Juan B. Blanco

发表

6- N,N -Dimethylamino-2,3-Naphthalimide a New Environment-Sensitive Fluorescent Probe in δ -Selective and μ -Selective Opioid Peptides

S. Salvadori, G. Balboni, M. Vázquez, 2007 .

Photophysics and biological applications of the environment-sensitive fluorophore 6-N,N-dimethylamino-2,3-naphthalimide.

B. Imperiali, M. Vázquez, Juan B Blanco, 2005, Journal of the American Chemical Society.

Specific DNA recognition by a synthetic, monomeric Cys2His2 zinc-finger peptide conjugated to a minor-groove binder.

M. Vázquez, J. Mascareñas, L. Castedo, 2007, Angewandte Chemie.

Sequence-specific DNA binding by noncovalent peptide-tripyrrole conjugates.

M. Vázquez, J. Mascareñas, V. Dodero, 2006, Angewandte Chemie.

6-N,N-Dimethylamino-2,3-naphthalimide: A New Environment-Sensitive Fluorescent Probe in δ- and μ-Selective Opioid Peptides

S. Salvadori, G. Balboni, R. Argazzi, 2006 .

6-N,N-dimethylamino-2,3-naphthalimide: a new environment-sensitive fluorescent probe in delta- and mu-selective opioid peptides.

S. Salvadori, G. Balboni, R. Argazzi, 2006, Journal of medicinal chemistry.

Sequence-specific DNA binding by noncovalent peptide-tripyrrole conjugates.

M. Vázquez, J. Mascareñas, V. Dodero, 2006, Angewandte Chemie.

Sequence‐Specific DNA Recognition by Monomeric bZIP Basic Regions Equipped with a Tripyrrole Unit on the N‐Terminal Side. Towards the Development of Synthetic Mimics of Skn‐1

M. Vázquez, J. Mascareñas, L. Castedo, 2005, Chembiochem : a European journal of chemical biology.

High affinity, sequence specific DNA binding by synthetic tripyrrole-peptide conjugates.

J. Martínez‐Costas, J. Mascareñas, L. Castedo, 2005, Chemistry.

A synthetic miniprotein that binds specific DNA sequences by contacting both the major and the minor groove.

M. Vázquez, J. Mascareñas, L. Castedo, 2003, Chemistry & biology.