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Journal Abstract Search

145 related items for PubMed ID: 7668341

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  • 2. Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease).
    Palmer DN, Fearnley IM, Walker JE, Hall NA, Lake BD, Wolfe LS, Haltia M, Martinus RD, Jolly RD.
    Am J Med Genet; 1992 Feb 15; 42(4):561-7. PubMed ID: 1535179
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  • 3. Specific delay of degradation of mitochondrial ATP synthase subunit c in late infantile neuronal ceroid lipofuscinosis (Batten disease).
    Ezaki J, Wolfe LS, Higuti T, Ishidoh K, Kominami E.
    J Neurochem; 1995 Feb 15; 64(2):733-41. PubMed ID: 7830067
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  • 4. New insight into lysosomal protein storage disease: delayed catabolism of ATP synthase subunit c in Batten disease.
    Kominami E, Ezaki J, Wolfe LS.
    Neurochem Res; 1995 Nov 15; 20(11):1305-9. PubMed ID: 8786816
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  • 8. [Batten disease (Neuronal ceroid lipofuscinoses)--accumulation of ATP synthase subunit c caused by the delay of lysosomal degradation].
    Ezaki J, Kominami E.
    Nihon Rinsho; 1995 Dec 15; 53(12):3055-61. PubMed ID: 8577058
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  • 13. Submitochondrial distribution and delayed proteolysis of subunit c of the H+-transporting ATP-synthase in ovine ceroid-lipofuscinosis.
    Hughes SM, Moroni-Rawson P, Jolly RD, Jordan TW.
    Electrophoresis; 2001 May 15; 22(9):1785-94. PubMed ID: 11425233
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  • 17. The ovine model of neuronal ceroid lipofuscinosis (NCL): its contribution to understanding the pathogenesis of Batten disease.
    Jolly RD.
    Neuropediatrics; 1997 Feb 15; 28(1):60-2. PubMed ID: 9151325
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