Mai M - Search Results

1

p73 mutations are not detected in sporadic and hereditary breast cancer.

Schwartz DI, Lindor NM, Walsh-Vockley C, Roche PC, Mai M, Smith DI, Liu W, Couch FJ. Schwartz DI, et al. Among authors: mai m. Breast Cancer Res Treat. 1999 Nov;58(1):25-9. doi: 10.1023/a:1006237031070. Breast Cancer Res Treat. 1999. PMID: 10634515

2

Activation of p73 silent allele in lung cancer.

Mai M, Yokomizo A, Qian C, Yang P, Tindall DJ, Smith DI, Liu W. Mai M, et al. Cancer Res. 1998 Jun 1;58(11):2347-9. Cancer Res. 1998. PMID: 9622072

3

Genomic organization and mutation analysis of p73 in oligodendrogliomas with chromosome 1 p-arm deletions.

Mai M, Huang H, Reed C, Qian C, Smith JS, Alderete B, Jenkins R, Smith DI, Liu W. Mai M, et al. Genomics. 1998 Aug 1;51(3):359-63. doi: 10.1006/geno.1998.5387. Genomics. 1998. PMID: 9721206

4

Loss of imprinting and allele switching of p73 in renal cell carcinoma.

Mai M, Qian C, Yokomizo A, Tindall DJ, Bostwick D, Polychronakos C, Smith DI, Liu W. Mai M, et al. Oncogene. 1998 Oct 1;17(13):1739-41. doi: 10.1038/sj.onc.1202099. Oncogene. 1998. PMID: 9796703

5

Overexpression of the wild type p73 gene in human bladder cancer.

Yokomizo A, Mai M, Tindall DJ, Cheng L, Bostwick DG, Naito S, Smith DI, Liu W. Yokomizo A, et al. Among authors: mai m. Oncogene. 1999 Feb 25;18(8):1629-33. doi: 10.1038/sj.onc.1202474. Oncogene. 1999. PMID: 10102633

6

Mutation and expression analysis of the p73 gene in prostate cancer.

Yokomizo A, Mai M, Bostwick DG, Tindall DJ, Qian J, Cheng L, Jenkins RB, Smith DI, Liu W. Yokomizo A, et al. Among authors: mai m. Prostate. 1999 May;39(2):94-100. doi: 10.1002/(sici)1097-0045(19990501)39:2<94::aid-pros3>3.0.co;2-w. Prostate. 1999. PMID: 10221564

7

Differential expression and allelotyping of the p73 gene in neuroblastoma.

Liu W, Mai M, Yokomizo A, Qian C, Tindall DJ, Smith DI, Thibodeau SN. Liu W, et al. Among authors: mai m. Int J Oncol. 2000 Jan;16(1):181-5. Int J Oncol. 2000. PMID: 10601564

8

Cloning of the human homolog of conductin (AXIN2), a gene mapping to chromosome 17q23-q24.

Mai M, Qian C, Yokomizo A, Smith DI, Liu W. Mai M, et al. Genomics. 1999 Feb 1;55(3):341-4. doi: 10.1006/geno.1998.5650. Genomics. 1999. PMID: 10049590

9

Mutations in AXIN2 cause colorectal cancer with defective mismatch repair by activating beta-catenin/TCF signalling.

Liu W, Dong X, Mai M, Seelan RS, Taniguchi K, Krishnadath KK, Halling KC, Cunningham JM, Boardman LA, Qian C, Christensen E, Schmidt SS, Roche PC, Smith DI, Thibodeau SN. Liu W, et al. Among authors: mai m. Nat Genet. 2000 Oct;26(2):146-7. doi: 10.1038/79859. Nat Genet. 2000. PMID: 11017067 No abstract available.

10

Genomic structure, chromosome mapping and expression analysis of the human AXIN2 gene.

Dong X, Seelan RS, Qian C, Mai M, Liu W. Dong X, et al. Among authors: mai m. Cytogenet Cell Genet. 2001;93(1-2):26-8. doi: 10.1159/000056942. Cytogenet Cell Genet. 2001. PMID: 11474173

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