Thermodynamic studies of base pairing involving 2,6-diaminopurine.
about
Quantitative assessment of the use of modified nucleoside triphosphates in expression profiling: differential effects on signal intensities and impacts on expression ratios.Structural Basis for Promoter −10 Element Recognition by the Bacterial RNA Polymerase σ SubunitAPOBEC3A is implicated in a novel class of G-to-A mRNA editing in WT1 transcriptsPyrazolo[3,4-d]pyrimidine nucleic acids: adjustment of dA-dT to dG-dC base pair stability.Binding specificity and stability of duplexes formed by modified oligonucleotides with a 4096-hexanucleotide microarrayHomopolymer tail-mediated ligation PCR: a streamlined and highly efficient method for DNA cloning and library construction.Recombination R-triplex: H-bonds contribution to stability as revealed with minor base substitutions for adenine.Improved templated fluorogenic probes enhance the analysis of closely related pathogenic bacteria by microscopy and flow cytometry.Substrate mimicry: HIV-1 reverse transcriptase recognizes 6-modified-3'-azido-2',3'-dideoxyguanosine-5'-triphosphates as adenosine analogs.Comparative NMR analysis of the decadeoxynucleotide d-(GCATTAATGC)2 and an analogue containing 2-aminoadenine.Role of pK(a) of nucleobases in the origins of chemical evolutionDNA probes: applications of the principles of nucleic acid hybridization.Strings of contiguous modified pentanucleotides with increased DNA-binding affinity can be used for DNA sequencing by primer walking.Structural destabilization of DNA duplexes containing single-base lesions investigated by nanopore measurementsIntroduction of 2,6-Diaminopurines into Serinol Nucleic Acid Improves Anti-miRNA Performance.Roles of the amino group of purine bases in the thermodynamic stability of DNA base pairing.Antisense oligonucleotides containing modified bases inhibit in vitro translation of Leishmania amazonensis mRNAs by invading the mini-exon hairpin.Biochemical Characterization of the Active Anti-Hepatitis C Virus Metabolites of 2,6-Diaminopurine Ribonucleoside Prodrug Compared to Sofosbuvir and BMS-986094.Labelling oligonucleotides to high specific activity (I).Structural context effects in the oxidation of 8-oxo-7,8-dihydro-2'-deoxyguanosine to hydantoin products: electrostatics, base stacking, and base pairingMechanisms of base selection by the Escherichia coli mispaired uracil glycosylase.Importance of minor groove functional groups for the stability of DNA duplexes.Pyrazolo[3,4-d]pyrimidine nucleic acids: adjustment of the dA-dT to the dG-dC base pair stability.Formation of supramolecular assemblies and liquid crystals by purine nucleobases and cyanuric acid in water: implications for the possible origins of RNA.
P2860
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P2860
Thermodynamic studies of base pairing involving 2,6-diaminopurine.
description
1988 nî lūn-bûn
@nan
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
1988年论文
@zh
1988年论文
@zh-cn
name
Thermodynamic studies of base pairing involving 2,6-diaminopurine.
@ast
Thermodynamic studies of base pairing involving 2,6-diaminopurine.
@en
type
label
Thermodynamic studies of base pairing involving 2,6-diaminopurine.
@ast
Thermodynamic studies of base pairing involving 2,6-diaminopurine.
@en
prefLabel
Thermodynamic studies of base pairing involving 2,6-diaminopurine.
@ast
Thermodynamic studies of base pairing involving 2,6-diaminopurine.
@en
P2093
P2860
P356
P1476
Thermodynamic studies of base pairing involving 2,6-diaminopurine.
@en
P2093
P2860
P304
P356
10.1093/NAR/16.11.5115
P407
P577
1988-06-01T00:00:00Z