Le Beau MM - Search Results

1

Molecular genetics of myeloid leukemia: identification of the commonly deleted segment of chromosome 20.

Roulston D, Espinosa R 3rd, Stoffel M, Bell GI, Le Beau MM. Roulston D, et al. Among authors: le beau mm. Blood. 1993 Dec 1;82(11):3424-9. Blood. 1993. PMID: 8241509 Free article.

2

Interleukin-4 and interleukin-5 map to human chromosome 5 in a region encoding growth factors and receptors and are deleted in myeloid leukemias with a del(5q).

Le Beau MM, Lemons RS, Espinosa R 3rd, Larson RA, Arai N, Rowley JD. Le Beau MM, et al. Blood. 1989 Feb 15;73(3):647-50. Blood. 1989. PMID: 2783863 Free article.

3

Localization of the glucagon receptor gene to human chromosome band 17q25.

Menzel S, Stoffel M, Espinosa R 3rd, Fernald AA, Le Beau MM, Bell GI. Menzel S, et al. Among authors: le beau mm. Genomics. 1994 Mar 15;20(2):327-8. doi: 10.1006/geno.1994.1179. Genomics. 1994. PMID: 8020989

4

Human G-protein-coupled inwardly rectifying potassium channel (GIRK1) gene (KCNJ3): localization to chromosome 2 and identification of a simple tandem repeat polymorphism.

Stoffel M, Espinosa R 3rd, Powell KL, Philipson LH, Le Beau MM, Bell GI. Stoffel M, et al. Among authors: le beau mm. Genomics. 1994 May 1;21(1):254-6. doi: 10.1006/geno.1994.1253. Genomics. 1994. PMID: 8088798

5

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: le beau mm. Genomics. 1993 Sep;17(3):785-6. doi: 10.1006/geno.1993.1410. Genomics. 1993. PMID: 8244401

6

Heterogeneity of breakpoints of 11q23 rearrangements in hematologic malignancies identified with fluorescence in situ hybridization.

Kobayashi H, Espinosa R 3rd, Thirman MJ, Gill HJ, Fernald AA, Diaz MO, Le Beau MM, Rowley JD. Kobayashi H, et al. Among authors: le beau mm. Blood. 1993 Jul 15;82(2):547-51. Blood. 1993. PMID: 8329710 Free article.

7

Human glucagon-like peptide-1 receptor gene. Localization to chromosome band 6p21 by fluorescence in situ hybridization and linkage of a highly polymorphic simple tandem repeat DNA polymorphism to other markers on chromosome 6.

Stoffel M, Espinosa R 3rd, Le Beau MM, Bell GI. Stoffel M, et al. Among authors: le beau mm. Diabetes. 1993 Aug;42(8):1215-8. doi: 10.2337/diab.42.8.1215. Diabetes. 1993. PMID: 8392011

8

Involvement of the AML1 gene in the t(3;21) in therapy-related leukemia and in chronic myeloid leukemia in blast crisis.

Nucifora G, Birn DJ, Espinosa R 3rd, Erickson P, LeBeau MM, Roulston D, McKeithan TW, Drabkin H, Rowley JD. Nucifora G, et al. Blood. 1993 May 15;81(10):2728-34. Blood. 1993. PMID: 8490181 Free article.

9

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: le beau mm. Blood. 1993 Jun 1;81(11):3027-33. Blood. 1993. PMID: 8499638 Free article.

10

Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases.

Le Beau MM, Espinosa R 3rd, Neuman WL, Stock W, Roulston D, Larson RA, Keinanen M, Westbrook CA. Le Beau MM, et al. Proc Natl Acad Sci U S A. 1993 Jun 15;90(12):5484-8. doi: 10.1073/pnas.90.12.5484. Proc Natl Acad Sci U S A. 1993. PMID: 8516290 Free PMC article.

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