BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

215 related articles for article (PubMed ID: 11574484)

  • 1. Structure and function of the N-terminal 40 kDa fragment of human PMS2: a monomeric GHL ATPase.
    Guarné A; Junop MS; Yang W
    EMBO J; 2001 Oct; 20(19):5521-31. PubMed ID: 11574484
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutations within the hMLH1 and hPMS2 subunits of the human MutLalpha mismatch repair factor affect its ATPase activity, but not its ability to interact with hMutSalpha.
    Räschle M; Dufner P; Marra G; Jiricny J
    J Biol Chem; 2002 Jun; 277(24):21810-20. PubMed ID: 11948175
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Contribution of human mlh1 and pms2 ATPase activities to DNA mismatch repair.
    Tomer G; Buermeyer AB; Nguyen MM; Liskay RM
    J Biol Chem; 2002 Jun; 277(24):21801-9. PubMed ID: 11897781
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The interacting domains of three MutL heterodimers in man: hMLH1 interacts with 36 homologous amino acid residues within hMLH3, hPMS1 and hPMS2.
    Kondo E; Horii A; Fukushige S
    Nucleic Acids Res; 2001 Apr; 29(8):1695-702. PubMed ID: 11292842
    [TBL] [Abstract][Full Text] [Related]  

  • 5. HNPCC mutations in the human DNA mismatch repair gene hMLH1 influence assembly of hMutLalpha and hMLH1-hEXO1 complexes.
    Jäger AC; Rasmussen M; Bisgaard HC; Singh KK; Nielsen FC; Rasmussen LJ
    Oncogene; 2001 Jun; 20(27):3590-5. PubMed ID: 11429708
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The PMS2 subunit of human MutLalpha contains a metal ion binding domain of the iron-dependent repressor protein family.
    Kosinski J; Plotz G; Guarné A; Bujnicki JM; Friedhoff P
    J Mol Biol; 2008 Oct; 382(3):610-27. PubMed ID: 18619468
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Structure and function of mismatch repair proteins.
    Yang W
    Mutat Res; 2000 Aug; 460(3-4):245-56. PubMed ID: 10946232
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Somatic mutation of hPMS2 as a possible cause of sporadic human colon cancer with microsatellite instability.
    Ma AH; Xia L; Littman SJ; Swinler S; Lader G; Polinkovsky A; Olechnowicz J; Kasturi L; Lutterbaugh J; Modrich P; Veigl ML; Markowitz SD; Sedwick WD
    Oncogene; 2000 Apr; 19(18):2249-56. PubMed ID: 10822375
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Conditional nuclear localization of hMLH3 suggests a minor activity in mismatch repair and supports its role as a low-risk gene in HNPCC.
    Korhonen MK; Raevaara TE; Lohi H; Nyström M
    Oncol Rep; 2007 Feb; 17(2):351-4. PubMed ID: 17203173
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Human mismatch-repair protein MutL homologue 1 (MLH1) interacts with Escherichia coli MutL and MutS in vivo and in vitro: a simple genetic system to assay MLH1 function.
    Quaresima B; Alifano P; Tassone P; Avvedimento EV; Costanzo FS; Venuta S
    Biochem J; 2003 Apr; 371(Pt 1):183-9. PubMed ID: 12513688
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Crystal structure and ATPase activity of MutL: implications for DNA repair and mutagenesis.
    Ban C; Yang W
    Cell; 1998 Nov; 95(4):541-52. PubMed ID: 9827806
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of a second MutL DNA mismatch repair complex (hPMS1 and hMLH1) in human epithelial cells.
    Leung WK; Kim JJ; Wu L; Sepulveda JL; Sepulveda AR
    J Biol Chem; 2000 May; 275(21):15728-32. PubMed ID: 10748105
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A Lynch syndrome-associated mutation at a Bergerat ATP-binding fold destabilizes the structure of the DNA mismatch repair endonuclease MutL.
    Izuhara K; Fukui K; Murakawa T; Baba S; Kumasaka T; Uchiyama K; Yano T
    J Biol Chem; 2020 Aug; 295(33):11643-11655. PubMed ID: 32571878
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations of two PMS homologues in hereditary nonpolyposis colon cancer.
    Nicolaides NC; Papadopoulos N; Liu B; Wei YF; Carter KC; Ruben SM; Rosen CA; Haseltine WA; Fleischmann RD; Fraser CM
    Nature; 1994 Sep; 371(6492):75-80. PubMed ID: 8072530
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The human PMS2L proteins do not interact with hMLH1, a major DNA mismatch repair protein.
    Kondo E; Horii A; Fukushige S
    J Biochem; 1999 Apr; 125(4):818-25. PubMed ID: 10101297
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Adenosine triphosphate stimulates Aquifex aeolicus MutL endonuclease activity.
    Mauris J; Evans TC
    PLoS One; 2009 Sep; 4(9):e7175. PubMed ID: 19777055
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Dimerization of MLH1 and PMS2 limits nuclear localization of MutLalpha.
    Wu X; Platt JL; Cascalho M
    Mol Cell Biol; 2003 May; 23(9):3320-8. PubMed ID: 12697830
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of hMutLbeta, a heterodimer of hMLH1 and hPMS1.
    Räschle M; Marra G; Nyström-Lahti M; Schär P; Jiricny J
    J Biol Chem; 1999 Nov; 274(45):32368-75. PubMed ID: 10542278
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Transformation of MutL by ATP binding and hydrolysis: a switch in DNA mismatch repair.
    Ban C; Junop M; Yang W
    Cell; 1999 Apr; 97(1):85-97. PubMed ID: 10199405
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Conservation of functional asymmetry in the mammalian MutLα ATPase.
    Johnson JR; Erdeniz N; Nguyen M; Dudley S; Liskay RM
    DNA Repair (Amst); 2010 Nov; 9(11):1209-13. PubMed ID: 20864418
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.