234 related articles for article (PubMed ID: 26753533)
1. An intact Pms2 ATPase domain is not essential for male fertility.
Fischer JM; Dudley S; Miller AJ; Liskay RM
DNA Repair (Amst); 2016 Mar; 39():46-51. PubMed ID: 26753533
[TBL] [Abstract][Full Text] [Related]
2. Changes in the expression profile of the meiosis-involved mismatch repair genes in impaired human spermatogenesis.
Terribas E; Bonache S; García-Arévalo M; Sánchez J; Franco E; Bassas L; Larriba S
J Androl; 2010; 31(4):346-57. PubMed ID: 20075417
[TBL] [Abstract][Full Text] [Related]
3. 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; 5(3):347-61. PubMed ID: 16338176
[TBL] [Abstract][Full Text] [Related]
4. Contributions by MutL homologues Mlh3 and Pms2 to DNA mismatch repair and tumor suppression in the mouse.
Chen PC; Dudley S; Hagen W; Dizon D; Paxton L; Reichow D; Yoon SR; Yang K; Arnheim N; Liskay RM; Lipkin SM
Cancer Res; 2005 Oct; 65(19):8662-70. PubMed ID: 16204034
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Meiotic arrest and aneuploidy in MLH3-deficient mice.
Lipkin SM; Moens PB; Wang V; Lenzi M; Shanmugarajah D; Gilgeous A; Thomas J; Cheng J; Touchman JW; Green ED; Schwartzberg P; Collins FS; Cohen PE
Nat Genet; 2002 Aug; 31(4):385-90. PubMed ID: 12091911
[TBL] [Abstract][Full Text] [Related]
7. Nuclear import of human MLH1, PMS2, and MutLalpha: redundancy is the key.
Leong V; Lorenowicz J; Kozij N; Guarné A
Mol Carcinog; 2009 Aug; 48(8):742-50. PubMed ID: 19148896
[TBL] [Abstract][Full Text] [Related]
8. 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; 9(6):e100523. PubMed ID: 24971578
[TBL] [Abstract][Full Text] [Related]
9. 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; 9():382. PubMed ID: 19863800
[TBL] [Abstract][Full Text] [Related]
10. 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; 31(8):975-82. PubMed ID: 20533529
[TBL] [Abstract][Full Text] [Related]
11. Elevated levels of the mismatch repair protein PMS2 are associated with prostate cancer.
Norris AM; Woodruff RD; D'Agostino RB; Clodfelter JE; Scarpinato KD
Prostate; 2007 Feb; 67(2):214-25. PubMed ID: 17044039
[TBL] [Abstract][Full Text] [Related]
12. Differing patterns of genetic instability in mice deficient in the mismatch repair genes Pms2, Mlh1, Msh2, Msh3 and Msh6.
Hegan DC; Narayanan L; Jirik FR; Edelmann W; Liskay RM; Glazer PM
Carcinogenesis; 2006 Dec; 27(12):2402-8. PubMed ID: 16728433
[TBL] [Abstract][Full Text] [Related]
13. Different mutator phenotypes in Mlh1- versus Pms2-deficient mice.
Yao X; Buermeyer AB; Narayanan L; Tran D; Baker SM; Prolla TA; Glazer PM; Liskay RM; Arnheim N
Proc Natl Acad Sci U S A; 1999 Jun; 96(12):6850-5. PubMed ID: 10359802
[TBL] [Abstract][Full Text] [Related]
14. Localization of MMR proteins on meiotic chromosomes in mice indicates distinct functions during prophase I.
Kolas NK; Svetlanov A; Lenzi ML; Macaluso FP; Lipkin SM; Liskay RM; Greally J; Edelmann W; Cohen PE
J Cell Biol; 2005 Nov; 171(3):447-58. PubMed ID: 16260499
[TBL] [Abstract][Full Text] [Related]
15. Multivariate analysis of MLH1 c.1664T>C (p.Leu555Pro) mismatch repair gene variant demonstrates its pathogenicity.
Farrell MP; Hughes DJ; Drost M; Wallace AJ; Cummins RJ; Fletcher TA; Meany MA; Kay EW; de Wind N; Power DG; Andrews EJ; Green AJ; Gallagher DJ
Fam Cancer; 2013 Dec; 12(4):741-7. PubMed ID: 23712482
[TBL] [Abstract][Full Text] [Related]
16. Epigenetic repression of DNA mismatch repair by inflammation and hypoxia in inflammatory bowel disease-associated colorectal cancer.
Edwards RA; Witherspoon M; Wang K; Afrasiabi K; Pham T; Birnbaumer L; Lipkin SM
Cancer Res; 2009 Aug; 69(16):6423-9. PubMed ID: 19638594
[TBL] [Abstract][Full Text] [Related]
17. DNA mismatch repair and colon cancer.
Marra G; Jiricny J
Adv Exp Med Biol; 2005; 570():85-123. PubMed ID: 18727499
[No Abstract] [Full Text] [Related]
18. Apoptosis and mutation in the murine small intestine: loss of Mlh1- and Pms2-dependent apoptosis leads to increased mutation in vivo.
Sansom OJ; Bishop SM; Court H; Dudley S; Liskay RM; Clarke AR
DNA Repair (Amst); 2003 Sep; 2(9):1029-39. PubMed ID: 12967659
[TBL] [Abstract][Full Text] [Related]
19. Concomitant mutation and epimutation of the MLH1 gene in a Lynch syndrome family.
Cini G; Carnevali I; Quaia M; Chiaravalli AM; Sala P; Giacomini E; Maestro R; Tibiletti MG; Viel A
Carcinogenesis; 2015 Apr; 36(4):452-8. PubMed ID: 25742745
[TBL] [Abstract][Full Text] [Related]
20. DNA mismatch repair deficiency in breast carcinoma: a pilot study of triple-negative and non-triple-negative tumors.
Wen YH; Brogi E; Zeng Z; Akram M; Catalano J; Paty PB; Norton L; Shia J
Am J Surg Pathol; 2012 Nov; 36(11):1700-8. PubMed ID: 22992699
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]