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Identification of De Novo Chromosomal Translocations Disrupting NIPBL in a Patient With Cornelia de Lange Syndrome by Full Genome Analysis. [PDF]
Mol Genet Genomic MedKao HJ +8 more
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PHILADELPHIA CHROMOSOME BY TRANSLOCATION
The Lancet, 1973SCOPUS: le.j ; info:eu-repo/semantics ...
Petit, Paul, Cauchie, Charles
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Chromosomal translocations and sarcomas
Current Opinion in Oncology, 2002This review examines how the identification of tumor-specific translocations and fusion proteins has advanced the basic scientific and clinical understanding of sarcomas. Recent genetic advances, including the ASPL-TFE3 fusion of alveolar soft part sarcoma, the JAZF1-JJAZ1 fusion of endometrial stromal sarcoma, and HMGIC fusions in liposarcoma, are ...
Frederic G. Barr +1 more
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Sex chromosome translocations and speciation [PDF]
Nature, 1976 SPECIATION is the primary process of cladogenetic evolution. It is generally agreed that genetic divergence sufficient to produce reproductive isolation among populations is acquired in the allopatric state1–4. One of the major problems of evolutionary genetics is, then, characterisation of the genetic differences which actually produce the ...
S. A. Espinet, M. L. Tracey
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Chromosomal translocations in cancer
Biochimica et Biophysica Acta (BBA) - Reviews on Cancer, 2008Genetic 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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, 2016
Synovial sarcoma, the most common soft-tissue sarcoma in young adults bears a t(X;18) translocation that generates a fusion between SS18 (formerly SYT) and an SSX gene. SS18-SSX1 and SS18-SSX2 differ by only 13 amino acids.
Kevin B. Jones +4 more
semanticscholar +1 more source
Synovial sarcoma, the most common soft-tissue sarcoma in young adults bears a t(X;18) translocation that generates a fusion between SS18 (formerly SYT) and an SSX gene. SS18-SSX1 and SS18-SSX2 differ by only 13 amino acids.
Kevin B. Jones +4 more
semanticscholar +1 more source
Reciprocal translocation and the Philadelphia chromosome
Human Genetics, 1978We 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
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Mechanisms of oncogenic chromosomal translocations
Annals of the New York Academy of Sciences, 2014Chromosome 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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Chromosome Translocation in Peripheral Neuroepithelioma
New England Journal of Medicine, 1984PERIPHERAL 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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