Genetic modification of the dilated cardiomyopathy and neonatal lethality phenotype of mice lacking manganese superoxide dismutase
- 1 April 1998
- journal article
- Published by Springer Science and Business Media LLC in AGE
- Vol. 21 (2), 83-84
- https://doi.org/10.1007/s11357-998-0011-y
Abstract
No abstract availableThis publication has 20 references indexed in Scilit:
- Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factorNature Genetics, 1996
- Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutaseNature Genetics, 1995
- Targeted Disruption of Mouse EGF receptor: Effect of Genetic Background on Mutant PhenotypeScience, 1995
- Oxidative damage in neurodegenerative diseaseThe Lancet, 1994
- Oxidative injury in reoxygenated and reperfused heartsFree Radical Biology & Medicine, 1994
- Extension of Life-Span by Overexpression of Superoxide Dismutase and Catalase in Drosophila melanogasterScience, 1994
- Oxygen Radicals in Focal Cerebral IschemiaBrain Pathology, 1994
- Relationship between mitochondrial superoxide and hydrogen peroxide production and longevity of mammalian speciesFree Radical Biology & Medicine, 1993
- NMDA-dependent superoxide production and neurotoxicityNature, 1993
- The Role of Oxygen Radicals in Human Disease, with Particular Reference to the Vascular SystemPathophysiology of Haemostasis and Thrombosis, 1993