<p>Mapping of markers belonging to <i>in silico</i> chromosomes TcChr7 (<b>Panel A</b>) and TcChr22 (<b>Panel B</b>). Identification of chromosomal rearrangements involving one band in the G strain and two bands in clone D11 (<b>Panel A</b>) or vice versa (<b>Panel B</b>). The positions of the markers used as radiolabeled probes are indicated in the diagrammatic representation of the <i>in silico</i> chromosomes. Markers from TcChr7 are XM_799116, XM_803657, TryP and NLI. Markers from TcChr22 are XM_801648, XM_801647, Bpp-1 and XM_801649. Gene identification and GenBank accession number of each marker are shown in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0063738#pone-0063738-t001" target="_blank">Table 1</a>.</p
The 11q23 chromosome band is frequently associated with chromosomal aberrations in human leukemias. ...
© 2001 Nature Publishing GroupWe have placed 7,600 cytogenetically defined landmarks on the draft se...
Introduction: Congenital anomalies, namely caused by chromosome rearrangements, are a leading cause ...
<p>Selected markers belonging to <i>in silico</i> chromosomes TcChr37 (<b>Panel A</b>) and TcChr39 (...
<p>Hybridization profile of specific chromosomal markers hybridized to one or more bands of similar ...
<p><b>Panel A</b>) Mapping of the α-tubulin gene on chromosomal bands of the G strain and clone D11 ...
<div><p>A genetic map of Chromosome 11 indicating the loci analysed is given on the left (<i>Xist</i...
<p><b>A)</b> Late passage of T25 clone expressing endogenous level of TOP2A. <b>B)</b> Late passage ...
(A) The complex chromosomal rearrangement identified in Case 1, t(2;8;15)(q34;q23.3;q21.3). A schema...
Fluorescence In Situ Hybridization (FISH) studies with chromosome-specific libraries and repetitive ...
The original objective of the work described in this thesis was the development of genetic and physi...
The work concerns the molecular characterization of the breakpoints of an engineered human minichrom...
With the advent of new cytogenetic techniques, more questions can be answered concerning chromosoma...
It has been clear for the last 15 years that cloning translocation breakpoints in both AML de novo a...
<p>Each probe set (i.e. collection of all probes hybridizing to USA300 genes) is represented by a si...
The 11q23 chromosome band is frequently associated with chromosomal aberrations in human leukemias. ...
© 2001 Nature Publishing GroupWe have placed 7,600 cytogenetically defined landmarks on the draft se...
Introduction: Congenital anomalies, namely caused by chromosome rearrangements, are a leading cause ...
<p>Selected markers belonging to <i>in silico</i> chromosomes TcChr37 (<b>Panel A</b>) and TcChr39 (...
<p>Hybridization profile of specific chromosomal markers hybridized to one or more bands of similar ...
<p><b>Panel A</b>) Mapping of the α-tubulin gene on chromosomal bands of the G strain and clone D11 ...
<div><p>A genetic map of Chromosome 11 indicating the loci analysed is given on the left (<i>Xist</i...
<p><b>A)</b> Late passage of T25 clone expressing endogenous level of TOP2A. <b>B)</b> Late passage ...
(A) The complex chromosomal rearrangement identified in Case 1, t(2;8;15)(q34;q23.3;q21.3). A schema...
Fluorescence In Situ Hybridization (FISH) studies with chromosome-specific libraries and repetitive ...
The original objective of the work described in this thesis was the development of genetic and physi...
The work concerns the molecular characterization of the breakpoints of an engineered human minichrom...
With the advent of new cytogenetic techniques, more questions can be answered concerning chromosoma...
It has been clear for the last 15 years that cloning translocation breakpoints in both AML de novo a...
<p>Each probe set (i.e. collection of all probes hybridizing to USA300 genes) is represented by a si...
The 11q23 chromosome band is frequently associated with chromosomal aberrations in human leukemias. ...
© 2001 Nature Publishing GroupWe have placed 7,600 cytogenetically defined landmarks on the draft se...
Introduction: Congenital anomalies, namely caused by chromosome rearrangements, are a leading cause ...