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Mylène Amherdt

Researcher at University of Geneva

Publications -  61
Citations -  9648

Mylène Amherdt is an academic researcher from University of Geneva. The author has contributed to research in topics: Golgi apparatus & Vesicle. The author has an hindex of 43, co-authored 61 publications receiving 9454 citations. Previous affiliations of Mylène Amherdt include Memorial Sloan Kettering Cancer Center.

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COPII: a membrane coat formed by Sec proteins that drive vesicle budding from the endoplasmic reticulum.

TL;DR: In vitro synthesis of endoplasmic reticulum-derived transport vesicles has been reconstituted with washed membranes and three soluble proteins and it is proposed that the coat structures be called COPI and COPII.
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Brefeldin A's effects on endosomes, lysosomes, and the TGN suggest a general mechanism for regulating organelle structure and membrane traffic

TL;DR: Evidence is provided that suggests BFA's effects are not limited to the Golgi apparatus but are reiterated throughout the central vacuolar system.
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COPII-Coated Vesicle Formation Reconstituted with Purified Coat Proteins and Chemically Defined Liposomes

TL;DR: Observations suggest that the assembly of the COPII coat on the ER occurs by a sequential binding of coat proteins to specific lipids and that this assembly promotes the budding of COPII-coated vesicles.
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Brefeldin A, a drug that blocks secretion, prevents the assembly of non-clathrin-coated buds on Golgi cisternae

TL;DR: It is reported that brefeldin A prevents the assembly of non-clathrin-coated vesicles from Golgi cisternae in a cell-free system, and extensive tubule networks form that connect previously separate cisternAE and stacks into a single topological unit, allowing the intermixing of contents of Golgi bisternae by lateral diffusion.
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Bidirectional Transport by Distinct Populations of COPI-Coated Vesicles

TL;DR: Electron microscope immunocytochemistry reveals that both anterograde-directed and retrograde-directed cargo are present in COPI-coated vesicles budding from every level of the Golgi stack in whole cells; however, they comprise two distinct populations that together can account for at least 80% of the vesicle budding from Golgi cisternae.