Netherlands Cancer Institute.

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The IS4 family of insertion sequences : evidence for a conserved transposase motif

TL;DR: Comparison with all the proka‐ryotic transposable elements sequenced so far revealed that the IS231 transposases share two conserved regions with those of 35 other insertion sequences of wide origins.
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Overexpression of adiponectin targeted to adipose tissue in transgenic mice: impaired adipocyte differentiation.

TL;DR: Impaired adipocyte differentiation contributes to the anti-adiposity effect of ApN, and a transgenic mouse model allowing persistent and moderate overexpression of native full-length ApN targeted to white adipose tissue is generated.
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Cellular uptake of Antennapedia Penetratin peptides is a two-step process in which phase transfer precedes a tryptophan-dependent translocation.

TL;DR: Biophysical studies demonstrate that entry of Penetratin into cells requires its binding to surface lipids but that binding and translocation are differentially affected by modifications of some physico-chemical properties of the peptide, like helical amphipathicity or net charge, and that internalization requires both lipid binding and other specific properties.
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Cellular and molecular insights into Hox protein action.

TL;DR: The molecular and cellular scale mechanisms underlying the diverse roles of the Hox transcription factors during morphogenesis and organogenesis are discussed.
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IS231 and other Bacillus thuringiensis transposable elements: a review.

TL;DR: Functional data gathered from IS231 A inEscherichia coli indicate a non-replicative mode of transposition, with a marked preference for specific targets, and a working model for DNA-protein interactions at the target site is proposed.