897 related articles for article (PubMed ID: 16888742)
1. Nanoswitches based on DNA base pairs: why adenine-thymine is less suitable than guanine-cytosine.
Fonseca Guerra C; van der Wijst T; Bickelhaupt FM
Chemphyschem; 2006 Sep; 7(9):1971-9. PubMed ID: 16888742
[TBL] [Abstract][Full Text] [Related]
2. Supramolecular switches based on the guanine-cytosine (GC) Watson-Crick pair: effect of neutral and ionic substituents.
Fonseca Guerra C; van der Wijst T; Bickelhaupt FM
Chemistry; 2006 Apr; 12(11):3032-42. PubMed ID: 16453355
[TBL] [Abstract][Full Text] [Related]
3. Direct assessment of interresidue forces in Watson-Crick base pairs using theoretical compliance constants.
Grunenberg J
J Am Chem Soc; 2004 Dec; 126(50):16310-1. PubMed ID: 15600318
[TBL] [Abstract][Full Text] [Related]
4. Double-proton transfer in adenine-thymine and guanine-cytosine base pairs. A post-Hartree-Fock ab initio study.
Gorb L; Podolyan Y; Dziekonski P; Sokalski WA; Leszczynski J
J Am Chem Soc; 2004 Aug; 126(32):10119-29. PubMed ID: 15303888
[TBL] [Abstract][Full Text] [Related]
5. True stabilization energies for the optimal planar hydrogen-bonded and stacked structures of guanine...cytosine, adenine...thymine, and their 9- and 1-methyl derivatives: complete basis set calculations at the MP2 and CCSD(T) levels and comparison with experiment.
Jurecka P; Hobza P
J Am Chem Soc; 2003 Dec; 125(50):15608-13. PubMed ID: 14664608
[TBL] [Abstract][Full Text] [Related]
6. Interaction energy contributions of H-bonded and stacked structures of the AT and GC DNA base pairs from the combined density functional theory and intermolecular perturbation theory approach.
Hesselmann A; Jansen G; Schütz M
J Am Chem Soc; 2006 Sep; 128(36):11730-1. PubMed ID: 16953592
[TBL] [Abstract][Full Text] [Related]
7. Stabilization energies of the hydrogen-bonded and stacked structures of nucleic acid base pairs in the crystal geometries of CG, AT, and AC DNA steps and in the NMR geometry of the 5'-d(GCGAAGC)-3' hairpin: Complete basis set calculations at the MP2 and CCSD(T) levels.
Dabkowska I; Gonzalez HV; Jurecka P; Hobza P
J Phys Chem A; 2005 Feb; 109(6):1131-6. PubMed ID: 16833422
[TBL] [Abstract][Full Text] [Related]
8. Density functional theory-symmetry adapted perturbation treatment energy decomposition of nucleic acid base pairs taken from DNA crystal geometry.
Sedlák R; Jurecka P; Hobza P
J Chem Phys; 2007 Aug; 127(7):075104. PubMed ID: 17718635
[No Abstract] [Full Text] [Related]
9. Binding of gold clusters with DNA base pairs: a density functional study of neutral and anionic GC-Aun and AT-Aun (n = 4, 8) complexes.
Kumar A; Mishra PC; Suhai S
J Phys Chem A; 2006 Jun; 110(24):7719-27. PubMed ID: 16774220
[TBL] [Abstract][Full Text] [Related]
10. A theoretical study of structures and electron affinities of radical anions of guanine-cytosine, adenine-thymine, and hypoxanthine-cytosine base pairs.
Kumar A; Knapp-Mohammady M; Mishra PC; Suhai S
J Comput Chem; 2004 Jun; 25(8):1047-59. PubMed ID: 15067680
[TBL] [Abstract][Full Text] [Related]
11. On the aromatic character of the heterocyclic bases of DNA and RNA.
Cyrański MK; Gilski M; Jaskólski M; Krygowski TM
J Org Chem; 2003 Oct; 68(22):8607-13. PubMed ID: 14575493
[TBL] [Abstract][Full Text] [Related]
12. Coupling between hydrogen atoms transfer and stacking interaction in adenine-thymine/guanine-cytosine complexes: a theoretical study.
Villani G
J Phys Chem B; 2014 May; 118(20):5439-52. PubMed ID: 24813562
[TBL] [Abstract][Full Text] [Related]
13. A TDDFT study of the optical response of DNA bases, base pairs, and their tautomers in the gas phase.
Tsolakidis A; Kaxiras E
J Phys Chem A; 2005 Mar; 109(10):2373-80. PubMed ID: 16839008
[TBL] [Abstract][Full Text] [Related]
14. Hydrogen bonding in mimics of Watson-Crick base pairs involving C-H proton donor and F proton acceptor groups: a theoretical study.
Guerra CF; Bickelhaupt FM; Baerends EJ
Chemphyschem; 2004 Apr; 5(4):481-7. PubMed ID: 15139221
[TBL] [Abstract][Full Text] [Related]
15. FTIR and UV spectroscopy of parallel-stranded DNAs with mixed A*T/G*C sequences and their A*T/I*C analogues.
Mohammadi S; Klement R; Shchyolkina AK; Liquier J; Jovin TM; Taillandier E
Biochemistry; 1998 Nov; 37(47):16529-37. PubMed ID: 9843419
[TBL] [Abstract][Full Text] [Related]
16. Propeller-twisted adenine.thymine and guanine.cytosine base pairs tend to buckle and stagger in opposite directions.
Jursa J; Kypr J
Gen Physiol Biophys; 1991 Aug; 10(4):373-81. PubMed ID: 1769516
[TBL] [Abstract][Full Text] [Related]
17. Does the A.T or G.C base-pair possess enhanced stability? Quantifying the effects of CH...O interactions and secondary interactions on base-pair stability using a phenomenological analysis and ab initio calculations.
Quinn JR; Zimmerman SC; Del Bene JE; Shavitt I
J Am Chem Soc; 2007 Jan; 129(4):934-41. PubMed ID: 17243830
[TBL] [Abstract][Full Text] [Related]
18. Marked influences on the adenine-cytosine base pairs by electron attachment and ionization.
Tian SX
J Phys Chem A; 2005 Jun; 109(23):5153-9. PubMed ID: 16833870
[TBL] [Abstract][Full Text] [Related]
19. Theoretical investigation of the proton transfer mechanism in guanine-cytosine and adenine-thymine base pairs.
Xiao S; Wang L; Liu Y; Lin X; Liang H
J Chem Phys; 2012 Nov; 137(19):195101. PubMed ID: 23181336
[TBL] [Abstract][Full Text] [Related]
20. Prediction of interaction energies of substituted hydrogen-bonded Watson-Crick cytosine:guanine(8X) base pairs.
Xue C; Popelier PL
J Phys Chem B; 2009 Mar; 113(10):3245-50. PubMed ID: 19260717
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]