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Chromosomal translocations in cancer

Biochimica et Biophysica Acta (BBA) - Reviews on Cancer, 2008
Genetic alterations in DNA can lead to cancer when it is present in proto-oncogenes, tumor suppressor genes, DNA repair genes etc. Examples of such alterations include deletions, inversions and chromosomal translocations. Among these rearrangements chromosomal translocations are considered as the primary cause for many cancers including lymphoma ...
Nambiar, Mridula   +2 more
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Reciprocal translocation and the Philadelphia chromosome

Human Genetics, 1978
We examined metaphases from three patients with chronic myeloid leukaemia and a typical Philadelphia chromosome with one chromosome 9 as the recipient to determine whether the 9q+22q- translocation is reciprocal. Good quality G-banded photographs of the chromosomes concerned were subjected to light absorption density analysis.
Brenda M. Page, Jessie L. Watt
openaire   +3 more sources

Mechanisms of oncogenic chromosomal translocations

Annals of the New York Academy of Sciences, 2014
Chromosome translocations are caused by inappropriate religation of two DNA double‐strand breaks (DSBs) in heterologous chromosomes. These DSBs can be generated by endogenous or exogenous sources. Endogenous sources of DSBs leading to translocations include inappropriate recombination activating gene (RAG) or activation‐induced deaminase (AID) activity
Jac A. Nickoloff   +7 more
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Sex Chromosome Translocations

2018
The sex chromosomes (gonosomes) are different, and sex chromosome translocations need to be considered separately from translocations between autosomes. A sex chromosome can engage in translocation with an autosome, with the other sex chromosome, or even with its homolog.
R. J McKinlay Gardner, David J. Amor
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Chromosome Translocation in Peripheral Neuroepithelioma

New England Journal of Medicine, 1984
PERIPHERAL neuroepithelioma (peripheral neuroblastoma) is an uncommon malignant tumor of the peripheral nervous system with a histologic appearance similar to that of classical childhood neuroblast...
Mark A. Israel   +5 more
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Nondisjunction of a translocation-chromosome t(4;13)

Human Genetics, 1981
We have studied a male infant with multiple congenital anomalies due to a double derivative chromosome 13 resulting from an inherited balanced reciprocal translocation t(4;13)(q23;q12).
M. Westmeier   +5 more
openaire   +3 more sources

Histone influences on chromosomal translocations [PDF]

open access: possibleNature Reviews Genetics, 2015
A new report shows that histone modification patterns influence the occurrence of chromosomal translocations.
openaire   +4 more sources

DNA Repair and Chromosomal Translocations

2015
The balance between DNA damage, especially double strand breaks, and DNA damage repair is a critical determinant of chromosomal translocation frequency. The non-homologous end-joining repair (NHEJ) pathways seem to play the major role in the generation of chromosomal translocations.
Purvi M. Kakadia, Stefan K. Bohlander
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Complex chromosomal translocations in the Philadelphia chromosome leukemias

Cancer Genetics and Cytogenetics, 1991
Joining of the BCR and ABL genes is an essential feature of the group of human leukemias characterized by the Philadelphia chromosome and there is recent evidence that the human BCR-ABL fusion gene induces leukemia in experimental animals. Joining of these two genes is the result of cytogenetic translocation, usually the t(9;22)(q34;q11), but sometimes
Christine M. Morris, Peter H. Fitzgerald
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The mystery of chromosomal translocations in cancer

Cytogenetic and Genome Research, 2007
Chromosomal translocations in human cancer may result in products that can be suppressed by targeting drugs. An example is bcr-abl tyrosine kinase in chronic myelogenous leukemia that can be treated with imatinib mesylate. However, the mechanisms of translocations or exchanges of chromosomal segments are virtually unknown.
openaire   +3 more sources

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