BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

129 related articles for article (PubMed ID: 1627355)

  • 1. Heterogeneity in cblG: differential retention of cobalamin on methionine synthase.
    Sillaots SL; Hall CA; Hurteloup V; Rosenblatt DS
    Biochem Med Metab Biol; 1992 Jun; 47(3):242-9. PubMed ID: 1627355
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Methionine auxotrophy in inborn errors of cobalamin metabolism.
    Garovic-Kocic V; Rosenblatt DS
    Clin Invest Med; 1992 Aug; 15(4):395-400. PubMed ID: 1516297
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Functionally null mutations in patients with the cblG-variant form of methionine synthase deficiency.
    Wilson A; Leclerc D; Saberi F; Campeau E; Hwang HY; Shane B; Phillips JA; Rosenblatt DS; Gravel RA
    Am J Hum Genet; 1998 Aug; 63(2):409-14. PubMed ID: 9683607
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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; Berghaüser 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]  

  • 8. Defects in auxiliary redox proteins lead to functional methionine synthase deficiency.
    Gulati S; Chen Z; Brody LC; Rosenblatt DS; Banerjee R
    J Biol Chem; 1997 Aug; 272(31):19171-5. PubMed ID: 9235907
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Interaction between methionine synthase isoforms and MMACHC: characterization in cblG-variant, cblG and cblC inherited causes of megaloblastic anaemia.
    Fofou-Caillierez MB; Mrabet NT; Chéry C; Dreumont N; Flayac J; Pupavac M; Paoli J; Alberto JM; Coelho D; Camadro JM; Feillet F; Watkins D; Fowler B; Rosenblatt DS; Guéant JL
    Hum Mol Genet; 2013 Nov; 22(22):4591-601. PubMed ID: 23825108
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical onset and course, response to treatment and outcome in 24 patients with the cblE or cblG remethylation defect complemented by genetic and in vitro enzyme study data.
    Huemer M; Bürer C; Ješina P; Kožich V; Landolt MA; Suormala T; Fowler B; Augoustides-Savvopoulou P; Blair E; Brennerova K; Broomfield A; De Meirleir L; Gökcay G; Hennermann J; Jardine P; Koch J; Lorenzl S; Lotz-Havla AS; Noss J; Parini R; Peters H; Plecko B; Ramos FJ; Schlune A; Tsiakas K; Zerjav Tansek M; Baumgartner MR
    J Inherit Metab Dis; 2015 Sep; 38(5):957-67. PubMed ID: 25526710
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Folate-responsive homocystinuria and megaloblastic anaemia in a female patient with functional methionine synthase deficiency (cblE disease).
    Fowler B; Schutgens RB; Rosenblatt DS; Smit GP; Lindemans J
    J Inherit Metab Dis; 1997 Nov; 20(6):731-41. PubMed ID: 9427140
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Methionine synthase and methionine synthase reductase interact with MMACHC and with MMADHC.
    Bassila C; Ghemrawi R; Flayac J; Froese DS; Baumgartner MR; Guéant JL; Coelho D
    Biochim Biophys Acta Mol Basis Dis; 2017 Jan; 1863(1):103-112. PubMed ID: 27771510
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. Analysis of fibroblasts from patients with cblC and cblG genetic defects of cobalamin metabolism reveals global dysregulation of alternative splicing.
    Rashka C; Hergalant S; Dreumont N; Oussalah A; Camadro JM; Marchand V; Hassan Z; Baumgartner MR; Rosenblatt DS; Feillet F; Guéant JL; Flayac J; Coelho D
    Hum Mol Genet; 2020 Jul; 29(12):1969-1985. PubMed ID: 32068834
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 1244(2-3):395-403. PubMed ID: 7599160
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Intracellular binding of radioactive hydroxocobalamin to cobalamin-dependent apoenzymes in rat liver.
    Mellman IS; Youngdahl-Turner P; Willard HF; Rosenberg LE
    Proc Natl Acad Sci U S A; 1977 Mar; 74(3):916-20. PubMed ID: 15258
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.