Results 11 to 20 of about 160,061 (270)

BCR (breakpoint cluster region) [PDF]

open access: bronzeAtlas of Genetics and Cytogenetics in Oncology and Haematology, 2011
Review on BCR (breakpoint cluster region), with data on DNA, on the protein encoded, and where the gene is implicated.
Ali G. Turhan
semanticscholar   +5 more sources

Comparative Expression Analysis of Breakpoint Cluster Region-Abelson Oncogene in Leukemia Patients. [PDF]

open access: goldACS Omega, 2023
Leukemia is a proliferative disorder of myeloid and lymphoid cells that may lead to death. Different types of leukemia have been reported, and several genetic and environmental factors are involved in their development. The Philadelphia chromosome causes the most common mutation known as breakpoint cluster region-Abelson oncogene (BCR-ABL1), which ...
Arshad F   +9 more
europepmc   +4 more sources

Nucleolytic Cleavage of the Mixed Lineage Leukemia Breakpoint Cluster Region during Apoptosis [PDF]

open access: hybridJournal of Biological Chemistry, 2001
VP-16 (etoposide) has recently been shown to induce topoisomerase II (TOP2)-mediated DNA cleavage within the mixed lineage leukemia (MLL) breakpoint cluster region (bcr), suggesting a role of TOP2 in MLL gene rearrangement.
Sai-Peng Sim, Leroy F. Liu
semanticscholar   +6 more sources

Detection of a second t(14;18) breakpoint cluster region in human follicular lymphomas. [PDF]

open access: bronzeThe Journal of experimental medicine, 1986
Our results indicate that there are two major breakpoint cluster regions in chromosome 18 DNA for t(14;18) translocations in follicular lymphomas. The absence of a pFL-1 homologous transcript in a cell line containing a pFL-2-detectable translocation ...
Michael L. Cleary   +2 more
semanticscholar   +5 more sources

Two novel translocation breakpoints upstream of SOX9 define borders of the proximal and distal breakpoint cluster region in campomelic dysplasia [PDF]

open access: bronzeClinical Genetics, 2006
The semilethal skeletal malformation syndrome campomelic dysplasia (CD) with or without XY sex reversal is caused by mutations within the SOX9 gene on 17q24.3 or by chromosomal aberrations (translocations, inversions or deletions) with breakpoints outside the SOX9 coding region.
M. Leipoldt   +10 more
semanticscholar   +6 more sources

Mutations in the breakpoint cluster region-Abelson murine leukemia 1 gene in Brazilian patients with chronic myeloid leukemia [PDF]

open access: yesHematology, Transfusion and Cell Therapy, 2018
Introduction: Mutations in the breakpoint cluster region-Abelson murine leukemia 1 gene are the leading cause of resistance to treatment with tyrosine kinase inhibitors in chronic myeloid leukemia patients.
Heloísa Zorzi Costa   +5 more
doaj   +2 more sources

Id1 Transcription Inhibitor–Matrix Metalloproteinase 9 Axis Enhances Invasiveness of the Breakpoint Cluster Region/Abelson Tyrosine Kinase–Transformed Leukemia Cells [PDF]

open access: bronzeCancer Research, 2006
Breakpoint cluster region/Abelson (BCR/ABL) tyrosine kinase enhances the ability of leukemia cells to infiltrate various organs. We show here that expression of the helix-loop-helix transcription factor Id1 is enhanced by BCR/ABL in a signal transducer ...
Margaret Nieborowska-Skorska   +6 more
openalex   +2 more sources

Nucleotide sequence of a t(14;18) chromosomal breakpoint in follicular lymphoma and demonstration of a breakpoint-cluster region near a transcriptionally active locus on chromosome 18.

open access: greenProceedings of the National Academy of Sciences of the United States of America, 1985
The t(14;18)(q32;21) chromosomal translocation characteristic of follicular lymphomas is the most common cytogenetic abnormality known to be associated with any specific type of hematolymphoid malignancy.
Michael L. Cleary, Jeffrey Sklar
openalex   +2 more sources

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