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 *

146 related articles for article (PubMed ID: 7830067)

  • 41. 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]  

  • 42. 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]  

  • 43. Tissue and cellular distribution of subunit c of ATP synthase in Batten disease (neuronal ceroid-lipofuscinosis).
    Rowan SA; Lake BD
    Am J Med Genet; 1995 Jun; 57(2):172-6. PubMed ID: 7668325
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Rapid detection of subunit c of mitochondrial ATP synthase in urine as a diagnostic screening method for neuronal ceroid-lipofuscinoses.
    Wisniewski KE; Kaczmarski W; Golabek AA; Kida E
    Am J Med Genet; 1995 Jun; 57(2):246-9. PubMed ID: 7668339
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Lysosomal proteinosis based on decreased degradation of a specific protein, mitochondrial ATP synthase subunit C: Batten disease.
    Ezaki J; Wolfe LS; Ishidoh K; Muno D; Ueno T; Kominami E
    Adv Exp Med Biol; 1996; 389():121-8. PubMed ID: 8861001
    [No Abstract]   [Full Text] [Related]  

  • 46. Biochemical characterization of a lysosomal protease deficient in classical late infantile neuronal ceroid lipofuscinosis (LINCL) and development of an enzyme-based assay for diagnosis and exclusion of LINCL in human specimens and animal models.
    Sohar I; Sleat DE; Jadot M; Lobel P
    J Neurochem; 1999 Aug; 73(2):700-11. PubMed ID: 10428067
    [TBL] [Abstract][Full Text] [Related]  

  • 47. 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]  

  • 48. Recent biochemical and genetic advances in our understanding of Batten's disease (ceroid-lipofuscinosis).
    Hall NA; Lake BD; Patrick AD
    Dev Neurosci; 1991; 13(4-5):339-44. PubMed ID: 1840101
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Abnormal lysosomal cathepsin activities in leukocytes and cultured skin fibroblasts in late infantile, but not in juvenile neuronal ceroid-lipofuscinosis (Batten disease).
    Bennett MJ; Chern L; Carpenter KH; Sladky JT
    Clin Chim Acta; 1992 Jun; 208(1-2):111-7. PubMed ID: 1638746
    [No Abstract]   [Full Text] [Related]  

  • 50. Lysosomal Storage of Subunit c of Mitochondrial ATP Synthase in Brain-Specific Atp13a2-Deficient Mice.
    Sato S; Koike M; Funayama M; Ezaki J; Fukuda T; Ueno T; Uchiyama Y; Hattori N
    Am J Pathol; 2016 Dec; 186(12):3074-3082. PubMed ID: 27770614
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Accumulation of the adenosine triphosphate synthase subunit C in the mnd mutant mouse. A model for neuronal ceroid lipofuscinosis.
    Pardo CA; Rabin BA; Palmer DN; Price DL
    Am J Pathol; 1994 Apr; 144(4):829-35. PubMed ID: 8160780
    [TBL] [Abstract][Full Text] [Related]  

  • 52. 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]  

  • 53. Ovine ceroid lipofuscinosis. The major lipopigment protein and the lipid-binding subunit of mitochondrial ATP synthase have the same NH2-terminal sequence.
    Palmer DN; Martinus RD; Cooper SM; Midwinter GG; Reid JC; Jolly RD
    J Biol Chem; 1989 Apr; 264(10):5736-40. PubMed ID: 2522438
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Variant late infantile neuronal ceroid-lipofuscinosis: pathology and biochemistry.
    Tyynelä J; Suopanki J; Santavuori P; Baumann M; Haltia M
    J Neuropathol Exp Neurol; 1997 Apr; 56(4):369-75. PubMed ID: 9100667
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Alterations in ROS activity and lysosomal pH account for distinct patterns of macroautophagy in LINCL and JNCL fibroblasts.
    Vidal-Donet JM; Cárcel-Trullols J; Casanova B; Aguado C; Knecht E
    PLoS One; 2013; 8(2):e55526. PubMed ID: 23408996
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Pathological study on sibling autopsy cases of the late infantile form of neuronal ceroid lipofuscinosis.
    Kurata K; Hayashi M; Satoh J; Kojima H; Nagata J; Tamagawa K; Shinohara T; Morimatsu Y; Kominami E
    Brain Dev; 1999 Jan; 21(1):63-7. PubMed ID: 10082255
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Tissue culture loading test with storage granules from animal models of neuronal ceroid-lipofuscinosis (Batten disease): testing their lysosomal degradability by normal and Batten cells.
    Elleder M; Drahota Z; Lisá V; Mares V; Mandys V; Müller J; Palmer DN
    Am J Med Genet; 1995 Jun; 57(2):213-21. PubMed ID: 7668332
    [TBL] [Abstract][Full Text] [Related]  

  • 58. 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]  

  • 59. Abnormal cathepsin B activity in Batten disease.
    Dawson G; Glaser PT
    Am J Med Genet Suppl; 1988; 5():209-20. PubMed ID: 3146318
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Sheep and other animals with ceroid-lipofuscinoses: their relevance to Batten disease.
    Jolly RD; Martinus RD; Palmer DN
    Am J Med Genet; 1992 Feb; 42(4):609-14. PubMed ID: 1535180
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.