| The clathrin-binding domain of CALM-AF10 alters the phenotype of myeloid neoplasms in mice. Stoddart A., Tennant T.R., Fernald A.A., Anastasi J., Brodsky F.M., Le Beau M.M.
Oncogene 31:494-506(2012) · Mapped (14) |
| Haploinsufficiency of Apc leads to ineffective hematopoiesis. Wang J., Fernald A.A., Anastasi J., Le Beau M.M., Qian Z.
Blood 115:3481-3488(2010) · Mapped (7) |
| A critical role for Apc in hematopoietic stem and progenitor cell survival. Qian Z., Chen L., Fernald A.A., Williams B.O., Le Beau M.M.
J. Exp. Med. 205:2163-2175(2008) · Mapped (11) |
| Haploinsufficiency of EGR1, a candidate gene in the del(5q), leads to the development of myeloid disorders. Joslin J.M., Fernald A.A., Tennant T.R., Davis E.M., Kogan S.C., Anastasi J., Crispino J.D., Le Beau M.M.
Blood 110:719-726(2007) · Mapped (13) |
| Transcript map and comparative analysis of the 1.5-Mb commonly deleted segment of human 5q31 in malignant myeloid diseases with a del(5q). Lai F., Godley L.A., Joslin J., Fernald A.A., Liu J., Espinosa R. III, Zhao N., Pamintuan L., Till B.G., Larson R.A. et al.
Genomics 71:235-245(2001) · UniProtKB (1) |
| cDNA cloning and genomic structure of three genes localized to human chromosome band 5q31 encoding potential nuclear proteins. Lai F., Godley L.A., Fernald A.A., Orelli B.J., Pamintuan L., Zhao N., Le Beau M.M.
Genomics 70:123-130(2000) · UniProtKB (3) |
| Molecular characterization of KLHL3, a human homologue of the Drosophila kelch gene. Lai F., Orelli B.J., Till B.G., Godley L.A., Fernald A.A., Pamintuan L., Le Beau M.M.
Genomics 66:65-75(2000) · UniProtKB (1) |
| cDNA cloning, expression pattern, genomic structure and chromosomal location of RAB6KIFL, a human kinesin-like gene. Lai F., Fernald A.A., Zhao N., Le Beau M.M.
Gene 248:117-125(2000) · UniProtKB (1) |
| Human CDC23: cDNA cloning, mapping to 5q31, genomic structure, and evaluation as a candidate tumor suppressor gene in myeloid leukemias. Zhao N., Lai F., Fernald A.A., Eisenbart J.D., Espinosa R., Wang P.W., Le Beau M.M.
Genomics 53:184-190(1998) · UniProtKB (1) · Mapped (1) |
| Identification and characterization of the gene encoding a second proteolipid subunit of human vacuolar H(+)-ATPase (ATP6F). Nishigori H., Yamada S., Tomura H., Fernald A.A., le Beau M.M., Takeuchi T., Takeda J.
Genomics 50:222-228(1998) · UniProtKB (1) · Mapped (1) |
| Comparison of the human and mouse genes encoding the telomeric protein, TRF1: chromosomal localization, expression and conserved protein domains. Broccoli D., Chong L., Oelmann S., Fernald A.A., Marziliano N., van Steensel B., Kipling D., le Beau M.M., de Lange T.
Hum. Mol. Genet. 6:69-76(1997) · UniProtKB (1) · Mapped (2) |
| Sequence of human hexokinase III cDNA and assignment of the human hexokinase III gene (HK3) to chromosome band 5q35.2 by fluorescence in situ hybridization. Furuta H., Nishi S., Le Beau M.M., Fernald A.A., Yano H., Bell G.I.
Genomics 36:206-209(1996) · UniProtKB (1) |
| Structural organization and mapping of the human mitochondrial glycerol phosphate dehydrogenase-encoding gene and pseudogene. Brown L.J., Stoffel M., Moran S.M., Fernald A.A., Lehn D.A., LeBeau M.M., MacDonald M.J.
Gene 172:309-312(1996) · UniProtKB (1) · Mapped (1) |
| The human gene CGT encoding the UDP-galactose ceramide galactosyl transferase (cerebroside synthase): cloning, characterization, and assignment to human chromosome 4, band q26. Bosio A., Binczek E., Lebeau M.M., Fernald A.A., Stoffel W.
Genomics 34:69-75(1996) · UniProtKB (1) |
| Localization of the glucagon receptor gene to human chromosome band 17q25. Menzel S., Stoffel M., Espinosa R. III, Fernald A.A., Le Beau M.M., Bell G.I.
Genomics 20:327-328(1994) · UniProtKB (1) |
| Human fructose-1,6-bisphosphatase gene (FBP1): exon-intron organization, localization to chromosome bands 9q22.2-q22.3, and mutation screening in subjects with fructose-1,6-bisphosphatase deficiency. El-Maghrabi M.R., Lang A.J., Jiang W., Yamagata K., Stoffel M., Takeda J., Fernald A.A., le Beau M.M., Bell G.I., Baker L. et al.
Genomics 27:520-525(1995) · UniProtKB (1) |
| Receptor tyrosine kinase specific for the skeletal muscle lineage: expression in embryonic muscle, at the neuromuscular junction, and after injury. Valenzuela D.M., Stitt T.N., DiStefano P.S., Rojas E., Mattsson K., Compton D.L., Nunez L., Park J.S., Stark J.L., Gies D.R. et al.
Neuron 15:573-584(1995) · UniProtKB (2) · Mapped (27) |
