GT198 Splice Variants Display Dominant-Negative Activities and Are Induced by Inactivating Mutations
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چکیده
منابع مشابه
Cloning and characterization of dominant negative splice variants of the human histamine H4 receptor.
The H(4)R (histamine H(4) receptor) is the latest identified member of the histamine receptor subfamily of GPCRs (G-protein-coupled receptors) with potential functional implications in inflammatory diseases and cancer. The H(4)R is primarily expressed in eosinophils and mast cells and has the highest homology with the H(3)R. The occurrence of at least twenty different hH(3)R (human H(3)R) isofo...
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The molecular defects which lead to multistep incidences of human T-cell leukemia have yet to be identified. The DNA-binding protein Helios (known as IKZF2), a member of the Ikaros family of Krüppel-like zinc-finger proteins, functions pivotally in T-cell differentiation and activation. In this study, we identify three novel short Helios splice variants which are T-cell leukemic specific, and d...
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Stat5 was initially identified as a prolactin-induced member of the signal transducer and activator of transcription (Stat) family in sheep. However, Stat5 is also activated in the response to a variety of cytokines. In mice, and possibly in other species, there exist two Stat5 genes (Stat5a and Stat5b) that encode proteins of 92 and 94 kDa that are 95% identical. In the studies described here,...
متن کاملVariants Terminal Deoxynucleotidyltransferase Splice Distinct and Opposite Activities of Human
متن کامل
Distinct and opposite activities of human terminal deoxynucleotidyltransferase splice variants.
Evidence for potential human TdT (hTdT) isoforms derived from hTdT genomic sequences led us to identify the short isoform (hTdTS), as well as mature long transcripts containing exon XII (hTdTL1) and another including exon VII (hTdTL2) in lymphoid cells. Normal B and T lymphocytes express exclusively hTdTS and hTdTL2, whereas hTdTL1 expression appears to be restricted to transformed lymphoid cel...
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ژورنال
عنوان ژورنال: Genes & Cancer
سال: 2013
ISSN: 1947-6019,1947-6027
DOI: 10.1177/1947601913486345