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Bruce A. Bamber

Researcher at University of Toledo

Publications -  29
Citations -  7816

Bruce A. Bamber is an academic researcher from University of Toledo. The author has contributed to research in topics: GABA receptor & GABAA receptor. The author has an hindex of 17, co-authored 28 publications receiving 6768 citations. Previous affiliations of Bruce A. Bamber include University of Utah.

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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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Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotes

Daniel J. Klionsky, +235 more
- 16 Feb 2008 - 
TL;DR: A set of guidelines for the selection and interpretation of the methods that can be used by investigators who are attempting to examine macroautophagy and related processes, as well as by reviewers who need to provide realistic and reasonable critiques of papers that investigate these processes are presented.
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Regulation of presynaptic terminal organization by C. elegans RPM-1, a putative guanine nucleotide exchanger with a RING-H2 finger domain.

TL;DR: The RPM-1 protein has an RCC1-like guanine nucleotide exchange factor (GEF) domain and a RING-H2 finger and may regulate the spatial arrangement, or restrict the formation, of presynaptic structures.
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The Caenorhabditis elegans unc-49 Locus Encodes Multiple Subunits of a Heteromultimeric GABA Receptor

TL;DR: C. elegans is able to encode a heteromeric GABA receptor with a single locus and the cloned unc-49 possesses an unusual overlapping gene structure, suggesting that the three UNC-49 subunits are coordinately rescued and therefore might coassemble to form a heteromultimeric GABA receptors.
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Presynaptic Terminals Independently Regulate Synaptic Clustering and Autophagy of GABAA Receptors in Caenorhabditis elegans

TL;DR: It is shown that GABAA receptors traffic to autophagosomes after endocytic removal from the cell surface and that acetylcholine receptors in the same cells do not traffic toAutophagy can degrade cell-surface receptors and can do so selectively, and a novel function for autophagy is demonstrated in GAB AA receptor degradative trafficking.