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Journal Abstract Search

127 related items for PubMed ID: 9247091

  • 1. Late-infantile ceroid-lipofuscinosis: lysine methylation of mitochondrial ATP synthase subunit c from lysosomal storage bodies.
    Katz ML, Siakotos AN, Gao Q, Freiha B, Chin DT.
    Biochim Biophys Acta; 1997 Jul 10; 1361(1):66-74. PubMed ID: 9247091
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  • 2. Lysine methylation of mitochondrial ATP synthase subunit c stored in tissues of dogs with hereditary ceroid lipofuscinosis.
    Katz ML, Christianson JS, Norbury NE, Gao CL, Siakotos AN, Koppang N.
    J Biol Chem; 1994 Apr 01; 269(13):9906-11. PubMed ID: 8144584
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  • 3. Mitochondrial ATP synthase subunit c stored in hereditary ceroid-lipofuscinosis contains trimethyl-lysine.
    Katz ML, Gao CL, Tompkins JA, Bronson RT, Chin DT.
    Biochem J; 1995 Sep 15; 310 ( Pt 3)(Pt 3):887-92. PubMed ID: 7575423
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  • 4. Lysosomal storage of the DCCD reactive proteolipid subunit of mitochondrial ATP synthase in human and ovine ceroid lipofuscinoses.
    Palmer DN, Fearnley IM, Medd SM, Walker JE, Martinus RD, Bayliss SL, Hall NA, Lake BD, Wolfe LS, Jolly RD.
    Adv Exp Med Biol; 1989 Sep 15; 266():211-22; discussion 223. PubMed ID: 2535017
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  • 5. 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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  • 6. 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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  • 8. Specific storage of subunit c of mitochondrial ATP synthase in lysosomes of neuronal ceroid lipofuscinosis (Batten's disease).
    Kominami E, Ezaki J, Muno D, Ishido K, Ueno T, Wolfe LS.
    J Biochem; 1992 Feb 15; 111(2):278-82. PubMed ID: 1533218
    [Abstract] [Full Text] [Related]

  • 9. Methylated lysine in storage body protein of sheep with hereditary ceroid-lipofuscinosis.
    Katz ML, Gerhardt KO.
    Biochim Biophys Acta; 1992 Feb 14; 1138(2):97-108. PubMed ID: 1540666
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  • 11. Lysine 43 is trimethylated in subunit C from bovine mitochondrial ATP synthase and in storage bodies associated with batten disease.
    Chen R, Fearnley IM, Palmer DN, Walker JE.
    J Biol Chem; 2004 May 21; 279(21):21883-7. PubMed ID: 15010464
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  • 13. Canine hereditary ceroid-lipofuscinosis: evidence for a defect in the carnitine biosynthetic pathway.
    Katz ML, Siakotos AN.
    Am J Med Genet; 1995 Jun 05; 57(2):266-71. PubMed ID: 7668343
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  • 14. Lysosomal storage of subunit c of mitochondrial ATP synthase in Batten's disease (ceroid-lipofuscinosis).
    Hall NA, Lake BD, Dewji NN, Patrick AD.
    Biochem J; 1991 Apr 01; 275 ( Pt 1)(Pt 1):269-72. PubMed ID: 1826833
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  • 15. Tripeptidyl peptidase I, the late infantile neuronal ceroid lipofuscinosis gene product, initiates the lysosomal degradation of subunit c of ATP synthase.
    Ezaki J, Takeda-Ezaki M, Kominami E.
    J Biochem; 2000 Sep 01; 128(3):509-16. PubMed ID: 10965052
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  • 18. [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 01; 53(12):3055-61. PubMed ID: 8577058
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  • 20. A lysosomal proteinase, the late infantile neuronal ceroid lipofuscinosis gene (CLN2) product, is essential for degradation of a hydrophobic protein, the subunit c of ATP synthase.
    Ezaki J, Tanida I, Kanehagi N, Kominami E.
    J Neurochem; 1999 Jun 01; 72(6):2573-82. PubMed ID: 10349869
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