Searching journal content for articles similar to Shen et al. 21 (9): 1478.

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  1. ...: 3150–3161. Shen Y, VenuRC,Nobuta K,WuX,Notibala V,Demirci C,Meyers BC,Wang GL, Ji G, Li QQ. 2011. Transcriptome dynamics through alternative polyadenylation in developmental and environmental responses in plants revealed by deep sequencing. Genome Res 21: 1478–1486. Shepard PJ, Choi EA, Lu J, Flanagan...
  2. ...isoforms from the same gene increases vastly the complexity of the transcriptome and proteome in eukaryotes (Keren et al. 2010; Nilsen and Graveley 2010). Alternative isoforms with different coding sequences can be generated through multiple types of alternative splicing (AS) events (Naftaly et al. 2021...
  3. ...to other plants, is needed.In the transcriptomic landscape, alternative splicing (AS) is regarded as an important mechanism for increasing the coding capacity of s (James et al. 2012; Rühl et al. 2012). Its identification and characterization in plants are widely considered a milestone to understanding...
  4. ...Deep RNA sequencing at single base-pair resolution reveals high complexity of the rice transcriptome Guojie Zhang 1 , 2 , 6 , Guangwu Guo 1 , 6 , Xueda Hu 1 , 6 , Yong Zhang 1 , 6 , Qiye Li 1 , 3 , Ruiqiang Li 1 , 4...
  5. ...alternative polyadenylation in developmental and environmental responses in plants revealed by deep sequencing. Genome Res 21: 1478–1486. Simpson GG, Dijkwel PP, Quesada V, Henderson I, Dean C. 2003. FY is an RNA 3′ end-processing factor that interacts with FCA to control the Arabidopsis floral transition...
  6. ...M, Schulz MH, Richard H, Magen A, Klingenhoff A, Scherf M, Seifert M, Borodina T, Soldatov A, Parkhomchuk D, et al. 2008. A global view of gene activity and alternative splicing by deep sequencing of the human transcriptome. Science 321: 956–960. Trapnell C, Pachter L, Salzberg SL. 2009. Top...
  7. ...of regulation by DNA methylation, depending on factors such as cell type, developmental stage, and environmental conditions (Gardiner-Garden and Frommer 1987; Jaenisch and Bird 2003; Illingworth and Bird 2009; Loyfer et al. 2023). CG-rich sequences are predominantly found in the 5′-flanking regions of genes...
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  8. ...to environmental and cell-autonomous stimuli. It also highlights the possibility of the same enhancer site being active at a distinct time of day to regulate the subsequent tissue-specific gene expression.View larger version: In this window In a new window Figure 3. Dynamic H3K27ac occupancy based on time...
  9. ...the other two identical Class I RNAs, DfiR-12 and DdR-50, could not be properly assessed because of the lack of available sequence surrounding DfiR-12.Class I RNAs are unique to dictyostelid social amoebasThe omnipresence of Class I RNAs within Dictyostelia, their developmental regulation, as well...
  10. ...RNAs as histone modifications influence Pol II dynamics and its interaction with RNA modifying components, such as the capping enzyme or the spliceosome.Paramecium tetraurelia is a unicellular organism belonging to the SAR clade (including Stramenophiles, alveolates, and Rhizaria), which is as distant to plants...
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