Orientation preferences of backbone secondary amide functional groups in peptide nucleic acid complexes: quantum chemical calculations reveal an intrinsic preference of cationic D-amino acid-based chiral PNA analogues for the P-form.
about
Evaluating the effect of ionic strength on duplex stability for PNA having negatively or positively charged side chains.The DNA and RNA sugar-phosphate backbone emerges as the key player. An overview of quantum-chemical, structural biology and simulation studies.Effect of chirality in gamma-PNA: PNA interaction, another piece in the picturePNAs grafted with (α/γ, R/S)-aminomethylene pendants: regio and stereo specific effects on DNA binding and improved cell uptake.Molecular dynamics simulations of cyclohexyl modified peptide nucleic acids (PNA).Synthesis and structural characterization of monomeric and dimeric peptide nucleic acids prepared by using microwave-promoted multicomponent reactions
P2860
Orientation preferences of backbone secondary amide functional groups in peptide nucleic acid complexes: quantum chemical calculations reveal an intrinsic preference of cationic D-amino acid-based chiral PNA analogues for the P-form.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Orientation preferences of bac ...... PNA analogues for the P-form.
@ast
Orientation preferences of bac ...... PNA analogues for the P-form.
@en
type
label
Orientation preferences of bac ...... PNA analogues for the P-form.
@ast
Orientation preferences of bac ...... PNA analogues for the P-form.
@en
prefLabel
Orientation preferences of bac ...... PNA analogues for the P-form.
@ast
Orientation preferences of bac ...... PNA analogues for the P-form.
@en
P2860
P1433
P1476
Orientation preferences of bac ...... l PNA analogues for the P-form
@en
P2093
Christopher M Topham
P2860
P304
P356
10.1529/BIOPHYSJ.105.079723
P407
P577
2006-10-27T00:00:00Z