These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

451 related articles for article (PubMed ID: 6511919)

  • 1. 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]  

  • 2. Homocystinuria and megaloblastic anemia responsive to vitamin B12 therapy. An inborn error of metabolism due to a defect in cobalamin metabolism.
    Schuh S; Rosenblatt DS; Cooper BA; Schroeder ML; Bishop AJ; Seargeant LE; Haworth JC
    N Engl J Med; 1984 Mar; 310(11):686-90. PubMed ID: 6700644
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Vitamin B12 responsive homocystinuria and megaloblastic anemia: heterogeneity in methylcobalamin deficiency.
    Rosenblatt DS; Thomas IT; Watkins D; Cooper BA; Erbe RW
    Am J Med Genet; 1987 Feb; 26(2):377-83. PubMed ID: 3812589
    [TBL] [Abstract][Full Text] [Related]  

  • 4. New disorder of vitamin B12 metabolism (cobalamin F) presenting as methylmalonic aciduria.
    Rosenblatt DS; Laframboise R; Pichette J; Langevin P; Cooper BA; Costa T
    Pediatrics; 1986 Jul; 78(1):51-4. PubMed ID: 3725502
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic heterogeneity among patients with methylcobalamin deficiency. Definition of two complementation groups, cblE and cblG.
    Watkins D; Rosenblatt DS
    J Clin Invest; 1988 Jun; 81(6):1690-4. PubMed ID: 3384945
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Vitamin B12 in health and disease: part I--inherited disorders of function, absorption, and transport.
    Kapadia CR
    Gastroenterologist; 1995 Dec; 3(4):329-44. PubMed ID: 8775094
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Functional methionine synthase deficiency (cblE and cblG): clinical and biochemical heterogeneity.
    Watkins D; Rosenblatt DS
    Am J Med Genet; 1989 Nov; 34(3):427-34. PubMed ID: 2688421
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 34(5):483-96. PubMed ID: 43301
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Vitamin B12-responsive neonatal megaloblastic anemia and homocystinuria with associated reduced methionine synthase activity.
    Hallam LJ; Sawyer M; Clark AC; Van der Weyden MB
    Blood; 1987 Apr; 69(4):1128-33. PubMed ID: 3828532
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A cobalamin metabolic defect with homocystinuria, methylmalonic aciduria and macrocytic anemia.
    Mamlok RJ; Isenberg JN; Rassin DK; Norcross K; Tallan HH
    Neuropediatrics; 1986 May; 17(2):94-9. PubMed ID: 2873525
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Perturbation of methionine metabolism in sheep with nitrous-oxide-induced inactivation of cobalamin.
    Xue GP; Snoswell AM; Runciman WB
    Biochem Int; 1986 Jan; 12(1):61-9. PubMed ID: 2868723
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cobalamin inactivation decreases purine and methionine synthesis in cultured lymphoblasts.
    Boss GR
    J Clin Invest; 1985 Jul; 76(1):213-8. PubMed ID: 2862163
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Development and reversion of methionine dependence in a human glioma cell line: relation to homocysteine remethylation and cobalamin status.
    Fiskerstrand T; Christensen B; Tysnes OB; Ueland PM; Refsum H
    Cancer Res; 1994 Sep; 54(18):4899-906. PubMed ID: 8069855
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Methionine synthase inactivation by nitrous oxide during methionine loading of normal human fibroblasts. Homocysteine remethylation as determinant of enzyme inactivation and homocysteine export.
    Christensen B; Ueland PM
    J Pharmacol Exp Ther; 1993 Dec; 267(3):1298-303. PubMed ID: 8263793
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Effect of methionine and nitrous oxide on homocysteine export and remethylation in fibroblasts from cystathionine synthase-deficient, cb1G, and cb1E patients.
    Christensen B; Rosenblatt DS; Chu RC; Ueland PM
    Pediatr Res; 1994 Jan; 35(1):3-9. PubMed ID: 8134195
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Functional methionine synthase deficiency due to cblG disorder: a report of two patients and a review.
    Harding CO; Arnold G; Barness LA; Wolff JA; Rosenblatt DS
    Am J Med Genet; 1997 Sep; 71(4):384-90. PubMed ID: 9286442
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 23.