Nanopore native RNA sequencing of a human poly(A) transcriptome
bioRxiv, 2018 High-throughput complementary DNA sequencing technologies have advanced our understanding of transcriptome complexity and regulation. However, these methods lose information contained in biological RNA because the copied reads are often short and ...
R. Workman +21 more
semanticscholar +1 more source
Localization Properties of Electronic States in Polaron Model of poly(dG)-poly(dC) and poly(dA)-poly(dT) DNA polymers [PDF]
, 2004 We numerically investigate localization properties of electronic states in a static model of poly(dG)-poly(dC) and poly(dA)-poly(dT) DNA polymers with realistic parameters obtained by quantum-chemical calculation.
Barnett +23 more
core +2 more sources
The use of aluminum trialkoxide for synthesis of poly (ε-caprolactone) and poly (δ-valerolactone): A comparative study [PDF]
Songklanakarin Journal of Science and Technology (SJST), 2018 Four aluminum(III) trialkoxides, namely Al(III) ethoxide (1), Al(III) isopropoxide (2), Al(III) tert-butoxide (3), and Al(III) sec.-butoxide (4), were employed as initiators for the bulk ring-opening polymerizations of δ-valerolactone (VL) and ...
Jitrayut Jitonnom +3 more
doaj +1 more source
The Dynamic Poly(A) Tail Acts as a Signal Hub in mRNA Metabolism
Cells, 2023 In eukaryotes, mRNA metabolism requires a sophisticated signaling system. Recent studies have suggested that polyadenylate tail may play a vital role in such a system.
Guiying Zhang +4 more
doaj +1 more source
Exchange reactions of poly(arylene ether ketone) dithioketals with aliphatic diols: formation and deprotection of poly(arylene ether ketal)s [PDF]
, 2017 The dithioketal derivatives of industrially important, semi-crystalline poly(arylene ether ketone)s undergo facile exchange with aliphatic diols in the presence of N-bromo-succinimide to give a range of novel poly(arylene ether ketal)s.
Colquhoun, Howard +2 more
core +1 more source
Poly A- transcripts expressed in HeLa cells. [PDF]
PLoS ONE, 2008 Transcripts expressed in eukaryotes are classified as poly A+ transcripts or poly A- transcripts based on the presence or absence of the 3' poly A tail.
Qingfa Wu +9 more
doaj +1 more source
Poly(rA) ioinos poly(rG) poly(rC) to form a tripie helix [PDF]
Nucleic Acids Research, 1992 Poly(rA) binds poly(rG).poly(rC) to form a triple helix. Evidence for this structure includes ultraviolet absorbance mixing curves and melting curves, and circular dichroism spectroscopy. The formation of the triple helix depends on the length of the poly(rC) strand. Triple helix forms when the average length is around 100 nucleotides but does not form
M, Chastain, I, Tinoco
openaire +2 more sources
iCLIP analysis of RNA substrates of the archaeal exosome
BMC Genomics, 2020 Background The archaeal exosome is an exoribonucleolytic multiprotein complex, which degrades single-stranded RNA in 3′ to 5′ direction phosphorolytically. In a reverse reaction, it can add A-rich tails to the 3′-end of RNA.
Jochen Bathke +9 more
doaj +1 more source
Poly(A)-Driven and Poly(A)-Assisted Termination: Two Different Modes of Poly(A)-Dependent Transcription Termination [PDF]
Molecular and Cellular Biology, 1998 We mapped the elements that mediate termination of transcription downstream of the chicken betaH- and betaA-globin gene poly(A) sites. We found no unique element and no segment of 3'-flanking DNA to be significantly more effective than any other. When we replaced the native 3'-flanking DNA with bacterial DNA, it too supported transcription termination.
G, Yeung +6 more
openaire +2 more sources
Inkjet printed metal insulator semiconductor (MIS) diodes for organic and flexible electronic application [PDF]
, 2017 All inkjet printed rectifying diodes based on a metal-insulator-semiconductor (MIS) layer stack are presented. The rectifying properties were optimized by careful selection of the insulator interlayer thickness and the layout structure.
Baumann, Reinhard R. +7 more
core +1 more source