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Cancer Genetics and Cytogenetics|March 1, 1987
Cytogenetic studies of a human medullary thyroid carcinoma cell lineK Tanaka, S B Baylin, B D Nelkin, et al.Cytogenetics and Cell Genetics|January 1, 1996
Chromosome mapping of the mouse Akt2 gene and Akt2 pseudogeneD A Altomare, C A Kozak, G Sonoda, et al.Cytogenetics and Cell Genetics|January 1, 1996
Structures and chromosome locations of the human MEF2A gene and a pseudogene MEF2APE Suzuki, J Lowry, G Sonoda, et al.Science (New York, N.Y.)|October 11, 1991
A retroviral oncogene, akt, encoding a serine-threonine kinase containing an SH2-like regionA Bellacosa, J R Testa, S P Staal, et al.Proceedings of the National Academy of Sciences of the United States of America|August 15, 1993
The 3;21 translocation in myelodysplasia results in a fusion transcript between the AML1 gene and the gene for EAP, a highly conserved protein associated with the Epstein-Barr virus small RNA EBER 1G Nucifora, C R Begy, P Erickson, et al.Genes, Chromosomes & Cancer|April 1, 1997
A t(6;12)(q23;p13) results in the fusion of ETV6 to a novel gene, STL, in a B-cell ALL cell lineY Suto, Y Sato, S D Smith, et al.Nature|November 1, 1984
Evidence for two distinct c-src loci on human chromosomes 1 and 20M M Le Beau, C A Westbrook, M O Diaz, et al.Blood|October 1, 1982
Nonrandom chromosome abnormalities in angioimmunoblastic lymphadenopathyY Kaneko, R A Larson, D Variakojis, et al.Proceedings of the National Academy of Sciences of the United States of America|October 1, 1985
c-src is consistently conserved in the chromosomal deletion (20q) observed in myeloid disordersM M Le Beau, C A Westbrook, M O Diaz, et al.Genomics|December 1, 1994
Molecular cloning and localization of the human GAX gene to 7p21D F LePage, D A Altomare, J R Testa, et al.Pageof 431