Results 11 to 20 of about 159,072 (309)
Prevalence of Gene Rearrangement by Multiplex PCR in De Novo Acute Myeloid Leukemia in Adult Iraqi Patients. [PDF]
Ali AlJabban, Jaffar Alalsaidissa Department of Pathology, College of Medicine, University of Baghdad, Baghdad, IraqCorrespondence: Ali AlJabban, Department of Pathology, College of medicine, University of Baghdad, Baghdad, Iraq, Tel +9647706056226 ...
AlJabban A, Alalsaidissa J.
europepmc +3 more sources
Gene rearrangement of the mitochondrial genome of insects, especially the rearrangement of protein-coding genes, has long been a hot topic for entomologists.
Xinyu Ge, Haoming Zang, Lang Peng
exaly +3 more sources
Gene conversion in human rearranged immunoglobulin genes [PDF]
Over the past 20 years, many DNA sequences have been published suggesting that all or part of the V<sub>H</sub> segment of a rearranged immunoglobulin gene may be replaced in vivo. Two different mechanisms appear to be operating. One of these
Darlow, J.M. +3 more
core +3 more sources
Lack of ROS1 Gene Rearrangement in Glioblastoma Multiforme. [PDF]
Glioblastoma multiforme (GBM) is the most aggressive type of brain tumor, and the prognosis remains poor. Rearrangement of ROS1 gene, which was shown to have an oncogenic potential, was previously discovered in GBM cell lines.
Sun Min Lim +17 more
core +4 more sources
Case Report: Experience of a rare case of primary acute mast cell leukemia with FGFR1 gene rearrangement. [PDF]
Mast cell leukemia represents the most malignant subtype of systemic mastocytosis, characterized by a dire clinical prognosis. Currently, no standard treatment regimen exists, with allogeneic hematopoietic stem cell transplantation being the sole option ...
Liu Y, Gao S, Du H, Ji H, Li Z.
europepmc +2 more sources
Acute lymphoblastic leukemia (ALL) is a relatively rare disease during pregnancy, accounting for about 15% of all cases of pregnancy-associated leukemia.
Ahmed, Syed Osman +17 more
core +2 more sources
Marfan syndrome with a complex chromosomal rearrangement including deletion of the
Background The majority of Marfan syndrome (MFS) cases is caused by mutations in the fibrillin-1 gene (FBN1), mapped to chromosome 15q21.1. Only few reports on deletions including the whole FBN1 gene, detected by molecular cytogenetic techniques, were ...
Luciana RJ da Silva +26 more
core +2 more sources
Ki67 deficiency impedes chromatin accessibility and BCR gene rearrangement. [PDF]
The proliferation marker Ki67 has been attributed critical functions in maintaining mitotic chromosome morphology and heterochromatin organization during the cell cycle, indicating a potential role in developmental processes requiring rigid cell-cycle ...
Ding Z +16 more
europepmc +2 more sources
Rearranging Detection of Gene Rearrangements [PDF]
®ecent years have witnessed a dramatic expansion in our knowledge of the genetic diversity of non–small-cell lung cancer (NSCLC), and in particular adenocarcinoma. This appreciation of the genetic landscape of the disease has resulted in the development of targeted therapies that are directed to ward activated oncogenes.
Davies, Kurtis D. +2 more
openaire +2 more sources
Extensive gene rearrangement is characteristic in the mitogenomes of thrips (Thysanoptera), but the historical process giving rise to the contemporary gene rearrangement pattern remains unclear.
Qiaoqiao Liu +5 more
doaj +1 more source

