AbstractA characteristic DNA rearrangement, the loss of an EcoRI cleavage site next to the 3́-end of the human c-mos gene, has been found to be frequently present in DNA from transformed hematopoietic cells of the myeloid lineage but not in DNA from either normal or transformed cells of different tissue types. Three established cell lines, respectively a pro-monocytic line (CM-S) and two precursor granulocytic lines (My/Kl and My/K5), carry the same genome rearrangement, but not fibroblasts obtained from the marrow of the same patients. This DNA rearrangement is maintained in three different hybridomas derived by fusion of CM-S cells with normal human embryo hepatocytes.Proto-oncogenec-mosDNA rearrangementMyeloid leukemi
Microsatellites are short tandem repeat sequences dispersed throughout the genome. Their instability...
At diagnosis, about 5% of Chronic Myeloid Leukemia (CML) patients lacks Philadelphia chromosome (Ph)...
The t(9;22)(q34;q11), generating the Philadelphia chromosome, is found in more than 90% of patients ...
AbstractA characteristic DNA rearrangement, the loss of an EcoRI cleavage site next to the 3́...
We report the molecular analysis of an 8;14 reciprocal chromsome translocation in a case of acute ly...
The structure of the c-myc locus and the flanking chromosomal region was investigated by Southern bl...
The chromosomal localization of c-myc sequences was determined by in situ hybridization in HL-60 cel...
By combining somatic cell genetics, in situ hybridization and Southern hybridization, we found that ...
Chronic myeloid leukemia (CML) is a rare myeloproliferative disorder caused by the reciprocal transl...
Amplification is one of the mechanisms by which cellular oncogenes may be altered in their function,...
The translocation (6;9)(p23;q34) is mainly found in specific subtypes of acute myeloid leukemia (AML...
whether duplication of the c-fes gene occurs in the M3 subtypes exhibiting translocation t(15; 17) o...
A new complex rearrangement involving chromosome bands 5q13, 12p13, 22q11, and 3q12 was identified a...
Genomic deletions on the derivative chromosomes bearing the reciprocal fusion gene have recently bee...
A new complex rearrangement involving chromosome bands 5q13, 12p13, 22q11, and 3q12 was identified a...
Microsatellites are short tandem repeat sequences dispersed throughout the genome. Their instability...
At diagnosis, about 5% of Chronic Myeloid Leukemia (CML) patients lacks Philadelphia chromosome (Ph)...
The t(9;22)(q34;q11), generating the Philadelphia chromosome, is found in more than 90% of patients ...
AbstractA characteristic DNA rearrangement, the loss of an EcoRI cleavage site next to the 3́...
We report the molecular analysis of an 8;14 reciprocal chromsome translocation in a case of acute ly...
The structure of the c-myc locus and the flanking chromosomal region was investigated by Southern bl...
The chromosomal localization of c-myc sequences was determined by in situ hybridization in HL-60 cel...
By combining somatic cell genetics, in situ hybridization and Southern hybridization, we found that ...
Chronic myeloid leukemia (CML) is a rare myeloproliferative disorder caused by the reciprocal transl...
Amplification is one of the mechanisms by which cellular oncogenes may be altered in their function,...
The translocation (6;9)(p23;q34) is mainly found in specific subtypes of acute myeloid leukemia (AML...
whether duplication of the c-fes gene occurs in the M3 subtypes exhibiting translocation t(15; 17) o...
A new complex rearrangement involving chromosome bands 5q13, 12p13, 22q11, and 3q12 was identified a...
Genomic deletions on the derivative chromosomes bearing the reciprocal fusion gene have recently bee...
A new complex rearrangement involving chromosome bands 5q13, 12p13, 22q11, and 3q12 was identified a...
Microsatellites are short tandem repeat sequences dispersed throughout the genome. Their instability...
At diagnosis, about 5% of Chronic Myeloid Leukemia (CML) patients lacks Philadelphia chromosome (Ph)...
The t(9;22)(q34;q11), generating the Philadelphia chromosome, is found in more than 90% of patients ...