Results 1 to 10 of about 365,481 (368)

Nucleic Acid Conformation Influences Postsynthetic Suzuki-Miyaura Labeling of Oligonucleotides. [PDF]

open access: greenBioconjug Chem, 2020
Chemoselective transformations that work under physiological conditions have emerged as powerful tools to label nucleic acids in cell-free and cellular environments.
Walunj MB, Srivatsan SG.
europepmc   +4 more sources

Global Studies of Single-Stranded Nucleic Acid Conformation [PDF]

open access: bronzeBiophysical Journal, 2013
Unstructured regions of RNA molecules require flexibility to accomplish many biological tasks such as conformational switching and protein recognition. Due to its highly charged backbone, the flexibility of single-stranded RNA is influenced by counterions.
Julie L. Sutton   +3 more
semanticscholar   +4 more sources

Dependence of interferon induction on nucleic acid conformation. [PDF]

open access: greenProceedings of the National Academy of Sciences, 1976
UV and circular dichroism characteristics of duplex analogs belonging to the (A)n-(U)n and (I)n-(C)n series were determined to assign qualitatively the nature of conformational differences caused by 5-pyrimidine and c7 purine substitutions in such duplexes.
Albert M. Bobst   +3 more
semanticscholar   +5 more sources

Sensing the structural and conformational properties of single-stranded nucleic acids using electrometry and molecular simulations [PDF]

open access: goldScientific Reports
Inferring the 3D structure and conformation of disordered biomolecules, e.g., single stranded nucleic acids (ssNAs), remains challenging due to their conformational heterogeneity in solution.
Rowan Walker-Gibbons   +4 more
doaj   +3 more sources

Rigid spin-labeled nucleoside Ç: a nonperturbing EPR probe of nucleic acid conformation [PDF]

open access: goldNucleic Acids Research, 2008
Rigid spin-labeled nucleoside Ç, an analog of deoxycytidine that base-pairs with deoxyguanosine, was incorporated into DNA oligomers by chemical synthesis.
Pavol Čekan   +4 more
openalex   +2 more sources

Conformational analysis of nucleic acids revisited: Curves+ [PDF]

open access: goldNucleic Acids Research, 2009
We describe Curves+, a new nucleic acid conformational analysis program which is applicable to a wide range of nucleic acid structures, including those with up to four strands and with either canonical or modified bases and backbones. The program is algorithmically simpler and computationally much faster than the earlier Curves approach, although it ...
Richard Lavery   +4 more
openalex   +6 more sources

The electrostatic field of DNA: the role of the nucleic acid conformation

open access: yesNucleic Acids Research, 1982
Calculations of the electrostatic field of DNA in two very different double helical conformations, A and Z, are reported and compared with the results previously obtained for B-DNA. Striking contrasts between these fields and the associated electrostatic potentials are brought into evidence.
Lavery, R., Pullman, B.
openaire   +7 more sources

Methylation Effects on Nucleic Acid Conformations [PDF]

open access: green, 1978
Chemical modification of nucleic acids by alkylating agents continues to be extensively explored from the perspective of chemical mutagenesis and carcinogenesis. Largely through the pioneering in vitro and in vivo studies of Lawley (1961), Lawley and Brookes (1963), Singer (1972), and Reese and coworkers (1965), coupled with theoretical predictions of ...
S. Danyluk   +2 more
openalex   +3 more sources

Nucleic Acid Reactivity and Conformation

open access: hybridJournal of Biological Chemistry, 1973
Treatment of calf thymus DNA with sodium bisulfite gave no deamination of cytosine to uracil, under conditions where 68% of the cytosines of heat-denatured DNA were converted to uracil. This implies that the mutagenic properties of bisulfite are due to reaction with single-stranded DNA.
Robert Shapiro   +3 more
openalex   +4 more sources

A Nonafluoro Nucleoside as a Sensitive 19F NMR Probe of Nucleic Acid Conformation [PDF]

open access: greenOrganic Letters, 2008
A nucleoside carrying a perfluorinated tert-butyl group ( 4) was prepared by a Sonogashira coupling of 5-iodo-2'-deoxyuridine with 4,4,4-trifluoro-3,3-bis(trifluoromethyl)-1-butyne in nearly quantitative yield and subsequently incorporated into DNA ...
Nivrutti B. Barhate   +4 more
openalex   +2 more sources

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