N. Graciani

发表

Matrix metalloproteinase–activated doxorubicin prodrugs inhibit HT1080 xenograft growth better than doxorubicin with less toxicity

G. Trainor, R. Copeland, S. P. Seitz, 2005, Molecular Cancer Therapeutics.

Analysis of protein-peptide interaction by a miniaturized fluorescence polarization assay using cyclin-dependent kinase 2/cyclin E as a model system.

I. Kariv, K. Oldenburg, N. Graciani, 1999, Analytical biochemistry.

A continuous fluorometric assay of myristoyl-coenzyme A:protein N-myristoyltransferase.

N. Georgopapadakou, D. Pompliano, C. Pennise, 2002, Analytical Biochemistry.

Discovery of matrix metalloproteases selective and activated peptide-doxorubicin prodrugs as anti-tumor agents.

G. Trainor, S. P. Seitz, C. Albright, 2010, Bioorganic & medicinal chemistry letters.

Solid-phase synthesis of a selective αvβ3 integrin antagonist library

W. DeGrado, S. Mousa, N. Graciani, 1997 .

Nucleated Antiparallel β-Sheet That Folds and Undergoes Self-Assembly: A Template Promoted Folding Strategy toward Controlled Molecular Architectures

J. Kelly, J. Schneider, N. Graciani, 1996 .

Phosphomonoesters and phosphodiesters derived from the photohydrolysis of 2-methoxy-5-nitrophenyl substituted phosphotriesters

J. Kelly, N. Graciani, Daniel S. Swanson, 1995 .

HYDROPHOBIC CLUSTER FORMATION IS NECESSARY FOR DIBENZOFURAN-BASED AMINO ACIDS TO FUNCTION AS BETA -SHEET NUCLEATORS

J. Kelly, H. Díaz, Jeffery W. Kelly, 1994 .

Mechanism of Inhibition of β-Site Amyloid Precursor Protein-cleaving Enzyme (BACE) by a Statine-based Peptide*

Y. Luo, J. Marcinkeviciene, R. Copeland, 2001, The Journal of Biological Chemistry.

Amino acids that specify structure through hydrophobic clustering and histidine-aromatic interactions lead to biologically active peptidomimetics.

J. Kelly, N. Graciani, K. Tsang, 1994, Bioorganic & medicinal chemistry.

Antagonism of CRF2 receptors produces anxiolytic behavior in animal models of anxiety

L. Takahashi, S. Arneric, N. Graciani, 2001, Brain Research.

Comparative studies of active site-ligand interactions among various recombinant constructs of human beta-amyloid precursor protein cleaving enzyme.

M. Wittekind, M. Witmer, J. Yanchunas, 2003, Archives of biochemistry and biophysics.

Novel progesterone receptor modulators with gene selective and context-dependent partial agonism.

R. Winneker, S. Nagpal, S. Jelinsky, 2009, Biochemical pharmacology.

Formation of unusual glutamate conjugates of 1-[3-(aminomethyl)phenyl]-N-[3-fluoro-2'-(methylsulfonyl)-[1,1'-biphenyl]-4-yl]-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide (DPC 423) and its analogs: the role of gamma-glutamyltranspeptidase in the biotransformation of benzylamines.

A. Mutlib, J. Shockcor, L. Gan, 2001, Drug metabolism and disposition: the biological fate of chemicals.

Disposition of glutathione conjugates in rats by a novel glutamic acid pathway: characterization of unique peptide conjugates by liquid chromatography/mass spectrometry and liquid chromatography/NMR.

A. Mutlib, J. Shockcor, L. Gan, 2000, The Journal of pharmacology and experimental therapeutics.