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James G. Evans

Researcher at Massachusetts Institute of Technology

Publications -  10
Citations -  2531

James G. Evans is an academic researcher from Massachusetts Institute of Technology. The author has contributed to research in topics: Cell morphology & Podosome. The author has an hindex of 8, co-authored 10 publications receiving 2346 citations.

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A Mitochondrial Protein Compendium Elucidates Complex I Disease Biology

TL;DR: This work predicts 19 proteins to be important for the function of complex I (CI) of the electron transport chain and validate a subset of these predictions using RNAi, including C8orf38, which is shown to have an inherited mutation in a lethal, infantile CI deficiency.
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Insulin Causes Fatty Acid Transport Protein Translocation and Enhanced Fatty Acid Uptake in Adipocytes

TL;DR: In adipocytes, insulin induces plasma membrane translocation of FATPs from an intracellular perinuclear compartment to the plasma membrane, which may play an important role in energy homeostasis and metabolic disorders such as type 2 diabetes.
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Macrophage podosomes assemble at the leading lamella by growth and fragmentation.

TL;DR: Because daughter podosomes and podosome cluster precursors are preferentially located at the leading edge, they may play a critical role in continually generating new sites of cell adhesion.
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The differential roles of budding yeast Tem1p, Cdc15p, and Bub2p protein dynamics in mitotic exit.

TL;DR: Spindle pole penetration into the bud activates mitotic exit, resulting in Tem1p and Cdc15p persistence at the dSPB to initiate the MEN signal cascade, and fluorescence recovery after photobleaching (FRAP) measurements revealedTem1p-GFP is dynamic at thedSPB in late anaphase.
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Visualization of replication initiation and elongation in Drosophila.

TL;DR: It is found that initiation and elongation occur during separate developmental stages, thus permitting analysis of these two phases of replication in vivo, and the pre–replication complex component, double-parked protein/cell division cycle 10–dependent transcript 1, is not only necessary for proper MCM2–7 localization, but, unexpectedly, is present during elongation.