A complex genetic rearrangement in a t(10;14)(q24;q11) associated with T-cell acute lymphoblastic leukemia
Author:
Publisher
Wiley
Subject
Cancer Research,Genetics
Reference21 articles.
1. The mechanism of chromosomal translocation t(11;14) involving the T-cell receptor C delta locus on human chromosome 14q11 and a transcribed region of chromosome 11p15.
2. Alternating purine-pyrimidine tracts may promote chromosomal translocations seen in a variety of human lymphoid tumours.
3. Coding sequences of the tal-1 gene are disrupted by chromosome translocation in human T cell leukemia.
4. A new translocation, t(10;14)(q24;q11), in T cell neoplasia
5. A novel human homeobox gene lies at the chromosome 10 breakpoint in lymphoid neoplasias with chromosomal translocation t(10;14)
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1. G-Quadruplex Structures Formed at the HOX11 Breakpoint Region Contribute to Its Fragility during t(10;14) Translocation in T-Cell Leukemia;Molecular and Cellular Biology;2013-09-03
2. Genomic Aberrations and Survival in Cutaneous T Cell Lymphomas;Journal of Investigative Dermatology;2004-03
3. Defining the breakpoints of proximal chromosome 14q rearrangements in nine patients using flow-sorted chromosomes;American Journal of Medical Genetics;2001
4. Loss of heterozygosity on 10q and microsatellite instability in advanced stages of primary cutaneous T-cell lymphoma and possible association with homozygous deletion of PTEN;Blood;2000-05-01
5. Molecular characterization of a complex chromosomal translocation breakpoint t(10;14) including the HOX11 oncogene locus;Leukemia;1999-06
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