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 *

191 related articles for article (PubMed ID: 1540666)

  • 1. Methylated lysine in storage body protein of sheep with hereditary ceroid-lipofuscinosis.
    Katz ML; Gerhardt KO
    Biochim Biophys Acta; 1992 Feb; 1138(2):97-108. PubMed ID: 1540666
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 310 ( Pt 3)(Pt 3):887-92. PubMed ID: 7575423
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Juvenile ceroid lipofuscinosis. Evidence for methylated lysine in neural storage body protein.
    Katz ML; Rodrigues M
    Am J Pathol; 1991 Feb; 138(2):323-32. PubMed ID: 1899540
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 1361(1):66-74. PubMed ID: 9247091
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Storage protein in hereditary ceroid-lipofuscinosis contains S-methylated methionine.
    Katz ML; Gerhardt KO
    Mech Ageing Dev; 1990 Apr; 53(3):277-90. PubMed ID: 2376986
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 266():211-22; discussion 223. PubMed ID: 2535017
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 268(3):751-8. PubMed ID: 2141977
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 42(4):561-7. PubMed ID: 1535179
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Decreased plasma carnitine and trimethyl-L-lysine levels associated with lysosomal accumulation of a trimethyl-L-lysine containing protein in Batten disease.
    Katz ML
    Biochim Biophys Acta; 1996 Dec; 1317(3):192-8. PubMed ID: 8988235
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A mouse gene knockout model for juvenile ceroid-lipofuscinosis (Batten disease).
    Katz ML; Shibuya H; Liu PC; Kaur S; Gao CL; Johnson GS
    J Neurosci Res; 1999 Aug; 57(4):551-6. PubMed ID: 10440905
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Dietary carnitine supplements slow disease progression in a putative mouse model for hereditary ceroid-lipofuscinosis.
    Katz ML; Rice LM; Gao CL
    J Neurosci Res; 1997 Oct; 50(1):123-32. PubMed ID: 9379488
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Inhibition of storage pathology in prenatal CLN5-deficient sheep neural cultures by lentiviral gene therapy.
    Hughes SM; Hope KM; Xu JB; Mitchell NL; Palmer DN
    Neurobiol Dis; 2014 Feb; 62():543-50. PubMed ID: 24269732
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Characterization of disease-specific brain fluorophores in ceroid-lipofuscinosis.
    Katz ML; Eldred GE; Siakotos AN; Koppang N
    Am J Med Genet Suppl; 1988; 5():253-64. PubMed ID: 3146323
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hereditary ceroid-lipofuscinosis: methylated amino acids in storage body proteins.
    Katz ML
    J Inherit Metab Dis; 1993; 16(2):305-7. PubMed ID: 8411987
    [No Abstract]   [Full Text] [Related]  

  • 17. Profound infantile neuroretinal dysfunction in a heterozygote for the CLN3 genetic defect.
    de los Reyes E; Dyken PR; Phillips P; Brodsky M; Bates S; Glasier C; Mrak RE
    J Child Neurol; 2004 Jan; 19(1):42-6. PubMed ID: 15032383
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Analysis of dolichyl pyrophosphoryl oligosaccharides in purified storage cytosomes from ovine ceroid-lipofuscinosis.
    Hall NA; Jolly RD; Palmer DN; Lake BD; Patrick AD
    Biochim Biophys Acta; 1989 Dec; 993(2-3):245-51. PubMed ID: 2597696
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Accumulation of glial fibrillary acidic protein and histone H4 in brain storage bodies of Tibetan terriers with hereditary neuronal ceroid lipofuscinosis.
    Katz ML; Sanders DN; Mooney BP; Johnson GS
    J Inherit Metab Dis; 2007 Nov; 30(6):952-63. PubMed ID: 18004671
    [TBL] [Abstract][Full Text] [Related]  

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

    [Next]    [New Search]
    of 10.