Literature DB >> 3470108

Role of heterochromatin during preferential 9q;22q translocation in chronic myelogenous leukemia.

R S Verma, J Rodriguez, A Babu, S Chemitiganti, M Coleman, R T Silver, H Dosik.   

Abstract

The secondary constriction region (h) of human chromosome 9 was evaluated in 55 chronic myelogenous leukemia (CML) patients with respect to its size and position. Each case was examined by C-banding and distamycin A-4,6-diamidino-2-phenylindole techniques for the expression of the h regions. When one h region of chromosome 9 was larger, it was more frequently involved in the reciprocal translocation with chromosome 22. In addition, there was a higher incidence of pericentric inversions in the h regions in the translocated chromosome 9 when compared with normal homologues. The role of the constitutive heterochromatin of chromosome 9 as a possible influencing factor during 9q;22q translocation in CML is suggested.

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Year:  1986        PMID: 3470108     DOI: 10.1139/g86-138

Source DB:  PubMed          Journal:  Can J Genet Cytol        ISSN: 0008-4093


  2 in total

1.  Acquired pericentric inversion of chromosome 9 in essential thrombocythemia.

Authors:  T S Wan; S K Ma; L C Chan
Journal:  Hum Genet       Date:  2000-06       Impact factor: 4.132

2.  Centromeric alpha satellite DNA amplification and translocation in an unusually large chromosome 14p+ variant.

Authors:  S Dale; E Earle; L Voullaire; J Rogers; K H Choo
Journal:  Hum Genet       Date:  1989-05       Impact factor: 4.132

  2 in total

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