BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

134 related articles for article (PubMed ID: 36511274)

  • 1. Development of a system adapted for the diagnosis and evaluation of peroxisomal disorders by measuring bile acid intermediates.
    Kawai H; Takashima S; Ohba A; Toyoshi K; Kubota K; Ohnishi H; Shimozawa N
    Brain Dev; 2023 Jan; 45(1):58-69. PubMed ID: 36511274
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Plasma analysis of di- and trihydroxycholestanoic acid diastereoisomers in peroxisomal alpha-methylacyl-CoA racemase deficiency.
    Ferdinandusse S; Overmars H; Denis S; Waterham HR; Wanders RJ; Vreken P
    J Lipid Res; 2001 Jan; 42(1):137-41. PubMed ID: 11160375
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Importance of peroxisomes in the formation of chenodeoxycholic acid in human liver. Metabolism of 3 alpha,7 alpha-dihydroxy-5 beta-cholestanoic acid in Zellweger syndrome.
    Kase BF; Pedersen JI; Wathne KO; Gustafsson J; Björkhem I
    Pediatr Res; 1991 Jan; 29(1):64-9. PubMed ID: 2000261
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Liver disease caused by failure to racemize trihydroxycholestanoic acid: gene mutation and effect of bile acid therapy.
    Setchell KD; Heubi JE; Bove KE; O'Connell NC; Brewsaugh T; Steinberg SJ; Moser A; Squires RH
    Gastroenterology; 2003 Jan; 124(1):217-32. PubMed ID: 12512044
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Measurement of bile acid CoA esters by high-performance liquid chromatography-electrospray ionisation tandem mass spectrometry (HPLC-ESI-MS/MS).
    Gan-Schreier H; Okun JG; Kohlmueller D; Langhans CD; Peters V; Ten Brink HJ; Verhoeven NM; Jakobs C; Voelkl A; Hoffmann GF
    J Mass Spectrom; 2005 Jul; 40(7):882-9. PubMed ID: 15892178
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Plasma bile acids in patients with peroxisomal dysfunction syndromes: analysis by capillary gas chromatography-mass spectrometry.
    Clayton PT; Lake BD; Hall NA; Shortland DB; Carruthers RA; Lawson AM
    Eur J Pediatr; 1987 Mar; 146(2):166-73. PubMed ID: 2436918
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The role of alpha-methylacyl-CoA racemase in bile acid synthesis.
    Cuebas DA; Phillips C; Schmitz W; Conzelmann E; Novikov DK
    Biochem J; 2002 May; 363(Pt 3):801-7. PubMed ID: 11964182
    [TBL] [Abstract][Full Text] [Related]  

  • 8. In vivo and vitro studies on formation of bile acids in patients with Zellweger syndrome. Evidence that peroxisomes are of importance in the normal biosynthesis of both cholic and chenodeoxycholic acid.
    Kase BF; Pedersen JI; Strandvik B; Björkhem I
    J Clin Invest; 1985 Dec; 76(6):2393-402. PubMed ID: 4077985
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Peroxisomes, peroxisomal diseases, and the hepatotoxicity induced by peroxisomal metabolites.
    Wanders RJ; Ferdinandusse S
    Curr Drug Metab; 2012 Dec; 13(10):1401-11. PubMed ID: 22978395
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Bile acid profiles in a peroxisomal D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency.
    Une M; Konishi M; Suzuki Y; Akaboshi S; Yoshii M; Kuramoto T; Fujimura K
    J Biochem; 1997 Sep; 122(3):655-8. PubMed ID: 9348098
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Sensitive analysis of serum 3alpha, 7alpha, 12alpha,24-tetrahydroxy- 5beta-cholestan-26-oic acid diastereomers using gas chromatography-mass spectrometry and its application in peroxisomal D-bifunctional protein deficiency.
    Vreken P; van Rooij A; Denis S; van Grunsven EG; Cuebas DA; Wanders RJ
    J Lipid Res; 1998 Dec; 39(12):2452-8. PubMed ID: 9831634
    [TBL] [Abstract][Full Text] [Related]  

  • 12. ATP-dependent transport of bile acid intermediates across rat liver peroxisomal membranes.
    Une M; Iguchi Y; Sakamoto T; Tomita T; Suzuki Y; Morita M; Imanaka T
    J Biochem; 2003 Aug; 134(2):225-30. PubMed ID: 12966071
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rapid quantification of conjugated and unconjugated bile acids and C27 precursors in dried blood spots and small volumes of serum.
    Janzen N; Sander S; Terhardt M; Das AM; Sass JO; Kraetzner R; Rosewich H; Peter M; Sander J
    J Lipid Res; 2010 Jun; 51(6):1591-8. PubMed ID: 20093478
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hyperpipecolic acidaemia: a diagnostic tool for peroxisomal disorders.
    Peduto A; Baumgartner MR; Verhoeven NM; Rabier D; Spada M; Nassogne MC; Poll-The BT; Bonetti G; Jakobs C; Saudubray JM
    Mol Genet Metab; 2004 Jul; 82(3):224-30. PubMed ID: 15234336
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Bile acid profiles in peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency.
    Clayton PT; Patel E; Lawson AM; Carruthers RA; Collins J
    J Clin Invest; 1990 Apr; 85(4):1267-73. PubMed ID: 2318981
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Defective peroxisomal cleavage of the C27-steroid side chain in the cerebro-hepato-renal syndrome of Zellweger.
    Kase BF; Björkhem I; Hågå P; Pedersen JI
    J Clin Invest; 1985 Feb; 75(2):427-35. PubMed ID: 3973012
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The optimized use of gas chromatography-mass spectrometry and high performance liquid chromatography to analyse the serum bile acids of patients with metabolic cholestasis and peroxisomal disorders.
    Courillon F; Gerhardt MF; Myara A; Rocchiccioli F; Trivin F
    Eur J Clin Chem Clin Biochem; 1997 Dec; 35(12):919-22. PubMed ID: 9476620
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Dried blood spot-based newborn screening for bile acid synthesis disorders, Zellweger spectrum disorder, and Niemann-Pick type C1 by detection of bile acid metabolites.
    Muto Y; Suzuki M; Takei H; Saito N; Mori J; Sugimoto S; Imagawa K; Nambu R; Oguri S; Itonaga T; Ihara K; Hayashi H; Murayama K; Kakiyama G; Nittono H; Shimizu T
    Mol Genet Metab; 2023; 140(1-2):107703. PubMed ID: 37802748
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The metabolism of 3alpha, 7alpha, 12alpha-trihydorxy-5beta-cholestan-26-oic acid in two siblings with cholestasis due to intrahepatic bile duct anomalies. An apparent inborn error of cholic acid synthesis.
    Hanson RF; Isenberg JN; Williams GC; Hachey D; Szczepanik P; Klein PD; Sharp HL
    J Clin Invest; 1975 Sep; 56(3):577-87. PubMed ID: 1159074
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Oral bile acid treatment and the patient with Zellweger syndrome.
    Setchell KD; Bragetti P; Zimmer-Nechemias L; Daugherty C; Pelli MA; Vaccaro R; Gentili G; Distrutti E; Dozzini G; Morelli A
    Hepatology; 1992 Feb; 15(2):198-207. PubMed ID: 1735522
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.