Year |
Citation |
Score |
2022 |
Ghosh P, Kropp HM, Betz K, Ludmann S, Diederichs K, Marx A, Srivatsan SG. Microenvironment-Sensitive Fluorescent Nucleotide Probes from Benzofuran, Benzothiophene, and Selenophene as Substrates for DNA Polymerases. Journal of the American Chemical Society. 144: 10556-10569. PMID 35666775 DOI: 10.1021/jacs.2c03454 |
0.494 |
|
2020 |
George JT, Srivatsan SG. Bioorthogonal chemistry-based RNA labeling technologies: evolution and current state. Chemical Communications (Cambridge, England). PMID 33026365 DOI: 10.1039/D0Cc05228K |
0.352 |
|
2020 |
George JT, Srivatsan SG. Responsive fluorescent nucleotides serve as efficient substrates to probe terminal uridylyl transferase. Chemical Communications (Cambridge, England). PMID 32939524 DOI: 10.1039/D0Cc05092J |
0.375 |
|
2020 |
Walunj MB, Srivatsan SG. Posttranscriptional Suzuki-Miyaura Cross-Coupling Yields Labeled RNA for Conformational Analysis and Imaging. Methods in Molecular Biology (Clifton, N.J.). 2166: 473-486. PMID 32710426 DOI: 10.1007/978-1-0716-0712-1_27 |
0.408 |
|
2020 |
George JT, Azhar M, Aich M, Sinha D, Ambi UB, Maiti S, Chakraborty D, Srivatsan SG. Terminal Uridylyl Transferase Mediated Site-Directed Access to Clickable Chromatin Employing CRISPR-dCas9. Journal of the American Chemical Society. PMID 32658470 DOI: 10.1021/Jacs.0C06541 |
0.316 |
|
2020 |
Sontakke VA, Srivatsan SG. A dual-app nucleoside probe reports G-quadruplex formation and ligand binding in the long terminal repeat of HIV-1 proviral genome. Bioorganic & Medicinal Chemistry Letters. 30: 127345. PMID 32631544 DOI: 10.1016/J.Bmcl.2020.127345 |
0.336 |
|
2020 |
Nuthanakanti A, Srivatsan SG. Synthesis of DNA and RNA Oligonucleotides Containing a Dual-Purpose Selenium-Modified Fluorescent Nucleoside Probe. Current Protocols in Nucleic Acid Chemistry. 81: e106. PMID 32311240 DOI: 10.1002/Cpnc.106 |
0.409 |
|
2019 |
Nuthanakanti A, Ahmed I, Khatik SY, Saikrishnan K, Srivatsan SG. Probing G-quadruplex topologies and recognition concurrently in real time and 3D using a dual-app nucleoside probe. Nucleic Acids Research. PMID 31216006 DOI: 10.1093/Nar/Gkz516 |
0.349 |
|
2019 |
Manna S, Srivatsan SG. Synthesis and Enzymatic Incorporation of a Responsive Ribonucleoside Probe That Enables Quantitative Detection of Metallo-Base Pairs. Organic Letters. PMID 31184159 DOI: 10.1021/Acs.Orglett.9B01544 |
0.398 |
|
2018 |
Manna S, Srivatsan SG. Fluorescence-based tools to probe G-quadruplexes in cell-free and cellular environments. Rsc Advances. 8: 25673-25694. PMID 30210793 DOI: 10.1039/C8Ra03708F |
0.36 |
|
2018 |
Manna S, Sarkar D, Srivatsan SG. A Dual-App Nucleoside Probe Provides Structural Insights into the Human Telomeric Overhang in Live Cells. Journal of the American Chemical Society. PMID 30192541 DOI: 10.1021/Jacs.8B08436 |
0.339 |
|
2018 |
Sabale PM, Tanpure AA, Srivatsan SG. Probing the competition between duplex and G-quadruplex/i-motif structures using a conformation-sensitive fluorescent nucleoside probe. Organic & Biomolecular Chemistry. 16: 4141-4150. PMID 29781489 DOI: 10.1039/C8Ob00646F |
0.345 |
|
2018 |
Walunj MB, Tanpure AA, Srivatsan SG. Post-transcriptional labeling by using Suzuki-Miyaura cross-coupling generates functional RNA probes. Nucleic Acids Research. 46: e65. PMID 29546376 DOI: 10.1093/Nar/Gky185 |
0.386 |
|
2018 |
Sabale PM, Ambi UB, Srivatsan SG. A Lucifer-Based Environment-Sensitive Fluorescent PNA Probe for Imaging Poly(A) RNAs. Chembiochem : a European Journal of Chemical Biology. 19: 826-835. PMID 29396904 DOI: 10.1002/Cbic.201700661 |
0.419 |
|
2018 |
Sawant AA, Galande S, Srivatsan SG. Imaging Newly Transcribed RNA in Cells by Using a Clickable Azide-Modified UTP Analog. Methods in Molecular Biology (Clifton, N.J.). 1649: 359-371. PMID 29130210 DOI: 10.1007/978-1-4939-7213-5_24 |
0.385 |
|
2018 |
Sabale PM, Ambi UB, Srivatsan SG. Cover Feature: A Lucifer-Based Environment-Sensitive Fluorescent PNA Probe for Imaging Poly(A) RNAs (ChemBioChem 8/2018) Chembiochem. 19: 767-767. DOI: 10.1002/Cbic.201800140 |
0.373 |
|
2017 |
Nuthanakanti A, Srivatsan SG. Surface-Tuned and Metal-Ion-Responsive Supramolecular Gels Based on Nucleolipids. Acs Applied Materials & Interfaces. 9: 22864-22874. PMID 28614659 DOI: 10.1021/Acsami.7B06037 |
0.318 |
|
2017 |
Manna S, Panse CH, Sontakke VA, Sangamesh S, Srivatsan SG. Probing Human Telomeric DNA and RNA Topology and Ligand Binding in a Cellular Model by Using Responsive Fluorescent Nucleoside Probes. Chembiochem : a European Journal of Chemical Biology. 18: 1604-1615. PMID 28569423 DOI: 10.1002/Cbic.201700283 |
0.409 |
|
2017 |
George JT, Srivatsan SG. Vinyluridine as a Versatile Chemoselective Handle for the Posttranscriptional Chemical Functionalization of RNA. Bioconjugate Chemistry. PMID 28406614 DOI: 10.1021/Acs.Bioconjchem.7B00169 |
0.384 |
|
2017 |
George JT, Srivatsan SG. Posttranscriptional chemical labeling of RNA by using bioorthogonal chemistry. Methods (San Diego, Calif.). PMID 28215631 DOI: 10.1016/J.Ymeth.2017.02.004 |
0.355 |
|
2017 |
Nuthanakanti A, Boerneke MA, Hermann T, Srivatsan SG. Structure of the Ribosomal RNA Decoding Site Containing a Selenium-Modified Responsive Fluorescent Ribonucleoside Probe. Angewandte Chemie (International Ed. in English). PMID 28156044 DOI: 10.1002/Anie.201611700 |
0.387 |
|
2016 |
Sabale PM, Srivatsan SG. Responsive Fluorescent PNA Analogue as a Tool for Detecting G-quadruplex Motifs of Oncogenes and Activity of Toxic Ribosome-Inactivating Proteins. Chembiochem : a European Journal of Chemical Biology. 17: 1665-73. PMID 27271025 DOI: 10.1002/Cbic.201600192 |
0.415 |
|
2016 |
Sawant AA, Mukherjee PP, Jangid RK, Galande S, Srivatsan SG. A clickable UTP analog for the posttranscriptional chemical labeling and imaging of RNA. Organic & Biomolecular Chemistry. PMID 27173127 DOI: 10.1039/C6Ob00576D |
0.37 |
|
2016 |
Nuthanakanti A, Srivatsan SG. Hierarchical self-assembly of switchable nucleolipid supramolecular gels based on environmentally-sensitive fluorescent nucleoside analogs. Nanoscale. 8: 3607-19. PMID 26804191 DOI: 10.1039/C5Nr07490H |
0.362 |
|
2015 |
Sawant AA, Tanpure AA, Mukherjee PP, Athavale S, Kelkar A, Galande S, Srivatsan SG. A versatile toolbox for posttranscriptional chemical labeling and imaging of RNA. Nucleic Acids Research. PMID 26384420 DOI: 10.1093/Nar/Gkv903 |
0.377 |
|
2015 |
Tanpure AA, Srivatsan SG. Conformation-sensitive nucleoside analogues as topology-specific fluorescence turn-on probes for DNA and RNA G-quadruplexes. Nucleic Acids Research. 43: e149. PMID 26202965 DOI: 10.1093/Nar/Gkv743 |
0.414 |
|
2014 |
Sabale PM, George JT, Srivatsan SG. A base-modified PNA-graphene oxide platform as a turn-on fluorescence sensor for the detection of human telomeric repeats. Nanoscale. 6: 10460-9. PMID 24981293 DOI: 10.1039/C4Nr00878B |
0.33 |
|
2014 |
Tanpure AA, Srivatsan SG. Synthesis, photophysical properties and incorporation of a highly emissive and environment-sensitive uridine analogue based on the Lucifer chromophore. Chembiochem : a European Journal of Chemical Biology. 15: 1309-16. PMID 24861713 DOI: 10.1002/Cbic.201402052 |
0.372 |
|
2013 |
Pawar MG, Srivatsan SG. Environment-responsive fluorescent nucleoside analogue probe for studying oligonucleotide dynamics in a model cell-like compartment. The Journal of Physical Chemistry. B. 117: 14273-82. PMID 24161106 DOI: 10.1021/Jp4071168 |
0.405 |
|
2013 |
Peters JP, Yelgaonkar SP, Srivatsan SG, Tor Y, James Maher L. Mechanical properties of DNA-like polymers. Nucleic Acids Research. 41: 10593-604. PMID 24013560 DOI: 10.1093/Nar/Gkt808 |
0.521 |
|
2013 |
Pawar MG, Nuthanakanti A, Srivatsan SG. Heavy atom containing fluorescent ribonucleoside analog probe for the fluorescence detection of RNA-ligand binding. Bioconjugate Chemistry. 24: 1367-77. PMID 23841942 DOI: 10.1021/Bc400194G |
0.412 |
|
2013 |
Tanpure AA, Pawar MG, Srivatsan SG. Fluorescent Nucleoside Analogs: Probes for Investigating Nucleic Acid Structure and Function Israel Journal of Chemistry. 53: 366-378. DOI: 10.1002/Ijch.201300010 |
0.391 |
|
2012 |
Tanpure AA, Srivatsan SG. Synthesis and photophysical characterisation of a fluorescent nucleoside analogue that signals the presence of an abasic site in RNA. Chembiochem : a European Journal of Chemical Biology. 13: 2392-9. PMID 23070860 DOI: 10.1002/Cbic.201200408 |
0.427 |
|
2012 |
Rao H, Tanpure AA, Sawant AA, Srivatsan SG. Enzymatic incorporation of an azide-modified UTP analog into oligoribonucleotides for post-transcriptional chemical functionalization. Nature Protocols. 7: 1097-112. PMID 22576108 DOI: 10.1038/Nprot.2012.046 |
0.334 |
|
2012 |
Tanpure AA, Patheja P, Srivatsan SG. Label-free fluorescence detection of the depurination activity of ribosome inactivating protein toxins. Chemical Communications (Cambridge, England). 48: 501-3. PMID 22105782 DOI: 10.1039/C1Cc16667K |
0.361 |
|
2012 |
Rao H, Sawant AA, Tanpure AA, Srivatsan SG. Posttranscriptional chemical functionalization of azide-modified oligoribonucleotides by bioorthogonal click and Staudinger reactions. Chemical Communications (Cambridge, England). 48: 498-500. PMID 22006199 DOI: 10.1039/C1Cc15659D |
0.388 |
|
2011 |
Tanpure AA, Srivatsan SG. A microenvironment-sensitive fluorescent pyrimidine ribonucleoside analogue: synthesis, enzymatic incorporation, and fluorescence detection of a DNA abasic site. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 12820-7. PMID 21956450 DOI: 10.1002/Chem.201101194 |
0.435 |
|
2011 |
Pawar MG, Srivatsan SG. Synthesis, photophysical characterization, and enzymatic incorporation of a microenvironment-sensitive fluorescent uridine analog. Organic Letters. 13: 1114-7. PMID 21275418 DOI: 10.1021/Ol103147T |
0.408 |
|
2011 |
Srivatsan SG, Sawant AA. Fluorescent ribonucleoside analogues as probes for investigating RNA structure and function Pure and Applied Chemistry. 83: 213-232. DOI: 10.1351/Pac-Con-10-09-16 |
0.423 |
|
2009 |
Srivatsan SG, Tor Y. Enzymatic incorporation of emissive pyrimidine ribonucleotides. Chemistry, An Asian Journal. 4: 419-27. PMID 19072942 DOI: 10.1002/Asia.200800370 |
0.573 |
|
2008 |
Srivatsan SG, Greco NJ, Tor Y. A highly emissive fluorescent nucleoside that signals the activity of toxic ribosome-inactivating proteins. Angewandte Chemie (International Ed. in English). 47: 6661-5. PMID 18683267 DOI: 10.1002/Anie.200802199 |
0.695 |
|
2008 |
Fusz S, Srivatsan SG, Ackermann D, Famulok M. Photocleavable initiator nucleotide substrates for an aldolase ribozyme. The Journal of Organic Chemistry. 73: 5069-77. PMID 18517252 DOI: 10.1021/Jo800639P |
0.689 |
|
2008 |
Srivatsan SG, Weizman H, Tor Y. A highly fluorescent nucleoside analog based on thieno[3,4-d]pyrimidine senses mismatched pairing. Organic & Biomolecular Chemistry. 6: 1334-8. PMID 18385838 DOI: 10.1039/B801054D |
0.582 |
|
2008 |
Srivatsan S, Greco N, Tor Y. Cover Picture: A Highly Emissive Fluorescent Nucleoside that Signals the Activity of Toxic Ribosome-Inactivating Proteins (Angew. Chem. Int. Ed. 35/2008) Angewandte Chemie International Edition. 47: 6495-6495. DOI: 10.1002/Anie.200890170 |
0.7 |
|
2008 |
Srivatsan S, Greco N, Tor Y. Titelbild: A Highly Emissive Fluorescent Nucleoside that Signals the Activity of Toxic Ribosome-Inactivating Proteins (Angew. Chem. 35/2008) Angewandte Chemie. 120: 6595-6595. DOI: 10.1002/Ange.200890224 |
0.7 |
|
2007 |
Srivatsan SG, Tor Y. Using an emissive uridine analogue for assembling fluorescent HIV-1 TAR constructs. Tetrahedron. 63: 3601-3607. PMID 18431440 DOI: 10.1016/J.Tet.2007.01.074 |
0.586 |
|
2007 |
Srivatsan SG, Famulok M. Functional nucleic acids in high throughput screening and drug discovery. Combinatorial Chemistry & High Throughput Screening. 10: 698-705. PMID 18045081 DOI: 10.2174/138620707782507359 |
0.65 |
|
2007 |
Srivatsan SG, Tor Y. Synthesis and enzymatic incorporation of a fluorescent pyrimidine ribonucleotide. Nature Protocols. 2: 1547-55. PMID 17571062 DOI: 10.1038/Nprot.2007.222 |
0.614 |
|
2007 |
Srivatsan SG, Tor Y. Fluorescent pyrimidine ribonucleotide: synthesis, enzymatic incorporation, and utilization. Journal of the American Chemical Society. 129: 2044-53. PMID 17256858 DOI: 10.1021/Ja066455R |
0.611 |
|
2007 |
Tor Y, Del Valle S, Jaramillo D, Srivatsan SG, Rios A, Weizman H. Designing new isomorphic fluorescent nucleobase analogues: the thieno[3,2-d]pyrimidine core Tetrahedron. 63: 3608-3614. DOI: 10.1016/J.Tet.2007.01.075 |
0.73 |
|
2006 |
Hafner M, Schmitz A, Grüne I, Srivatsan SG, Paul B, Kolanus W, Quast T, Kremmer E, Bauer I, Famulok M. Inhibition of cytohesins by SecinH3 leads to hepatic insulin resistance. Nature. 444: 941-4. PMID 17167487 DOI: 10.1038/Nature05415 |
0.7 |
|
2005 |
Fusz S, Eisenführ A, Srivatsan SG, Heckel A, Famulok M. A ribozyme for the aldol reaction. Chemistry & Biology. 12: 941-50. PMID 16125106 DOI: 10.1016/J.Chembiol.2005.06.008 |
0.686 |
|
2004 |
Chandrasekhar V, Deria P, Krishnan V, Athimoolam A, Singh S, Madhavaiah C, Srivatsan SG, Verma S. Metalated hybrid polymers as catalytic reagents for phosphate ester hydrolysis and plasmid modification. Bioorganic & Medicinal Chemistry Letters. 14: 1559-62. PMID 15006403 DOI: 10.1016/J.Bmcl.2003.12.082 |
0.67 |
|
2004 |
Srivatsan SG. Modeling prebiotic catalysis with nucleic acid-like polymers and its implications for the proposed RNA world Pure and Applied Chemistry. 76: 2085-2099. DOI: 10.1351/Pac200476122085 |
0.376 |
|
2004 |
Saxena A, Srivatsan SG, Saxena V, Verma S. Bioinspired Modification of Polystyryl Matrix: Single-step Chemical Evolution to a Moderately Conducting Polymer Chemistry Letters. 33: 740-741. DOI: 10.1246/Cl.2004.740 |
0.627 |
|
2003 |
Srivatsan SG, Parvez M, Verma S. Adenine-copper coordination polymer as an oxidative nucleozyme: implications for simple prebiotic catalytic units. Journal of Inorganic Biochemistry. 97: 340-4. PMID 14568238 DOI: 10.1016/S0162-0134(03)00285-X |
0.654 |
|
2003 |
Mukhopadhyay R, Srivatsan SG, Verma S. Surface trapping and AFM detection of DNA topological intermediates generated from an oxidative chemical nuclease Biochemical and Biophysical Research Communications. 308: 165-169. PMID 12890496 DOI: 10.1016/S0006-291X(03)01351-2 |
0.602 |
|
2003 |
Verma S, Srivatsan SG, Claussen CA, Long EC. DNA strand scission by a Cu(I).adenylated polymeric template: preliminary mechanistic and recycling studies. Bioorganic & Medicinal Chemistry Letters. 13: 2501-4. PMID 12852952 DOI: 10.1016/S0960-894X(03)00501-8 |
0.642 |
|
2003 |
Madhavaiah C, Srivatsan S, Verma S. Heterogeneously active nucleolytic reagents: flexible design of reusable catalysts for nucleic acid scission Catalysis Communications. 4: 237-241. DOI: 10.1016/S1566-7367(03)00050-5 |
0.646 |
|
2002 |
Srivatsan SG, Parvez M, Verma S. Modeling of prebiotic catalysis with adenylated polymeric templates: crystal structure studies and kinetic characterization of template-assisted phosphate ester hydrolysis. Chemistry (Weinheim An Der Bergstrasse, Germany). 8: 5184-91. PMID 12613036 DOI: 10.1002/1521-3765(20021115)8:22<5184::Aid-Chem5184>3.0.Co;2-2 |
0.655 |
|
2002 |
Chandrasekhar V, Athimoolam A, Srivatsan SG, Sundaram PS, Verma S, Steiner A, Zacchini S, Butcher R. Pyrazolylcyclotriphosphazene containing pendant polymers: synthesis, characterization, and phosphate ester hydrolysis using a Cu(II)-metalated cross-linked polymeric catalyst. Inorganic Chemistry. 41: 5162-73. PMID 12354050 DOI: 10.1021/Ic011159V |
0.624 |
|
2002 |
Srivatsan SG, Verma S, Parvez M. 4-Vinylbenzyl analogs of adenine and uracil: reactive monomers for nucleobase polymeric resins. Acta Crystallographica. Section C, Crystal Structure Communications. 58: o378-80. PMID 12094051 DOI: 10.1107/S0108270102007515 |
0.595 |
|
2002 |
Srivatsan SG, Kingsley S, Verma S. Self-Assembly of 9-Allyladenine Hydrochloride in Crystalline State: Formation of Infinitely Stacked Supramolecular SheetsviaHydrogen Bonding Network Chemistry Letters. 31: 240-241. DOI: 10.1246/Cl.2002.240 |
0.599 |
|
2002 |
Madhavaiah C, Srivatsan S, Verma S. Kinetic and mechanistic investigations of phosphodiester cleavage catalyzed by uranyl ion impregnated adenylated homopolymer Catalysis Communications. 3: 299-303. DOI: 10.1016/S1566-7367(02)00134-6 |
0.614 |
|
2001 |
Srivatsan SG, Verma S. Nucleobase-containing metallated polymeric resins as artificial phosphodiesterases: kinetics of hydrolysis, pH dependence, and catalyst recycling. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 828-33. PMID 11288874 DOI: 10.1002/1521-3765(20010216)7:4<828::Aid-Chem828>3.0.Co;2-Z |
0.648 |
|
2001 |
Madhavaiah C, Srivatsan S, Verma S. Ruthenium-metallated adenine nucleobase polymers as novel reagents for catalytic cleavage of phosphate esters Catalysis Communications. 2: 95-99. DOI: 10.1016/S1566-7367(01)00014-0 |
0.656 |
|
2001 |
Srivatsan S, Nigam P, Rao M, Verma S. Phenol oxidation by copper-metallated 9-allyladenine-DVB polymer: reaction catalysis and polymer recycling Applied Catalysis a: General. 209: 327-334. DOI: 10.1016/S0926-860X(00)00765-1 |
0.647 |
|
2000 |
Srivatsan SG, Verma S. Synthetic dephosphorylation reagents: rate enhancement of phosphate monoester hydrolysis by Cu(II)-metallated adenine nucleobase polymers Chemical Communications. 515-516. DOI: 10.1039/B000348O |
0.646 |
|
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