These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

130 related articles for article (PubMed ID: 7668344)

  • 21. Increased expression of subunit c of mitochondrial ATP synthase in brain tissue from neuronal ceroid lipofuscinoses and mucopolysaccharidosis cases but not in long-term fibroblast cultures.
    Kida E; Wisniewski KE; Golabek AA
    Neurosci Lett; 1993 Dec; 164(1-2):121-4. PubMed ID: 8152585
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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; 269(13):9906-11. PubMed ID: 8144584
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Variant proteins in ovine ceroid-lipofuscinosis.
    Moroni-Rawson P; Palmer DN; Jolly RD; Jordan TW
    Am J Med Genet; 1995 Jun; 57(2):279-84. PubMed ID: 7668345
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [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; 53(12):3055-61. PubMed ID: 8577058
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Increased urine concentration of subunit c of mitochondrial ATP synthase in neuronal ceroid lipofuscinoses patients.
    Wisniewski KE; Golabek AA; Kida E
    J Inherit Metab Dis; 1994; 17(2):205-10. PubMed ID: 7967475
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Light and electron microscopic studies on subunit c in cultured fibroblasts in late infantile and juvenile Batten disease.
    Lake BD; Rowan SA
    Neuropediatrics; 1997 Feb; 28(1):56-9. PubMed ID: 9151324
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Disease-specific pathology in neurons cultured from sheep affected with ceroid lipofuscinosis.
    Hughes SM; Kay GW; Jordan TW; Rickards GK; Palmer DN
    Mol Genet Metab; 1999 Apr; 66(4):381-6. PubMed ID: 10191133
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Different patterns of hydrophobic protein storage in different forms of neuronal ceroid lipofuscinosis (NCL, Batten disease).
    Palmer DN; Jolly RD; van Mil HC; Tyynelä J; Westlake VJ
    Neuropediatrics; 1997 Feb; 28(1):45-8. PubMed ID: 9151321
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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; 93(4):379-90. PubMed ID: 9113203
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Ion pores made of mitochondrial ATP synthase subunit c in the neuronal plasma membrane and Batten disease.
    McGeoch JE; Palmer DN
    Mol Genet Metab; 1999 Apr; 66(4):387-92. PubMed ID: 10191134
    [TBL] [Abstract][Full Text] [Related]  

  • 31. ATP synthase subunit C storage in the polymorphonucleocytes of late infantile and juvenile batten patients.
    Ansari NH; Cook JD; Khanna P; Srivastava SK
    Int J Dev Neurosci; 1995 Aug; 13(5):455-62. PubMed ID: 7484216
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Decreased lysosomal subunit c-degrading activity in fibroblasts from patients with late infantile neuronal ceroid lipofuscinosis.
    Ezaki J; Wolfe LS; Kominami E
    Neuropediatrics; 1997 Feb; 28(1):53-5. PubMed ID: 9151323
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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; 64(2):733-41. PubMed ID: 7830067
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Comparative biology of the neuronal ceroid-lipofuscinoses (NCL): an overview.
    Jolly RD
    Am J Med Genet; 1995 Jun; 57(2):307-11. PubMed ID: 7668352
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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; 67(4):1677-87. PubMed ID: 8858953
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Palmitate oxidation in muscle mitochondria of patients with the juvenile form of neuronal ceroid-lipofuscinosis.
    Majander A; Pihko H; Santavuori P
    Am J Med Genet; 1995 Jun; 57(2):298-300. PubMed ID: 7668349
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Batten disease (ceroid-lipofuscinosis): the enigma of subunit c of mitochondrial ATP synthase accumulation.
    Jolly RD
    Neurochem Res; 1995 Nov; 20(11):1301-4. PubMed ID: 8786815
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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; 279(21):21883-7. PubMed ID: 15010464
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Progress in neuropathology of the neuronal ceroid lipofuscinoses.
    Goebel HH; Schochet SS; Jaynes M; Brück W; Kohlschütter A; Hentati F
    Mol Genet Metab; 1999 Apr; 66(4):367-72. PubMed ID: 10191130
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Decreased activity of the mitochondrial ATP-synthase in fibroblasts from children with late-infantile and juvenile neuronal ceroid lipofuscinosis.
    Das AM; Kohlschütter A
    J Inherit Metab Dis; 1996; 19(2):130-2. PubMed ID: 8739947
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.