Metabolic Profiling of Genetic Disorders: A Multitissue 1H Nuclear Magnetic Resonance Spectroscopic and Pattern Recognition Study into Dystrophic Tissue
- 1 June 2001
- journal article
- research article
- Published by Elsevier in Analytical Biochemistry
- Vol. 293 (1) , 16-21
- https://doi.org/10.1006/abio.2001.5096
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Regeneration and myogenic cell proliferation correlate with taurine levels in dystrophin- and MyoD-Deficient musclesThe Anatomical Record, 1998
- Increased cerebral choline-compounds in Duchenne muscular dystrophyNeuroReport, 1997
- Brain metabolism is abnormal in the mdx model of Duchenne muscular dystrophyBrain, 1996
- Components of energy expenditure in themdx mouse model of Duchenne muscular dystrophyPflügers Archiv - European Journal of Physiology, 1996
- Brain abnormalities in Duchenne muscular dystrophy: phosphorus-31 magnetic resonance spectroscopy and neuropsychological studyThe Lancet, 1995
- Defective regulation of energy metabolism in mdx-mouse skeletal musclesBiochemical Journal, 1994
- A 71-kilodalton protein is a major product of the Duchenne muscular dystrophy gene in brain and other nonmuscle tissues.Proceedings of the National Academy of Sciences, 1992
- Passive avoidance behaviour deficit in the mdx mouseNeuromuscular Disorders, 1991
- Duchenne muscular dystrophy gene product is not identical in muscle and brainNature, 1989
- X chromosome-linked muscular dystrophy (mdx) in the mouse.Proceedings of the National Academy of Sciences, 1984