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Jennifer Lippincott-Schwartz

Researcher at National Institutes of Health

Publications -  281
Citations -  65042

Jennifer Lippincott-Schwartz is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Golgi apparatus & Endoplasmic reticulum. The author has an hindex of 112, co-authored 264 publications receiving 59277 citations. Previous affiliations of Jennifer Lippincott-Schwartz include Johns Hopkins University & Howard Hughes Medical Institute.

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Imaging intracellular fluorescent proteins at nanometer resolution.

Eric Betzig, +8 more
- 15 Sep 2006 - 
TL;DR: This work introduced a method for optically imaging intracellular proteins at nanometer spatial resolution and used this method to image specific target proteins in thin sections of lysosomes and mitochondria and in fixed whole cells to image retroviral protein Gag at the plasma membrane.
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Guidelines for the use and interpretation of assays for monitoring autophagy

Daniel J. Klionsky, +1287 more
- 01 Apr 2012 - 
TL;DR: These guidelines are presented for the selection and interpretation of methods for use by investigators who aim to examine macroautophagy 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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Brefeldin A: insights into the control of membrane traffic and organelle structure.

Richard D. Klausner, +2 more
- 01 Mar 1992 - 
TL;DR: The relationship between the control of membrane traffic and the maintenance of organelle structure has been investigated with the use of a remarkable drug, brefeldin A (BFA), and some speculative models concerning the mechanism and regulation ofmembrane traffic within the central vacuolar system are proposed.
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Rapid redistribution of Golgi proteins into the ER in cells treated with brefeldin A: evidence for membrane cycling from Golgi to ER.

Jennifer Lippincott-Schwartz, +3 more
- 10 Mar 1989 - 
TL;DR: It is suggested that BFA disrupts a dynamic membrane-recycling pathway between the ER and cis/medial Golgi, effectively blocking membrane transport out of but not back to the ER.
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A Photoactivatable GFP for Selective Photolabeling of Proteins and Cells

George H. Patterson, +1 more
- 13 Sep 2002 - 
TL;DR: A photoactivatable variant of the Aequorea victoria green fluorescent protein is reported that, after intense irradiation with 413-nanometer light, increases fluorescence 100 times when excited by 488-nanometers light and remains stable for days under aerobic conditions.