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Jeffery S. Cox

Researcher at University of California, Berkeley

Publications -  88
Citations -  20902

Jeffery S. Cox is an academic researcher from University of California, Berkeley. The author has contributed to research in topics: Mycobacterium tuberculosis & Secretion. The author has an hindex of 51, co-authored 84 publications receiving 19016 citations. Previous affiliations of Jeffery S. Cox include University of California, San Francisco & Albert Einstein College of Medicine.

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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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Transcriptional induction of genes encoding endoplasmic reticulum resident proteins requires a transmembrane protein kinase

TL;DR: IRE1 encodes a transmembrane serine/threonine kinase that it is proposed transmits the unfolded protein signal across the ER or inner nuclear membrane, suggesting that the induction of ER resident proteins is coupled to the biogenesis of new ER membrane.
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A novel mechanism for regulating activity of a transcription factor that controls the unfolded protein response.

TL;DR: It is proposed that the complex regulation of Hac1p expression serves to provide multiple levels at which the UPR can be controlled.
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Complex lipid determines tissue-specific replication of Mycobacterium tuberculosis in mice

TL;DR: Using signature-tagged mutagenesis, three attenuated M. tuberculosis mutants are isolated that cannot synthesize or transport a complex, cell wall-associated lipid called phthiocerol dimycocerosate (PDIM) which is found only in pathogenic mycobacteria.
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Type VII secretion — mycobacteria show the way

TL;DR: Given the unique composition of this secretion system, and its general importance, it is proposed that, in line with the accepted nomenclature, it should be called type VII secretion.