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Anne K. Kenworthy

Researcher at University of Virginia

Publications -  125
Citations -  14569

Anne K. Kenworthy is an academic researcher from University of Virginia. The author has contributed to research in topics: Fluorescence recovery after photobleaching & Lipid raft. The author has an hindex of 42, co-authored 108 publications receiving 13296 citations. Previous affiliations of Anne K. Kenworthy include Duke University & Johns Hopkins University.

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Journal ArticleDOI

Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

Daniel J. Klionsky, +2522 more
- 21 Jan 2016 - 
TL;DR: In this paper, the authors present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macro-autophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
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Studying protein dynamics in living cells.

TL;DR: Live cell imaging, in combination with photobleaching, energy transfer or fluorescence correlation spectroscopy are providing unprecedented insights into the movement of proteins and their interactions with cellular components.
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Imaging Protein-Protein Interactions Using Fluorescence Resonance Energy Transfer Microscopy

TL;DR: A FRET microscopy method that can be used to determine whether proteins that are colocalized at the level of light microscopy interact with one another, implemented using digital microscopy systems such as a confocal microscope or a wide-field fluorescence microscope coupled to a charge-coupled camera.
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Rapid Cycling of Lipid Raft Markers between the Cell Surface and Golgi Complex

TL;DR: It is shown that different GPI-anchored proteins have different intracellular distributions; some accumulate in transferrin-containing compartments, others accumulate in the Golgi apparatus.
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Distribution of a glycosylphosphatidylinositol-anchored protein at the apical surface of MDCK cells examined at a resolution of <100 A using imaging fluorescence resonance energy transfer.

TL;DR: The data imply that most 5′ NT molecules are randomly distributed across the apical surface of MDCK cells, which constrain current models for lipid rafts and the membrane organization of GPI-anchored proteins.