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Journal Abstract Search

226 related items for PubMed ID: 7936829

  • 1.
    ; . PubMed ID:
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  • 2. Combined defect of long-chain 3-hydroxyacyl-CoA dehydrogenase, 2-enoyl-CoA hydratase and 3-oxoacyl-CoA thiolase.
    Jackson S, Kler RS, Bartlett K, Pourfarzam M, Aynsley-Green A, Bindoff LA, Turnbull DM.
    Prog Clin Biol Res; 1992; 375():327-37. PubMed ID: 1438378
    [No Abstract] [Full Text] [Related]

  • 3. Mitochondrial trifunctional protein deficiency. Catalytic heterogeneity of the mutant enzyme in two patients.
    Kamijo T, Wanders RJ, Saudubray JM, Aoyama T, Komiyama A, Hashimoto T.
    J Clin Invest; 1994 Apr; 93(4):1740-7. PubMed ID: 8163672
    [Abstract] [Full Text] [Related]

  • 4. Novel fatty acid beta-oxidation enzymes in rat liver mitochondria. II. Purification and properties of enoyl-coenzyme A (CoA) hydratase/3-hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase trifunctional protein.
    Uchida Y, Izai K, Orii T, Hashimoto T.
    J Biol Chem; 1992 Jan 15; 267(2):1034-41. PubMed ID: 1730633
    [Abstract] [Full Text] [Related]

  • 5. Histidine-450 is the catalytic residue of L-3-hydroxyacyl coenzyme A dehydrogenase associated with the large alpha-subunit of the multienzyme complex of fatty acid oxidation from Escherichia coli.
    He XY, Yang SY.
    Biochemistry; 1996 Jul 23; 35(29):9625-30. PubMed ID: 8755745
    [Abstract] [Full Text] [Related]

  • 6. Molecular cloning of the cDNAs for the subunits of rat mitochondrial fatty acid beta-oxidation multienzyme complex. Structural and functional relationships to other mitochondrial and peroxisomal beta-oxidation enzymes.
    Kamijo T, Aoyama T, Miyazaki J, Hashimoto T.
    J Biol Chem; 1993 Dec 15; 268(35):26452-60. PubMed ID: 8253773
    [Abstract] [Full Text] [Related]

  • 7. Combined enzyme defect of mitochondrial fatty acid oxidation.
    Jackson S, Kler RS, Bartlett K, Briggs H, Bindoff LA, Pourfarzam M, Gardner-Medwin D, Turnbull DM.
    J Clin Invest; 1992 Oct 15; 90(4):1219-25. PubMed ID: 1401059
    [Abstract] [Full Text] [Related]

  • 8. Clinical and biochemical presentation of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.
    Hagenfeldt L, Venizelos N, von Döbeln U.
    J Inherit Metab Dis; 1995 Oct 15; 18(2):245-8. PubMed ID: 7564259
    [No Abstract] [Full Text] [Related]

  • 9. Differentiation of long-chain fatty acid oxidation disorders using alternative precursors and acylcarnitine profiling in fibroblasts.
    Roe DS, Yang BZ, Vianey-Saban C, Struys E, Sweetman L, Roe CR.
    Mol Genet Metab; 2006 Jan 15; 87(1):40-7. PubMed ID: 16297647
    [Abstract] [Full Text] [Related]

  • 10. General mitochondrial trifunctional protein (TFP) deficiency as a result of either alpha- or beta-subunit mutations exhibits similar phenotypes because mutations in either subunit alter TFP complex expression and subunit turnover.
    Spiekerkoetter U, Khuchua Z, Yue Z, Bennett MJ, Strauss AW.
    Pediatr Res; 2004 Feb 15; 55(2):190-6. PubMed ID: 14630990
    [Abstract] [Full Text] [Related]

  • 11. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: high frequency of the G1528C mutation with no apparent correlation with the clinical phenotype.
    Ijlst L, Uskikubo S, Kamijo T, Hashimoto T, Ruiter JP, de Klerk JB, Wanders RJ.
    J Inherit Metab Dis; 1995 Feb 15; 18(2):241-4. PubMed ID: 7564258
    [No Abstract] [Full Text] [Related]

  • 12. Intact alpha-subunit is required for membrane-binding of human mitochondrial trifunctional beta-oxidation protein, but is not necessary for conferring 3-ketoacyl-CoA thiolase activity to the beta-subunit.
    Weinberger MJ, Rinaldo P, Strauss AW, Bennett MJ.
    Biochem Biophys Res Commun; 1995 Apr 06; 209(1):47-52. PubMed ID: 7726862
    [Abstract] [Full Text] [Related]

  • 13. Structural and functional characterization of the recombinant human mitochondrial trifunctional protein.
    Fould B, Garlatti V, Neumann E, Fenel D, Gaboriaud C, Arlaud GJ.
    Biochemistry; 2010 Oct 05; 49(39):8608-17. PubMed ID: 20825197
    [Abstract] [Full Text] [Related]

  • 14. Glutamate 139 of the large alpha-subunit is the catalytic base in the dehydration of both D- and L-3-hydroxyacyl-coenzyme A but not in the isomerization of delta 3, delta 2-enoyl-coenzyme A catalyzed by the multienzyme complex of fatty acid oxidation from Escherichia coli.
    Yang SY, He XY, Schulz H.
    Biochemistry; 1995 May 16; 34(19):6441-7. PubMed ID: 7756275
    [Abstract] [Full Text] [Related]

  • 15. Structure of mycobacterial β-oxidation trifunctional enzyme reveals its altered assembly and putative substrate channeling pathway.
    Venkatesan R, Wierenga RK.
    ACS Chem Biol; 2013 May 17; 8(5):1063-73. PubMed ID: 23496842
    [Abstract] [Full Text] [Related]

  • 16. Importance of the gamma-carboxyl group of glutamate-462 of the large alpha-subunit for the catalytic function and the stability of the multienzyme complex of fatty acid oxidation from Escherichia coli.
    He XY, Deng H, Yang SY.
    Biochemistry; 1997 Jan 07; 36(1):261-8. PubMed ID: 8993342
    [Abstract] [Full Text] [Related]

  • 17. Enzymes of fatty acid beta-oxidation in developing brain.
    Reichmann H, Maltese WA, DeVivo DC.
    J Neurochem; 1988 Aug 07; 51(2):339-44. PubMed ID: 2899130
    [Abstract] [Full Text] [Related]

  • 18. Complementation analysis of fibroblasts from peroxisomal fatty acid oxidation deficient patients shows high frequency of bifunctional enzyme deficiency plus intragenic complementation: unequivocal evidence for differential defects in the same enzyme protein.
    van Grunsven EG, van Roermund CW, Denis S, Wanders RJ.
    Biochem Biophys Res Commun; 1997 Jun 09; 235(1):176-9. PubMed ID: 9196058
    [Abstract] [Full Text] [Related]

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