247 related articles for article (PubMed ID: 26493165)
1. GREM1 and POLE variants in hereditary colorectal cancer syndromes.
Rohlin A; Eiengård F; Lundstam U; Zagoras T; Nilsson S; Edsjö A; Pedersen J; Svensson J; Skullman S; Karlsson BG; Björk J; Nordling M
Genes Chromosomes Cancer; 2016 Jan; 55(1):95-106. PubMed ID: 26493165
[TBL] [Abstract][Full Text] [Related]
2. POLE and POLD1 screening in 155 patients with multiple polyps and early-onset colorectal cancer.
Esteban-Jurado C; Giménez-Zaragoza D; Muñoz J; Franch-Expósito S; Álvarez-Barona M; Ocaña T; Cuatrecasas M; Carballal S; López-Cerón M; Marti-Solano M; Díaz-Gay M; van Wezel T; Castells A; Bujanda L; Balmaña J; Gonzalo V; Llort G; Ruiz-Ponte C; Cubiella J; Balaguer F; Aligué R; Castellví-Bel S
Oncotarget; 2017 Apr; 8(16):26732-26743. PubMed ID: 28423643
[TBL] [Abstract][Full Text] [Related]
3. Identification of a novel GREM1 duplication in a patient with multiple colon polyps.
McKenna DB; Van Den Akker J; Zhou AY; Ryan L; Leon A; O'Connor R; Shah PD; Rustgi AK; Katona BW
Fam Cancer; 2019 Jan; 18(1):63-66. PubMed ID: 29804199
[TBL] [Abstract][Full Text] [Related]
4. POLE and POLD1 mutations in 529 kindred with familial colorectal cancer and/or polyposis: review of reported cases and recommendations for genetic testing and surveillance.
Bellido F; Pineda M; Aiza G; Valdés-Mas R; Navarro M; Puente DA; Pons T; González S; Iglesias S; Darder E; Piñol V; Soto JL; Valencia A; Blanco I; Urioste M; Brunet J; Lázaro C; Capellá G; Puente XS; Valle L
Genet Med; 2016 Apr; 18(4):325-32. PubMed ID: 26133394
[TBL] [Abstract][Full Text] [Related]
5. Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas.
Spier I; Holzapfel S; Altmüller J; Zhao B; Horpaopan S; Vogt S; Chen S; Morak M; Raeder S; Kayser K; Stienen D; Adam R; Nürnberg P; Plotz G; Holinski-Feder E; Lifton RP; Thiele H; Hoffmann P; Steinke V; Aretz S
Int J Cancer; 2015 Jul; 137(2):320-31. PubMed ID: 25529843
[TBL] [Abstract][Full Text] [Related]
6. Features of Patients With Hereditary Mixed Polyposis Syndrome Caused by Duplication of GREM1 and Implications for Screening and Surveillance.
Lieberman S; Walsh T; Schechter M; Adar T; Goldin E; Beeri R; Sharon N; Baris H; Ben Avi L; Half E; Lerer I; Shirts BH; Pritchard CC; Tomlinson I; King MC; Levy-Lahad E; Peretz T; Goldberg Y
Gastroenterology; 2017 Jun; 152(8):1876-1880.e1. PubMed ID: 28242209
[TBL] [Abstract][Full Text] [Related]
7. New insights into POLE and POLD1 germline mutations in familial colorectal cancer and polyposis.
Valle L; Hernández-Illán E; Bellido F; Aiza G; Castillejo A; Castillejo MI; Navarro M; Seguí N; Vargas G; Guarinos C; Juarez M; Sanjuán X; Iglesias S; Alenda C; Egoavil C; Segura Á; Juan MJ; Rodriguez-Soler M; Brunet J; González S; Jover R; Lázaro C; Capellá G; Pineda M; Soto JL; Blanco I
Hum Mol Genet; 2014 Jul; 23(13):3506-12. PubMed ID: 24501277
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Polymerase proofreading-associated polyposis: a new, dominantly inherited syndrome of hereditary colorectal cancer predisposition.
Church JM
Dis Colon Rectum; 2014 Mar; 57(3):396-7. PubMed ID: 24509466
[TBL] [Abstract][Full Text] [Related]
10. Low frequency of POLD1 and POLE exonuclease domain variants in patients with multiple colorectal polyps.
Elsayed FA; Tops CMJ; Nielsen M; Ruano D; Vasen HFA; Morreau H; J Hes F; van Wezel T
Mol Genet Genomic Med; 2019 Apr; 7(4):e00603. PubMed ID: 30827058
[TBL] [Abstract][Full Text] [Related]
11. Clinicopathological features of a kindred with SCG5-GREM1-associated hereditary mixed polyposis syndrome.
Plesec T; Brown K; Allen C; A Burke C; Church J; Kalady M; LaGuardia L; O'Malley M; Heald B
Hum Pathol; 2017 Feb; 60():75-81. PubMed ID: 27984123
[TBL] [Abstract][Full Text] [Related]
12. Exome sequencing in diagnostic evaluation of colorectal cancer predisposition in young patients.
Tanskanen T; Gylfe AE; Katainen R; Taipale M; Renkonen-Sinisalo L; Mecklin JP; Järvinen H; Tuupanen S; Kilpivaara O; Vahteristo P; Aaltonen LA
Scand J Gastroenterol; 2013 Jun; 48(6):672-8. PubMed ID: 23544471
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Defining the polyposis/colorectal cancer phenotype associated with the Ashkenazi GREM1 duplication: counselling and management recommendations.
Ziai J; Matloff E; Choi J; Kombo N; Materin M; Bale AE
Genet Res (Camb); 2016 Mar; 98():e5. PubMed ID: 26947005
[TBL] [Abstract][Full Text] [Related]
15. POLE and POLD1 germline exonuclease domain pathogenic variants, a rare event in colorectal cancer from the Middle East.
Siraj AK; Bu R; Iqbal K; Parvathareddy SK; Masoodi T; Siraj N; Al-Rasheed M; Kong Y; Ahmed SO; Al-Obaisi KAS; Victoria IG; Arshad M; Al-Dayel F; Abduljabbar A; Ashari LH; Al-Kuraya KS
Mol Genet Genomic Med; 2020 Aug; 8(8):e1368. PubMed ID: 32567205
[TBL] [Abstract][Full Text] [Related]
16. The first mutations in the MYH gene reported in Moroccan colon cancer patients.
Laarabi FZ; Cherkaoui Jaouad I; Baert-Desurmont S; Ouldim K; Ibrahimi A; Kanouni N; Frebourg T; Sefiani A
Gene; 2012 Mar; 496(1):55-8. PubMed ID: 22266422
[TBL] [Abstract][Full Text] [Related]
17. Genome-wide scan identifies a copy number variable region at 3q26 that regulates PPM1L in APC mutation-negative familial colorectal cancer patients.
Thean LF; Loi C; Ho KS; Koh PK; Eu KW; Cheah PY
Genes Chromosomes Cancer; 2010 Feb; 49(2):99-106. PubMed ID: 19847890
[TBL] [Abstract][Full Text] [Related]
18. Scarce evidence of the causal role of germline mutations in UNC5C in hereditary colorectal cancer and polyposis.
Mur P; Sánchez-Cuartielles E; Aussó S; Aiza G; Valdés-Mas R; Pineda M; Navarro M; Brunet J; Urioste M; Lázaro C; Moreno V; Capellá G; Puente XS; Valle L
Sci Rep; 2016 Feb; 6():20697. PubMed ID: 26852919
[TBL] [Abstract][Full Text] [Related]
19. A novel POLE mutation associated with cancers of colon, pancreas, ovaries and small intestine.
Hansen MF; Johansen J; Bjørnevoll I; Sylvander AE; Steinsbekk KS; Sætrom P; Sandvik AK; Drabløs F; Sjursen W
Fam Cancer; 2015 Sep; 14(3):437-48. PubMed ID: 25860647
[TBL] [Abstract][Full Text] [Related]
20. Hereditary mixed polyposis syndrome is caused by a 40-kb upstream duplication that leads to increased and ectopic expression of the BMP antagonist GREM1.
Jaeger E; Leedham S; Lewis A; Segditsas S; Becker M; Cuadrado PR; Davis H; Kaur K; Heinimann K; Howarth K; ; East J; Taylor J; Thomas H; Tomlinson I
Nat Genet; 2012 May; 44(6):699-703. PubMed ID: 22561515
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]