204 related articles for article (PubMed ID: 36502525)
1. AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancer.
Leclerc J; Beaumont M; Vibert R; Pinson S; Vermaut C; Flament C; Lovecchio T; Delattre L; Demay C; Coulet F; Guillerm E; Hamzaoui N; Benusiglio PR; Brahimi A; Cornelis F; Delhomelle H; Fert-Ferrer S; Fournier BPJ; Hovnanian A; Legrand C; Lortholary A; Malka D; Petit F; Saurin JC; Lejeune S; Colas C; Buisine MP
Genes Chromosomes Cancer; 2023 Apr; 62(4):210-222. PubMed ID: 36502525
[TBL] [Abstract][Full Text] [Related]
2. Rare germline variants in the AXIN2 gene in families with colonic polyposis and colorectal cancer.
Chan JM; Clendenning M; Joseland S; Georgeson P; Mahmood K; Walker R; Como J; Joo JE; Preston S; Hutchinson RA; Pope BJ; Metz A; Beard C; Purvis R; Arnold J; Vijay V; Konycheva G; Atkinson N; Parry S; Jenkins MA; Macrae FA; Rosty C; Winship IM; Buchanan DD
Fam Cancer; 2022 Oct; 21(4):399-413. PubMed ID: 34817745
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Phenotypic confirmation of oligodontia, colorectal polyposis and cancer in a family carrying an exon 7 nonsense variant in the AXIN2 gene.
Beard C; Purvis R; Winship IM; Macrae FA; Buchanan DD
Fam Cancer; 2019 Jul; 18(3):311-315. PubMed ID: 30671715
[TBL] [Abstract][Full Text] [Related]
5. Familial colorectal cancer and tooth agenesis caused by an AXIN2 variant: how do we detect families with rare cancer predisposition syndromes?
Jensen JM; Skakkebæk A; Gaustadness M; Sommerlund M; Gjørup H; Ljungmann K; Lautrup CK; Sunde L
Fam Cancer; 2022 Jul; 21(3):325-332. PubMed ID: 34637023
[TBL] [Abstract][Full Text] [Related]
6. A novel AXIN2 germline variant associated with attenuated FAP without signs of oligondontia or ectodermal dysplasia.
Rivera B; Perea J; Sánchez E; Villapún M; Sánchez-Tomé E; Mercadillo F; Robledo M; Benítez J; Urioste M
Eur J Hum Genet; 2014 Mar; 22(3):423-6. PubMed ID: 23838596
[TBL] [Abstract][Full Text] [Related]
7. Case report expanding the germline AXIN2- related phenotype to include olfactory neuroblastoma and gastric adenoma.
Macklin-Mantia SK; Hines SL; Chaichana KL; Donaldson AM; Ko SL; Zhai Q; Samadder NJ; Riegert-Johnson DL
BMC Med Genet; 2020 Aug; 21(1):161. PubMed ID: 32807118
[TBL] [Abstract][Full Text] [Related]
8. Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing.
Rohlin A; Rambech E; Kvist A; Törngren T; Eiengård F; Lundstam U; Zagoras T; Gebre-Medhin S; Borg Å; Björk J; Nilbert M; Nordling M
Fam Cancer; 2017 Apr; 16(2):195-203. PubMed ID: 27696107
[TBL] [Abstract][Full Text] [Related]
9. Genetic Polymorphisms in APC, DVL2, and AXIN1 Are Associated with Susceptibility, Advanced TNM Stage or Tumor Location in Colorectal Cancer.
Rosales-Reynoso MA; Saucedo-Sariñana AM; Contreras-Díaz KB; Márquez-González RM; Barros-Núñez P; Pineda-Razo TD; Marin-Contreras ME; Durán-Anguiano Ó; Gallegos-Arreola MP; Flores-Martínez SE; Sánchez-Corona J
Tohoku J Exp Med; 2019 Nov; 249(3):173-183. PubMed ID: 31723073
[TBL] [Abstract][Full Text] [Related]
10. An AXIN2 Mutant Allele Associated With Predisposition to Colorectal Neoplasia Has Context-Dependent Effects on AXIN2 Protein Function.
Mazzoni SM; Petty EM; Stoffel EM; Fearon ER
Neoplasia; 2015 May; 17(5):463-72. PubMed ID: 26025668
[TBL] [Abstract][Full Text] [Related]
11. different Roles for the axin interactions with the SAMP versus the second twenty amino acid repeat of adenomatous polyposis coli.
Schneikert J; Ruppert JG; Behrens J; Wenzel EM
PLoS One; 2014; 9(4):e94413. PubMed ID: 24722208
[TBL] [Abstract][Full Text] [Related]
12. Paired Somatic-Germline Testing of 15 Polyposis and Colorectal Cancer-Predisposing Genes Highlights the Role of APC Mosaicism in de Novo Familial Adenomatous Polyposis.
Rofes P; González S; Navarro M; Moreno-Cabrera JM; Solanes A; Darder E; Carrasco E; Iglesias S; Salinas M; Gómez C; Velasco À; Tuset N; Varela M; Llort G; Ramon Y Cajal T; Grau È; Dueñas N; de la Ossa Merlano N; Matías-Guiu X; Rivera B; Balmaña J; Pineda M; Brunet J; Capellá G; Del Valle J; Lázaro C
J Mol Diagn; 2021 Nov; 23(11):1452-1459. PubMed ID: 34454113
[TBL] [Abstract][Full Text] [Related]
13. Update on genetic predisposition to colorectal cancer and polyposis.
Valle L; de Voer RM; Goldberg Y; Sjursen W; Försti A; Ruiz-Ponte C; Caldés T; Garré P; Olsen MF; Nordling M; Castellvi-Bel S; Hemminki K
Mol Aspects Med; 2019 Oct; 69():10-26. PubMed ID: 30862463
[TBL] [Abstract][Full Text] [Related]
14. miR-155 Is Downregulated in Familial Adenomatous Polyposis and Modulates WNT Signaling by Targeting AXIN1 and TCF4.
Prossomariti A; Piazzi G; D'Angelo L; Miccoli S; Turchetti D; Alquati C; Montagna C; Bazzoli F; Ricciardiello L
Mol Cancer Res; 2018 Dec; 16(12):1965-1976. PubMed ID: 30072583
[TBL] [Abstract][Full Text] [Related]
15. [Mechanism of Wnt signaling pathway regulation by a truncated mutant of Axin2 in colorectal cancer].
Wang FW; Wen L; Zhu SW; Yao Q; Cai YM; Ma G
Ai Zheng; 2007 Oct; 26(10):1041-6. PubMed ID: 17927870
[TBL] [Abstract][Full Text] [Related]
16. Germline mutations of the adenomatous polyposis coli (APC) gene in Algerian familial adenomatous polyposis cohort: first report.
Khider F; Cherbal F; Boumehdi AL; Layaida K; Mahfouf H; Zebboudj F; Maaoui M
Mol Biol Rep; 2022 May; 49(5):3823-3837. PubMed ID: 35142982
[TBL] [Abstract][Full Text] [Related]
17. Germline variation in the oxidative DNA repair genes NUDT1 and OGG1 is not associated with hereditary colorectal cancer or polyposis.
Mur P; Jemth AS; Bevc L; Amaral N; Navarro M; Valdés-Mas R; Pons T; Aiza G; Urioste M; Valencia A; Lázaro C; Moreno V; Puente XS; Stenmark P; Warpman-Berglund U; Capellá G; Helleday T; Valle L
Hum Mutat; 2018 Sep; 39(9):1214-1225. PubMed ID: 29900613
[TBL] [Abstract][Full Text] [Related]
18. APC germline mutations in individuals being evaluated for familial adenomatous polyposis: a review of the Mayo Clinic experience with 1591 consecutive tests.
Kerr SE; Thomas CB; Thibodeau SN; Ferber MJ; Halling KC
J Mol Diagn; 2013 Jan; 15(1):31-43. PubMed ID: 23159591
[TBL] [Abstract][Full Text] [Related]
19. Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis.
Spier I; Kerick M; Drichel D; Horpaopan S; Altmüller J; Laner A; Holzapfel S; Peters S; Adam R; Zhao B; Becker T; Lifton RP; Holinski-Feder E; Perner S; Thiele H; Nöthen MM; Hoffmann P; Timmermann B; Schweiger MR; Aretz S
Fam Cancer; 2016 Apr; 15(2):281-8. PubMed ID: 26780541
[TBL] [Abstract][Full Text] [Related]
20. Role of rare variants in undetermined multiple adenomatous polyposis and early-onset colorectal cancer.
Lefevre JH; Bonilla C; Colas C; Winney B; Johnstone E; Tonks S; Day T; Hutnik K; Boumertit A; Soubrier F; Midgley R; Kerr D; Parc Y; Bodmer WF
J Hum Genet; 2012 Nov; 57(11):709-716. PubMed ID: 22875147
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]