@article { ISI:000359962900040,
	title = {Glycine-linked nucleoside-beta-amino acids: polyamide analogues of nucleic acids},
	journal = {Bioconjugate Chemistry},
	volume = {26},
	number = {8},
	year = {2015},
	month = {AUG},
	pages = {1737-1742},
	publisher = {AMER CHEMICAL SOC},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>3{\textquoteright}-5{\textquoteright}-Deoxyribose-sugar-phoshate backbone in DNA is completely replaced by 2{\textquoteright}-deoxyribonucleoside-based beta-amino acids interlinked by glycine to create uncharged polyamide DNA with 3{\textquoteright}-5{\textquoteright}-directionality. These oligomers as conjugates of alpha-amino acids and nucleoside-beta-amino acids bind strongly and sequence-specifically only to the antiparallel complementary RNA and DNA.</p>},
	issn = {1043-1802},
	doi = {10.1021/acs.bioconjchem.5b00296},
	author = {Banerjee, Anjan and Seema Bagmare and Varada, Manojkumar and Kumar, Vaijayanti A.}
}
