Work

Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblasts

Year: 2009

Type: article

Source: Neuromuscular Disorders

DOI: 10.1016/j.nmd.2009.08.003

Authors: Jouni Vesa, Hailing Su, Giles D. Watts, Sabine Krause, Maggie C. Walter, Barbara Martin, Charles Smith, Douglas C. Wallace, Virginia E. Kimonis

Institutions: University of California, Irvine, Boston Children's Hospital, Harvard University, Ludwig-Maximilians-Universität München, University of Kentucky

Language: English

Topic: Muscle Physiology and Disorders

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

Funders: Muscular Dystrophy Association, Bundesministerium für Bildung und Forschung, National Institutes of Health, National Institute on Aging, National Institute of Neurological Disorders and Stroke, National Institute of Arthritis and Musculoskeletal and Skin Diseases

Awards: G2718742063, Imaging Brain Function/Structure in Presymptomatic FTD, G322054087, G3376850671, G3534085635, Adaptive Physiology of mtDNA Longevity Mutations, The Alzheimer's Disease Research Center at the University of California, Irvine, G5484089957, Genetic basis of myopathy with Paget disease of bone, Mitochondrial Inborn Errors in Metabolism, G731271158, ANT Defects in Neurodegenerative Diseases, Mitochondrial Genetics and Aging, G9000153835

OpenAlex ID: W2169201164

FWCI: 2.5

Cites: 42

Cited by: 61

Related to: 10