D
David W. Piston
Researcher at Washington University in St. Louis
Publications - 248
Citations - 19927
David W. Piston is an academic researcher from Washington University in St. Louis. The author has contributed to research in topics: Islet & Insulin. The author has an hindex of 66, co-authored 230 publications receiving 18364 citations. Previous affiliations of David W. Piston include Uniformed Services University of the Health Sciences & University of Washington.
Papers
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Journal ArticleDOI
An improved cyan fluorescent protein variant useful for FRET.
TL;DR: Cerulean is 2.5-fold brighter than ECFP and replacement of ECFP with Cerulean substantially improves the signal-to-noise ratio of a FRET-based sensor for glucokinase activation.
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Use of the green fluorescent protein and its mutants in quantitative fluorescence microscopy.
TL;DR: No single GFP variant is ideal for every application, but each one offers advantages and disadvantages for quantitative imaging in living cells.
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Fluorescent protein FRET: the good, the bad and the ugly
David W. Piston,Gert-Jan Kremers +1 more
TL;DR: The physical basis of FRET and the fluorescent proteins appropriate for these experiments are described and the approaches that can be used to measure FRET are reviewed, with particular emphasis on the potential artifacts associated with each approach.
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Bone morphogenetic proteins (BMPs) as regulators of dorsal forebrain development
TL;DR: Evidence is provided that BMPs function during regional morphogenesis of the dorsal telencephalon by regulating specific gene expression, cell proliferation and local cell death.
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Ablation of PRDM16 and Beige Adipose Causes Metabolic Dysfunction and a Subcutaneous to Visceral Fat Switch
Paul Cohen,Julia D. Levy,Yingying Zhang,Andrea Frontini,Dmitriy Kolodin,Katrin J. Svensson,James C. Lo,James C. Lo,Xing Zeng,Li Ye,Melin J. Khandekar,Jun Wu,Subhadra C. Gunawardana,Alexander S. Banks,Joao Paulo Camporez,Michael J. Jurczak,Shingo Kajimura,David W. Piston,Diane Mathis,Saverio Cinti,Gerald I. Shulman,Patrick Seale,Bruce M. Spiegelman +22 more
TL;DR: It is shown that adipocyte-specific deletion of the coregulatory protein PRDM16 caused minimal effects on classical brown fat but markedly inhibited beige adipocyte function in subcutaneous fat following cold exposure or β3-agonist treatment, indicating that PRDM 16 and beige fat cells are required for the "browning" of white fat and the healthful effects of sub cutaneous adipose tissue.