Le Beau MM - Search Results

1

Increased genetic instability of the common fragile site at 3p14 after integration of exogenous DNA.

Rassool FV, Le Beau MM, Neilly ME, van Melle E, Espinosa R 3rd, McKeithan TW. Rassool FV, et al. Among authors: le beau mm. Am J Hum Genet. 1992 Jun;50(6):1243-51. Am J Hum Genet. 1992. PMID: 1317992 Free PMC article.

2

Identification of unstable sequences within the common fragile site at 3p14.2: implications for the mechanism of deletions within fragile histidine triad gene/common fragile site at 3p14.2 in tumors.

Corbin S, Neilly ME, Espinosa R 3rd, Davis EM, McKeithan TW, Le Beau MM. Corbin S, et al. Among authors: le beau mm. Cancer Res. 2002 Jun 15;62(12):3477-84. Cancer Res. 2002. PMID: 12067991

3

Localization of the Chinese hamster MHC locus to chromosome 1q17-->q18 by fluorescence in situ hybridization.

Rassool FV, Neilly ME, McGuire KL, McKeithan TW, Le Beau MM. Rassool FV, et al. Among authors: le beau mm. Cytogenet Cell Genet. 1995;71(1):62-3. doi: 10.1159/000134064. Cytogenet Cell Genet. 1995. PMID: 7606930

4

Direct cloning of DNA sequences from the common fragile site region at chromosome band 3p14.2.

Rassool FV, Le Beau MM, Shen ML, Neilly ME, Espinosa R 3rd, Ong ST, Boldog F, Drabkin H, McCarroll R, McKeithan TW. Rassool FV, et al. Among authors: le beau mm. Genomics. 1996 Jul 1;35(1):109-17. doi: 10.1006/geno.1996.0329. Genomics. 1996. PMID: 8661111

5

Precise localization of the FHIT gene to the common fragile site at 3p14.2 (FRA3B) and characterization of homozygous deletions within FRA3B that affect FHIT transcription in tumor cell lines.

Ong ST, Fong KM, Bader SA, Minna JD, Le Beau MM, McKeithan TW, Rassool FV. Ong ST, et al. Among authors: le beau mm. Genes Chromosomes Cancer. 1997 Sep;20(1):16-23. doi: 10.1002/(sici)1098-2264(199709)20:1<16::aid-gcc3>3.0.co;2-c. Genes Chromosomes Cancer. 1997. PMID: 9290949

6

Replication of a common fragile site, FRA3B, occurs late in S phase and is delayed further upon induction: implications for the mechanism of fragile site induction.

Le Beau MM, Rassool FV, Neilly ME, Espinosa R 3rd, Glover TW, Smith DI, McKeithan TW. Le Beau MM, et al. Hum Mol Genet. 1998 Apr;7(4):755-61. doi: 10.1093/hmg/7.4.755. Hum Mol Genet. 1998. PMID: 9499431

7

An FHIT tumor suppressor gene?

Le Beau MM, Drabkin H, Glover TW, Gemmill R, Rassool FV, McKeithan TW, Smith DI. Le Beau MM, et al. Genes Chromosomes Cancer. 1998 Apr;21(4):281-9. doi: 10.1002/(sici)1098-2264(199804)21:4<281::aid-gcc1>3.0.co;2-v. Genes Chromosomes Cancer. 1998. PMID: 9559339 Review.

8

Preferential integration of marker DNA into the chromosomal fragile site at 3p14: an approach to cloning fragile sites.

Rassool FV, McKeithan TW, Neilly ME, van Melle E, Espinosa R 3rd, Le Beau MM. Rassool FV, et al. Among authors: le beau mm. Proc Natl Acad Sci U S A. 1991 Aug 1;88(15):6657-61. doi: 10.1073/pnas.88.15.6657. Proc Natl Acad Sci U S A. 1991. PMID: 1862089 Free PMC article.

9

An (8;14)(q24;q11) translocation involving the T-cell receptor alpha-chain gene and the MYC oncogene 3' region in a B-cell lymphoma.

Park JK, McKeithan TW, Le Beau MM, Bitter MA, Franklin WA, Rowley JD, Diaz MO. Park JK, et al. Among authors: le beau mm. Genes Chromosomes Cancer. 1989 Sep;1(1):15-22. doi: 10.1002/gcc.2870010105. Genes Chromosomes Cancer. 1989. PMID: 2535034

10

Regional localization of the human thrombomodulin gene to 20p12-cen.

Espinosa R 3rd, Sadler JE, Le Beau MM. Espinosa R 3rd, et al. Among authors: le beau mm. Genomics. 1989 Oct;5(3):649-50. doi: 10.1016/0888-7543(89)90038-4. Genomics. 1989. PMID: 2559025 No abstract available.

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