Comparative genomic hybridization reveals previously undescribed amplifications and deletions in the chronic myeloid leukemia-derived K-562 cell line

This publication has 22 references indexed in Scilit:

• Integration of physical, breakpoint and genetic maps of chromosome 22. Localization of 587 yeast artificial chromosomes with 238 mapped markers
  Human Molecular Genetics, 1995
• Identification of cryptic sites of DNA sequence amplification in human breast cancer by chromosome microdissection
  Nature Genetics, 1994
• Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization
  Human Genetics, 1993
• Complete nucleotide sequence of the gene for human heparin cofactor II and mapping to chromosomal band 22q11
  Biochemistry, 1991
• A simple method for DNA purification from peripheral blood
  Analytical Biochemistry, 1988
• Linear order of the four BCR-related loci in 22q11
  Genomics, 1988
• The chronic myelocytic cell line K562 contains a breakpoint in bcr and produces a chimeric bcr/c-abl transcript.
  Molecular and Cellular Biology, 1986
• Modal karyotype of human leukemia cell line, K562 (ATCC CCL 243)
  Cancer Genetics and Cytogenetics, 1985
• Localization of the c-abl oncogene adjacent to a translocation break point in chronic myelocytic leukaemia
  Nature, 1983
• Rearrangement and amplification of c-abl sequences in the human chronic myelogenous leukemia cell line K-562.
  Proceedings of the National Academy of Sciences, 1983