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Journal Abstract Search

106 related items for PubMed ID: 20371198

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  • 4. Misfolding, degradation, and aggregation of variant proteins. The molecular pathogenesis of short chain acyl-CoA dehydrogenase (SCAD) deficiency.
    Pedersen CB, Bross P, Winter VS, Corydon TJ, Bolund L, Bartlett K, Vockley J, Gregersen N.
    J Biol Chem; 2003 Nov 28; 278(48):47449-58. PubMed ID: 14506246
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  • 10. Handling of human short-chain acyl-CoA dehydrogenase (SCAD) variant proteins in transgenic mice.
    Kragh PM, Pedersen CB, Schmidt SP, Winter VS, Vajta G, Gregersen N, Bolund L, Corydon TJ.
    Mol Genet Metab; 2007 Jun 28; 91(2):128-37. PubMed ID: 17462936
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  • 11. Short-chain acyl-CoA dehydrogenase deficiency: from gene to cell pathology and possible disease mechanisms.
    Nochi Z, Olsen RKJ, Gregersen N.
    J Inherit Metab Dis; 2017 Sep 28; 40(5):641-655. PubMed ID: 28516284
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  • 16. High prevalence of short-chain acyl-CoA dehydrogenase deficiency in the Netherlands, but no association with epilepsy of unknown origin in childhood.
    van Maldegem BT, Kloosterman SF, Janssen WJ, Augustijn PB, van der Lee JH, Ijlst L, Waterham HR, Duran R, Wanders RJ, Wijburg FA.
    Neuropediatrics; 2011 Feb 28; 42(1):13-7. PubMed ID: 21500142
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  • 19. Role of common gene variations in the molecular pathogenesis of short-chain acyl-CoA dehydrogenase deficiency.
    Corydon MJ, Vockley J, Rinaldo P, Rhead WJ, Kjeldsen M, Winter V, Riggs C, Babovic-Vuksanovic D, Smeitink J, De Jong J, Levy H, Sewell AC, Roe C, Matern D, Dasouki M, Gregersen N.
    Pediatr Res; 2001 Jan 28; 49(1):18-23. PubMed ID: 11134486
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