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 *

168 related articles for article (PubMed ID: 1840101)

  • 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. 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]  

  • 23. BTN1, a yeast gene corresponding to the human gene responsible for Batten's disease, is not essential for viability, mitochondrial function, or degradation of mitochondrial ATP synthase.
    Pearce DA; Sherman F
    Yeast; 1997 Jun; 13(8):691-7. PubMed ID: 9219333
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Normal dolichol concentration in urine sediments from four patients with neuronal ceroid lipofuscinosis (Batten's disease).
    Paton BC; Poulos A
    J Inherit Metab Dis; 1987; 10(1):28-32. PubMed ID: 3106713
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Submitochondrial distribution and delayed proteolysis of subunit c of the H+-transporting ATP-synthase in ovine ceroid-lipofuscinosis.
    Hughes SM; Moroni-Rawson P; Jolly RD; Jordan TW
    Electrophoresis; 2001 May; 22(9):1785-94. PubMed ID: 11425233
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The neuronal ceroid-lipofuscinoses.
    Goebel HH
    J Child Neurol; 1995 Nov; 10(6):424-37. PubMed ID: 8576551
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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; 57(2):254-9. PubMed ID: 7668341
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The neuronal ceroid-lipofuscinoses (Batten disease): comparative aspects.
    Jolly RD; Palmer DN
    Neuropathol Appl Neurobiol; 1995 Feb; 21(1):50-60. PubMed ID: 7770121
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Defect of proteolysis of mitochondrial ATP synthase subunit C in neuronal ceroid lipofuscinosis.
    Ezaki J; Wolfe LS; Kominami E
    Gerontology; 1995; 41 Suppl 2():259-69. PubMed ID: 8821337
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Adult type of neuronal ceroid lipofuscinosis.
    Martin JJ
    Dev Neurosci; 1991; 13(4-5):331-8. PubMed ID: 1817040
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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; 66(4):349-55. PubMed ID: 10191128
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. 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]  

  • 34. Batten disease and the ATP synthase subunit c turnover pathway: raising antibodies to subunit c.
    Palmer DN; Bayliss SL; Westlake VJ
    Am J Med Genet; 1995 Jun; 57(2):260-5. PubMed ID: 7668342
    [TBL] [Abstract][Full Text] [Related]  

  • 35. You say lipofuscin, we say ceroid: defining autofluorescent storage material.
    Seehafer SS; Pearce DA
    Neurobiol Aging; 2006 Apr; 27(4):576-88. PubMed ID: 16455164
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Autosomal dominant adult neuronal ceroid lipofuscinosis: a novel form of NCL with granular osmiophilic deposits without palmitoyl protein thioesterase 1 deficiency.
    Nijssen PC; Ceuterick C; van Diggelen OP; Elleder M; Martin JJ; Teepen JL; Tyynelä J; Roos RA
    Brain Pathol; 2003 Oct; 13(4):574-81. PubMed ID: 14655761
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. 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]  

  • 40. 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; 269(13):10150-5. PubMed ID: 8144516
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.