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Phillip A. Sharp

Researcher at Massachusetts Institute of Technology

Publications -  618
Citations -  125567

Phillip A. Sharp is an academic researcher from Massachusetts Institute of Technology. The author has contributed to research in topics: RNA & Gene. The author has an hindex of 172, co-authored 614 publications receiving 117126 citations. Previous affiliations of Phillip A. Sharp include McGovern Institute for Brain Research & Medical Research Council.

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Journal ArticleDOI

Genome-wide identification of Ago2 binding sites from mouse embryonic stem cells with and without mature microRNAs

TL;DR: In this article, photo-cross-linking immunoprecipitation using antibodies to Argonaute (Ago2) followed by deep sequencing of RNAs (CLIP-seq) was performed to identify endogenous miRNA binding sites in mouse embryonic stem cells.
Journal ArticleDOI

HIV-1 Tat protein trans-activates transcription in vitro

TL;DR: Analysis of Tat trans-activation in vitro will provide new mechanistic insights into this process and allow a more detailed study of the relationship between Tat protein structure and function.
Book ChapterDOI

In vitro transcription: whole-cell extract.

TL;DR: This chapter focuses on three classes of nuclear DNA-dependent RNA polymerases that have been identified in eukaryotic cells, finding that short runoff transcripts have a higher optimum DNA concentration than longer runoff transcripts.
Journal ArticleDOI

Sustained Small Interfering RNA-Mediated Human Immunodeficiency Virus Type 1 Inhibition in Primary Macrophages

TL;DR: In this paper, the authors investigated if sustained siRNA-mediated silencing of human immunodeficiency virus type 1 (HIV-1) is possible in terminally differentiated macrophages, which constitute an important reservoir of HIV in vivo.
Journal ArticleDOI

Nramp2 Expression Is Associated with pH-dependent Iron Uptake across the Apical Membrane of Human Intestinal Caco-2 Cells

TL;DR: It is demonstrated that Nramp2 is expressed in the apical membrane of the human intestinal epithelial cell line, Caco 2 TC7, and is associated with functional iron transport in these cells with a substrate preference for iron over other divalent cations, suggesting that the expression of the Nramps2 transporter in human enterocytes may play an important role in intestinal iron absorption.