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6. Inherited disorders of cobalamin metabolism. Qureshi AA; Rosenblatt DS; Cooper BA Crit Rev Oncol Hematol; 1994 Oct; 17(2):133-51. PubMed ID: 7818787 [No Abstract] [Full Text] [Related]
7. 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 [TBL] [Abstract][Full Text] [Related]
8. Inborn errors of cobalamin absorption and metabolism. Watkins D; Rosenblatt DS Am J Med Genet C Semin Med Genet; 2011 Feb; 157C(1):33-44. PubMed ID: 21312325 [TBL] [Abstract][Full Text] [Related]
9. Cobalt-vitamin B12 deficiency and the activity of methylmalonyl CoA mutase and methionine synthase in cattle. Kennedy DG; Young PB; Kennedy S; Scott JM; Molloy AM; Weir DG; Price J Int J Vitam Nutr Res; 1995; 65(4):241-7. PubMed ID: 8789620 [TBL] [Abstract][Full Text] [Related]
10. Cobalamin deficiency and the pathogenesis of nervous system disease. Metz J Annu Rev Nutr; 1992; 12():59-79. PubMed ID: 1354465 [TBL] [Abstract][Full Text] [Related]
11. Selective inactivation of vitamin B12 in rats by nitrous oxide. Deacon R; Lumb M; Perry J; Chanarin I; Minty B; Halsey MJ; Nunn JF Lancet; 1978 Nov; 2(8098):1023-4. PubMed ID: 82036 [TBL] [Abstract][Full Text] [Related]
13. The cblD defect causes either isolated or combined deficiency of methylcobalamin and adenosylcobalamin synthesis. Suormala T; Baumgartner MR; Coelho D; Zavadakova P; Kozich V; Koch HG; BerghaĆ¼ser M; Wraith JE; Burlina A; Sewell A; Herwig J; Fowler B J Biol Chem; 2004 Oct; 279(41):42742-9. PubMed ID: 15292234 [TBL] [Abstract][Full Text] [Related]
14. 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; 93(11):5550-5. PubMed ID: 8643613 [TBL] [Abstract][Full Text] [Related]
15. 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 [TBL] [Abstract][Full Text] [Related]
16. 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 [TBL] [Abstract][Full Text] [Related]
17. [Effects of cobalamin analogues produced by reaction between OHB12 and ascorbic acid upon absorption, plasma transport, organ distribution and B12 dependent enzymes]. Kondo H; Terada H; Iseki T; Iwasa S; Okuda K; Kanazawa S; Okuda K Nihon Ketsueki Gakkai Zasshi; 1986 Nov; 49(7):1338-46. PubMed ID: 2881421 [No Abstract] [Full Text] [Related]
19. Identification and perturbation of mutant human fibroblasts based on measurements of methylmalonic acid and total homocysteine in the culture media. Kolhouse JF; Stabler SP; Allen RH Arch Biochem Biophys; 1993 Jun; 303(2):355-60. PubMed ID: 8099783 [TBL] [Abstract][Full Text] [Related]