420 related articles for article (PubMed ID: 10375116)
1. Deletion analysis of the adenomatous polyposis coli and PTCH gene loci in patients with sporadic and nevoid basal cell carcinoma syndrome-associated medulloblastoma.
Vortmeyer AO; Stavrou T; Selby D; Li G; Weil RJ; Park WS; Moon YW; Chandra R; Goldstein AM; Zhuang Z
Cancer; 1999 Jun; 85(12):2662-7. PubMed ID: 10375116
[TBL] [Abstract][Full Text] [Related]
2. Correlation of loss of heterozygosity at chromosome 9q with histological subtype in medulloblastomas.
Schofield D; West DC; Anthony DC; Marshal R; Sklar J
Am J Pathol; 1995 Feb; 146(2):472-80. PubMed ID: 7856756
[TBL] [Abstract][Full Text] [Related]
3. Mutations in the human homologue of the Drosophila segment polarity gene patched (PTCH) in sporadic basal cell carcinomas of the skin and primitive neuroectodermal tumors of the central nervous system.
Wolter M; Reifenberger J; Sommer C; Ruzicka T; Reifenberger G
Cancer Res; 1997 Jul; 57(13):2581-5. PubMed ID: 9205058
[TBL] [Abstract][Full Text] [Related]
4. Somatic mutations in the human homologue of Drosophila patched in primitive neuroectodermal tumours.
Vorechovský I; Tingby O; Hartman M; Strömberg B; Nister M; Collins VP; Toftgård R
Oncogene; 1997 Jul; 15(3):361-6. PubMed ID: 9233770
[TBL] [Abstract][Full Text] [Related]
5. Deletions of AXIN1, a component of the WNT/wingless pathway, in sporadic medulloblastomas.
Dahmen RP; Koch A; Denkhaus D; Tonn JC; Sörensen N; Berthold F; Behrens J; Birchmeier W; Wiestler OD; Pietsch T
Cancer Res; 2001 Oct; 61(19):7039-43. PubMed ID: 11585731
[TBL] [Abstract][Full Text] [Related]
6. Nevoid basal cell carcinoma syndrome: relation with desmoplastic medulloblastoma in infancy. A population-based study and review of the literature.
Amlashi SF; Riffaud L; Brassier G; Morandi X
Cancer; 2003 Aug; 98(3):618-24. PubMed ID: 12879481
[TBL] [Abstract][Full Text] [Related]
7. Genetic testing for germline mutations of the APC gene in patients with apparently sporadic desmoid tumors but a family history of colorectal carcinoma.
Brueckl WM; Ballhausen WG; Förtsch T; Günther K; Fiedler W; Gentner B; Croner R; Boxberger F; Kirchner T; Hahn EG; Hohenberger W; Wein A
Dis Colon Rectum; 2005 Jun; 48(6):1275-81. PubMed ID: 15793634
[TBL] [Abstract][Full Text] [Related]
8. The molecular basis of Turcot's syndrome.
Hamilton SR; Liu B; Parsons RE; Papadopoulos N; Jen J; Powell SM; Krush AJ; Berk T; Cohen Z; Tetu B
N Engl J Med; 1995 Mar; 332(13):839-47. PubMed ID: 7661930
[TBL] [Abstract][Full Text] [Related]
9. Mutations in SUFU predispose to medulloblastoma.
Taylor MD; Liu L; Raffel C; Hui CC; Mainprize TG; Zhang X; Agatep R; Chiappa S; Gao L; Lowrance A; Hao A; Goldstein AM; Stavrou T; Scherer SW; Dura WT; Wainwright B; Squire JA; Rutka JT; Hogg D
Nat Genet; 2002 Jul; 31(3):306-10. PubMed ID: 12068298
[TBL] [Abstract][Full Text] [Related]
10. Should children at risk for familial adenomatous polyposis be screened for hepatoblastoma and children with apparently sporadic hepatoblastoma be screened for APC germline mutations?
Aretz S; Koch A; Uhlhaas S; Friedl W; Propping P; von Schweinitz D; Pietsch T
Pediatr Blood Cancer; 2006 Nov; 47(6):811-8. PubMed ID: 16317745
[TBL] [Abstract][Full Text] [Related]
11. Detection of APC gene deletion by double competitive polymerase chain reaction in patients with familial adenomatous polyposis.
Takahashi M; Kikuchi M; Ohkura N; Yaguchi H; Nagamura Y; Ohnami S; Ushiama M; Yoshida T; Sugano K; Iwama T; Kosugi S; Tsukada T
Int J Oncol; 2006 Aug; 29(2):413-21. PubMed ID: 16820884
[TBL] [Abstract][Full Text] [Related]
12. Somatic mutations of the APC gene in sporadic hepatoblastomas.
Oda H; Imai Y; Nakatsuru Y; Hata J; Ishikawa T
Cancer Res; 1996 Jul; 56(14):3320-3. PubMed ID: 8764128
[TBL] [Abstract][Full Text] [Related]
13. Mutation analysis of the adenomatous polyposis coli (APC) gene in northwest Spanish patients with familial adenomatous polyposis (FAP) and sporadic colorectal cancer.
Ruiz-Ponte C; Vega A; Carracedo A; Barros F
Hum Mutat; 2001 Oct; 18(4):355. PubMed ID: 11668620
[TBL] [Abstract][Full Text] [Related]
14. Genotype-phenotype correlations in 19 Dutch cases with APC gene deletions and a literature review.
Nielsen M; Bik E; Hes FJ; Breuning MH; Vasen HF; Bakker E; Tops CM; Weiss MM
Eur J Hum Genet; 2007 Oct; 15(10):1034-42. PubMed ID: 17568392
[TBL] [Abstract][Full Text] [Related]
15. APC mutations in sporadic medulloblastomas.
Huang H; Mahler-Araujo BM; Sankila A; Chimelli L; Yonekawa Y; Kleihues P; Ohgaki H
Am J Pathol; 2000 Feb; 156(2):433-7. PubMed ID: 10666372
[TBL] [Abstract][Full Text] [Related]
16. Medulloblastoma in the nevoid basal-cell carcinoma syndrome: case reports and review of the literature.
Lacombe D; Chateil JF; Fontan D; Battin J
Genet Couns; 1990; 1(3-4):273-7. PubMed ID: 2098052
[TBL] [Abstract][Full Text] [Related]
17. Low prevalence of loss of heterozygosity and SMAD4 mutations in sporadic and familial juvenile polyposis syndrome-associated juvenile polyps.
Fogt F; Brown CA; Badizadegan K; Zimmerman RL; Odze R
Am J Gastroenterol; 2004 Oct; 99(10):2025-31. PubMed ID: 15447767
[TBL] [Abstract][Full Text] [Related]
18. Sporadic medulloblastomas contain oncogenic beta-catenin mutations.
Zurawel RH; Chiappa SA; Allen C; Raffel C
Cancer Res; 1998 Mar; 58(5):896-9. PubMed ID: 9500446
[TBL] [Abstract][Full Text] [Related]
19. Promoter hypermethylation leads to decreased APC mRNA expression in familial polyposis and sporadic colorectal tumours, but does not substitute for truncating mutations.
Segditsas S; Sieber OM; Rowan A; Setien F; Neale K; Phillips RK; Ward R; Esteller M; Tomlinson IP
Exp Mol Pathol; 2008 Dec; 85(3):201-6. PubMed ID: 18977219
[TBL] [Abstract][Full Text] [Related]
20. Refining the relation between 'first hits' and 'second hits' at the APC locus: the 'loose fit' model and evidence for differences in somatic mutation spectra among patients.
Crabtree M; Sieber OM; Lipton L; Hodgson SV; Lamlum H; Thomas HJ; Neale K; Phillips RK; Heinimann K; Tomlinson IP
Oncogene; 2003 Jul; 22(27):4257-65. PubMed ID: 12833148
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
