Fernald A - Search Results

1

Fluorescence in situ hybridization: a sensitive method for trisomy 8 detection in bone marrow specimens.

Jenkins RB, Le Beau MM, Kraker WJ, Borell TJ, Stalboerger PG, Davis EM, Penland L, Fernald A, Espinosa R 3rd, Schaid DJ, et al. Jenkins RB, et al. Among authors: fernald a. Blood. 1992 Jun 15;79(12):3307-15. Blood. 1992. PMID: 1596571 Free article.

2

Detection of trisomy 12 in chronic lymphocytic leukemia by fluorescence in situ hybridization to interphase cells: a simple and sensitive method.

Anastasi J, Le Beau MM, Vardiman JW, Fernald AA, Larson RA, Rowley JD. Anastasi J, et al. Among authors: fernald aa. Blood. 1992 Apr 1;79(7):1796-801. Blood. 1992. PMID: 1558972 Free article.

3

Haploinsufficiency of EGR1, a candidate gene in the del(5q), leads to the development of myeloid disorders.

Joslin JM, Fernald AA, Tennant TR, Davis EM, Kogan SC, Anastasi J, Crispino JD, Le Beau MM. Joslin JM, et al. Among authors: fernald aa. Blood. 2007 Jul 15;110(2):719-26. doi: 10.1182/blood-2007-01-068809. Epub 2007 Apr 9. Blood. 2007. PMID: 17420284 Free PMC article.

4

Haploinsufficiency of Apc leads to ineffective hematopoiesis.

Wang J, Fernald AA, Anastasi J, Le Beau MM, Qian Z. Wang J, et al. Among authors: fernald aa. Blood. 2010 Apr 29;115(17):3481-8. doi: 10.1182/blood-2009-11-251835. Epub 2010 Jan 11. Blood. 2010. PMID: 20065296 Free PMC article.

5

Inhibition of WNT signaling in the bone marrow niche prevents the development of MDS in the Apc^del/+ MDS mouse model.

Stoddart A, Wang J, Hu C, Fernald AA, Davis EM, Cheng JX, Le Beau MM. Stoddart A, et al. Among authors: fernald aa. Blood. 2017 Jun 1;129(22):2959-2970. doi: 10.1182/blood-2016-08-736454. Epub 2017 Mar 27. Blood. 2017. PMID: 28348148 Free PMC article.

6

Analysis of deletions of the long arm of chromosome 11 in hematologic malignancies with fluorescence in situ hybridization.

Kobayashi H, Espinosa R 3rd, Fernald AA, Begy C, Diaz MO, Le Beau MM, Rowley JD. Kobayashi H, et al. Among authors: fernald aa. Genes Chromosomes Cancer. 1993 Dec;8(4):246-52. doi: 10.1002/gcc.2870080407. Genes Chromosomes Cancer. 1993. PMID: 7512368

7

Do terminal deletions of 11q23 exist? Identification of undetected translocations with fluorescence in situ hybridization.

Kobayashi H, Espinosa R 3rd, Thirman MJ, Fernald AA, Shannon K, Diaz MO, Le Beau MM, Rowley JD. Kobayashi H, et al. Among authors: fernald aa. Genes Chromosomes Cancer. 1993 Aug;7(4):204-8. doi: 10.1002/gcc.2870070404. Genes Chromosomes Cancer. 1993. PMID: 7692945

8

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: fernald aa. Blood. 1993 Jul 15;82(2):547-51. Blood. 1993. PMID: 8329710 Free article.

9

Sequence-independent amplification and labeling of yeast artificial chromosomes for fluorescence in situ hybridization.

Bohlander SK, Espinosa R 3rd, Fernald AA, Rowley JD, Le Beau MM, Díaz MO. Bohlander SK, et al. Among authors: fernald aa. Cytogenet Cell Genet. 1994;65(1-2):108-10. doi: 10.1159/000133612. Cytogenet Cell Genet. 1994. PMID: 8404060

10

Haploinsufficiency of del(5q) genes, Egr1 and Apc, cooperate with Tp53 loss to induce acute myeloid leukemia in mice.

Stoddart A, Fernald AA, Wang J, Davis EM, Karrison T, Anastasi J, Le Beau MM. Stoddart A, et al. Among authors: fernald aa. Blood. 2014 Feb 13;123(7):1069-78. doi: 10.1182/blood-2013-07-517953. Epub 2013 Dec 31. Blood. 2014. PMID: 24381225 Free PMC article.

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