Fishel R - Search Results

1

Female embryonic lethality in mice nullizygous for both Msh2 and p53.

Cranston A, Bocker T, Reitmair A, Palazzo J, Wilson T, Mak T, Fishel R. Cranston A, et al. Among authors: fishel r. Nat Genet. 1997 Sep;17(1):114-8. doi: 10.1038/ng0997-114. Nat Genet. 1997. PMID: 9288110

2

MutS homologs in mammalian cells.

Fishel R, Wilson T. Fishel R, et al. Curr Opin Genet Dev. 1997 Feb;7(1):105-13. doi: 10.1016/s0959-437x(97)80117-7. Curr Opin Genet Dev. 1997. PMID: 9024626 Review.

3

Mutator phenotype in Msh2-deficient murine embryonic fibroblasts.

Reitmair AH, Risley R, Bristow RG, Wilson T, Ganesh A, Jang A, Peacock J, Benchimol S, Hill RP, Mak TW, Fishel R, Meuth M. Reitmair AH, et al. Among authors: fishel r. Cancer Res. 1997 Sep 1;57(17):3765-71. Cancer Res. 1997. PMID: 9288785

4

Severe attenuation of the B cell immune response in Msh2-deficient mice.

Vora KA, Tumas-Brundage KM, Lentz VM, Cranston A, Fishel R, Manser T. Vora KA, et al. Among authors: fishel r. J Exp Med. 1999 Feb 1;189(3):471-82. doi: 10.1084/jem.189.3.471. J Exp Med. 1999. PMID: 9927509 Free PMC article.

5

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

Bocker T, Rüschoff J, Fishel R. Bocker T, et al. Among authors: fishel r. Biochim Biophys Acta. 1999 May 31;1423(3):O1-O10. doi: 10.1016/s0304-419x(99)00008-6. Biochim Biophys Acta. 1999. PMID: 10382540 Review.

6

Female embryonic lethality in Msh2-Trp53 nullizygous mice is strain dependent.

Cranston A, Fishel R. Cranston A, et al. Among authors: fishel r. Mamm Genome. 1999 Oct;10(10):1020-2. doi: 10.1007/s003359901151. Mamm Genome. 1999. PMID: 10501974 No abstract available.

7

Spontaneous and mutagen-induced transformation of primary cultures of Msh2-/- p53-/- colonocytes.

Sevignani C, Cranston A, Iozzo RV, Fishel R, Calabretta B. Sevignani C, et al. Among authors: fishel r. Cancer Res. 1999 Dec 1;59(23):5882-6. Cancer Res. 1999. PMID: 10606228

8

HNPCC mutations in hMSH2 result in reduced hMSH2-hMSH6 molecular switch functions.

Heinen CD, Wilson T, Mazurek A, Berardini M, Butz C, Fishel R. Heinen CD, et al. Among authors: fishel r. Cancer Cell. 2002 Jun;1(5):469-78. doi: 10.1016/s1535-6108(02)00073-9. Cancer Cell. 2002. PMID: 12124176 Free article.

9

Interactions of human hMSH2 with hMSH3 and hMSH2 with hMSH6: examination of mutations found in hereditary nonpolyposis colorectal cancer.

Guerrette S, Wilson T, Gradia S, Fishel R. Guerrette S, et al. Among authors: fishel r. Mol Cell Biol. 1998 Nov;18(11):6616-23. doi: 10.1128/MCB.18.11.6616. Mol Cell Biol. 1998. PMID: 9774676 Free PMC article.

10

MLH1 promoter methylation and gene silencing is the primary cause of microsatellite instability in sporadic endometrial cancers.

Simpkins SB, Bocker T, Swisher EM, Mutch DG, Gersell DJ, Kovatich AJ, Palazzo JP, Fishel R, Goodfellow PJ. Simpkins SB, et al. Among authors: fishel r. Hum Mol Genet. 1999 Apr;8(4):661-6. doi: 10.1093/hmg/8.4.661. Hum Mol Genet. 1999. PMID: 10072435

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