Triple fluorescence in situ hybridization with a plasmid DNA library from sorted human chromosomes 8 in combination with bacteriophage clones flanking the breakpoint in 8q24 of the Burkitt lymphoma cell line Jl was used for the specific delineation of this breakpoint in individual tumor cells. With this approach, tumor-specific breakpoints in translocation chromosomes can be detected at all stages of the cell cycle with high specificity
The detection of chromosomal translocations by fluorescence in situ hybridization (FISH) is widely p...
A method of in situ hybridization for visualizing individual human chromosomes from pter to qter, bo...
In about 80% of Burkitt's lymphoma cases, the tumour cell harbours a reciprocal chromosomal tran...
Triple fluorescence in situ hybridization with a plasmid DNA library from sorted human chromosomes 8...
Triple fluorescence in situ hybridization with a plasmid DNA library from sorted human chromosomes 8...
Triple fluorescence in situ hybridization with a plasmid DNA library from sorted human chromosomes 8...
In 6 different Burkitt lymphoma cell lines with t(2;8) variant translocations (J1, LY66, LY91, BL21,...
Non-random chromosomal translocations are specifically involved in the pathogenesis of many non-Hodg...
Rearrangements within the chromosome 11q13 region are frequent in hematologic malignancies. 50% of 7...
Structural chromosome aberrations are hallmarks of many human genetic diseases. The precise mapping ...
Structural chromosome aberrations are hallmarks of many human genetic diseases. The precise mapping ...
The detection of chromosomal translocations by fluorescence in situ hybridization (FISH) is widely p...
A method of in situ hybridization for visualizing individual human chromosomes from pter to qter, bo...
In about 80% of Burkitt's lymphoma cases, the tumour cell harbours a reciprocal chromosomal tran...
Triple fluorescence in situ hybridization with a plasmid DNA library from sorted human chromosomes 8...
Triple fluorescence in situ hybridization with a plasmid DNA library from sorted human chromosomes 8...
Triple fluorescence in situ hybridization with a plasmid DNA library from sorted human chromosomes 8...
In 6 different Burkitt lymphoma cell lines with t(2;8) variant translocations (J1, LY66, LY91, BL21,...
Non-random chromosomal translocations are specifically involved in the pathogenesis of many non-Hodg...
Rearrangements within the chromosome 11q13 region are frequent in hematologic malignancies. 50% of 7...
Structural chromosome aberrations are hallmarks of many human genetic diseases. The precise mapping ...
Structural chromosome aberrations are hallmarks of many human genetic diseases. The precise mapping ...
The detection of chromosomal translocations by fluorescence in situ hybridization (FISH) is widely p...
A method of in situ hybridization for visualizing individual human chromosomes from pter to qter, bo...
In about 80% of Burkitt's lymphoma cases, the tumour cell harbours a reciprocal chromosomal tran...