Results 251 to 260 of about 158,249 (312)

Genetic dissection reveals distinct contributions of the eS31 N‐terminal domain to translational accuracy in Saccharomyces cerevisiae

open access: yesThe FEBS Journal, EarlyView.
The eukaryote‐specific N‐terminal domain (NTD) of eS31 uses two distinct strategies to maintain translation fidelity. During elongation, a positively charged “hotspot” fine‐tunes the selection of incoming aa‐tRNA. During termination, the entire NTD acts as a structural scaffold to ensure the correct positioning of the release factor eRF1.
Qingxuan Gao   +3 more
wiley   +1 more source

Chromosomal Translocation Formation Is Sufficient to Produce Fusion Circular RNAs Specific to Patient Tumor Cells.

open access: yesiScience, 2018
Babin L   +8 more
europepmc   +1 more source

Chromosomal translocations

1997
Abstract To generate chromosomal translocations in ES cells using the Cre/loxP system two consecutive homologous recombination events are necessary. In the first step, a positive selection marker gene with one loxP site (e.g. loxP-neo) must be introduced by homologous recombination on one chromosome and a second selection marker with ...
Raul M Torres, Ralf Kühn
openaire   +1 more source

Chromosomal translocations and sarcomas

Current Opinion in Oncology, 2002
This 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 ...
Jeannette L, Bennicelli   +1 more
openaire   +2 more sources

PHILADELPHIA CHROMOSOME BY TRANSLOCATION

The Lancet, 1973
SCOPUS: le.j ; info:eu-repo/semantics ...
Petit, Paul, Cauchie, Charles
openaire   +2 more sources

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
openaire   +2 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
Michael, Byrne   +7 more
openaire   +2 more sources

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...
J, Whang-Peng   +5 more
openaire   +2 more sources

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