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This is reflected in the complex transcript patterns encountered when performing chloroplast RNA gel blot hybridization experiments.
For this to be a useful method, it will need to be applicable to other complex transcript sets.
This improvement allows for the identification of complex transcript structures – such as genes in operons – as well as novel short transcripts – such as small RNAs – that would be missed by previous low-density arrays (Reppas et al., 2006).
The results of our study demonstrate a complex transcript pattern for bovine skin and suggest a possible functional relevance of novel transcripts, including lncRNA, in the modulation of pigmentation processes.
Comparing with other lincRNAs, hES lincRNAs generally had more complex transcript structure with longer transcript length (1,215 nt versus 906 nt, p-value < 2.2e-16), morexonsns per transcript (3.44 versus 3.00, p-value = 2.2e-06 2.2e-06re andernative isoformoreer gene (2.76 versus 1.42, p-valternative-16).
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We began by segmenting the complex transcripts into more manageable units.
Subsequently, the long-standing conventional definition of a gene is fading and it is now realized that the genome is full of overlapping and other complex transcripts [2].
In addition, many of the adaptor-related protein complex transcripts are strongly downregulated, AP1B1 (⇓2.29), AP2A2 (⇓2.25), AP2S1 (⇓3.35), AP3D1 (⇓2.67) and AP4B1 (⇓2), and these also play a key role in the transport of vesicles from the GA to the endosomal sorting pathway.
Currently we do not understand the reasons for the increased levels of the MHC protein complex transcripts in aneuploid cells.
This is likely the most important factor that contributes to the relative pyrimidine-richness of mitochondrial membrane complex transcripts.
The A subcluster from the array analysis did include achaete and scute as well as the Notch pathway components Enhancer of spilt complex transcripts m7, m4, and γ.
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