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Items: 20

1.

Analysis of hMLH1 and hMSH2 gene dosage alterations in hereditary nonpolyposis colorectal cancer patients by novel methods.

Baudhuin LM, Mai M, French AJ, Kruckeberg KE, Swanson RL, Winters JL, Courteau LK, Thibodeau SN.

J Mol Diagn. 2005 May;7(2):226-35.

2.

Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability.

Umar A, Boland CR, Terdiman JP, Syngal S, de la Chapelle A, Rüschoff J, Fishel R, Lindor NM, Burgart LJ, Hamelin R, Hamilton SR, Hiatt RA, Jass J, Lindblom A, Lynch HT, Peltomaki P, Ramsey SD, Rodriguez-Bigas MA, Vasen HF, Hawk ET, Barrett JC, Freedman AN, Srivastava S.

J Natl Cancer Inst. 2004 Feb 18;96(4):261-8.

3.

A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United States.

Lynch HT, Coronel SM, Okimoto R, Hampel H, Sweet K, Lynch JF, Barrows A, Wijnen J, van der Klift H, Franken P, Wagner A, Fodde R, de la Chapelle A.

JAMA. 2004 Feb 11;291(6):718-24.

PMID:
14871915
4.
5.

Clinical significance of early-onset "sporadic" colorectal cancer with microsatellite instability.

Jass JR.

Dis Colon Rectum. 2003 Oct;46(10):1305-9. No abstract available.

PMID:
14530666
6.
7.

Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene.

Wagner A, Barrows A, Wijnen JT, van der Klift H, Franken PF, Verkuijlen P, Nakagawa H, Geugien M, Jaghmohan-Changur S, Breukel C, Meijers-Heijboer H, Morreau H, van Puijenbroek M, Burn J, Coronel S, Kinarski Y, Okimoto R, Watson P, Lynch JF, de la Chapelle A, Lynch HT, Fodde R.

Am J Hum Genet. 2003 May;72(5):1088-100. Epub 2003 Mar 25.

8.

Hereditary colorectal cancer.

Lynch HT, de la Chapelle A.

N Engl J Med. 2003 Mar 6;348(10):919-32. Review. No abstract available.

9.

2002 William Allan Award Address. Inherited human diseases: victories, challenges, disappointments.

de la Chapelle A.

Am J Hum Genet. 2003 Feb;72(2):236-40. No abstract available.

10.

Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approach.

Gille JJ, Hogervorst FB, Pals G, Wijnen JT, van Schooten RJ, Dommering CJ, Meijer GA, Craanen ME, Nederlof PM, de Jong D, McElgunn CJ, Schouten JP, Menko FH.

Br J Cancer. 2002 Oct 7;87(8):892-7.

11.

Allele separation facilitates interpretation of potential splicing alterations and genomic rearrangements.

Nakagawa H, Yan H, Lockman J, Hampel H, Kinzler KW, Vogelstein B, De La Chapelle A.

Cancer Res. 2002 Aug 15;62(16):4579-82.

12.

Immunohistochemistry versus microsatellite instability testing in phenotyping colorectal tumors.

Lindor NM, Burgart LJ, Leontovich O, Goldberg RM, Cunningham JM, Sargent DJ, Walsh-Vockley C, Petersen GM, Walsh MD, Leggett BA, Young JP, Barker MA, Jass JR, Hopper J, Gallinger S, Bapat B, Redston M, Thibodeau SN.

J Clin Oncol. 2002 Feb 15;20(4):1043-8.

PMID:
11844828
13.

The role of hPMS1 and hPMS2 in predisposing to colorectal cancer.

Liu T, Yan H, Kuismanen S, Percesepe A, Bisgaard ML, Pedroni M, Benatti P, Kinzler KW, Vogelstein B, Ponz de Leon M, Peltomäki P, Lindblom A.

Cancer Res. 2001 Nov 1;61(21):7798-802.

14.

Phenotypic analysis of hMSH2 mutations in mouse cells carrying human chromosomes.

Marra G, D'Atri S, Yan H, Perrera C, Cannavo' E, Vogelstein B, Jiricny J.

Cancer Res. 2001 Nov 1;61(21):7719-21.

15.

Conversion of diploidy to haploidy.

Yan H, Papadopoulos N, Marra G, Perrera C, Jiricny J, Boland CR, Lynch HT, Chadwick RB, de la Chapelle A, Berg K, Eshleman JR, Yuan W, Markowitz S, Laken SJ, Lengauer C, Kinzler KW, Vogelstein B.

Nature. 2000 Feb 17;403(6771):723-4. No abstract available.

PMID:
10693791
16.

New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.

Vasen HF, Watson P, Mecklin JP, Lynch HT.

Gastroenterology. 1999 Jun;116(6):1453-6. No abstract available.

PMID:
10348829
17.

A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer.

Boland CR, Thibodeau SN, Hamilton SR, Sidransky D, Eshleman JR, Burt RW, Meltzer SJ, Rodriguez-Bigas MA, Fodde R, Ranzani GN, Srivastava S.

Cancer Res. 1998 Nov 15;58(22):5248-57. Review.

18.

Genetic instability occurs in the majority of young patients with colorectal cancer.

Liu B, Farrington SM, Petersen GM, Hamilton SR, Parsons R, Papadopoulos N, Fujiwara T, Jen J, Kinzler KW, Wyllie AH, Vogelstein B, Dunlop MG, et al.

Nat Med. 1995 Apr;1(4):348-52.

PMID:
7585065
19.

Monoallelic mutation analysis (MAMA) for identifying germline mutations.

Papadopoulos N, Leach FS, Kinzler KW, Vogelstein B.

Nat Genet. 1995 Sep;11(1):99-102.

PMID:
7550326
20.

The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC).

Vasen HF, Mecklin JP, Khan PM, Lynch HT.

Dis Colon Rectum. 1991 May;34(5):424-5. No abstract available.

PMID:
2022152

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