DNA triple-helix formation at pyrimidine-purine inversion sites


Autoria(s): Parel, S. P.; Marfurt, J.; Leumann, Christian
Data(s)

2001

Resumo

A systematic investigation of a series of triplex forming oligonucleotides (TFOs) containing alpha- and beta-thymidine, alpha- and beta-N7-hypoxanthine, and alpha- and beta- N7 and N9 aminopurine nucleosides, designed to bind to T-A inversion sites in DNA target sequences was performed. Data obtained from gel mobility assays indicate that t-A recognition in the antiparallel triple-helical binding motif is possible if the nucleoside alpha N9-aminopurine is used opposite to the inversion site in the TFO.

Formato

application/pdf

Identificador

http://boris.unibe.ch/68586/1/8824635.pdf

Parel, S. P.; Marfurt, J.; Leumann, Christian (2001). DNA triple-helix formation at pyrimidine-purine inversion sites. Nucleosides, nucleotides & nucleic acids, 20(4-7), pp. 411-417. Taylor & Francis 10.1081/NCN-100002315 <http://dx.doi.org/10.1081/NCN-100002315>

doi:10.7892/boris.68586

info:doi:10.1081/NCN-100002315

info:pmid:11563056

urn:issn:1525-7770

Idioma(s)

eng

Publicador

Taylor & Francis

Relação

http://boris.unibe.ch/68586/

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Parel, S. P.; Marfurt, J.; Leumann, Christian (2001). DNA triple-helix formation at pyrimidine-purine inversion sites. Nucleosides, nucleotides & nucleic acids, 20(4-7), pp. 411-417. Taylor & Francis 10.1081/NCN-100002315 <http://dx.doi.org/10.1081/NCN-100002315>

Palavras-Chave #570 Life sciences; biology #540 Chemistry
Tipo

info:eu-repo/semantics/article

info:eu-repo/semantics/publishedVersion

PeerReviewed