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 *

81 related articles for article (PubMed ID: 12014007)

  • 1. [Mitochondrial acyl-CoA dehydrogenases (VLCAD, LCAD, MCAD, SCAD)].
    Yamaguchi S
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():94-7. PubMed ID: 12014007
    [No Abstract]   [Full Text] [Related]  

  • 2. Synergistic heterozygosity in mice with inherited enzyme deficiencies of mitochondrial fatty acid beta-oxidation.
    Schuler AM; Gower BA; Matern D; Rinaldo P; Vockley J; Wood PA
    Mol Genet Metab; 2005 May; 85(1):7-11. PubMed ID: 15862275
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Mitochondrial 3-hydroxyacyl-CoA dehydrogenase (SCHAD, LCHAD)].
    Yamaguchi S
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():101-4. PubMed ID: 12013827
    [No Abstract]   [Full Text] [Related]  

  • 4. [Mitochondrial 3-ketoacyl-CoA thiolase].
    Yamaguchi S; Kanai R
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():105-8. PubMed ID: 12013828
    [No Abstract]   [Full Text] [Related]  

  • 5. Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship.
    Gregersen N; Andresen BS; Corydon MJ; Corydon TJ; Olsen RK; Bolund L; Bross P
    Hum Mutat; 2001 Sep; 18(3):169-89. PubMed ID: 11524729
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Mitochondrial enoyl-CoA hydratase].
    Yamaguchi S
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():98-100. PubMed ID: 12014008
    [No Abstract]   [Full Text] [Related]  

  • 7. New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency.
    Stanley CA
    Adv Pediatr; 1987; 34():59-88. PubMed ID: 3318304
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Influence of dietary fatty acid chain-length on metabolic tolerance in mouse models of inherited defects in mitochondrial fatty acid beta-oxidation.
    Schuler AM; Gower BA; Matern D; Rinaldo P; Wood PA
    Mol Genet Metab; 2004 Dec; 83(4):322-9. PubMed ID: 15589119
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis of mitochondrial fatty acid oxidation defects.
    Nada MA; Vianey-Saban C; Roe CR; Ding JH; Mathieu M; Wappner RS; Bialer MG; McGlynn JA; Mandon G
    Prenat Diagn; 1996 Feb; 16(2):117-24. PubMed ID: 8650121
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Purification of human very-long-chain acyl-coenzyme A dehydrogenase and characterization of its deficiency in seven patients.
    Aoyama T; Souri M; Ushikubo S; Kamijo T; Yamaguchi S; Kelley RI; Rhead WJ; Uetake K; Tanaka K; Hashimoto T
    J Clin Invest; 1995 Jun; 95(6):2465-73. PubMed ID: 7769092
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Structural basis for substrate fatty acyl chain specificity: crystal structure of human very-long-chain acyl-CoA dehydrogenase.
    McAndrew RP; Wang Y; Mohsen AW; He M; Vockley J; Kim JJ
    J Biol Chem; 2008 Apr; 283(14):9435-43. PubMed ID: 18227065
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel disease with deficiency of mitochondrial very-long-chain acyl-CoA dehydrogenase.
    Aoyama T; Uchida Y; Kelley RI; Marble M; Hofman K; Tonsgard JH; Rhead WJ; Hashimoto T
    Biochem Biophys Res Commun; 1993 Mar; 191(3):1369-72. PubMed ID: 8466512
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Long-chain acyl-CoA dehydrogenase is a key enzyme in the mitochondrial beta-oxidation of unsaturated fatty acids.
    Lea W; Abbas AS; Sprecher H; Vockley J; Schulz H
    Biochim Biophys Acta; 2000 May; 1485(2-3):121-8. PubMed ID: 10832093
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Quantitative analysis of urinary acylglycines for the diagnosis of beta-oxidation defects using GC-NCI-MS.
    Costa CG; Guérand WS; Struys EA; Holwerda U; ten Brink HJ; Tavares de Almeida I; Duran M; Jakobs C
    J Pharm Biomed Anal; 2000 Jan; 21(6):1215-24. PubMed ID: 10708405
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A case of impairment of mitochondrial fatty acid beta-oxidation.
    Hasegawa T; Hori N; Du W
    Keio J Med; 2002 Jun; 51(2):100-6. PubMed ID: 12125906
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Disorders of mitochondrial fatty acyl-CoA beta-oxidation.
    Wanders RJ; Vreken P; den Boer ME; Wijburg FA; van Gennip AH; IJlst L
    J Inherit Metab Dis; 1999 Jun; 22(4):442-87. PubMed ID: 10407780
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Effect of heat stress and bezafibrate on mitochondrial beta-oxidation: comparison between cultured cells from normal and mitochondrial fatty acid oxidation disorder children using in vitro probe acylcarnitine profiling assay.
    Li H; Fukuda S; Hasegawa Y; Kobayashi H; Purevsuren J; Mushimoto Y; Yamaguchi S
    Brain Dev; 2010 May; 32(5):362-70. PubMed ID: 19589653
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Encephalomyopathy due to a beta oxidation deficiency. Report of a new case].
    Balestri P; Mostardini R
    Minerva Pediatr; 1991 Mar; 43(3):93-5. PubMed ID: 1870532
    [No Abstract]   [Full Text] [Related]  

  • 19. Is autism a disorder of fatty acid metabolism? Possible dysfunction of mitochondrial beta-oxidation by long chain acyl-CoA dehydrogenase.
    Clark-Taylor T; Clark-Taylor BE
    Med Hypotheses; 2004; 62(6):970-5. PubMed ID: 15142659
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The reductive half reaction in the acyl-CoA dehydrogenases.
    Thorpe C
    Prog Clin Biol Res; 1990; 321():91-105. PubMed ID: 2183245
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.