Work

CMT-associated mutations in glycyl- and tyrosyl-tRNA synthetases exhibit similar pattern of toxicity and share common genetic modifiers in Drosophila

Year: 2014

Type: article

Source: Neurobiology of Disease

DOI: 10.1016/j.nbd.2014.04.020

Authors: Biljana Ermanoska, William W. Motley, Ricardo Leitão-Gonçalves, Bob Asselbergh, LaTasha H. Lee, Peter De Rijk, Kristel Sleegers, Tinne Ooms, Tanja A. Godenschwege, Vincent Timmerman, Kenneth H. Fischbeck, Albena Jordanova

Institutions: University of Antwerp, Institute Born-Bunge, National Institutes of Health, National Institute of Neurological Disorders and Stroke, University of Pennsylvania, Florida Atlantic University

Language: English

Topic: Hereditary Neurological Disorders

Subfield: Cellular and Molecular Neuroscience

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

Funders: Muscular Dystrophy Association, Association Belge contre les Maladies Neuro-Musculaires, Universiteit Antwerpen, National Institutes of Health, National Institute of Neurological Disorders and Stroke, National Institute of Child Health and Human Development, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: FUNCTIONAL ANALYSES OF NEUROGLIAN/L1 IN SYNAPTOGENESIS, Studies of Hereditary Neurological Disease: Disease Mechanisms, G7252857446

OpenAlex ID: W2007693243

FWCI: 2.589

Cites: 62

Cited by: 41

Related to: 10