Davis E - Search Results

1

A consistent pattern of RIN1 rearrangements in oral squamous cell carcinoma cell lines supports a breakage-fusion-bridge cycle model for 11q13 amplification.

Shuster MI, Han L, Le Beau MM, Davis E, Sawicki M, Lese CM, Park NH, Colicelli J, Gollin SM. Shuster MI, et al. Among authors: davis e. Genes Chromosomes Cancer. 2000 Jun;28(2):153-63. Genes Chromosomes Cancer. 2000. PMID: 10825000

2

Refinement of the commonly deleted segment in myeloid leukemias with a del(20q).

Wang PW, Iannantuoni K, Davis EM, Espinosa R 3rd, Stoffel M, Le Beau MM. Wang PW, et al. Among authors: davis em. Genes Chromosomes Cancer. 1998 Feb;21(2):75-81. Genes Chromosomes Cancer. 1998. PMID: 9491317

3

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

4

dic(5;17): a recurring abnormality in malignant myeloid disorders associated with mutations of TP53.

Wang P, Spielberger RT, Thangavelu M, Zhao N, Davis EM, Iannantuoni K, Larson RA, Le Beau MM. Wang P, et al. Among authors: davis em. Genes Chromosomes Cancer. 1997 Nov;20(3):282-91. doi: 10.1002/(sici)1098-2264(199711)20:3<282::aid-gcc9>3.0.co;2-z. Genes Chromosomes Cancer. 1997. PMID: 9365836

5

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

6

t(1;3)(p36;p21) is a recurring therapy-related translocation.

Sato Y, Izumi T, Kanamori H, Davis EM, Miura Y, Larson RA, Le Beau MM, Ozawa K, Rowley JD. Sato Y, et al. Genes Chromosomes Cancer. 2002 Jun;34(2):186-92. doi: 10.1002/gcc.10055. Genes Chromosomes Cancer. 2002. PMID: 11979552

7

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.

8

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. Cancer Res. 2002 Oct 1;62(19):5523-7. Cancer Res. 2002. PMID: 12359763

9

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

10

Identification of a novel metastasis-suppressor region on human chromosome 12.

Luu HH, Zagaja GP, Dubauskas Z, Chen SL, Smith RC, Watabe K, Ichikawa Y, Ichikawa T, Davis EM, Le Beau MM, Rinker-Schaeffer CW. Luu HH, et al. Among authors: davis em. Cancer Res. 1998 Aug 15;58(16):3561-5. Cancer Res. 1998. PMID: 9721861

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