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Items: 1 to 20 of 114

1.

Drastic genetic instability of tumors and normal tissues in Turcot syndrome.

Miyaki M, Nishio J, Konishi M, Kikuchi-Yanoshita R, Tanaka K, Muraoka M, Nagato M, Chong JM, Koike M, Terada T, Kawahara Y, Fukutome A, Tomiyama J, Chuganji Y, Momoi M, Utsunomiya J.

Oncogene. 1997 Dec 4;15(23):2877-81.

2.

Germ-line and somatic mutations of the APC gene in patients with Turcot syndrome and analysis of APC mutations in brain tumors.

Mori T, Nagase H, Horii A, Miyoshi Y, Shimano T, Nakatsuru S, Aoki T, Arakawa H, Yanagisawa A, Ushio Y, et al.

Genes Chromosomes Cancer. 1994 Mar;9(3):168-72.

PMID:
7515658
4.

Attenuated familial adenomatous polyposis and Muir-Torre syndrome linked to compound biallelic constitutional MYH gene mutations.

Ponti G, Ponz de Leon M, Maffei S, Pedroni M, Losi L, Di Gregorio C, Gismondi V, Scarselli A, Benatti P, Roncari B, Seidenari S, Pellacani G, Varotti C, Prete E, Varesco L, Roncucci L.

Clin Genet. 2005 Nov;68(5):442-7.

PMID:
16207212
5.
6.

Nine novel APC mutations in Italian FAP patients.

Resta N, Stella A, Susca F, Montera M, Gentile M, Cariola F, Prete F, Tenconi R, Tibiletti MG, Logrieco G, Mattina T, Andriulli G, Caruso ML, Fiorente P, Russo S, Caputi-Jambrenghi O, Mareni C, Guanti G.

Hum Mutat. 2001 May;17(5):434-5.

PMID:
11317365
7.

Alterations of repeated sequences in 5' upstream and coding regions in colorectal tumors from patients with hereditary nonpolyposis colorectal cancer and Turcot syndrome.

Miyaki M, Iijima T, Shiba K, Aki T, Kita Y, Yasuno M, Mori T, Kuroki T, Iwama T.

Oncogene. 2001 Aug 23;20(37):5215-8.

8.

Analysis of somatic molecular changes, clinicopathological features, family history, and germline mutations in colorectal cancer families: evidence for efficient diagnosis of HNPCC and for the existence of distinct groups of non-HNPCC families.

Johnson V, Lipton LR, Cummings C, Eftekhar Sadat AT, Izatt L, Hodgson SV, Talbot IC, Thomas HJ, Silver AJ, Tomlinson IP.

J Med Genet. 2005 Oct;42(10):756-62. Epub 2005 Mar 23.

9.

Mutations of the adenomatous polyposis coli and p53 genes in a child with Turcot's syndrome.

Barel D, Cohen IJ, Mor C, Stern S, Shapiro R, Shomrat R, Galanti Y, Legum C, Zaizov R, Avigad S.

Cancer Lett. 1998 Oct 23;132(1-2):119-25.

PMID:
10397462
10.

Genetic alterations in a patient with Turcot's syndrome.

Suzui M, Yoshimi N, Hara A, Morishita Y, Tanaka T, Mori H.

Pathol Int. 1998 Feb;48(2):126-33.

PMID:
9589476
11.

The genetics of hereditary colon cancer.

Rustgi AK.

Genes Dev. 2007 Oct 15;21(20):2525-38. Review.

12.

Germline and somatic mutations in exon 15 of the APC gene and K-ras mutations in duodenal adenomas in patients with familial adenomatous polyposis.

Norheim Andersen S, Løvig T, Fausa O, Rognum TO.

Scand J Gastroenterol. 1999 Jun;34(6):611-7.

PMID:
10440612
13.

A germline mutation at the extreme 3' end of the APC gene results in a severe desmoid phenotype and is associated with overexpression of beta-catenin in the desmoid tumor.

Couture J, Mitri A, Lagace R, Smits R, Berk T, Bouchard HL, Fodde R, Alman B, Bapat B.

Clin Genet. 2000 Mar;57(3):205-12.

PMID:
10782927
14.
15.

Germline MUTYH (MYH) mutations in Portuguese individuals with multiple colorectal adenomas.

Isidro G, Laranjeira F, Pires A, Leite J, Regateiro F, Castro e Sousa F, Soares J, Castro C, Giria J, Brito MJ, Medeira A, Teixeira R, Morna H, Gaspar I, Marinho C, Jorge R, Brehm A, Ramos JS, Boavida MG.

Hum Mutat. 2004 Oct;24(4):353-4.

PMID:
15366000
16.

APC gene mutations and colorectal adenomatosis in familial adenomatous polyposis.

Ficari F, Cama A, Valanzano R, Curia MC, Palmirotta R, Aceto G, Esposito DL, Crognale S, Lombardi A, Messerini L, Mariani-Costantini R, Tonelli F, Battista P.

Br J Cancer. 2000 Jan;82(2):348-53.

17.

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; PAFNORD Group, Porchet N, Manouvrier S, Buisine MP.

Hum Mutat. 2006 Oct;27(10):1064.

PMID:
16941501
18.

Analysis of somatic APC mutations in rare extracolonic tumors of patients with familial adenomatous polyposis coli.

Bläker H, Sutter C, Kadmon M, Otto HF, Von Knebel-Doeberitz M, Gebert J, Helmke BM.

Genes Chromosomes Cancer. 2004 Oct;41(2):93-8.

PMID:
15287021
19.

Inactivation of germline mutant APC alleles by attenuated somatic mutations: a molecular genetic mechanism for attenuated familial adenomatous polyposis.

Su LK, Barnes CJ, Yao W, Qi Y, Lynch PM, Steinbach G.

Am J Hum Genet. 2000 Sep;67(3):582-90. Epub 2000 Aug 3.

20.

[Muir-Torre syndrome].

Körber J, Djawari D.

Hautarzt. 2001 Dec;52(12):1107-10. German.

PMID:
11910863

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