Arun Tanpure

Visiting Scientist

Research Group Home Page:: Balasubramanian Group

Work address:: Cancer Research UK Cambridge Institute University of Cambridge Li Ka Shing Centre Robinson Way Cambridge CB2 0RE

Publications:: Probing the competition between duplex and G-quadruplex/i-motif structures using a conformation-sensitive fluorescent nucleoside probe.

E-pub date: 06 Jun 2018; Post-transcriptional labeling by using Suzuki-Miyaura cross-coupling generates functional RNA probes.

E-pub date: 13 Mar 2018; Synthesis and Multiple Incorporations of 2′-O-Methyl-5-hydroxymethylcytidine, 5-Hydroxymethylcytidine and 5-Formylcytidine Monomers into RNA Oligonucleotides.

E-pub date: 16 Nov 2017; 2′-O-Methyl-5-hydroxymethylcytidine: A Second Oxidative Derivative of 5-Methylcytidine in RNA.

E-pub date: 08 Feb 2017; A versatile toolbox for posttranscriptional chemical labeling and imaging of RNA.

E-pub date: 29 Jan 2016; Conformation-sensitive nucleoside analogues as topology-specific fluorescence turn-on probes for DNA and RNA G-quadruplexes.

E-pub date: 15 Dec 2015; Synthesis, photophysical properties and incorporation of a highly emissive and environment-sensitive uridine analogue based on the Lucifer chromophore.

E-pub date: 16 Jun 2014; Synthesis and photophysical characterisation of a fluorescent nucleoside analogue that signals the presence of an abasic site in RNA.

E-pub date: 05 Nov 2012; Enzymatic incorporation of an azide-modified UTP analog into oligoribonucleotides for post-transcriptional chemical functionalization.

E-pub date: 10 May 2012; Posttranscriptional chemical functionalization of azide-modified oligoribonucleotides by bioorthogonal click and Staudinger reactions.

E-pub date: 14 Jan 2012; Label-free fluorescence detection of the depurination activity of ribosome inactivating protein toxins.

E-pub date: 14 Jan 2012; A microenvironment-sensitive fluorescent pyrimidine ribonucleoside analogue: synthesis, enzymatic incorporation, and fluorescence detection of a DNA abasic site.

E-pub date: 04 Nov 2011; Show all Hide all

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Cancer Research UK Cambridge Institute

Arun Tanpure

Visiting Scientist

Probing the competition between duplex and G-quadruplex/i-motif structures using a conformation-sensitive fluorescent nucleoside probe.

Post-transcriptional labeling by using Suzuki-Miyaura cross-coupling generates functional RNA probes.

Synthesis and Multiple Incorporations of 2′-O-Methyl-5-hydroxymethylcytidine, 5-Hydroxymethylcytidine and 5-Formylcytidine Monomers into RNA Oligonucleotides.

2′-O-Methyl-5-hydroxymethylcytidine: A Second Oxidative Derivative of 5-Methylcytidine in RNA.

A versatile toolbox for posttranscriptional chemical labeling and imaging of RNA.

Conformation-sensitive nucleoside analogues as topology-specific fluorescence turn-on probes for DNA and RNA G-quadruplexes.

Synthesis, photophysical properties and incorporation of a highly emissive and environment-sensitive uridine analogue based on the Lucifer chromophore.

Synthesis and photophysical characterisation of a fluorescent nucleoside analogue that signals the presence of an abasic site in RNA.

Enzymatic incorporation of an azide-modified UTP analog into oligoribonucleotides for post-transcriptional chemical functionalization.

Posttranscriptional chemical functionalization of azide-modified oligoribonucleotides by bioorthogonal click and Staudinger reactions.

Label-free fluorescence detection of the depurination activity of ribosome inactivating protein toxins.

A microenvironment-sensitive fluorescent pyrimidine ribonucleoside analogue: synthesis, enzymatic incorporation, and fluorescence detection of a DNA abasic site.

Tweets

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Contact CRUK CI

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Study at Cambridge

About the University

Research at Cambridge

Arun Tanpure

Visiting Scientist

Probing the competition between duplex and G-quadruplex/i-motif structures using a conformation-sensitive fluorescent nucleoside probe.

Post-transcriptional labeling by using Suzuki-Miyaura cross-coupling generates functional RNA probes.

Synthesis and Multiple Incorporations of 2′-O-Methyl-5-hydroxymethylcytidine, 5-Hydroxymethylcytidine and 5-Formylcytidine Monomers into RNA Oligonucleotides.

2′-O-Methyl-5-hydroxymethylcytidine: A Second Oxidative Derivative of 5-Methylcytidine in RNA.

A versatile toolbox for posttranscriptional chemical labeling and imaging of RNA.

Conformation-sensitive nucleoside analogues as topology-specific fluorescence turn-on probes for DNA and RNA G-quadruplexes.

Synthesis, photophysical properties and incorporation of a highly emissive and environment-sensitive uridine analogue based on the Lucifer chromophore.

Synthesis and photophysical characterisation of a fluorescent nucleoside analogue that signals the presence of an abasic site in RNA.

Enzymatic incorporation of an azide-modified UTP analog into oligoribonucleotides for post-transcriptional chemical functionalization.

Posttranscriptional chemical functionalization of azide-modified oligoribonucleotides by bioorthogonal click and Staudinger reactions.

Label-free fluorescence detection of the depurination activity of ribosome inactivating protein toxins.

A microenvironment-sensitive fluorescent pyrimidine ribonucleoside analogue: synthesis, enzymatic incorporation, and fluorescence detection of a DNA abasic site.

Tweets

CRUK CI staff links

Contact CRUK CI

Useful links

Study at Cambridge

About the University

Research at Cambridge

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