BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

160 related articles for article (PubMed ID: 8059925)

  • 21. Prenatal diagnosis of rhizomelic chondrodysplasia punctata.
    Hoefler S; Hoefler G; Moser AB; Watkins PA; Chen WW; Moser HW
    Prenat Diagn; 1988 Oct; 8(8):571-6. PubMed ID: 3205862
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A prenatal test for the cerebro-hepato-renal (Zellweger) syndrome by demonstration of the absence of catalase-containing particles (peroxisomes) in cultured amniotic fluid cells.
    Wanders RJ; Schrakamp G; van den Bosch H; Tager JM; Schutgens RB
    Eur J Pediatr; 1986 Apr; 145(1-2):136-8. PubMed ID: 3732317
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Peroxisomal disorders in neurology.
    Wanders RJ; Heymans HS; Schutgens RB; Barth PG; van den Bosch H; Tager JM
    J Neurol Sci; 1988 Dec; 88(1-3):1-39. PubMed ID: 3066850
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Biochemical features of a patient with Zellweger-like syndrome with normal PTS-1 and PTS-2 peroxisomal protein import systems: a new peroxisomal disease.
    Singh I; Voigt RG; Sheikh FG; Kremser K; Brown FR
    Biochem Mol Med; 1997 Aug; 61(2):198-207. PubMed ID: 9259985
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genetic diseases caused by peroxisomal dysfunction. New findings in clinical and biochemical studies.
    Schutgens RB; Wanders RJ; Nijenhuis A; van den Hoek CM; Heymans HS; Schrakamp G; Bleeker-Wagemakers EM; Delleman JW; Schram AW; Tager JM
    Enzyme; 1987; 38(1-4):161-76. PubMed ID: 3440444
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Molecular analysis of peroxisomal beta-oxidation enzymes in infants with peroxisomal disorders indicates heterogeneity of the primary defect.
    Guerroui S; Aubourg P; Chen WW; Hashimoto T; Scotto J
    Biochem Biophys Res Commun; 1989 May; 161(1):242-51. PubMed ID: 2471528
    [TBL] [Abstract][Full Text] [Related]  

  • 27. New insights in peroxisomal beta-oxidation. Implications for human peroxisomal disorders.
    Van Veldhoven PP
    Verh K Acad Geneeskd Belg; 1998; 60(3):195-214. PubMed ID: 9803880
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Peroxisomal very long-chain fatty acid beta-oxidation in human skin fibroblasts: activity in Zellweger syndrome and other peroxisomal disorders.
    Wanders RJ; van Roermund CW; van Wijland MJ; Heikoop J; Schutgens RB; Schram AW; Tager JM; van den Bosch H; Poll-Thé BT; Saudubray JM
    Clin Chim Acta; 1987 Jul; 166(2-3):255-63. PubMed ID: 2441904
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Formation of a novel arachidonic acid metabolite in peroxisomes.
    Gordon JA; Heller SK; Rhead WJ; Watkins PA; Spector AA
    Prostaglandins Leukot Essent Fatty Acids; 1995; 52(2-3):77-81. PubMed ID: 7540307
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Peroxisomal 3-ketoacyl-CoA thiolase is partially processed in fibroblasts from patients with rhizomelic chondrodysplasia punctata.
    Suzuki Y; Shimozawa N; Izai K; Uchida Y; Miura K; Akatsuka H; Nagaya M; Yamaguchi S; Orii T
    J Inherit Metab Dis; 1993; 16(5):868-71. PubMed ID: 8295403
    [No Abstract]   [Full Text] [Related]  

  • 31. Phytanic acid alpha-oxidation and complementation analysis of classical Refsum and peroxisomal disorders.
    Poll-The BT; Skjeldal OH; Stokke O; Poulos A; Demaugre F; Saudubray JM
    Hum Genet; 1989 Jan; 81(2):175-81. PubMed ID: 2463966
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Identification of the peroxisomal beta-oxidation enzymes involved in the biosynthesis of docosahexaenoic acid.
    Ferdinandusse S; Denis S; Mooijer PA; Zhang Z; Reddy JK; Spector AA; Wanders RJ
    J Lipid Res; 2001 Dec; 42(12):1987-95. PubMed ID: 11734571
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Peroxisomes of normal morphology but deficient in 3-oxoacyl-CoA thiolase in rhizomelic chondrodysplasia punctata fibroblasts.
    Heikoop JC; Van den Berg M; Strijland A; Weijers PJ; Schutgens RB; Just WW; Wanders RJ; Tager JM
    Biochim Biophys Acta; 1991 Jul; 1097(1):62-70. PubMed ID: 1677591
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Peroxisomal beta-oxidation enzyme proteins in adrenoleukodystrophy: distinction between X-linked adrenoleukodystrophy and neonatal adrenoleukodystrophy.
    Chen WW; Watkins PA; Osumi T; Hashimoto T; Moser HW
    Proc Natl Acad Sci U S A; 1987 Mar; 84(5):1425-8. PubMed ID: 3469675
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Peroxisomal beta-oxidation enzyme proteins in the Zellweger syndrome.
    Tager JM; Van der Beek WA; Wanders RJ; Hashimoto T; Heymans HS; Van den Bosch H; Schutgens RB; Schram AW
    Biochem Biophys Res Commun; 1985 Feb; 126(3):1269-75. PubMed ID: 3977916
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Peroxisome mosaicism in the livers of peroxisomal deficiency patients.
    Espeel M; Mandel H; Poggi F; Smeitink JA; Wanders RJ; Kerckaert I; Schutgens RB; Saudubray JM; Poll-The BT; Roels F
    Hepatology; 1995 Aug; 22(2):497-504. PubMed ID: 7635418
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Studies on the oxidation of phytanic acid and pristanic acid in human fibroblasts by acylcarnitine analysis.
    Verhoeven NM; Jakobs C; ten Brink HJ; Wanders RJ; Roe CR
    J Inherit Metab Dis; 1998 Oct; 21(7):753-60. PubMed ID: 9819705
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency.
    Schram AW; Goldfischer S; van Roermund CW; Brouwer-Kelder EM; Collins J; Hashimoto T; Heymans HS; van den Bosch H; Schutgens RB; Tager JM
    Proc Natl Acad Sci U S A; 1987 Apr; 84(8):2494-6. PubMed ID: 2882519
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A new type of peroxisomal disorder with variable expression in liver and fibroblasts.
    Mandel H; Espeel M; Roels F; Sofer N; Luder A; Iancu TC; Aizin A; Berant M; Wanders RJ; Schutgens RB
    J Pediatr; 1994 Oct; 125(4):549-55. PubMed ID: 7931872
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Molecular analysis of peroxisomal beta-oxidation enzymes in infants with Zellweger syndrome and Zellweger-like syndrome: further heterogeneity of the peroxisomal disorder.
    Suzuki Y; Shimozawa N; Orii T; Igarashi N; Kono N; Hashimoto T
    Clin Chim Acta; 1988 Feb; 172(1):65-76. PubMed ID: 2452040
    [TBL] [Abstract][Full Text] [Related]  

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