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Items: 1 to 20 of 77

1.

Aspirin suppresses the mutator phenotype associated with hereditary nonpolyposis colorectal cancer by genetic selection.

Rüschoff J, Wallinger S, Dietmaier W, Bocker T, Brockhoff G, Hofstädter F, Fishel R.

Proc Natl Acad Sci U S A. 1998 Sep 15;95(19):11301-6.

2.

Prevalence of germline mutations of hMLH1, hMSH2, hPMS1, hPMS2, and hMSH6 genes in 75 French kindreds with nonpolyposis colorectal cancer.

Wang Q, Lasset C, Desseigne F, Saurin JC, Maugard C, Navarro C, Ruano E, Descos L, Trillet-Lenoir V, Bosset JF, Puisieux A.

Hum Genet. 1999 Jul-Aug;105(1-2):79-85.

PMID:
10480359
3.

Characterization of mutator phenotype in familial colorectal cancer patients not fulfilling amsterdam criteria.

Kim JC, Lee KH, Ka IH, Koo KH, Roh SA, Kim HC, Yu CS, Kim TW, Chang HM, Gong GY, Kim JS.

Clin Cancer Res. 2004 Sep 15;10(18 Pt 1):6159-68.

4.

Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations.

Wijnen J, Khan PM, Vasen H, van der Klift H, Mulder A, van Leeuwen-Cornelisse I, Bakker B, Losekoot M, Møller P, Fodde R.

Am J Hum Genet. 1997 Aug;61(2):329-35.

5.

Transient mismatch repair gene transfection for functional analysis of genetic hMLH1 and hMSH2 variants.

Brieger A, Trojan J, Raedle J, Plotz G, Zeuzem S.

Gut. 2002 Nov;51(5):677-84.

6.

Altered expression of hMSH2 and hMLH1 in tumors with microsatellite instability and genetic alterations in mismatch repair genes.

Thibodeau SN, French AJ, Roche PC, Cunningham JM, Tester DJ, Lindor NM, Moslein G, Baker SM, Liskay RM, Burgart LJ, Honchel R, Halling KC.

Cancer Res. 1996 Nov 1;56(21):4836-40.

7.

Identification of concurrent germ-line mutations in hMSH2 and/or hMLH1 in Japanese hereditary nonpolyposis colorectal cancer kindreds.

Nakahara M, Yokozaki H, Yasui W, Dohi K, Tahara E.

Cancer Epidemiol Biomarkers Prev. 1997 Dec;6(12):1057-64.

8.

Replication error in colorectal carcinoma: association with loss of heterozygosity at mismatch repair loci and clinicopathological variables.

Johannsdottir JT, Bergthorsson JT, Gretarsdottir S, Kristjansson AK, Ragnarsson G, Jonasson JG, Egilsson V, Ingvarsson S.

Anticancer Res. 1999 May-Jun;19(3A):1821-6.

PMID:
10470121
9.

[Aspirin suppresses microsatellite instability].

Wallinger S, Dietmaier W, Beyser K, Bocker T, Hofstädter F, Fishel R, Rüschoff J.

Verh Dtsch Ges Pathol. 1999;83:240-6. German.

PMID:
10714217
10.

Microsatellite instability and mutation of DNA mismatch repair genes in gliomas.

Leung SY, Chan TL, Chung LP, Chan AS, Fan YW, Hung KN, Kwong WK, Ho JW, Yuen ST.

Am J Pathol. 1998 Oct;153(4):1181-8.

11.

Undectable expression of hMLH1 protein in sporadic colorectal cancer with replication error phenotype.

Koike J, Yamada K, Takano S, Kikuchi Y, Hemmi H, Koi M, Tsujita K, Yanagita K, Yoshio T, Shimatake H.

Dis Colon Rectum. 1997 Oct;40(10 Suppl):S23-8.

PMID:
9378008
12.

Hypermethylation of the hMLH1 promoter in colon cancer with microsatellite instability.

Cunningham JM, Christensen ER, Tester DJ, Kim CY, Roche PC, Burgart LJ, Thibodeau SN.

Cancer Res. 1998 Aug 1;58(15):3455-60.

13.

Unbalanced germ-line expression of hMLH1 and hMSH2 alleles in hereditary nonpolyposis colorectal cancer.

Curia MC, Palmirotta R, Aceto G, Messerini L, Verì MC, Crognale S, Valanzano R, Ficari F, Fracasso P, Stigliano V, Tonelli F, Casale V, Guadagni F, Battista P, Mariani-Costantini R, Cama A.

Cancer Res. 1999 Aug 1;59(15):3570-5.

14.

Molecular diagnostics of cancer predisposition: hereditary non-polyposis colorectal carcinoma and mismatch repair defects.

Bocker T, Rüschoff J, Fishel R.

Biochim Biophys Acta. 1999 May 31;1423(3):O1-O10. Review.

PMID:
10382540
15.

Etiology, natural history, management and molecular genetics of hereditary nonpolyposis colorectal cancer (Lynch syndromes): genetic counseling implications.

Lynch HT, Lemon SJ, Karr B, Franklin B, Lynch JF, Watson P, Tinley S, Lerman C, Carter C.

Cancer Epidemiol Biomarkers Prev. 1997 Dec;6(12):987-91.

16.

Novel hMLH1 and hMSH2 germline mutations in African Americans with colorectal cancer.

Weber TK, Chin HM, Rodriguez-Bigas M, Keitz B, Gilligan R, O'Malley L, Urf E, Diba N, Pazik J, Petrelli NJ.

JAMA. 1999 Jun 23-30;281(24):2316-20.

PMID:
10386556
17.

Mismatch repair deficiency in hematological malignancies with microsatellite instability.

Gu L, Cline-Brown B, Zhang F, Qiu L, Li GM.

Oncogene. 2002 Aug 22;21(37):5758-64.

18.
19.

hMLH1, hMSH2 and hMSH6 mutations in hereditary non-polyposis colorectal cancer families from southern Sweden.

Planck M, Koul A, Fernebro E, Borg A, Kristoffersson U, Olsson H, Wenngren E, Mangell P, Nilbert M.

Int J Cancer. 1999 Oct 8;83(2):197-202.

20.

Microsatellite instability and expression of MLH1 and MSH2 in normal and malignant endometrial and ovarian epithelium in hereditary nonpolyposis colorectal cancer family members.

Ichikawa Y, Lemon SJ, Wang S, Franklin B, Watson P, Knezetic JA, Bewtra C, Lynch HT.

Cancer Genet Cytogenet. 1999 Jul 1;112(1):2-8.

PMID:
10432927

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