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Journal Abstract Search

139 related items for PubMed ID: 172988

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  • 2. Oxidative phosphorylation at various stages of genetically determined cardiomyopathy in the Syrian hamster.
    Wrogemann K, Blanchaer MC, Jacobson BE.
    Recent Adv Stud Cardiac Struct Metab; 1973; 3():467-78. PubMed ID: 4377606
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  • 5. Hereditary polymyopathy and cardiomyopathy in the Syrian hamster. II. Development of heart necrotic changes in relation to defective mitochondrial function.
    Proschek L, Jasmin G.
    Muscle Nerve; 1982 Jan; 5(1):26-32. PubMed ID: 7057802
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  • 6. Serum CK, calcium, magnesium, and oxidative phosphorylation in mdx mouse muscular dystrophy.
    Glesby MJ, Rosenmann E, Nylen EG, Wrogemann K.
    Muscle Nerve; 1988 Aug; 11(8):852-6. PubMed ID: 3173410
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  • 10. On the mechanism of a calcium-associated defect of oxidative phosphorylation in progessive muscular dystrophy.
    Wrogemann K, Jacobson BE, Blanchaer MC.
    Arch Biochem Biophys; 1973 Nov; 159(1):267-78. PubMed ID: 4361547
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  • 15. Fragmented sarcoplasmic reticulum of the cardiomyopathic Syrian hamster: lipid composition, Ca++ transport, and Ca++-stimulated ATPase.
    Owens K, Ruth RC, Weglicki WB, Stam AC, Sonnenblick EH.
    Recent Adv Stud Cardiac Struct Metab; 1974 Nov; 4():541-50. PubMed ID: 4283223
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  • 16. Mitochondrial calcium content and oxidative phosphorylation in heart and skeletal muscle of dystrophic mice.
    Nylen EG, Wrogemann K.
    Exp Neurol; 1983 Apr; 80(1):69-80. PubMed ID: 6832274
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  • 18. Differing populations of mitochondria isolated from the skeletal muscle of normal and dystrophic hamsters.
    Mezon BJ, Wrogemann K, Blanchaer MC.
    Can J Biochem; 1974 Nov; 52(11):1024-32. PubMed ID: 4429865
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