Davis EM - Search Results

1

Human somatostatin receptor genes: localization of SSTR5 to human chromosome 20p11.2.

Yasuda K, Espinosa R 3rd, Davis EM, Le Beau MM, Bell GI. Yasuda K, et al. Among authors: davis em. Genomics. 1993 Sep;17(3):785-6. doi: 10.1006/geno.1993.1410. Genomics. 1993. PMID: 8244401

2

Assignment of the human ubiquitous receptor gene (UNR) to 19q13.3 using fluorescence in situ hybridization.

Le Beau MM, Song C, Davis EM, Hiipakka RA, Kokontis JM, Liao S. Le Beau MM, et al. Among authors: davis em. Genomics. 1995 Mar 1;26(1):166-8. doi: 10.1016/0888-7543(95)80100-z. Genomics. 1995. PMID: 7782080 No abstract available.

3

Localization of prostate cancer metastasis-suppressor activity on human chromosome 17.

Chekmareva MA, Hollowell CM, Smith RC, Davis EM, LeBeau MM, Rinker-Schaeffer CW. Chekmareva MA, et al. Among authors: davis em. Prostate. 1997 Dec 1;33(4):271-80. doi: 10.1002/(sici)1097-0045(19971201)33:4<271::aid-pros8>3.0.co;2-k. Prostate. 1997. PMID: 9397200

4

Refinement of the smallest commonly deleted segment of chromosome 20 in malignant myeloid diseases and development of a PAC-based physical and transcription map.

Wang PW, Eisenbart JD, Espinosa R 3rd, Davis EM, Larson RA, Le Beau MM. Wang PW, et al. Among authors: davis em. Genomics. 2000 Jul 1;67(1):28-39. doi: 10.1006/geno.2000.6215. Genomics. 2000. PMID: 10945467

5

Identification of novel cryptic translocations involving IGH in B-cell non-Hodgkin's lymphomas.

Gozzetti A, Davis EM, Espinosa R 3rd, Fernald AA, Anastasi J, Le Beau MM. Gozzetti A, et al. Among authors: davis em. Cancer Res. 2002 Oct 1;62(19):5523-7. Cancer Res. 2002. PMID: 12359763

6

TEL and KIP1 define the smallest region of deletions on 12p13 in hematopoietic malignancies.

Sato Y, Suto Y, Pietenpol J, Golub TR, Gilliland DG, Davis EM, Le Beau MM, Roberts JM, Vogelstein B, Rowley JD, et al. Sato Y, et al. Among authors: davis em. Blood. 1995 Aug 15;86(4):1525-33. Blood. 1995. PMID: 7632960 Free article.

7

Alternative splicing of human inwardly rectifying K+ channel ROMK1 mRNA.

Yano H, Philipson LH, Kugler JL, Tokuyama Y, Davis EM, Le Beau MM, Nelson DJ, Bell GI, Takeda J. Yano H, et al. Among authors: davis em. Mol Pharmacol. 1994 May;45(5):854-60. Mol Pharmacol. 1994. PMID: 8190102

8

Variability of 11q23 rearrangements in hematopoietic cell lines identified with fluorescence in situ hybridization.

Kobayashi H, Espinosa R 3rd, Thirman MJ, Davis EM, Diaz MO, Le Beau MM, Rowley JD. Kobayashi H, et al. Among authors: davis em. Blood. 1993 Jun 1;81(11):3027-33. Blood. 1993. PMID: 8499638 Free article.

9

Cytogenetic and molecular delineation of a region of chromosome 7 commonly deleted in malignant myeloid diseases.

Le Beau MM, Espinosa R 3rd, Davis EM, Eisenbart JD, Larson RA, Green ED. Le Beau MM, et al. Among authors: davis em. Blood. 1996 Sep 15;88(6):1930-5. Blood. 1996. PMID: 8822909 Free article.

10

Human mitochondrial enoyl-CoA hydratase gene (ECHS1): structural organization and assignment to chromosome 10q26.2-q26.3.

Janssen U, Davis EM, Le Beau MM, Stoffel W. Janssen U, et al. Among authors: davis em. Genomics. 1997 Mar 15;40(3):470-5. doi: 10.1006/geno.1996.4597. Genomics. 1997. PMID: 9073515

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