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Journal Abstract Search

130 related items for PubMed ID: 8440722

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  • 4. 3-Hydroxy-3-methylglutaryl coenzyme A lyase (HL): cloning and characterization of a mouse liver HL cDNA and subchromosomal mapping of the human and mouse HL genes.
    Wang S, Nadeau JH, Duncan A, Robert MF, Fontaine G, Schappert K, Johnson KR, Zietkiewicz E, Hruz P, Miziorko H.
    Mamm Genome; 1993; 4(7):382-7. PubMed ID: 8102917
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  • 5. A two-base deletion in exon 6 of the 3-hydroxy-3-methylglutaryl coenzyme A lyase (HL) gene producing the skipping of exons 5 and 6 determines 3-hydroxy-3-methylglutaric aciduria.
    Casals N, Pié J, Casale CH, Zapater N, Ribes A, Castro-Gago M, Rodriguez-Segade S, Wanders RJ, Hegardt FG.
    J Lipid Res; 1997 Nov; 38(11):2303-13. PubMed ID: 9392428
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  • 10. Rat mitochondrial and cytosolic 3-hydroxy-3-methylglutaryl-CoA synthases are encoded by two different genes.
    Ayté J, Gil-Gómez G, Haro D, Marrero PF, Hegardt FG.
    Proc Natl Acad Sci U S A; 1990 May; 87(10):3874-8. PubMed ID: 1971108
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  • 13. 3-Hydroxy-3-methylglutaryl coenzyme a lyase deficiency with reversible white matter changes after treatment.
    Zafeiriou DI, Vargiami E, Mayapetek E, Augoustidou-Savvopoulou P, Mitchell GA.
    Pediatr Neurol; 2007 Jul; 37(1):47-50. PubMed ID: 17628222
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  • 15. Molecular prenatal diagnosis of 3-hydroxy-3-methylglutaryl CoA lyase deficiency.
    Mitchell GA, Jakobs C, Gibson KM, Robert MF, Burlina A, Dionisi-Vici C, Dallaire L.
    Prenat Diagn; 1995 Aug; 15(8):725-9. PubMed ID: 7479590
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  • 16. 3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: review of 18 reported patients.
    Gibson KM, Breuer J, Nyhan WL.
    Eur J Pediatr; 1988 Dec; 148(3):180-6. PubMed ID: 3063529
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  • 20. Expression of chicken hepatic type I and type III iodothyronine deiodinases during embryonic development.
    Van der Geyten S, Sanders JP, Kaptein E, Darras VM, Kühn ER, Leonard JL, Visser TJ.
    Endocrinology; 1997 Dec; 138(12):5144-52. PubMed ID: 9389494
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