Smith DI - Search Results

1

Assignment of the human serotonin 1F receptor gene (HTR1F) to the short arm of chromosome 3 (3p13-p14.1).

Erdmann J, Shimron-Abarbanell D, Shridhar V, Smith DI, Propping P, Nöthen MM. Erdmann J, et al. Among authors: smith di. Mol Membr Biol. 1997 Jul-Sep;14(3):133-5. doi: 10.3109/09687689709048173. Mol Membr Biol. 1997. PMID: 9394293

2

Cloning and characterization of the human t(3;6)(p14;p11) translocation breakpoint associated with hematologic malignancies.

Smith SE, Joseph A, Nadeau S, Shridhar V, Gemmill R, Drabkin H, Knuutila S, Smith DI. Smith SE, et al. Among authors: smith di. Cancer Genet Cytogenet. 1993 Nov;71(1):15-21. doi: 10.1016/0165-4608(93)90197-t. Cancer Genet Cytogenet. 1993. PMID: 8275448

3

A gene from human chromosomal band 3p21.1 encodes a highly conserved arginine-rich protein and is mutated in renal cell carcinomas.

Shridhar V, Rivard S, Shridhar R, Mullins C, Bostick L, Sakr W, Grignon D, Miller OJ, Smith DI. Shridhar V, et al. Among authors: smith di. Oncogene. 1996 May 2;12(9):1931-9. Oncogene. 1996. PMID: 8649854

4

Isolation of two contigs of overlapping cosmids derived from human chromosomal band 3p21.1 and identification of 5 new 3p21.1 genes.

Shridhar V, Golembieski W, Kamat A, Smith SE, Phillips N, Miller OJ, Miller Y, Smith DI. Shridhar V, et al. Among authors: smith se, smith di. Somat Cell Mol Genet. 1994 Jul;20(4):255-65. doi: 10.1007/BF02254716. Somat Cell Mol Genet. 1994. PMID: 7974002

5

Genetic instability of microsatellite sequences in many non-small cell lung carcinomas.

Shridhar V, Siegfried J, Hunt J, del Mar Alonso M, Smith DI. Shridhar V, et al. Among authors: smith di. Cancer Res. 1994 Apr 15;54(8):2084-7. Cancer Res. 1994. PMID: 8174109

6

The human loci DNF15S2 and D3S94 have a high degree of sequence similarity to acyl-peptide hydrolase and are located at 3p21.3.

Ginzinger DG, Shridhar V, Baldini A, Taggart RT, Miller OJ, Smith DI. Ginzinger DG, et al. Among authors: smith di. Am J Hum Genet. 1992 Apr;50(4):826-33. Am J Hum Genet. 1992. PMID: 1550126 Free PMC article.

7

Loss of heterozygosity on the long arm of human chromosome 7 in sporadic renal cell carcinomas.

Shridhar V, Sun QC, Miller OJ, Kalemkerian GP, Petros J, Smith DI. Shridhar V, et al. Among authors: smith di. Oncogene. 1997 Nov 27;15(22):2727-33. doi: 10.1038/sj.onc.1201448. Oncogene. 1997. PMID: 9400999

8

Frequent breakpoints in the region surrounding FRA3B in sporadic renal cell carcinomas.

Shridhar V, Wang L, Rosati R, Paradee W, Shridhar R, Mullins C, Sakr W, Grignon D, Miller OJ, Sun QC, Petros J, Smith DI. Shridhar V, et al. Among authors: smith di. Oncogene. 1997 Mar 20;14(11):1269-77. doi: 10.1038/sj.onc.1201100. Oncogene. 1997. PMID: 9178887

9

Involvement of H-cadherin (CDH13) on 16q in the region of frequent deletion in ovarian cancer.

Kawakami M, Staub J, Cliby W, Hartmann L, Smith DI, Shridhar V. Kawakami M, et al. Among authors: smith di. Int J Oncol. 1999 Oct;15(4):715-20. doi: 10.3892/ijo.15.4.715. Int J Oncol. 1999. PMID: 10493953

10

Cloning and characterization of a senescence inducing and class II tumor suppressor gene in ovarian carcinoma at chromosome region 6q27.

Acquati F, Morelli C, Cinquetti R, Bianchi MG, Porrini D, Varesco L, Gismondi V, Rocchetti R, Talevi S, Possati L, Magnanini C, Tibiletti MG, Bernasconi B, Daidone MG, Shridhar V, Smith DI, Negrini M, Barbanti-Brodano G, Taramelli R. Acquati F, et al. Among authors: smith di. Oncogene. 2001 Feb 22;20(8):980-8. doi: 10.1038/sj.onc.1204178. Oncogene. 2001. PMID: 11314033

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