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 *

172 related articles for article (PubMed ID: 8729109)

  • 1. Very long-chain fatty acids in diagnosis, pathogenesis, and therapy of peroxisomal disorders.
    Moser HW; Moser AB
    Lipids; 1996 Mar; 31 Suppl():S141-4. PubMed ID: 8729109
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Peroxisomal disorders].
    Stradomska TJ
    Postepy Biochem; 2018 Dec; 64(4):359-367. PubMed ID: 30656921
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Very-long-chain polyunsaturated fatty acids accumulate in phosphatidylcholine of fibroblasts from patients with Zellweger syndrome and acyl-CoA oxidase1 deficiency.
    Abe Y; Honsho M; Nakanishi H; Taguchi R; Fujiki Y
    Biochim Biophys Acta; 2014 Apr; 1841(4):610-9. PubMed ID: 24418004
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Immunochemical and biochemical studies of fatty acid oxidation in fibroblasts of Zellweger and X-linked adrenoleukodystrophy patients.
    Reubsaet FA; Veerkamp JH; Brückwilder ML; Trijbels JM; Hashimoto T; Monnens LA
    Biochim Biophys Acta; 1991 Jun; 1083(3):305-9. PubMed ID: 2049396
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Plasma polyenoic very-long-chain fatty acids in peroxisomal disease: biochemical discrimination of Zellweger's syndrome from other phenotypes.
    Poulos A; Sharp P; Johnson D
    Neurology; 1989 Jan; 39(1):44-7. PubMed ID: 2462697
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phytanic acid and very long chain fatty acids in genetic peroxisomal disorders.
    Molzer B; Kainz-Korschinsky M; Sundt-Heller R; Bernheimer H
    J Clin Chem Clin Biochem; 1989 May; 27(5):309-14. PubMed ID: 2474624
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Very long-chain fatty acids in peroxisomal disease.
    Poulos A; Beckman K; Johnson DW; Paton BC; Robinson BS; Sharp P; Usher S; Singh H
    Adv Exp Med Biol; 1992; 318():331-40. PubMed ID: 1378993
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Straight-chain acyl-CoA oxidase knockout mouse accumulates extremely long chain fatty acids from alpha-linolenic acid: evidence for runaway carousel-type enzyme kinetics in peroxisomal beta-oxidation diseases.
    Infante JP; Tschanz CL; Shaw N; Michaud AL; Lawrence P; Brenna JT
    Mol Genet Metab; 2002 Feb; 75(2):108-19. PubMed ID: 11855929
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cytokine-induced accumulation of very long-chain fatty acids in rat C6 glial cells: implication for X-adrenoleukodystrophy.
    Khan M; Pahan K; Singh AK; Singh I
    J Neurochem; 1998 Jul; 71(1):78-87. PubMed ID: 9648853
    [TBL] [Abstract][Full Text] [Related]  

  • 11. DNA diagnosis of X-linked adrenoleukodystrophy.
    Seneca S; Lissens W
    J Inherit Metab Dis; 1995; 18 Suppl 1():34-44. PubMed ID: 9053554
    [TBL] [Abstract][Full Text] [Related]  

  • 12. X-linked adrenoleukodystrophy: defective peroxisomal oxidation of very long chain fatty acids but not of very long chain fatty acyl-CoA esters.
    Wanders RJ; van Roermund CW; van Wijland MJ; Nijenhuis AA; Tromp A; Schutgens RB; Brouwer-Kelder EM; Schram AW; Tager JM; van den Bosch H
    Clin Chim Acta; 1987 Jun; 165(2-3):321-9. PubMed ID: 3652454
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical and genetic aspects of X-linked adrenoleukodystrophy.
    Gärtner J; Braun A; Holzinger A; Roerig P; Lenard HG; Roscher AA
    Neuropediatrics; 1998 Feb; 29(1):3-13. PubMed ID: 9553942
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular species of phosphatidylcholine containing very long chain fatty acids in human brain: enrichment in X-linked adrenoleukodystrophy brain and diseases of peroxisome biogenesis brain.
    Sharp P; Johnson D; Poulos A
    J Neurochem; 1991 Jan; 56(1):30-7. PubMed ID: 1702833
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls.
    Moser AB; Kreiter N; Bezman L; Lu S; Raymond GV; Naidu S; Moser HW
    Ann Neurol; 1999 Jan; 45(1):100-10. PubMed ID: 9894883
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Profiles of very-long-chain fatty acids in plasma, fibroblasts, and blood cells in Zellweger syndrome, X-linked adrenoleukodystrophy, and rhizomelic chondrodysplasia punctata.
    Schutgens RB; Bouman IW; Nijenhuis AA; Wanders RJ; Frumau ME
    Clin Chem; 1993 Aug; 39(8):1632-7. PubMed ID: 8353949
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Peroxisomal neurologic diseases and Refsum disease: very long chain fatty acids and phytanic acid as diagnostic markers].
    Molzer B; Stöckler S; Bernheimer H
    Wien Klin Wochenschr; 1992; 104(21):665-70. PubMed ID: 1282286
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Dietary management of X-linked adrenoleukodystrophy.
    Moser HW; Borel J
    Annu Rev Nutr; 1995; 15():379-97. PubMed ID: 8527226
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Fatty acid composition of human myelin proteolipid protein in peroxisomal disorders.
    Bizzozero OA; Zuñiga G; Lees MB
    J Neurochem; 1991 Mar; 56(3):872-8. PubMed ID: 1704424
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [X-chromosomal adrenoleukodystrophy. A peroxisomal disease important for differential diagnosis in the internal medicine-neurological field].
    Wagdi P; Meier C
    Schweiz Med Wochenschr; 1990 Sep; 120(35):1247-52. PubMed ID: 2218446
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.