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Steven D. Harris

Researcher at University of Manitoba

Publications -  90
Citations -  8643

Steven D. Harris is an academic researcher from University of Manitoba. The author has contributed to research in topics: Aspergillus nidulans & Hyphal growth. The author has an hindex of 33, co-authored 86 publications receiving 7399 citations. Previous affiliations of Steven D. Harris include University of Connecticut Health Center & University of Windsor.

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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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Polarisome Meets Spitzenkörper: Microscopy, Genetics, and Genomics Converge

TL;DR: The impact of filamentous fungi on human welfare has never been greater and they are attaining increasing notoriety for their ability to cause life-threatening infections in humans.
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Structure and Biosynthesis of Heat-Stable Antifungal Factor (HSAF), a Broad-Spectrum Antimycotic with a Novel Mode of Action

TL;DR: The elucidation of the chemical structure of HSAF and the identification of the genetic locus for its biosynthesis establish the foundation for future exploitation of this group of compounds as new fungicides or antifungal drugs.
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Farnesol‐induced apoptosis in Aspergillus nidulans reveals a possible mechanism for antagonistic interactions between fungi

TL;DR: The data suggest that farnesol, in addition to its quorum‐sensing function that regulates morphogenesis, is also employed by C. albicans to reduce competition from other microbes.
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Polarity in filamentous fungi: moving beyond the yeast paradigm.

TL;DR: Recent polarity research from filamentous fungi is discussed, focusing on the position of germ tube emergence, the relaying of positional information via RhoGTPase modules, and the recruitment of morphogenetic machinery components including cytoskeleton, polarisome and ARP2/3 complexes, andThe vesicle trafficking system.