Arun A Tanpure
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Explore the profile of Arun A Tanpure including associated specialties, affiliations and a list of published articles.
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11
Citations
155
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Recent Articles
1.
Sabale P, Tanpure A, Srivatsan S
Org Biomol Chem
. 2018 May;
16(22):4141-4150.
PMID: 29781489
Double-stranded segments of a genome that can potentially form G-quadruplex (GQ) and/or i-motif (iM) structures are considered to be important regulatory elements. Hence, the development of a common probe that...
2.
Post-transcriptional labeling by using Suzuki-Miyaura cross-coupling generates functional RNA probes
Walunj M, Tanpure A, Srivatsan S
Nucleic Acids Res
. 2018 Mar;
46(11):e65.
PMID: 29546376
Pd-catalyzed C-C bond formation, an important vertebra in the spine of synthetic chemistry, is emerging as a valuable chemoselective transformation for post-synthetic functionalization of biomacromolecules. While methods are available for...
3.
Tanpure A, Balasubramanian S
Chembiochem
. 2017 Sep;
18(22):2236-2241.
PMID: 28901692
The synthesis of 2'-O-methyl-5-hydroxymethylcytidine (hm Cm), 5-hydroxymethylcytidine (hm C) and 5-formylcytidine (f C) phosphoramidite monomers has been developed. Optimisation of mild post-synthetic deprotection conditions enabled the synthesis of RNA containing...
4.
Sawant A, Tanpure A, Mukherjee P, Athavale S, Kelkar A, Galande S, et al.
Nucleic Acids Res
. 2015 Sep;
44(2):e16.
PMID: 26384420
Cellular RNA labeling strategies based on bioorthogonal chemical reactions are much less developed in comparison to glycan, protein and DNA due to its inherent instability and lack of effective methods...
5.
Tanpure A, Srivatsan S
Nucleic Acids Res
. 2015 Jul;
43(22):e149.
PMID: 26202965
Development of probes that can discriminate G-quadruplex (GQ) structures and indentify efficient GQ binders on the basis of topology and nucleic acid type is highly desired to advance GQ-directed therapeutic...
6.
Tanpure A, Srivatsan S
Chembiochem
. 2014 May;
15(9):1309-16.
PMID: 24861713
The majority of fluorescent nucleoside analogues used in nucleic acid studies have excitation maxima in the UV region and show very low fluorescence within oligonucleotides (ONs); hence, they cannot be...
7.
Tanpure A, Srivatsan S
Chembiochem
. 2012 Oct;
13(16):2392-9.
PMID: 23070860
The synthesis and site-specific incorporation of an environment-sensitive fluorescent nucleoside analogue (2), based on a 5-(benzofuran-2-yl)pyrimidine core, into DNA oligonucleotides (ONs), and its photophysical properties within these ONs are described....
8.
Rao H, Tanpure A, Sawant A, Srivatsan S
Nat Protoc
. 2012 May;
7(6):1097-112.
PMID: 22576108
This protocol describes the detailed experimental procedure for the synthesis of an azide-modified uridine triphosphate analog and its effective incorporation into an oligoribonucleotide by in vitro transcription reactions. Furthermore, procedures...
9.
Tanpure A, Patheja P, Srivatsan S
Chem Commun (Camb)
. 2011 Nov;
48(4):501-3.
PMID: 22105782
Development of a simple label-free fluorescence hybridization assay to monitor the depurination activity of toxic ribosome inactivating proteins by using a fluorescent ligand that specifically pseudo base pairs with a...
10.
Rao H, Sawant A, Tanpure A, Srivatsan S
Chem Commun (Camb)
. 2011 Oct;
48(4):498-500.
PMID: 22006199
Direct incorporation of azide groups into RNA oligonucleotides by in vitro transcription reactions in the presence of a new azide-modified UTP analogue, and subsequent posttranscriptional chemical labeling of azide-modified oligoribonucleotide...