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 *

135 related articles for article (PubMed ID: 9308370)

  • 1. Impaired folding and subunit assembly as disease mechanism: the example of medium-chain acyl-CoA dehydrogenase deficiency.
    Bross P; Andresen BS; Gregersen N
    Prog Nucleic Acid Res Mol Biol; 1998; 58():301-37. PubMed ID: 9308370
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutations causing medium-chain acyl-CoA dehydrogenase deficiency: a collaborative compilation of the data from 172 patients. Workshop on Molecular Aspects of MCAD Deficiency.
    Prog Clin Biol Res; 1992; 375():499-506. PubMed ID: 1438394
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 4. Characterization of medium-chain acyl-CoA dehydrogenase (MCAD) with a point mutation associated with MCAD deficiency.
    Bross P; Jensen T; Kräutle F; Winter V; Andresen BS; Engst S; Bolund L; Kølvraa S; Ghisla S; Rasched I
    Prog Clin Biol Res; 1992; 375():473-8. PubMed ID: 1438390
    [No Abstract]   [Full Text] [Related]  

  • 5. Molecular characterization of medium-chain acyl-CoA dehydrogenase deficiency causing sudden death.
    Kelly DP; Whelan AJ; Hale DE; Rinaldo P; Rutledge SL; Zhang Z; Strauss AW
    Prog Clin Biol Res; 1992; 375():463-72. PubMed ID: 1438388
    [No Abstract]   [Full Text] [Related]  

  • 6. Defective folding and rapid degradation of mutant proteins is a common disease mechanism in genetic disorders.
    Gregersen N; Bross P; Jørgensen MM; Corydon TJ; Andresen BS
    J Inherit Metab Dis; 2000 Jul; 23(5):441-7. PubMed ID: 10947197
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Rapid degradation of short-chain acyl-CoA dehydrogenase variants with temperature-sensitive folding defects occurs after import into mitochondria.
    Corydon TJ; Bross P; Jensen TG; Corydon MJ; Lund TB; Jensen UB; Kim JJ; Gregersen N; Bolund L
    J Biol Chem; 1998 May; 273(21):13065-71. PubMed ID: 9582344
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The molecular basis of medium chain acyl-CoA dehydrogenase deficiency: survey and evolution of 985A----G transition, and identification of five rare types of mutation within the medium chain acyl-CoA dehydrogenase gene.
    Yokota I; Coates PM; Hale DE; Rinaldo P; Tanaka K
    Prog Clin Biol Res; 1992; 375():425-40. PubMed ID: 1359563
    [No Abstract]   [Full Text] [Related]  

  • 9. Medium chain acyl-CoA dehydrogenase deficiency in the United Kingdom.
    Curtis D; Blakemore AI; Engel PC; Kolvraa S; Gregersen N; Pollitt RJ
    Prog Clin Biol Res; 1992; 375():489-94. PubMed ID: 1438392
    [No Abstract]   [Full Text] [Related]  

  • 10. Co-overexpression of bacterial GroESL chaperonins partly overcomes non-productive folding and tetramer assembly of E. coli-expressed human medium-chain acyl-CoA dehydrogenase (MCAD) carrying the prevalent disease-causing K304E mutation.
    Bross P; Andresen BS; Winter V; Kräutle F; Jensen TG; Nandy A; Kølvraa S; Ghisla S; Bolund L; Gregersen N
    Biochim Biophys Acta; 1993 Oct; 1182(3):264-74. PubMed ID: 8104486
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Effects of two mutations detected in medium chain acyl-CoA dehydrogenase (MCAD)-deficient patients on folding, oligomer assembly, and stability of MCAD enzyme.
    Bross P; Jespersen C; Jensen TG; Andresen BS; Kristensen MJ; Winter V; Nandy A; Kräutle F; Ghisla S; Bolundi L
    J Biol Chem; 1995 Apr; 270(17):10284-90. PubMed ID: 7730333
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A murine model for short-chain acyl-CoA dehydrogenase deficiency.
    Wood PA; Amendt BA; Rhead WJ; Armstrong D; Millington DS; Inoue F
    Prog Clin Biol Res; 1990; 321():427-34. PubMed ID: 2326304
    [No Abstract]   [Full Text] [Related]  

  • 13. Molecular analysis of medium-chain acyl-CoA dehydrogenase deficiency: a diagnostic approach.
    Gregersen N; Winter V; Kølvraa S; Andresen BS; Bross P; Blakemore A; Curtis D; Bolund L
    Prog Clin Biol Res; 1992; 375():441-52. PubMed ID: 1438387
    [No Abstract]   [Full Text] [Related]  

  • 14. Historical perspective of medium-chain acyl-CoA dehydrogenase deficiency: a decade of discovery.
    Coates PM
    Prog Clin Biol Res; 1992; 375():409-23. PubMed ID: 1438385
    [No Abstract]   [Full Text] [Related]  

  • 15. Medium chain acyl CoA dehydrogenase deficiency.
    Lancet; 1991 Aug; 338(8766):544-5. PubMed ID: 1678805
    [No Abstract]   [Full Text] [Related]  

  • 16. A novel mutation of late-onset very-long-chain acyl-CoA dehydrogenase deficiency.
    Straussberg R; Strauss AW
    Pediatr Neurol; 2002 Aug; 27(2):136-7. PubMed ID: 12213615
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Medium-chain acyl-CoA dehydrogenase deficiency in Spain.
    Martínez G; Ribes A; Briones P; Rodés M; Baldellou A; Pineda M; Rodrigo C; Lorente I; García-Silva MT; Riudor E; Jaraba P; Lopez-Casas J; Nuñez-Roldan A
    J Inherit Metab Dis; 1998 Aug; 21(6):693-4. PubMed ID: 9762615
    [No Abstract]   [Full Text] [Related]  

  • 18. Mitochondrial fatty acid oxidation defects--remaining challenges.
    Gregersen N; Andresen BS; Pedersen CB; Olsen RK; Corydon TJ; Bross P
    J Inherit Metab Dis; 2008 Oct; 31(5):643-57. PubMed ID: 18836889
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Medium chain acyl-CoA dehydrogenase deficiency caused by a deletion of exons 11 and 12.
    Morris AA; Taylor RW; Lightowlers RN; Aynsley-Green A; Bartlett K; Turnbull DM
    Hum Mol Genet; 1995 Apr; 4(4):747-9. PubMed ID: 7633427
    [No Abstract]   [Full Text] [Related]  

  • 20. The molecular basis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in compound heterozygous patients: is there correlation between genotype and phenotype?
    Andresen BS; Bross P; Udvari S; Kirk J; Gray G; Kmoch S; Chamoles N; Knudsen I; Winter V; Wilcken B; Yokota I; Hart K; Packman S; Harpey JP; Saudubray JM; Hale DE; Bolund L; Kølvraa S; Gregersen N
    Hum Mol Genet; 1997 May; 6(5):695-707. PubMed ID: 9158144
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.