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Two INT markers were found to have multiple chromosomal localisation (INT467 and INT290).
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The cells surviving such overreplication constitute a heterogeneous population with multiple chromosomal changes, including partial or complete endoreduplication of chromosomes, as well as a variety of chromosomal rearrangements.
Human TGCT are typically aneuploid with multiple chromosomal rearrangements (Oosterhuis et al., 1990).
Multiple chromosomal aberrations were identified, some of them located in regions with known tumor suppressor genes and oncogenes.
An exception is the hESC line, CH-ES1, derived from a blastomere of a cleavage stage embryo and containing multiple chromosomal rearrangements (Hovatta et al., 2010).
Many different functions have been proposed for the multiple chromosomal toxin/antitoxin systems [54].
Our data predict that multiple chromosomal regions are involved in overexpression of full-length ETV1.
HERV-W env sequences were encoded by multiple chromosomal encoding loci in primary human neurons compared with less chromosomal diversity in astrocytes and microglia (p<0.05).
The effects of AZD1152-HQPA on chromosomal localisation and structure were examined by immunofluorescence.
Testis-specific protein Y-encoded differs from the known CT antigens by its chromosomal localisation.
Also, the chromosomal localisation of the genes was verified using BLAT search within the GoldenPath human genome browser [ 38].
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