Work

High throughput gene complementation screening permits identification of a mammalian mitochondrial protein synthesis (ρ − ) mutant

Year: 2016

Type: article

Source: Biochimica et Biophysica Acta (BBA) - Bioenergetics

DOI: 10.1016/j.bbabio.2016.02.021

Authors: Prasanth Potluri, Vincent Procaccio, Immo E. Scheffler, Douglas C. Wallace

Institutions: Children's Hospital of Philadelphia, University of Pennsylvania, Centre Hospitalier Universitaire d'Angers, University of California San Diego

Language: English

Topic: Mitochondrial Function and Pathology

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: National Institutes of Health, National Cancer Institute, National Institute of Diabetes and Digestive and Kidney Diseases, National Institute of Neurological Disorders and Stroke

Awards: G2134882154, G3956112164, C-TERMINAL INTERACTIONS OF ALPHA1-ADRENOCEPTOR SUBTYPES, G5225833643, Mitochondrial Diabetes & Manganic Porphyrin Treatment, G6666980440, Mitochondrial Inborn Errors in Metabolism, Mouse models for mitochondrial disorders caused by mutations in mtDNA, A Mitochondrial Etiology of Autism, High-throughput on-chip platform for interrogation of mitochondrial membrane potential and apoptosis

OpenAlex ID: W2296723259

FWCI: 0.142

Cites: 47

Cited by: 2

Related to: 10