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Journal Abstract Search

127 related items for PubMed ID: 9375799

  • 1. Turnover of F1F0-ATP synthase subunit 9 and other proteolipids in normal and Batten disease fibroblasts.
    Tanner A, Shen BH, Dice JF.
    Biochim Biophys Acta; 1997 Oct 24; 1361(3):251-62. PubMed ID: 9375799
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  • 2. Specific delay in the degradation of mitochondrial ATP synthase subunit c in late infantile neuronal ceroid lipofuscinosis is derived from cellular proteolytic dysfunction rather than structural alteration of subunit c.
    Ezaki J, Wolfe LS, Kominami E.
    J Neurochem; 1996 Oct 24; 67(4):1677-87. PubMed ID: 8858953
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  • 5. Abnormal degradative pathway of mitochondrial ATP synthase subunit c in late infantile neuronal ceroid-lipofuscinosis (Batten disease).
    Ezaki J, Wolfe LS, Ishidoh K, Kominami E.
    Am J Med Genet; 1995 Jun 05; 57(2):254-9. PubMed ID: 7668341
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  • 6. Two related proteolipids and dolichol-linked oligosaccharides accumulate in motor neuron degeneration mice (mnd/mnd), a model for neuronal ceroid lipofuscinosis.
    Faust JR, Rodman JS, Daniel PF, Dice JF, Bronson RT.
    J Biol Chem; 1994 Apr 01; 269(13):10150-5. PubMed ID: 8144516
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  • 8. Batten disease fibroblasts in culture accumulate mitochondrial ATP synthase subunit 9.
    Tanner A, Dice JF.
    Cell Biol Int; 1995 Jan 01; 19(1):71-5. PubMed ID: 7613514
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  • 9. Anomalies of mitochondrial ATP synthase regulation in four different types of neuronal ceroid lipofuscinosis.
    Das AM, Jolly RD, Kohlschütter A.
    Mol Genet Metab; 1999 Apr 01; 66(4):349-55. PubMed ID: 10191128
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  • 13. 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 01; 20(11):1305-9. PubMed ID: 8786816
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  • 14. The sequence of the major protein stored in ovine ceroid lipofuscinosis is identical with that of the dicyclohexylcarbodiimide-reactive proteolipid of mitochondrial ATP synthase.
    Fearnley IM, Walker JE, Martinus RD, Jolly RD, Kirkland KB, Shaw GJ, Palmer DN.
    Biochem J; 1990 Jun 15; 268(3):751-8. PubMed ID: 2141977
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  • 16. [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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  • 18. Role of subunit-9 of mitochondrial ATP synthase in Batten disease.
    Johnson DW, Speier S, Qian WH, Lane S, Cook A, Suzuki K, Daniel P, Boustany RM.
    Am J Med Genet; 1995 Jun 05; 57(2):350-60. PubMed ID: 7668362
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  • 19. Follow-up study of subunit c of mitochondrial ATP synthase (SCMAS) in Batten disease and in unrelated lysosomal disorders.
    Elleder M, Sokolová J, Hrebícek M.
    Acta Neuropathol; 1997 Apr 05; 93(4):379-90. PubMed ID: 9113203
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