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Alexander Tarakhovsky

Researcher at Rockefeller University

Publications -  88
Citations -  16217

Alexander Tarakhovsky is an academic researcher from Rockefeller University. The author has contributed to research in topics: Regulation of gene expression & Cellular differentiation. The author has an hindex of 55, co-authored 86 publications receiving 14871 citations. Previous affiliations of Alexander Tarakhovsky include University of Cologne.

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Suppression of inflammation by a synthetic histone mimic

TL;DR: A synthetic compound (I-BET) is described that by ‘mimicking’ acetylated histones disrupts chromatin complexes responsible for the expression of key inflammatory genes in activated macrophages, and confers protection against lipopolysaccharide-induced endotoxic shock and bacteria-induced sepsis.
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Blimp1 is a critical determinant of the germ cell lineage in mice

TL;DR: It is shown that Blimp1 (also known as Prdm1), a known transcriptional repressor, has a critical role in the foundation of the mouse germ cell lineage, as its disruption causes a block early in the process of primordial germ cell formation.
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Essential Role of the Histone Methyltransferase G9a in Cocaine-induced Plasticity

TL;DR: Using conditional mutagenesis and viral-mediated gene transfer, it is found that G9a down-regulation increased the dendritic spine plasticity of nucleus accumbens neurons and enhanced the preference for cocaine, thereby establishing a crucial role for histone methylation in the long-term actions of cocaine.
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Ezh2 controls B cell development through histone H3 methylation and Igh rearrangement

TL;DR: Ezh2-dependent histone H3 methylation as a novel regulatory mechanism controlling Igh rearrangement during early murine B cell development and rearrangements of the immunoglobulin heavy chain gene (Igh) are suggested.
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Maternal microRNAs are essential for mouse zygotic development

TL;DR: The effects of the loss of maternal inheritance of miRNAs following specific deletion of Dicer from growing oocytes are shown, which demonstrates that the maternal mi RNAs are essential for the earliest stages of mouse embryonic development.