| Literature DB >> 30318245 |
Panagiotis D Velentzas1, Lejie Zhang2, Gautam Das1, Tsun-Kai Chang3, Charles Nelson4, William R Kobertz2, Eric H Baehrecke5.
1. Department of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
2. Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
3. Department of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA; Cancer Immunology, Genentech Inc, South San Francisco, CA 94080, USA.
4. Department of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA; Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA.
5. Department of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA. Electronic address: eric.baehrecke@umassmed.edu.
Abstract
Entities:
Keywords: Drosophila; autophagy; cell death; mTOR; monocarboxylate transporter; pyruvate
Mesh:
Animals
Autophagy/physiology
Drosophila Proteins/metabolism
Drosophila melanogaster/metabolism
HEK293 Cells/metabolism
Humans
Monocarboxylic Acid Transporters/metabolism
Proton Pumps
Protons
RNA-Binding Proteins/metabolism
Salivary Glands/cytology
Signal Transduction
TOR Serine-Threonine Kinases/metabolism
Substances:
Drosophila Proteins
Monocarboxylic Acid Transporters
Proton Pumps
Protons
RNA-Binding Proteins
SLC16A11 protein, human
hrm protein, Drosophila
TOR Serine-Threonine Kinases
Year: 2018 PMID: 30318245 PMCID: PMC6219939 DOI: 10.1016/j.devcel.2018.09.015
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270