BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

528 related articles for article (PubMed ID: 8643613)

  • 1. 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]  

  • 2. Homology modeling of human methylmalonyl-CoA mutase: a structural basis for point mutations causing methylmalonic aciduria.
    Thomä NH; Leadlay PF
    Protein Sci; 1996 Sep; 5(9):1922-7. PubMed ID: 8880917
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cobalamin-dependent methionine synthase: the structure of a methylcobalamin-binding fragment and implications for other B12-dependent enzymes.
    Drennan CL; Matthews RG; Ludwig ML
    Curr Opin Struct Biol; 1994 Dec; 4(6):919-29. PubMed ID: 7712296
    [TBL] [Abstract][Full Text] [Related]  

  • 4. How a protein binds B12: A 3.0 A X-ray structure of B12-binding domains of methionine synthase.
    Drennan CL; Huang S; Drummond JT; Matthews RG; Ludwig ML
    Science; 1994 Dec; 266(5191):1669-74. PubMed ID: 7992050
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clustering of mutations in methylmalonyl CoA mutase associated with mut- methylmalonic acidemia.
    Crane AM; Ledley FD
    Am J Hum Genet; 1994 Jul; 55(1):42-50. PubMed ID: 7912889
    [TBL] [Abstract][Full Text] [Related]  

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

  • 7. Structure-based perspectives on B12-dependent enzymes.
    Ludwig ML; Matthews RG
    Annu Rev Biochem; 1997; 66():269-313. PubMed ID: 9242908
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Human B
    Mascarenhas R; Gouda H; Ruetz M; Banerjee R
    Methods Enzymol; 2022; 668():309-326. PubMed ID: 35589199
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Crystal structure and mutagenesis of the metallochaperone MeaB: insight into the causes of methylmalonic aciduria.
    Hubbard PA; Padovani D; Labunska T; Mahlstedt SA; Banerjee R; Drennan CL
    J Biol Chem; 2007 Oct; 282(43):31308-16. PubMed ID: 17728257
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [A molecular study of methylmalonic aciduria: structure-function correlations].
    Rosenblatt DS; Ledley FD
    Bull Acad Natl Med; 1996 Oct; 180(7):1553-63; discussion 1563-4. PubMed ID: 9102141
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Importance of the histidine ligand to coenzyme B12 in the reaction catalyzed by methylmalonyl-CoA mutase.
    Vlasie M; Chowdhury S; Banerjee R
    J Biol Chem; 2002 May; 277(21):18523-7. PubMed ID: 11893736
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic characterization of a MUT locus mutation discriminating heterogeneity in mut0 and mut- methylmalonic aciduria by interallelic complementation.
    Raff ML; Crane AM; Jansen R; Ledley FD; Rosenblatt DS
    J Clin Invest; 1991 Jan; 87(1):203-7. PubMed ID: 1670635
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cloning and expression of a mutant methylmalonyl coenzyme A mutase with altered cobalamin affinity that causes mut- methylmalonic aciduria.
    Crane AM; Jansen R; Andrews ER; Ledley FD
    J Clin Invest; 1992 Feb; 89(2):385-91. PubMed ID: 1346616
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The reactivity of B12 cofactors: the proteins make a difference.
    Ludwig ML; Drennan CL; Matthews RG
    Structure; 1996 May; 4(5):505-12. PubMed ID: 8736549
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of ABC transporters acting in vitamin B
    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
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular studies in mutase-deficient (MUT) methylmalonic aciduria: identification of five novel mutations.
    Peters HL; Nefedov M; Lee LW; Abdenur JE; Chamoles NA; Kahler SG; Ioannou PA
    Hum Mutat; 2002 Nov; 20(5):406. PubMed ID: 12402345
    [TBL] [Abstract][Full Text] [Related]  

  • 19. mut0 methylmalonic acidemia: eleven novel mutations of the methylmalonyl CoA mutase including a deletion-insertion mutation.
    Fuchshuber A; Mucha B; Baumgartner ER; Vollmer M; Hildebrandt F
    Hum Mutat; 2000 Aug; 16(2):179. PubMed ID: 10923046
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 27.