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Paper Details

A Genome-wide CRISPR Death Screen Identifies Genes Essential for Oxidative Phosphorylation.
Cell Metab
202
2016
ATP, Deficiencies in OXPHOS, FASTKD2, NGRN, OXPHOS, OXPHOS diseases, RPUSD3, RPUSD4, TRUB2, WBSCR16, deficient in OXPHOS, dying cells, galactose, genes, glucose, human, human cells, human genes, humans, inborn errors of metabolism, mitochondrial 16S rRNA, mitochondrial or nuclear genomes
Author NameAffiliation
Sarah E CalvoDepartment of Molecular Biology and Howard Hughes Medical Institute, Massachusetts General Hospital, Harvard Medical School, USA Broad Institute of MIT and Harvard
John G DoenchBroad Institute of MIT and Harvard
David E RootBroad Institute of MIT and Harvard
David E RootBroad Institute of MIT and Harvard
Vamsi K MoothaDepartment of Molecular Biology and Howard Hughes Medical Institute, Massachusetts General Hospital, Harvard Medical School, USA Broad Institute of MIT and Harvard
Vamsi K MoothaDepartment of Molecular Biology and Howard Hughes Medical Institute, Massachusetts General Hospital, Harvard Medical School, USA Broad Institute of MIT and Harvard
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