biblio

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2014
S. Nahar, Bose, D., Panja, S. Kumar, Saha, S., and Maiti, S., “Anti-cancer therapeutic potential of quinazoline based small molecules via global upregulation of miRNAs”, Chemical Communications, vol. 50, no. 35, pp. 4639-4642, 2014.
2015
T. Bose, Banerjee, A., Nahar, S., Maiti, S., and Kumar, V. A., “Beta, gamma-Bis-substituted PNA with configurational and conformational switch: preferred binding to cDNA/RNA and cell-uptake studies”, Chemical Communications, vol. 51, no. 36, pp. 7693-7696, 2015.
S. Nahar, Bose, D., Pal, S., Chakraborty, T. Kanti, and Maiti, S., “Cyclic cationic peptides containing sugar amino acids selectively distinguishes and inhibits maturation of pre-mirnas of the same family”, Nucleic Acid Therapeutics, vol. 25, no. 6, pp. 323-329, 2015.
G. Gunanathan Jayaraj, Nahar, S., and Maiti, S., “Nonconventional chemical inhibitors of microRNA: therapeutic scope”, Chemical Communications, vol. 51, no. 5, pp. 820-831, 2015.
S. Nahar, Ranjan, N., Ray, A., Arya, D. P., and Maiti, S., “Potent inhibition of miR-27a by neomycin-bisbenzimidazole conjugates”, Chemical Science, vol. 6, no. 10, pp. 5837-5846, 2015.
D. Bose, Nahar, S., Rai, M. Kumar, Ray, A., Chakraborty, K., and Maiti, S., “Selective inhibition of miR-21 by phage display screened peptide”, Nucleic Acids Research, vol. 43, no. 8, pp. 4342-4352, 2015.
2016
S. Nahar, Kotikam, V., Kumar, V. A., and Maiti, S., “Inhibition of miR-21 by 3 `/5 `-serinyl-capped 2 `-O-Methyl RNA Interspersed with 2 `-O-(2-Amino-3-Methoxypropyl) uridine units”, Nucleic Acid Therapeutics, vol. 26, no. 5, pp. 327-334, 2016.
S. Nahar, Singh, A., Morihiro, K., Moai, Y., Kodama, T., Obika, S., and Maiti, S., “Systematic evaluation of biophysical and functional characteristics of selenomethylene-locked nucleic acid-mediated inhibition of miR-21”, Biochemistry, vol. 55, no. 50, pp. 7023-7032, 2016.
2018
S. Nahar, Sehgal, P., Azhar, M., Rai, M., Singh, A., Sivasubbu, S., Chakraborty, D., and Maiti, S., “G-quadruplex motif at the 3' end of sgRNAs improves CRISPR-Cas9 based genome editing efficiency”, Chemical Communications, vol. 54, no. 19, pp. 2377-2380, 2018.