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Mutation Research|August 1, 1985
Sister-chromatid exchanges in lymphocytes and mutagenicity in urine of nurses handling cytostatic drugsR Barale, G Sozzi, P Toniolo, et al.European Radiology|February 13, 2016
Low-dose computed tomography for lung cancer screening: comparison of performance between annual and biennial screenNicola Sverzellati, M Silva, G Calareso, et al.Giornale Italiano Di Cardiologia|January 1, 1979
[Single vessel coronary disease. I. Differences in clinical and prognostic aspects and in surgical results in isolated lesions of the anterior descending branch and of other coronary branches]L Campolo, G Cataldo, M Ferratini, et al.Blood|March 1, 1992
Molecular cloning of cDNAs for the human granulocyte colony-stimulating factor receptor from HL-60 and mapping of the gene to chromosome region 1p32-34D J Tweardy, K Anderson, L A Cannizzaro, et al.Proceedings of the National Academy of Sciences of the United States of America|August 1, 1982
Chromosomal assignment of the human homologues of feline sarcoma virus and avian myeloblastosis virus onc genesR Dalla-Favera, G Franchini, S Martinotti, et al.Cancer Research|September 15, 1996
ATM mutations in cancer familiesI Vorechovský, L Luo, A Lindblom, et al.Cytogenetics and Cell Genetics|November 27, 1999
Exon structure and promoter identification of STIM1 (alias GOK), a human gene causing growth arrest of the human tumor cell lines G401 and RDS Sabbioni, A Veronese, M Trubia, et al.Proceedings of the National Academy of Sciences of the United States of America|December 10, 1999
Genomic analysis of human and mouse TCL1 loci reveals a complex of tightly clustered genesC Hallas, Y Pekarsky, T Itoyama, et al.Cancer Research|January 15, 1996
Loss of heterozygosity for chromosome 11 in adenocarcinoma of the stomachR Baffa, M Negrini, B Mandes, et al.Cancer Research|July 1, 1995
Seven megabase yeast artificial chromosome contig at region 11p15: identification of a yeast artificial chromosome spanning the breakpoint of a chromosomal translocation found in a case of Beckwith-Wiedemann syndromeM Negrini, S Sabbioni, M Ohta, et al.Pageof 60