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Items: 1 to 20 of 152

1.

Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC.

Laken SJ, Petersen GM, Gruber SB, Oddoux C, Ostrer H, Giardiello FM, Hamilton SR, Hampel H, Markowitz A, Klimstra D, Jhanwar S, Winawer S, Offit K, Luce MC, Kinzler KW, Vogelstein B.

Nat Genet. 1997 Sep;17(1):79-83.

PMID:
9288102
2.

A search for germline APC mutations in early onset colorectal cancer or familial colorectal cancer with normal DNA mismatch repair.

Boardman LA, Schmidt S, Lindor NM, Burgart LJ, Cunningham JM, Price-Troska T, Snow K, Ahlquist DA, Thibodeau SN.

Genes Chromosomes Cancer. 2001 Feb;30(2):181-6.

PMID:
11135435
3.
4.

[Hereditary colorectal cancer: Molecular analysis of APC and MLH1 genes].

Bellolio R F, Alvarez V K, De la Fuente L M, León G F, Fullerton M DA, Soto D G, Carvallo de S Q P, López-Köstner F.

Rev Med Chil. 2006 Jul;134(7):841-8. Epub 2006 Aug 29. Spanish.

5.

Molecular genetic analysis of exons 1 to 6 of the APC gene in non-polyposis familial colorectal cancer.

Joyce JA, Froggatt NJ, Davies R, Evans DG, Trembath R, Barton DE, Maher ER.

Clin Genet. 1995 Dec;48(6):299-303.

PMID:
8835324
6.

[Hereditary colorectal cancer].

Park JG, Kim IJ.

Korean J Gastroenterol. 2005 Feb;45(2):78-87. Review. Korean.

7.
8.

Familial microsatellite-stable non-polyposis colorectal cancer: incidence and characteristics in a clinic-based population.

Rovella V, Carrara S, Crucitti SC, Coco C, Magistrelli P, Lucci-Cordisco E, Anti M, Neri G, Genuardi M.

Ann Oncol. 2001 Jun;12(6):813-8.

9.

Report of a family segregating mutations in both the APC and MSH2 genes: juvenile onset of colorectal cancer in a double heterozygote.

Uhrhammer N, Bignon YJ.

Int J Colorectal Dis. 2008 Nov;23(11):1131-5. doi: 10.1007/s00384-008-0526-9. Epub 2008 Jul 16.

PMID:
18629513
10.

The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population.

Foulkes WD, Thiffault I, Gruber SB, Horwitz M, Hamel N, Lee C, Shia J, Markowitz A, Figer A, Friedman E, Farber D, Greenwood CM, Bonner JD, Nafa K, Walsh T, Marcus V, Tomsho L, Gebert J, Macrae FA, Gaff CL, Paillerets BB, Gregersen PK, Weitzel JN, Gordon PH, MacNamara E, King MC, Hampel H, De La Chapelle A, Boyd J, Offit K, Rennert G, Chong G, Ellis NA.

Am J Hum Genet. 2002 Dec;71(6):1395-412. Epub 2002 Nov 26.

11.

Adenomatous polyposis coli I1307K mutation in Jewish patients with different ethnicity: prevalence and phenotype.

Drucker L, Shpilberg O, Neumann A, Shapira J, Stackievicz R, Beyth Y, Yarkoni S.

Cancer. 2000 Feb 15;88(4):755-60.

PMID:
10679643
12.

Molecular and clinical study of familial adenomatous polyposis for genetic testing and management.

Li G, Tamura K, Yamamoto Y, Sashio H, Utsunomiya J, Yamamura T, Shimoyama T, Furuyama J.

J Exp Clin Cancer Res. 1999 Dec;18(4):519-29. Erratum in: J Exp Clin Cancer Res 2000 Mar;19(1):126.

PMID:
10746979
13.

Genetic testing and counseling for hereditary forms of colorectal cancer.

Petersen GM, Brensinger JD, Johnson KA, Giardiello FM.

Cancer. 1999 Dec 1;86(11 Suppl):2540-50. Review.

PMID:
10630180
14.

Multistep carcinogenesis in colorectal cancers.

Takami K, Yana I, Kurahashi H, Nishisho I.

Southeast Asian J Trop Med Public Health. 1995;26 Suppl 1:190-6. Review.

PMID:
8629105
15.

APC haploinsufficiency, but not CTNNB1 or CDH1 gene mutations, accounts for a fraction of familial adenomatous polyposis patients without APC truncating mutations.

Venesio T, Balsamo A, Rondo-Spaudo M, Varesco L, Risio M, Ranzani GN.

Lab Invest. 2003 Dec;83(12):1859-66.

PMID:
14691304
16.

Genetic analyses in consecutive israeli jewish colorectal cancer patients.

Fidder HH, Figer A, Geva R, Flex D, Schayek H, Avidan B, Meir SB, Friedman E.

Am J Gastroenterol. 2005 Jun;100(6):1376-80.

PMID:
15929773
17.

Mouse models for colorectal cancer.

Heyer J, Yang K, Lipkin M, Edelmann W, Kucherlapati R.

Oncogene. 1999 Sep 20;18(38):5325-33. Review.

18.

[Genetics of colorectal cancer. I. Non-polyposis and polyposis forms of hereditary colorectal cancer].

Menko FH, Griffioen G, Wijnen JT, Tops CM, Fodde R, Vasen HF.

Ned Tijdschr Geneeskd. 1999 Jun 5;143(23):1201-6. Review. Dutch.

PMID:
10389534
19.

[Familial cancer: recent advances].

Baba S.

Gan To Kagaku Ryoho. 1999 May;26(6):735-43. Review. Japanese.

PMID:
10410140
20.

Regionally clustered APC mutations are associated with a severe phenotype and occur at a high frequency in new mutation cases of adenomatous polyposis coli.

Gayther SA, Wells D, SenGupta SB, Chapman P, Neale K, Tsioupra K, Delhanty JD.

Hum Mol Genet. 1994 Jan;3(1):53-6.

PMID:
8162051
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