Results 271 to 280 of about 32,025 (309)
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Partition Chromatography on Starch of Ribonucleosides
Nature, 1948DURING work on ribonucleic acid turnover with nitrogen-15 in this Department, we found it necessary to isolate the different nitrogen-containing substances from small amounts of ribonucleic acid. It was thought that partition chromatography on starch as introduced by Elsden and Synge1 might give a possible solution to our problem. Vischer and Chargaff2
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Engineering Ribonucleoside Triphosphate Specificity in a Thymidylyltransferase
Biochemistry, 2008Nature's glycosylation catalysts, glycosyltransferases, indirectly manipulate and control many important biological processes by transferring sugar nucleotide donors onto acceptors. Challenging chemical synthesis impedes synthetic access to sugar nucleotides and limits the study of many glycosyltransferases.
Jakeman, David L+6 more
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Analytical Biochemistry, 1972
Abstract A paper chromatographic method for the separation of 2′- O -methylated ribonucleosides from nonmethylated and base-methylated ribonucleosides, using paper impregnated with ammonium borate and a butanol/borate developing solvent, is presented.
Adhid Al-Arif, Michael B. Sporn
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Abstract A paper chromatographic method for the separation of 2′- O -methylated ribonucleosides from nonmethylated and base-methylated ribonucleosides, using paper impregnated with ammonium borate and a butanol/borate developing solvent, is presented.
Adhid Al-Arif, Michael B. Sporn
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Rapid Communications in Mass Spectrometry, 2011
The patterns and levels of urinary excreted ribonucleosides which reflect RNA turnover and metabolism in humans offer the potential for early detection of disease and monitoring of therapeutic intervention.
F. Teichert+6 more
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The patterns and levels of urinary excreted ribonucleosides which reflect RNA turnover and metabolism in humans offer the potential for early detection of disease and monitoring of therapeutic intervention.
F. Teichert+6 more
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Interrogating the transcriptome with metabolically incorporated ribonucleosides
Molecular Omics, 2021This review summarizes recent developments in metabolic labeling of RNA to study RNA synthesis and turnover, RNA binding proteins, and RNA modifications and modifying enzymes.
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Journal of Medicinal Chemistry, 2009
A series of novel 3-arylethynyltriazolyl ribonucleosides were synthesized and assessed for their anticancer activity on the drug-resistant pancreatic cancer cell line MiaPaCa-2.
Yi Xia+7 more
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A series of novel 3-arylethynyltriazolyl ribonucleosides were synthesized and assessed for their anticancer activity on the drug-resistant pancreatic cancer cell line MiaPaCa-2.
Yi Xia+7 more
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Ribonucleoside 2′,3′-orthocarbonates
J. Chem. Soc. D, 1969Ribonucleosides undergo acid-catalysed exchange with tetramethyl orthocarbonate to give 2′,3′-O-dimethoxymethylidene derivatives.
G. R. Niaz, C. B. Reese
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Journal of Organic Chemistry, 2009
The synthesis of a novel C4-linked C2-imidazole ribonucleoside phosphoramidite (ICN-C2-PA 1) with a two-carbon linker between imidazole and ribose moieties is described.
Lisa Araki+6 more
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The synthesis of a novel C4-linked C2-imidazole ribonucleoside phosphoramidite (ICN-C2-PA 1) with a two-carbon linker between imidazole and ribose moieties is described.
Lisa Araki+6 more
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American Journal of Physiology. Endocrinology and Metabolism, 2005
The studies described herein were designed to investigate the effects of 5-aminoimidazole-4-carboxamide-1-beta-D-ribonucleoside (AICAR), an activator of the AMP-activated protein kinase (AMPK), on the translational control of protein synthesis and ...
Ali K. Reiter+4 more
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The studies described herein were designed to investigate the effects of 5-aminoimidazole-4-carboxamide-1-beta-D-ribonucleoside (AICAR), an activator of the AMP-activated protein kinase (AMPK), on the translational control of protein synthesis and ...
Ali K. Reiter+4 more
semanticscholar +1 more source
STUDIES ON REACTION OF RIBONUCLEOSIDES WITH OXYPHOSPHORANE
Phosphorus, Sulfur, and Silicon and the Related Elements, 1996Abstract Ester exchange reaction of ribonucleosides (2) with oxyphosphorane (1) afforded spirooxyphosphoranes (3). After hydrolysis followed by acetylation, the labile spirooxyphosphoranes such as 3a were converted into stable nucleotide derivatives (4). The possible mechanism for the conversion was also discussed.
Yufen Zhao+3 more
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