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272 related items for PubMed ID: 30783

  • 1. Cobalamin binding and cobalamin-dependent enzyme activity in normal and mutant human fibroblasts.
    Mellman I, Willard HF, Rosenberg LE.
    J Clin Invest; 1978 Nov; 62(5):952-60. PubMed ID: 30783
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  • 3. Recognition of two intracellular cobalamin binding proteins and their identification as methylmalonyl-CoA mutase and methionine synthetase.
    Kolhouse JF, Allen RH.
    Proc Natl Acad Sci U S A; 1977 Mar; 74(3):921-5. PubMed ID: 15259
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  • 4. 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; 65(3):690-8. PubMed ID: 6101601
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  • 5. Congenital defect in intracellular cobalamin metabolism resulting in homocystinuria and methylmalonic aciduria. II. Biochemical investigations.
    Baumgartner ER, Wick H, Linnell JC, Gaull GE, Bachmann C, Steinmann B.
    Helv Paediatr Acta; 1979 Mar; 34(5):483-96. PubMed ID: 43301
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  • 6. Cobalamin metabolism in cultured human chorionic villus cells.
    Begley JA, Colligan PD, Chu RC, Hall CA.
    J Cell Physiol; 1993 Jul; 156(1):43-7. PubMed ID: 8100234
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  • 9. Altered vitamin B12 metabolism in fibroblasts from a patient with megaloblastic anemia and homocystinuria due to a new defect in methionine biosynthesis.
    Rosenblatt DS, Cooper BA, Pottier A, Lue-Shing H, Matiaszuk N, Grauer K.
    J Clin Invest; 1984 Dec; 74(6):2149-56. PubMed ID: 6511919
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  • 10. Cobalt: its role in health and disease.
    Yamada K.
    Met Ions Life Sci; 2013 Dec; 13():295-320. PubMed ID: 24470095
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  • 11. Cobalamin deficiency results in an abnormal increase in L-methylmalonyl-co-enzyme-A mutase expression in rat liver and COS-7 cells.
    Nakao M, Hironaka S, Harada N, Adachi T, Bito T, Yabuta Y, Watanabe F, Miura T, Yamaji R, Inui H, Nakano Y.
    Br J Nutr; 2009 Feb; 101(4):492-8. PubMed ID: 18710602
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  • 12. The nature of the defect in cobalamin G mutation.
    Hall CA, Lindenbaum RH, Arenson E, Begley JA, Chu RC.
    Clin Invest Med; 1989 Aug; 12(4):262-9. PubMed ID: 2535439
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  • 13. The regulatory roles of liver and kidney in cobalamin (vitamin B12) metabolism in the rat: the uptake and intracellular binding of cobalamin and the activity of the cobalamin-dependent enzymes in response to varying cobalamin supply.
    Scott JS, Treston AM, Bowman EP, Owens JA, Cooksley WG.
    Clin Sci (Lond); 1984 Sep; 67(3):299-306. PubMed ID: 6147223
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  • 14. Identification of ABC transporters acting in vitamin B12 metabolism in Caenorhabditis elegans.
    McDonald MK, Fritz JA, Jia D, Scheuchner D, Snyder FF, Stanislaus A, Curle J, Li L, Stabler SP, Allen RH, Mains PE, Gravel RA.
    Mol Genet Metab; 2017 Dec; 122(4):160-171. PubMed ID: 29153845
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  • 15. Enhanced levels of biochemical markers for cobalamin deficiency in totally gastrectomized rats: uncoupling of the enhancement from the severity of spongy vacuolation in spinal cord.
    Scalabrino G, Buccellato FR, Tredici G, Morabito A, Lorenzini EC, Allen RH, Lindenbaum J.
    Exp Neurol; 1997 Apr; 144(2):258-65. PubMed ID: 9168827
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  • 16. Glutathionylcobalamin as an intermediate in the formation of cobalamin coenzymes.
    Pezacka E, Green R, Jacobsen DW.
    Biochem Biophys Res Commun; 1990 Jun 15; 169(2):443-50. PubMed ID: 2357215
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  • 17. Cyclic activity of the receptors of cobalamin bound to transcobalamin II.
    Hall CA, Colligan PD, Begley JA.
    J Cell Physiol; 1987 Oct 15; 133(1):187-91. PubMed ID: 2822732
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  • 18. The dynamics of cobalamin utilization in L-1210 mouse leukemia cells: a model of cellular cobalamin metabolism.
    Quadros EV, Jacobsen DW.
    Biochim Biophys Acta; 1995 Jun 09; 1244(2-3):395-403. PubMed ID: 7599160
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  • 19. Nitrous oxide has multiple deleterious effects on cobalamin metabolism and causes decreases in activities of both mammalian cobalamin-dependent enzymes in rats.
    Kondo H, Osborne ML, Kolhouse JF, Binder MJ, Podell ER, Utley CS, Abrams RS, Allen RH.
    J Clin Invest; 1981 May 09; 67(5):1270-83. PubMed ID: 6112240
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  • 20. Molecular basis for dysfunction of some mutant forms of methylmalonyl-CoA mutase: deductions from the structure of methionine synthase.
    Drennan CL, Matthews RG, Rosenblatt DS, Ledley FD, Fenton WA, Ludwig ML.
    Proc Natl Acad Sci U S A; 1996 May 28; 93(11):5550-5. PubMed ID: 8643613
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