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 *

101 related articles for article (PubMed ID: 10191134)

  • 21. 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]  

  • 22. Action of BTN1, the yeast orthologue of the gene mutated in Batten disease.
    Pearce DA; Ferea T; Nosel SA; Das B; Sherman F
    Nat Genet; 1999 May; 22(1):55-8. PubMed ID: 10319861
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Bovine ceroid-lipofuscinosis (Batten's disease): the major component stored is the DCCD-reactive proteolipid, subunit C, of mitochondrial ATP synthase.
    Martinus RD; Harper PA; Jolly RD; Bayliss SL; Midwinter GG; Shaw GJ; Palmer DN
    Vet Res Commun; 1991; 15(2):85-94. PubMed ID: 1829867
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Batten disease and mitochondrial pathways of proteolysis.
    Tanner AJ; Dice JF
    Biochem Mol Med; 1996 Feb; 57(1):1-9. PubMed ID: 8812718
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Deficiency of the INCL protein Ppt1 results in changes in ectopic F1-ATP synthase and altered cholesterol metabolism.
    Lyly A; Marjavaara SK; Kyttälä A; Uusi-Rauva K; Luiro K; Kopra O; Martinez LO; Tanhuanpää K; Kalkkinen N; Suomalainen A; Jauhiainen M; Jalanko A
    Hum Mol Genet; 2008 May; 17(10):1406-17. PubMed ID: 18245779
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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; 275 ( Pt 1)(Pt 1):269-72. PubMed ID: 1826833
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Defective lysosomal arginine transport in juvenile Batten disease.
    Ramirez-Montealegre D; Pearce DA
    Hum Mol Genet; 2005 Dec; 14(23):3759-73. PubMed ID: 16251196
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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; 111(2):278-82. PubMed ID: 1533218
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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; 1361(3):251-62. PubMed ID: 9375799
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Molecular basis of lysosomal accumulation of subunit c of mitochondrial ATP synthase in neuronal ceroid-lipofuscinosis.
    Ezaki J; Wolfe LS; Kominami E
    J Inherit Metab Dis; 1993; 16(2):296-8. PubMed ID: 8411985
    [No Abstract]   [Full Text] [Related]  

  • 33. 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; 20(11):1305-9. PubMed ID: 8786816
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Storage bodies in the ceroid-lipofuscinoses (Batten disease): low-molecular-weight components, unusual amino acids and reconstitution of fluorescent bodies from non-fluorescent components.
    Palmer DN; Bayliss SL; Clifton PA; Grant VJ
    J Inherit Metab Dis; 1993; 16(2):292-5. PubMed ID: 8411984
    [No Abstract]   [Full Text] [Related]  

  • 35. Mitochondrial dysfunction in the neuronal ceroid-lipofuscinoses (Batten disease).
    Jolly RD; Brown S; Das AM; Walkley SU
    Neurochem Int; 2002 May; 40(6):565-71. PubMed ID: 11850114
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Preparative electrophoretic method for the purification of a hydrophobic membrane protein: subunit c of the mitochondrial ATP synthase from rat liver.
    Hagopian K
    Anal Biochem; 1999 Sep; 273(2):240-51. PubMed ID: 10469495
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Proton-translocating ATPases.
    Al-Awqati Q
    Annu Rev Cell Biol; 1986; 2():179-99. PubMed ID: 2435311
    [No Abstract]   [Full Text] [Related]  

  • 38. 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]  

  • 39. Electrospray ionisation mass spectrometry (ESI/MS) of ceroid lipofuscin protein; a model system for the study of F0 inhibitor interactions with mitochondrial subunit C.
    Ryan EM; Buzy A; Griffiths DE; Jennings KR; Palmer DN
    Biochem Soc Trans; 1996 May; 24(2):289S. PubMed ID: 8736947
    [No Abstract]   [Full Text] [Related]  

  • 40. Targeted disruption of the Cln3 gene provides a mouse model for Batten disease. The Batten Mouse Model Consortium [corrected].
    Mitchison HM; Bernard DJ; Greene ND; Cooper JD; Junaid MA; Pullarkat RK; de Vos N; Breuning MH; Owens JW; Mobley WC; Gardiner RM; Lake BD; Taschner PE; Nussbaum RL
    Neurobiol Dis; 1999 Oct; 6(5):321-34. PubMed ID: 10527801
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.