BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

472 related articles for article (PubMed ID: 1516297)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Metabolic cooperation among cell lines from patients with inborn errors of vitamin B12 metabolism: differential response of cblC and cblD.
    Byck S; Rosenblatt DS
    Clin Invest Med; 1991 Apr; 14(2):153-9. PubMed ID: 1676355
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Leukoencephalopathies associated with disorders of cobalamin and folate metabolism.
    Wilcken B
    Semin Neurol; 2012 Feb; 32(1):68-74. PubMed ID: 22422209
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 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. Inherited defects of cobalamin metabolism.
    Watkins D; Rosenblatt DS
    Vitam Horm; 2022; 119():355-376. PubMed ID: 35337626
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Changes in cobalamin metabolism are associated with the altered methionine auxotrophy of highly growth autonomous human melanoma cells.
    Liteplo RG; Hipwell SE; Rosenblatt DS; Sillaots S; Lue-Shing H
    J Cell Physiol; 1991 Nov; 149(2):332-8. PubMed ID: 1748723
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cobalamin metabolism in methionine-dependent human tumour and leukemia cell lines.
    Watkins D
    Clin Invest Med; 1998 Jun; 21(3):151-8. PubMed ID: 9627769
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The C-terminal domain of CblD interacts with CblC and influences intracellular cobalamin partitioning.
    Gherasim C; Hannibal L; Rajagopalan D; Jacobsen DW; Banerjee R
    Biochimie; 2013 May; 95(5):1023-32. PubMed ID: 23415655
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. SIRT1 activation rescues the mislocalization of RNA-binding proteins and cognitive defects induced by inherited cobalamin disorders.
    Ghemrawi R; Arnold C; Battaglia-Hsu SF; Pourié G; Trinh I; Bassila C; Rashka C; Wiedemann A; Flayac J; Robert A; Dreumont N; Feillet F; Guéant JL; Coelho D
    Metabolism; 2019 Dec; 101():153992. PubMed ID: 31672445
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Mitochondrial vitamin B12-binding proteins in patients with inborn errors of cobalamin metabolism.
    Moras E; Hosack A; Watkins D; Rosenblatt DS
    Mol Genet Metab; 2007 Feb; 90(2):140-7. PubMed ID: 17011224
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Acquired and inherited disorders of cobalamin and folate in children.
    Whitehead VM
    Br J Haematol; 2006 Jul; 134(2):125-36. PubMed ID: 16846473
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal diagnosis for methylmalonic acidemia and inborn errors of vitamin B12 metabolism and transport.
    Morel CF; Watkins D; Scott P; Rinaldo P; Rosenblatt DS
    Mol Genet Metab; 2005; 86(1-2):160-71. PubMed ID: 16150626
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Inborn Error of Cobalamin Metabolism Associated with the Intracellular Accumulation of Transcobalamin-Bound Cobalamin and Mutations in ZNF143, Which Codes for a Transcriptional Activator.
    Pupavac M; Watkins D; Petrella F; Fahiminiya S; Janer A; Cheung W; Gingras AC; Pastinen T; Muenzer J; Majewski J; Shoubridge EA; Rosenblatt DS
    Hum Mutat; 2016 Sep; 37(9):976-82. PubMed ID: 27349184
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 24.