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Frank C. Dorsey

Researcher at Eli Lilly and Company

Publications -  19
Citations -  9950

Frank C. Dorsey is an academic researcher from Eli Lilly and Company. The author has contributed to research in topics: Autophagy & Autophagy-related protein 13. The author has an hindex of 13, co-authored 18 publications receiving 8638 citations. Previous affiliations of Frank C. Dorsey include Scripps Research Institute.

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Journal ArticleDOI

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.
Journal ArticleDOI

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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Toll-like receptor signalling in macrophages links the autophagy pathway to phagocytosis

TL;DR: It is shown that a particle that engages TLRs on a murine macrophage while it is phagocytosed triggers the autophagosome marker LC3 to be rapidly recruited to the phagosome in a manner that depends on theAutophagy pathway proteins ATG5 and ATG7; this process is preceded by recruitment of beclin 1 and phosphoinositide-3-OH kinase activity.
Journal ArticleDOI

NIX is required for programmed mitochondrial clearance during reticulocyte maturation

TL;DR: It is shown that mitochondrial clearance in reticulocytes requires the BCL2-related protein NIX (BNIP3L) and a BAX- and BAK-independent role for a BCL3-relatedprotein in development, indicating that NIX does not function through established proapoptotic pathways.
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Mitochondrial dysfunction in ataxia-telangiectasia.

TL;DR: A model in which ATM plays direct roles in modulating mitochondrial homeostasis is supported and it is suggested that mitochondrial dysfunction and associated increases in mitochondrial reactive oxygen species contribute to the cancer-prone phenotype observed in organisms lacking ATM.