BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

130 related articles for article (PubMed ID: 8993564)

  • 21. Detection of unusual very-long-chain fatty acid and ether lipid derivatives in the fibroblasts and plasma of patients with peroxisomal diseases using liquid chromatography-mass spectrometry.
    Takashima S; Toyoshi K; Itoh T; Kajiwara N; Honda A; Ohba A; Takemoto S; Yoshida S; Shimozawa N
    Mol Genet Metab; 2017 Mar; 120(3):255-268. PubMed ID: 28089346
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Biochemistry of mammalian peroxisomes revisited.
    Wanders RJ; Waterham HR
    Annu Rev Biochem; 2006; 75():295-332. PubMed ID: 16756494
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Organelle interplay in peroxisomal disorders.
    Thoms S; Grønborg S; Gärtner J
    Trends Mol Med; 2009 Jul; 15(7):293-302. PubMed ID: 19560974
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Brain uptake and utilization of fatty acids: applications to peroxisomal biogenesis diseases.
    Watkins PA; Hamilton JA; Leaf A; Spector AA; Moore SA; Anderson RE; Moser HW; Noetzel MJ; Katz R
    J Mol Neurosci; 2001; 16(2-3):87-92; discussion 151-7. PubMed ID: 11478388
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clinical and Laboratory Diagnosis of Peroxisomal Disorders.
    Wanders RJ; Klouwer FC; Ferdinandusse S; Waterham HR; Poll-Thé BT
    Methods Mol Biol; 2017; 1595():329-342. PubMed ID: 28409475
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Genetic heterogeneity in patients with a disorder of peroxisomal beta-oxidation: a complementation study based on pristanic acid beta-oxidation suggesting different enzyme defects.
    van Grunsven EG; Wanders RJ
    J Inherit Metab Dis; 1997 Jul; 20(3):437-40. PubMed ID: 9266375
    [No Abstract]   [Full Text] [Related]  

  • 28. [Peroxisomal disorders; newer concept and recent studies].
    Kamoshita S
    Nihon Rinsho; 1990 Mar; 48(3):629-38. PubMed ID: 2192101
    [No Abstract]   [Full Text] [Related]  

  • 29. Peroxisomal fatty acid alpha- and beta-oxidation in health and disease: new insights.
    Wanders RJ; van Roermund CW; Visser WF; Ferdinandusse S; Jansen GA; van den Brink DM; Gloerich J; Waterham HR
    Adv Exp Med Biol; 2003; 544():293-302. PubMed ID: 14713243
    [No Abstract]   [Full Text] [Related]  

  • 30. Human disorders of peroxisome metabolism and biogenesis.
    Waterham HR; Ferdinandusse S; Wanders RJ
    Biochim Biophys Acta; 2016 May; 1863(5):922-33. PubMed ID: 26611709
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Atypical refsum disease with pipecolic acidemia and abnormal catalase distribution.
    Baumgartner MR; Jansen GA; Verhoeven NM; Mooyer PA; Jakobs C; Roels F; Espeel M; Fourmaintraux A; Bellet H; Wanders RJ; Saudubray JM
    Ann Neurol; 2000 Jan; 47(1):109-13. PubMed ID: 10632109
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Normal and defective neuronal membranes: structure and function: neuronal lesions in peroxisomal disorders.
    Powers JM
    J Mol Neurosci; 2001; 16(2-3):285-7; discussion 317-21. PubMed ID: 11478383
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Pre- and postnatal diagnosis of peroxisomal disorders using stable-isotope dilution gas chromatography--mass spectrometry.
    Verhoeven NM; Kulik W; van den Heuvel CM; Jakobs C
    J Inherit Metab Dis; 1995; 18 Suppl 1():45-60. PubMed ID: 9053555
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Peroxisome biogenesis disorders.
    Steinberg SJ; Dodt G; Raymond GV; Braverman NE; Moser AB; Moser HW
    Biochim Biophys Acta; 2006 Dec; 1763(12):1733-48. PubMed ID: 17055079
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Lipid biomarkers for the peroxisomal and lysosomal disorders: their formation, metabolism and measurement.
    Mashima R; Maekawa M
    Biomark Med; 2018 Jan; 12(1):83-95. PubMed ID: 29235891
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Identification and diagnostic value of phytanoyl- and pristanoyl-carnitine in plasma from patients with peroxisomal disorders.
    Herzog K; van Lenthe H; Wanders RJA; Vaz FM; Waterham HR; Ferdinandusse S
    Mol Genet Metab; 2017 Jul; 121(3):279-282. PubMed ID: 28566232
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Oxidation of pristanic acid in fibroblasts and its application to the diagnosis of peroxisomal beta-oxidation defects.
    Paton BC; Sharp PC; Crane DI; Poulos A
    J Clin Invest; 1996 Feb; 97(3):681-8. PubMed ID: 8609223
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Diagnosis of peroxisomal disorders with neurological involvement.
    Molzer B
    Padiatr Padol; 1993; 28(1):43-8. PubMed ID: 8446428
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Peroxisomes--functions and disturbances in human metabolism].
    Stradomska TJ
    Postepy Biochem; 2011; 57(2):183-90. PubMed ID: 21913419
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Fatty acid composition of tissues in Refsum's disease (herodopathia atactica polyneuritiformis). Estimation of total phytanic acid accumulation.
    Malmendier CL; Jonniaux G; Voet W; Van Den Bergen CJ
    Biomedicine; 1974 Nov; 20(6):398-407. PubMed ID: 4141904
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.