Evidence for whole chromosome 6 loss and duplication of the remaining chromosome in acute lymphoblastic leukemia

This publication has 24 references indexed in Scilit:

• Cloning and characterization of the common fragile site FRA6F harboring a replicative senescence gene and frequently deleted in human tumors
  Oncogene, 2002
• Intrinsic genetic instability of normal human lymphocytes and its implication for loss of heterozygosity
  Genes, Chromosomes and Cancer, 2001
• Chromosome loss is the most frequent mechanism contributing to HLA haplotype loss in human tumors
  International Journal of Cancer, 1999
• Mutations of the β₂‐microglobulin gene result in a lack of HLA class I molecules on melanoma cells of two patients immunized with MAGE peptides
  Tissue Antigens, 1998
• Chromosome loss with concomitant duplication and recombination both contribute most to loss of heterozygosity in vitro
  Genes, Chromosomes and Cancer, 1998
• Delineation of a 6 cM commonly deleted region in childhood acute lymphoblastic leukemia on the 6q chromosomal arm
  Leukemia, 1997
• SEN6, a locus for SV40-mediated immortalization of human cells, maps to 6q26-27
  Oncogene, 1997
• A human modifier of methylation for class I HLA genes (MEMO-1) maps to chromosomal bands 1p35-36.1
  Human Molecular Genetics, 1996
• Beta 2-microglobulin gene mutations: a study of established colorectal cell lines and fresh tumors.
  Proceedings of the National Academy of Sciences, 1994
• Cytogenetic analysis of lymphoblastoid cell lines
  Cytogenetic and Genome Research, 1986