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Journal Abstract Search

329 related items for PubMed ID: 21064154

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  • 4. Conservation of functional asymmetry in the mammalian MutLα ATPase.
    Johnson JR, Erdeniz N, Nguyen M, Dudley S, Liskay RM.
    DNA Repair (Amst); 2010 Nov 10; 9(11):1209-13. PubMed ID: 20864418
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  • 6. A novel interaction between human DNA polymerase eta and MutLalpha.
    Kanao R, Hanaoka F, Masutani C.
    Biochem Biophys Res Commun; 2009 Nov 06; 389(1):40-5. PubMed ID: 19703417
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  • 7. MutLα heterodimers modify the molecular phenotype of Friedreich ataxia.
    Ezzatizadeh V, Sandi C, Sandi M, Anjomani-Virmouni S, Al-Mahdawi S, Pook MA.
    PLoS One; 2014 Nov 06; 9(6):e100523. PubMed ID: 24971578
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  • 8. Modulation of microRNA processing by mismatch repair protein MutLα.
    Mao G, Lee S, Ortega J, Gu L, Li GM.
    Cell Res; 2012 Jun 06; 22(6):973-85. PubMed ID: 22290424
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  • 9. Truncation of the C-terminus of human MLH1 blocks intracellular stabilization of PMS2 and disrupts DNA mismatch repair.
    Mohd AB, Palama B, Nelson SE, Tomer G, Nguyen M, Huo X, Buermeyer AB.
    DNA Repair (Amst); 2006 Mar 07; 5(3):347-61. PubMed ID: 16338176
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  • 10. Functional characterization of MLH1 missense variants identified in Lynch syndrome patients.
    Andersen SD, Liberti SE, Lützen A, Drost M, Bernstein I, Nilbert M, Dominguez M, Nyström M, Hansen TV, Christoffersen JW, Jäger AC, de Wind N, Nielsen FC, Tørring PM, Rasmussen LJ.
    Hum Mutat; 2012 Dec 07; 33(12):1647-55. PubMed ID: 22753075
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  • 11. Identification of Lynch syndrome mutations in the MLH1-PMS2 interface that disturb dimerization and mismatch repair.
    Kosinski J, Hinrichsen I, Bujnicki JM, Friedhoff P, Plotz G.
    Hum Mutat; 2010 Aug 07; 31(8):975-82. PubMed ID: 20533529
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  • 12. CRM1-dependent nuclear export and dimerization with hMSH5 contribute to the regulation of hMSH4 subcellular localization.
    Neyton S, Lespinasse F, Lahaye F, Staccini P, Paquis-Flucklinger V, Santucci-Darmanin S.
    Exp Cell Res; 2007 Oct 15; 313(17):3680-93. PubMed ID: 17869244
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  • 13. 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 10; 382(3):610-27. PubMed ID: 18619468
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  • 14. Rhabdomyosarcoma in patients with constitutional mismatch-repair-deficiency syndrome.
    Kratz CP, Holter S, Etzler J, Lauten M, Pollett A, Niemeyer CM, Gallinger S, Wimmer K.
    J Med Genet; 2009 Jun 10; 46(6):418-20. PubMed ID: 19293170
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  • 15. The FANCJ/MutLalpha interaction is required for correction of the cross-link response in FA-J cells.
    Peng M, Litman R, Xie J, Sharma S, Brosh RM, Cantor SB.
    EMBO J; 2007 Jul 11; 26(13):3238-49. PubMed ID: 17581638
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  • 16. Assessing pathogenicity of MLH1 variants by co-expression of human MLH1 and PMS2 genes in yeast.
    Vogelsang M, Comino A, Zupanec N, Hudler P, Komel R.
    BMC Cancer; 2009 Oct 28; 9():382. PubMed ID: 19863800
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  • 17. An intact Pms2 ATPase domain is not essential for male fertility.
    Fischer JM, Dudley S, Miller AJ, Liskay RM.
    DNA Repair (Amst); 2016 Mar 28; 39():46-51. PubMed ID: 26753533
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  • 18. PMS2 involvement in patients suspected of Lynch syndrome.
    Niessen RC, Kleibeuker JH, Westers H, Jager PO, Rozeveld D, Bos KK, Boersma-van Ek W, Hollema H, Sijmons RH, Hofstra RM.
    Genes Chromosomes Cancer; 2009 Apr 28; 48(4):322-9. PubMed ID: 19132747
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  • 19. Human colon cancer cells surviving high doses of cisplatin or oxaliplatin in vitro are not defective in DNA mismatch repair proteins.
    Sergent C, Franco N, Chapusot C, Lizard-Nacol S, Isambert N, Correia M, Chauffert B.
    Cancer Chemother Pharmacol; 2002 Jun 28; 49(6):445-52. PubMed ID: 12107548
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  • 20. The MLH1 variants p.Arg265Cys and p.Lys618Ala affect protein stability while p.Leu749Gln affects heterodimer formation.
    Perera S, Bapat B.
    Hum Mutat; 2008 Feb 28; 29(2):332. PubMed ID: 18205192
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