McKeithan TW - Search Results

1

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: mckeithan tw. Cancer Res. 2002 Jun 15;62(12):3477-84. Cancer Res. 2002. PMID: 12067991

2

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: mckeithan tw. Am J Hum Genet. 1992 Jun;50(6):1243-51. Am J Hum Genet. 1992. PMID: 1317992 Free PMC article.

3

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: mckeithan tw. 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.

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: mckeithan tw. 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: mckeithan tw. 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. Among authors: mckeithan tw. 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. Among authors: mckeithan tw. 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

Molecular cloning of the breakpoints of a complex Philadelphia chromosome translocation: identification of a repeated region on chromosome 17.

McKeithan TW, Warshawsky L, Espinosa R 3rd, LeBeau MM. McKeithan TW, et al. Proc Natl Acad Sci U S A. 1992 Jun 1;89(11):4923-7. doi: 10.1073/pnas.89.11.4923. Proc Natl Acad Sci U S A. 1992. PMID: 1594595 Free PMC article.

9

Immunoglobulin gene rearrangements in acute lymphoblastic leukemia with the 9;11 translocation.

Lorenzana AN, Rubin CM, Le Beau MM, Nachman J, Connolly P, Subramanian U, Johnson FL, McKeithan TW. Lorenzana AN, et al. Among authors: mckeithan tw. Genes Chromosomes Cancer. 1991 Jan;3(1):74-7. doi: 10.1002/gcc.2870030113. Genes Chromosomes Cancer. 1991. PMID: 1906342

10

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: mckeithan tw. Genes Chromosomes Cancer. 1989 Sep;1(1):15-22. doi: 10.1002/gcc.2870010105. Genes Chromosomes Cancer. 1989. PMID: 2535034

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