Work

Mitochondrial fusion and function in Charcot–Marie–Tooth type 2A patient fibroblasts with mitofusin 2 mutations

Year: 2008

Type: article

Source: Experimental Neurology

DOI: 10.1016/j.expneurol.2008.01.010

Authors: Elizabeth A. Amiott, Paul Lott, Jamie Soto, Peter B. Kang, J. Michael McCaffery, Salvatore DiMauro, E. Dale Abel, Kevin M. Flanigan, Victoria H. Lawson, Janet M. Shaw

Institutions: University of Utah, Boston Children's Hospital, Harvard University, Johns Hopkins University, Columbia University Irving Medical Center

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: University of Utah, National Heart, Lung, and Blood Institute, National Institute of General Medical Sciences, National Institute of Neurological Disorders and Stroke, National Center for Research Resources, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: Amersham Typhoon 9410 Variable Model Imager, G2710467987, Zeiss LSM 510 META Confocal Microscope, G3852491282, FEI Tecnai 12 BioTWIN Transmission Electron Microscope, Characterization-Novel Subtypes-Inherited Neuropathies, Mechanisms of Mitochondrial Fission, G4594604145, General Clinical Research Center, Anatomic variations in muscle gene expression, Zeiss/31 Stallion DDI Multi-Dimensional Live-Cell Imaging Workstation, Training in Cardiovascular Research

OpenAlex ID: W2093662055

FWCI: 4.042

Cites: 52

Cited by: 110

Related to: 10