F. Hobbs

发表

A system for rapid DNA sequencing with fluorescent chain-terminating dideoxynucleotides.

J. M. Prober, G. Trainor, R. J. Dam, 1987, Science.

Identification of a Novel Inhibitor of Mitogen-activated Protein Kinase Kinase*

F. Hobbs, E. Manos, R. Copeland, 1998, The Journal of Biological Chemistry.

Potent antisense oligonucleotides to the human multidrug resistance-1 mRNA are rationally selected by mapping RNA-accessible sites with oligonucleotide libraries.

G. Trainor, F. Hobbs, B. Stone, 1996, Nucleic acids research.

MEK inhibitors: the chemistry and biological activity of U0126, its analogs, and cyclization products.

J. Wityak, G. Trainor, F. Hobbs, 1998, Bioorganic & medicinal chemistry letters.

Non-peptide corticotropin-releasing hormone antagonists: syntheses and structure-activity relationships of 2-anilinopyrimidines and -triazines.

E. D. De Souza, F. Hobbs, A. Cocuzza, 1999, Journal of medicinal chemistry.

Oxazolidinones Mechanism of Action: Inhibition of the First Peptide Bond Formation*

F. Hobbs, D. Pompliano, A. Slee, 2001, The Journal of Biological Chemistry.

Parallel synthesis of potent, pyrazole-based inhibitors of Helicobacter pylori dihydroorotate dehydrogenase.

J. Marcinkeviciene, G. Trainor, F. Hobbs, 2002, Journal of medicinal chemistry.

Synthesis, corticotropin-releasing factor receptor binding affinity, and pharmacokinetic properties of triazolo-, imidazo-, and pyrrolopyrimidines and -pyridines.

C. Hodge, Y. Wong, F. Hobbs, 1999, Journal of medicinal chemistry.

Selective inhibition of bacterial dihydroorotate dehydrogenases by thiadiazolidinediones.

T. Chung, J. Marcinkeviciene, G. Trainor, 2000, Biochemical pharmacology.

Biodistribution and metabolism of internally 3H-labeled oligonucleotides. I. Comparison of a phosphodiester and a phosphorothioate.

G. Trainor, F. Hobbs, A. Cocuzza, 1994, Molecular pharmacology.

Biodistribution and metabolism of internally 3H-labeled oligonucleotides. II. 3',5'-blocked oligonucleotides.

F. Hobbs, A. Cocuzza, H. Sands, 1995, Molecular pharmacology.

Helicobacter pylori-selective Antibacterials Based on Inhibition of Pyrimidine Biosynthesis*

J. Marcinkeviciene, G. Trainor, F. Hobbs, 2000, The Journal of Biological Chemistry.

Detection of single base differences using biotinylated nucleotides with very long linker arms.

K. Livak, F. Hobbs, R. Zagursky, 1992, Nucleic acids research.

Synthesis, structure-activity relationships, and in vivo evaluation of N3-phenylpyrazinones as novel corticotropin-releasing factor-1 (CRF1) receptor antagonists.

Joseph Payne, Vijay T. Ahuja, Yue-Zhong Shu, 2009, Journal of medicinal chemistry.