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Silver soldering of PNA:DNA duplexes: assembly of a triple duplex from bimodal PNAs with all-C on one face

Chemical communications (Cambridge, England), 2022-03, Vol.58 (25), p.483-486

2022

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Perfluoroalkylchain conjugation as a new tactic for enhancing cell permeability of peptide nucleic acids (PNAs) via reducing the nanoparticle size

Chemical communications (Cambridge, England), 2016-01, Vol.52 (3), p.521-524

2016

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A nanofiber assembly directed by the non-classical antiparallel β-structure from 4S-(OH) proline polypeptide

Chemical communications (Cambridge, England), 2016-04, Vol.52 (27), p.4884-4887

2016

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PNA C-C+ i-motif: superior stability of PNA TC8 tetraplexes compared to DNA TC8 tetraplexes at low pH

Chemical communications (Cambridge, England), 2005-09 (34), p.4330-4332

2005

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Two prolines with a difference: contrasting stereoelectronic effects of 4R/S-aminoproline on triplex stability in collagen peptides [pro(X)-pro(Y)-Gly]n

Chemical communications (Cambridge, England), 2003-10 (20), p.2606-2607

2003

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cis-Cyclopentyl PNA (cpPNA) as constrained chiral PNA analogues: stereochemical dependence of DNA/RNA hybridization

Chemical communications (Cambridge, England), 2004-04 (7), p.860-861

2004

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Expanding the repertoire of pyrrolidyl PNA analogues for DNA/RNA hybridization selectivity: aminoethylpyrrolidinone PNA (aepone-PNA)

Chemical communications (Cambridge, England), 2003-10 (19), p.2484-2485

2003

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Perfluoroalkylchain conjugation as a new tactic for enhancing cell permeability of peptide nucleic acids (PNAs) viareducing the nanoparticle size

Chemical communications (Cambridge, England), 2015-12, Vol.52 (3), p.521-524

2015

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cis-Cyclopentyl PNA (cpPNA) as constrained chiral PNA analogues: stereochemical dependence of DNA/RNA hybridizationElectronic Supplementary Information (ESI) available: Experimental procedures for the synthesis of compounds, 1H, 13C NMR, mass spectral data, crystal structural data and melting curves for triplexes. See http://www.rsc.org/suppdata/cc/b3/b317000d

Chemical communications (Cambridge, England), 2004-03 (7), p.860

2004

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Two prolines with a difference: contrasting stereoelectronic effects of 4R/S-aminoproline on triplex stability in collagen peptides [Pro(X)-Pro(Y)-Gly]nElectronic supplementary information (ESI) available: 1H NMR spectra and coupling constant analysis of 3 and 4; synthetic schemes for 3, 4, 5 and 6; FABMS of 3 and 4; MALDI-TOF MS of 5 and 6; HPLC of peptides 5 and 6. See http://www.rsc.org/suppdata/cc/b3/b308581c

Chemical communications (Cambridge, England), 2003-10 (20), p.2606

2003

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Sequential entrapment of PNA and DNA in lipid bilayers stacks

Chemical communications (Cambridge, England), 2001-12 (24), p.2622-2623

2001

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Cationic surfactant mediated hybridization and hydrophobization of DNA molecules at the liquid/liquid interface and their phase transfer

Chemical communications (Cambridge, England), 2001 (16), p.1434-1435

2001

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2-Aminopurine peptide nucleic acids (2-apPNA): intrinsic fluorescent PNA analogues for probing PNA–DNA interaction dynamics

Chemical communications (Cambridge, England), 1997 (19), p.1913

1997

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Silver soldering of PNA:DNA duplexes: assembly of a triple duplex from bimodal PNAs with all-C on one face

Perfluoroalkylchain conjugation as a new tactic for enhancing cell permeability of peptide nucleic acids (PNAs) via reducing the nanoparticle size

A nanofiber assembly directed by the non-classical antiparallel β-structure from 4S-(OH) proline polypeptide

PNA C-C+ i-motif: superior stability of PNA TC8 tetraplexes compared to DNA TC8 tetraplexes at low pH

Two prolines with a difference: contrasting stereoelectronic effects of 4R/S-aminoproline on triplex stability in collagen peptides [pro(X)-pro(Y)-Gly]n

cis-Cyclopentyl PNA (cpPNA) as constrained chiral PNA analogues: stereochemical dependence of DNA/RNA hybridization

Expanding the repertoire of pyrrolidyl PNA analogues for DNA/RNA hybridization selectivity: aminoethylpyrrolidinone PNA (aepone-PNA)

Perfluoroalkylchain conjugation as a new tactic for enhancing cell permeability of peptide nucleic acids (PNAs) viareducing the nanoparticle size

Sequential entrapment of PNA and DNA in lipid bilayers stacks

Cationic surfactant mediated hybridization and hydrophobization of DNA molecules at the liquid/liquid interface and their phase transfer

2-Aminopurine peptide nucleic acids (2-apPNA): intrinsic fluorescent PNA analogues for probing PNA–DNA interaction dynamics

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