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Peter E. Bayliss

Researcher at Harvard University

Publications -  13
Citations -  2325

Peter E. Bayliss is an academic researcher from Harvard University. The author has contributed to research in topics: Zebrafish & Senescence. The author has an hindex of 12, co-authored 12 publications receiving 2156 citations. Previous affiliations of Peter E. Bayliss include Princess Margaret Cancer Centre.

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A histone H3 lysine 27 demethylase regulates animal posterior development.

TL;DR: It is shown that the JmjC-domain-containing related proteins UTX and JMJD3 catalyse demethylation of H3K27me3/2, which identifies a small family of H 3K27 demethylases with important, evolutionarily conserved roles in H3k27 methylation regulation and in animal anterior–posterior development.
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The X-Linked Mental Retardation Gene SMCX/JARID1C Defines a Family of Histone H3 Lysine 4 Demethylases

TL;DR: A family of H3K4me3 demethylases are identified and a critical link between histone modifications and XLMR is uncovered, uncovering a role for SMCX in neuronal survival and dendritic development and a link to the demethylase activity.
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Dissection of angiogenic signaling in zebrafish using a chemical genetic approach.

TL;DR: Overexpression of AKT/PKB, a putative effector of vascular endothelial growth factor signaling, allowed blood vessels to form in the presence of drug, thus establishing the physiological relevance of AKt/P KB in the angiogenic process.
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Chemical modulation of receptor signaling inhibits regenerative angiogenesis in adult zebrafish

TL;DR: The utility of the adult zebrafish as a new model system for receptor signaling and chemical biology is illustrated, as an angiogenic limit to tissue regeneration was determined, as avascular tissue containing skin, pigment, neuronal axons and bone precursors could regenerate up to about 1 mm.
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The identification of zebrafish mutants showing alterations in senescence-associated biomarkers.

TL;DR: In this article, the same authors used the same SA-β-gal assay to screen chemically mutagenized zebrafish, each of which was heterozygous for lesions in multiple genes, under the sensitizing conditions of oxidative stress.