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Results: 1 to 20 of 105

Similar articles for PubMed (Select 8829664)

1.

Somatic mutations of a human mismatch repair gene, hMLH1, in tumors from patients with multiple primary cancers.

Sasaki S, Horii A, Shimada M, Han HJ, Yanagisawa A, Muto T, Nakamura Y.

Hum Mutat. 1996;7(3):275-8. No abstract available.

PMID:
8829664
3.

Clinical features and mismatch repair gene mutation screening in Chinese patients with hereditary nonpolyposis colorectal carcinoma.

Liu SR, Zhao B, Wang ZJ, Wan YL, Huang YT.

World J Gastroenterol. 2004 Sep 15;10(18):2647-51.

5.

Germline and somatic mutation analyses in the DNA mismatch repair gene MLH3: Evidence for somatic mutation in colorectal cancers.

Lipkin SM, Wang V, Stoler DL, Anderson GR, Kirsch I, Hadley D, Lynch HT, Collins FS.

Hum Mutat. 2001 May;17(5):389-96.

PMID:
11317354
6.

A core promoter and a frequent single-nucleotide polymorphism of the mismatch repair gene hMLH1.

Ito E, Yanagisawa Y, Iwahashi Y, Suzuki Y, Nagasaki H, Akiyama Y, Sugano S, Yuasa Y, Maruyama K.

Biochem Biophys Res Commun. 1999 Mar 24;256(3):488-94.

PMID:
10080925
7.

Mismatch repair gene defects contribute to the genetic basis of double primary cancers of the colorectum and endometrium.

Millar AL, Pal T, Madlensky L, Sherman C, Temple L, Mitri A, Cheng H, Marcus V, Gallinger S, Redston M, Bapat B, Narod S.

Hum Mol Genet. 1999 May;8(5):823-9.

8.

Mutational analysis of the hMLH1 gene using an automated two-dimensional DNA typing system.

Sasaki S, Tokino T, Miyatsu T, Muto T, Nakamura Y.

Hum Mutat. 1997;9(2):164-71.

PMID:
9067757
9.

Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer.

Bronner CE, Baker SM, Morrison PT, Warren G, Smith LG, Lescoe MK, Kane M, Earabino C, Lipford J, Lindblom A, et al.

Nature. 1994 Mar 17;368(6468):258-61.

PMID:
8145827
10.

The frequency of hereditary defective mismatch repair in a prospective series of unselected colorectal carcinomas.

Cunningham JM, Kim CY, Christensen ER, Tester DJ, Parc Y, Burgart LJ, Halling KC, McDonnell SK, Schaid DJ, Walsh Vockley C, Kubly V, Nelson H, Michels VV, Thibodeau SN.

Am J Hum Genet. 2001 Oct;69(4):780-90. Epub 2001 Aug 24. Erratum in: Am J Hum Genet 2001 Nov;69(5):1160.

11.

Missense mutations in hMLH1 associated with colorectal cancer.

Liu T, Tannergård P, Hackman P, Rubio C, Kressner U, Lindmark G, Hellgren D, Lambert B, Lindblom A.

Hum Genet. 1999 Nov;105(5):437-41.

PMID:
10598809
12.

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.

13.

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
14.
15.

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.

16.

HNPCC mutations in the human DNA mismatch repair gene hMLH1 influence assembly of hMutLalpha and hMLH1-hEXO1 complexes.

Jäger AC, Rasmussen M, Bisgaard HC, Singh KK, Nielsen FC, Rasmussen LJ.

Oncogene. 2001 Jun 14;20(27):3590-5.

17.

A novel germline mutation of hMLH1 in a patient with hereditary non-polyposis colorectal cancer.

Gonda K, Nomizu T, Fukayama N, Sugano K, Takenosita S.

Jpn J Clin Oncol. 2002 Jun;32(6):215-8.

18.

Germline hMLH1 promoter mutation in a Newfoundland HNPCC kindred.

Green RC, Green AG, Simms M, Pater A, Robb JD, Green JS.

Clin Genet. 2003 Sep;64(3):220-7.

PMID:
12919137
19.

Pathogenicity of the hereditary colorectal cancer mutation hMLH1 del616 linked to shortage of the functional protein.

Raevaara TE, Vaccaro C, Abdel-Rahman WM, Mocetti E, Bala S, Lönnqvist KE, Kariola R, Lynch HT, Peltomäki P, Nyström-Lahti M.

Gastroenterology. 2003 Aug;125(2):501-9.

PMID:
12891553
20.

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.

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