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Jyoti Chattopadhyaya

Jyoti Chattopadhyaya

D-Index & Metrics

Chemistry

D-Index
53
Citations
10498
World Ranking
13037
National Ranking
195

Overview

Jyoti Chattopadhyaya is affiliated with Uppsala University in Sweden. Their academic profile does not currently include records of recent papers, co-authors, or frequent publication venues. Additionally, there are no listed book publications associated with their name.

Information regarding primary fields of study, subfields, and main research topics for Jyoti Chattopadhyaya is not available in the dataset. There is also no record of awards received during their career.

Despite the limited data on publications and research areas, the association with Uppsala University suggests involvement in a research environment known for diverse scientific activities and disciplines. Further data would be required to provide a more detailed overview of their specific contributions and areas of expertise.

Best Publications

  • A large-scale chemical modification screen identifies design rules to generate siRNAs with high activity, high stability and low toxicity

    Jesper B. Bramsen;Maria B. Laursen;Anne F. Nielsen;Thomas B. Hansen

  • How do the gauche and anomeric effects drive the pseudorotational equilibrium of the pentofuranose moiety of nucleosides

    Janez Plavec;Weimin Tong;Jyoti Chattopadhyaya

  • A screen of chemical modifications identifies position-specific modification by UNA to most potently reduce siRNA off-target effects

    Jesper B. Bramsen;Malgorzata M. Pakula;Thomas B. Hansen;Claus Bus

  • Structure and toxicity of a peptide hepatotoxin from the cyanobacterium Oscillatoria agardhii.

    J.A.O. Meriluoto;A. Sandström;J.E. Eriksson;G. Remaud

  • Fine tuning of electrostatics around the internucleotidic phosphate through incorporation of modified 2',4'-carbocyclic-LNAs and -ENAs leads to significant modulation of antisense properties.

    Chuanzheng Zhou;Yi Liu;Mounir Andaloussi;Naresh Badgujar

  • A New Generalized Karplus-Type Equation Relating Vicinal Proton-Fluorine Coupling Constants to H−C−C−F Torsion Angles

    Christophe Thibaudeau;Janez Plavec;Jyoti Chattopadhyaya

  • A critical survey of the structure-function of the antisense oligo/RNA heteroduplex as substrate for RNase H.

    Edouard Zamaratski;P.I. Pradeepkumar;Jyoti Chattopadhyaya

  • Design, synthesis, biological evaluation and molecular modelling studies of novel quinoline derivatives against Mycobacterium tuberculosis.

    Ram Shankar Upadhayaya;Jaya Kishore Vandavasi;Nageswara Rao Vasireddy;Vivek Sharma

  • Allele-selective inhibition of mutant huntingtin expression with antisense oligonucleotides targeting the expanded CAG repeat.

    Keith T. Gagnon;Hannah M. Pendergraff;Glen F. Deleavey;Eric E. Swayze

  • Five- and Six-Membered Conformationally Locked 2',4'-Carbocyclic ribo-Thymidines: Synthesis, Structure, and Biochemical Studies

    Puneet Srivastava;Jharna Barman;Wimal Pathmasiri;Oleksandr Plashkevych

  • The pKa's of 2‘-Hydroxyl Group in Nucleosides and Nucleotides

    Irina Velikyan;Sandipta Acharya;Anna Trifonova;and Andras Földesi

  • Inhibition of the reverse transcriptase from HIV by 3'-azido-3'-deoxythymidine triphosphate and its threo analogue.

    Lotta Vrang;Hervé Bazin;Gerald Remaud;Jyoti Chattopadhyaya

  • Rapid and quantitative recovery of DNA fragments from gels by displacement electrophoresis (isotachophoresis).

    Lars-Göran Öfverstedt;Karin Hammarström;Neil Balgobin;Stellan Hjertén

  • How Does the Electronegativity of the Substituent Dictate the Strength of the Gauche Effect

    C. Thibaudeau;J. Plavec;N. Garg;A. Papchikhin

  • Single-stranded adenine-rich DNA and RNA retain structural characteristics of their respective double-stranded conformations and show directional differences in stacking pattern.

    Johan Isaksson;Sandipta Acharya;Jharna Barman;Pradeep Cheruku

  • Chemical synthesis of a tridecanucleoside dodecaphosphate sequence of SV40 DNA

    J.B. Chattopadhyaya;C.B. Reese

  • How Does the 2'-Hydroxy Group Drive the Pseudorotational Equilibrium in Nucleoside and Nucleotide by the Tuning of the 3'-Gauche Effect?

    Janez Plavec;Christophe Thibaudeau;Jyoti Chattopadhyaya

  • Quantitation of the pD Dependent Thermodynamics of the N ⇄ S Pseudorotational Equilibrium of the Pentofuranose Moiety in Nucleosides Gives a Direct Measurement of the Strength of the Tunable Anomeric Effect and the pKa of the Nucleobase†

    C. Thibaudeau;J. Plavec;J. Chattopadhyaya

  • Conformationally constrained 2'-N,4'-C-ethylene-bridged thymidine (aza-ENA-T): synthesis, structure, physical, and biochemical studies of aza-ENA-T-modified oligonucleotides.

    Oommen P. Varghese;Jharna Barman;Wimal Pathmasiri;Oleksandr Plashkevych

  • Measurement of nucleobase pKa values in model mononucleotides shows RNA-RNA duplexes to be more stable than DNA-DNA duplexes

    P Acharya;P Cheruku;S Chatterjee;S Acharya

  • How do the energetics of the stereoelectronic gauche and anomeric effects modulate the conformation of nucleos(t)ides

    J. Plavec;C. Thibaudeau;Jyoti Chattopadhyaya

Frequent Co-Authors

Colin B. Reese
Colin B. Reese University of Cambridge
Christopher J. Welch
Christopher J. Welch Indiana Consortium for Analytical Science & Engineering
Ivar Ugi
Ivar Ugi Technical University of Munich
Harri Lönnberg
Harri Lönnberg University of Turku
Akira Matsuda
Akira Matsuda Juntendo University
Stephen Neidle
Stephen Neidle University College London
Masad J. Damha
Masad J. Damha McGill University
Eric E. Swayze
Eric E. Swayze Ionis Pharmaceuticals (United States)
Jussi Meriluoto
Jussi Meriluoto Åbo Akademi University
Olov Sterner
Olov Sterner Lund University

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