Although inhibition mostly involved a transcript cleavage, the inhibition of translation was predicted for nine genes (HbERF-Ib5, HbERF-IIa1, HbERF-VI5, HbERF-VIIa4, HbERF-VIIIa7, HbERF-IXc3, HbERF-IXc5, HbERF-Xa1, HbSoloist3).
Although TICs could potentially be caused by a trans-splicing mechanism between two different transcripts, the proximity of the gene pairs makes a cis mechanism involving a single transcript more plausible.
Myeloproliferative disorders with PDGFR rearrangement show great sensitivity to IM and mostly require a lower dose of IM; this is especially true of chronic eosinophilic leukemia, which involves a fusion transcript of FIP1-like1 and PDGFRA [ 4].
Validation for fifteen gene transcripts involved a rigorous three-tiered quality control within tissue/development-specific contexts.
Thematic analysis of transcripts involved a process of coding and clustering of codes into categories with continuous comparisons and re-assessment to ensure validity.
The decision by Judge Arthur D. Spatt of Federal District Court in Uniondale, N.Y., which ended a trial that had spanned nearly four years and had produced a 10,000-page transcript, essentially involved a claim of trespassing on Federal land, the Jamaica Bay Wildlife Refuge.
RPL13a was reported to be involved in a transcript-specific translational control mechanism.
This redundancy had been continually masking the presence of another unexpected mechanism for heterochromatin silencing that is readily observable at the pericentromeric repeats, one that requires nascent RNA transcripts and involves a post-transcriptional gene silencing (PTGS) activity.
This analysis revealed that pairs involving a psoriasis-increased transcript in humans and an orthologous transcript decreased in K5-Tie2 or IMQ lesions were often associated with immunity (e.g., response to virus, innate immune response; see Figure S10).
Analysis of transcripts involved an initial process of open coding, which was also informed by the themes from the available literature 7 and the interview schedule.
Amplification of the transcripts involved an initial denaturation at 95°C for 30 seconds, followed by 40 cycles at 95°C for 5 seconds, 55°C for 30 seconds, and 72°C for 34 seconds.
