179 related articles for article (PubMed ID: 38196581)
1. A maternal germline mutator phenotype in a family affected by heritable colorectal cancer.
Young CL; Beichman AC; Mas-Ponte D; Hemker SL; Zhu L; Kitzman JO; Shirts B; Harris K
medRxiv; 2023 Dec; ():. PubMed ID: 38196581
[TBL] [Abstract][Full Text] [Related]
2. Frequency of the common germline MUTYH mutations p.G396D and p.Y179C in patients diagnosed with colorectal cancer in Southern Brazil.
Pitroski CE; Cossio SL; Koehler-Santos P; Graudenz M; Prolla JC; Ashton-Prolla P
Int J Colorectal Dis; 2011 Jul; 26(7):841-6. PubMed ID: 21424714
[TBL] [Abstract][Full Text] [Related]
3. Simplifying the detection of MUTYH mutations by high resolution melting analysis.
López-Villar I; Ayala R; Wesselink J; Morillas JD; López E; Marín JC; Díaz-Tasende J; González S; Robles L; Martínez-López J
BMC Cancer; 2010 Aug; 10():408. PubMed ID: 20687945
[TBL] [Abstract][Full Text] [Related]
4. Case Report: The Role of Molecular Analysis of the
Fabišíková K; Hamidová O; Behulová RL; Závodná K; Priščáková P; Repiská V
Front Genet; 2020; 11():590486. PubMed ID: 33384714
[No Abstract] [Full Text] [Related]
5. Analysis of MUTYH genotypes and colorectal phenotypes in patients With MUTYH-associated polyposis.
Nielsen M; Joerink-van de Beld MC; Jones N; Vogt S; Tops CM; Vasen HF; Sampson JR; Aretz S; Hes FJ
Gastroenterology; 2009 Feb; 136(2):471-6. PubMed ID: 19032956
[TBL] [Abstract][Full Text] [Related]
6. High prevalence of the c.1227_1228dup (p.Glu410GlyfsX43) mutation in Tunisian families affected with MUTYH-associated-polyposis.
Abdelmaksoud-Dammak R; Miladi-Abdennadher I; Amouri A; Tahri N; Ayadi L; Khabir A; Frikha F; Gargouri A; Mokdad-Gargouri R
Fam Cancer; 2012 Sep; 11(3):503-8. PubMed ID: 22744763
[TBL] [Abstract][Full Text] [Related]
7. Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene.
Win AK; Reece JC; Buchanan DD; Clendenning M; Young JP; Cleary SP; Kim H; Cotterchio M; Dowty JG; MacInnis RJ; Tucker KM; Winship IM; Macrae FA; Burnett T; Le Marchand L; Casey G; Haile RW; Newcomb PA; Thibodeau SN; Lindor NM; Hopper JL; Gallinger S; Jenkins MA
Fam Cancer; 2015 Dec; 14(4):575-83. PubMed ID: 26202870
[TBL] [Abstract][Full Text] [Related]
8. Epistasis between mutator alleles contributes to germline mutation spectra variability in laboratory mice.
Sasani TA; Quinlan AR; Harris K
bioRxiv; 2023 Nov; ():. PubMed ID: 37162999
[TBL] [Abstract][Full Text] [Related]
9. Epistasis between mutator alleles contributes to germline mutation spectrum variability in laboratory mice.
Sasani TA; Quinlan AR; Harris K
Elife; 2024 Feb; 12():. PubMed ID: 38381482
[TBL] [Abstract][Full Text] [Related]
10. Prevalence and phenotypes of APC and MUTYH mutations in patients with multiple colorectal adenomas.
Grover S; Kastrinos F; Steyerberg EW; Cook EF; Dewanwala A; Burbidge LA; Wenstrup RJ; Syngal S
JAMA; 2012 Aug; 308(5):485-492. PubMed ID: 22851115
[TBL] [Abstract][Full Text] [Related]
11. MUTYH-associated colorectal cancer and adenomatous polyposis.
Yamaguchi S; Ogata H; Katsumata D; Nakajima M; Fujii T; Tsutsumi S; Asao T; Sasaki K; Kuwano H; Kato H
Surg Today; 2014 Apr; 44(4):593-600. PubMed ID: 23605219
[TBL] [Abstract][Full Text] [Related]
12. Low frequency of AXIN2 mutations and high frequency of MUTYH mutations in patients with multiple polyposis.
Lejeune S; Guillemot F; Triboulet JP; Cattan S; Mouton C; ; Porchet N; Manouvrier S; Buisine MP
Hum Mutat; 2006 Oct; 27(10):1064. PubMed ID: 16941501
[TBL] [Abstract][Full Text] [Related]
13. The MUTYH hotspot mutations p.G396D and p.Y179C do not cause substantial genetic susceptibility to biliary cancer.
Casper M; Acalovschi M; Lammert F; Zimmer V
Fam Cancer; 2014 Jun; 13(2):243-7. PubMed ID: 24420788
[TBL] [Abstract][Full Text] [Related]
14. MUTYH hotspot mutations in unselected colonoscopy patients.
Casper M; Plotz G; Juengling B; Zeuzem S; Lammert F; Raedle J
Colorectal Dis; 2012 May; 14(5):e238-44. PubMed ID: 22469480
[TBL] [Abstract][Full Text] [Related]
15. Monoallelic deleterious MUTYH germline variants as a driver for tumorigenesis.
Barreiro RAS; Sabbaga J; Rossi BM; Achatz MIW; Bettoni F; Camargo AA; Asprino PF; A F Galante P
J Pathol; 2022 Feb; 256(2):214-222. PubMed ID: 34816434
[TBL] [Abstract][Full Text] [Related]
16. Spectrum of APC and MUTYH germ-line mutations in Russian patients with colorectal malignancies.
Yanus GA; Akhapkina TA; Ivantsov AO; Preobrazhenskaya EV; Aleksakhina SN; Bizin IV; Sokolenko AP; Mitiushkina NV; Kuligina ES; Suspitsin EN; Venina AR; Holmatov MM; Zaitseva OA; Yatsuk OS; Pashkov DV; Belyaev AM; Togo AV; Imyanitov EN; Iyevleva AG
Clin Genet; 2018 May; 93(5):1015-1021. PubMed ID: 29406563
[TBL] [Abstract][Full Text] [Related]
17. First evidence for digenic inheritance in hereditary colorectal cancer by mutations in the base excision repair genes.
Morak M; Massdorf T; Sykora H; Kerscher M; Holinski-Feder E
Eur J Cancer; 2011 May; 47(7):1046-55. PubMed ID: 21195604
[TBL] [Abstract][Full Text] [Related]
18. Impaired 8-hydroxyguanine repair activity of MUTYH variant p.Arg109Trp found in a Japanese patient with early-onset colorectal cancer.
Shinmura K; Goto M; Tao H; Kato H; Suzuki R; Nakamura S; Matsuda T; Yin G; Morita M; Kono S; Sugimura H
Oxid Med Cell Longev; 2014; 2014():617351. PubMed ID: 24799981
[TBL] [Abstract][Full Text] [Related]
19. Base excision repair deficiency signatures implicate germline and somatic
Thibodeau ML; Zhao EY; Reisle C; Ch'ng C; Wong HL; Shen Y; Jones MR; Lim HJ; Young S; Cremin C; Pleasance E; Zhang W; Holt R; Eirew P; Karasinska J; Kalloger SE; Taylor G; Majounie E; Bonakdar M; Zong Z; Bleile D; Chiu R; Birol I; Gelmon K; Lohrisch C; Mungall KL; Mungall AJ; Moore R; Ma YP; Fok A; Yip S; Karsan A; Huntsman D; Schaeffer DF; Laskin J; Marra MA; Renouf DJ; Jones SJM; Schrader KA
Cold Spring Harb Mol Case Stud; 2019 Apr; 5(2):. PubMed ID: 30833417
[TBL] [Abstract][Full Text] [Related]
20. Loss of MUTYH function in human cells leads to accumulation of oxidative damage and genetic instability.
Ruggieri V; Pin E; Russo MT; Barone F; Degan P; Sanchez M; Quaia M; Minoprio A; Turco E; Mazzei F; Viel A; Bignami M
Oncogene; 2013 Sep; 32(38):4500-8. PubMed ID: 23108399
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
