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Journal Abstract Search

147 related items for PubMed ID: 20894

  • 1. Inherited deficiencies of human methylmalonyl CaA mutase activity: reduced affinity of mutant apoenzyme for adenosylcobalamin.
    Willard HF, Rosenberg LE.
    Biochem Biophys Res Commun; 1977 Oct 10; 78(3):927-34. PubMed ID: 20894
    [No Abstract] [Full Text] [Related]

  • 2. Inherited methylmalonyl CoA mutase apoenzyme deficiency in human fibroblasts: evidence for allelic heterogeneity, genetic compounds, and codominant expression.
    Willard HF, Rosenberg LE.
    J Clin Invest; 1980 Mar 10; 65(3):690-8. PubMed ID: 6101601
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  • 3. A new variant of methylmalonic acidemia-defective coenzyme-apoenzyme binding in cultured fibroblasts.
    Morrow G, Revsin B, Clark R, Lebowitz J, Whelan DT.
    Clin Chim Acta; 1978 Apr 03; 85(1):67-72. PubMed ID: 25730
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  • 4. Cobalamin binding and cobalamin-dependent enzyme activity in normal and mutant human fibroblasts.
    Mellman I, Willard HF, Rosenberg LE.
    J Clin Invest; 1978 Nov 03; 62(5):952-60. PubMed ID: 30783
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  • 5. Inborn errors of cobalamin metabolism: effect of cobalamin supplementation in culture on methylmalonyl CoA mutase activity in normal and mutant human fibroblasts.
    Willard HF, Rosenberg LE.
    Biochem Genet; 1979 Feb 03; 17(1-2):57-75. PubMed ID: 36882
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  • 7. Immunochemical studies on cultured fibroblasts from patients with inherited methylmalonic acidemia.
    Kolhouse JF, Utley C, Fenton WA, Rosenberg LE.
    Proc Natl Acad Sci U S A; 1981 Dec 03; 78(12):7737-41. PubMed ID: 6121323
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  • 12. Heterogeneous alleles and expression of methylmalonyl CoA mutase in mut methylmalonic acidemia.
    Ledley FD, Crane AM, Lumetta M.
    Am J Hum Genet; 1990 Mar 03; 46(3):539-47. PubMed ID: 1968706
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  • 15. Cloning and expression of a mutant methylmalonyl coenzyme A mutase with altered cobalamin affinity that causes mut- methylmalonic aciduria.
    Crane AM, Jansen R, Andrews ER, Ledley FD.
    J Clin Invest; 1992 Feb 03; 89(2):385-91. PubMed ID: 1346616
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  • 18. [Isolated methylmalonyl-CoA mutase deficiency].
    Yoshino M.
    Ryoikibetsu Shokogun Shirizu; 1998 Feb 03; (18 Pt 1):269-72. PubMed ID: 9590044
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  • 19. Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant.
    Willard HF, Mellman IS, Rosenberg LE.
    Am J Hum Genet; 1978 Jan 03; 30(1):1-13. PubMed ID: 23678
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  • 20. Mutation eliminating mitochondrial leader sequence of methylmalonyl-CoA mutase causes muto methylmalonic acidemia.
    Ledley FD, Jansen R, Nham SU, Fenton WA, Rosenberg LE.
    Proc Natl Acad Sci U S A; 1990 Apr 03; 87(8):3147-50. PubMed ID: 1970180
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