Jennifer A. Williams

发表

Design and synthesis of arylaminoethyl amides as noncovalent inhibitors of cathepsin S. Part 1.

Jennifer L. Harris, R. Epple, B. Bursulaya, 2005, Bioorganic & medicinal chemistry letters.

The C-type Lectin Receptors CLEC-2 and Dectin-1, but Not DC-SIGN, Signal via a Novel YXXL-dependent Signaling Cascade*

Gemma L. J. Fuller, S. Watson, M. Tomlinson, 2007, Journal of Biological Chemistry.

Biochemical characterization of prostasin, a channel activating protease.

Aaron Shipway, Jennifer L. Harris, H. Danahay, 2004, Biochemical and biophysical research communications.

Recombinant adenovirus type 5 vectors that target DC-SIGN, ChemR23 and alpha(v)beta3 integrin efficiently transduce human dendritic cells and enhance presentation of vectored antigens.

S. Dewhurst, S. Ramirez, C. Maguire, 2006, Vaccine.

A strategy to profile prime and non-prime proteolytic substrate specificity.

H. M. Petrassi, Jennifer L. Harris, B. J. Backes, 2005, Bioorganic & medicinal chemistry letters.

Discovery of Tropifexor (LJN452), a Highly Potent Non-bile Acid FXR Agonist for the Treatment of Cholestatic Liver Diseases and Nonalcoholic Steatohepatitis (NASH).

P. McNamara, S. Joseph, B. Laffitte, 2017, Journal of medicinal chemistry.

Discovery of a potent and selective 5-ht5A receptor antagonist by high-throughput chemistry.

S. Bromidge, T. Heightman, D. F. Corbett, 2005, Bioorganic & medicinal chemistry letters.

Synthesis and SAR of succinamide peptidomimetic inhibitors of cathepsin S.

Jennifer L. Harris, A. Chatterjee, R. Epple, 2007, Bioorganic & medicinal chemistry letters.

The C-type Lectin Receptors CLEC-2 and Dectin-1, but Not DC-SIGN, Signal via a Novel YXXL-dependent

Gemma L. J. Fuller, S. Watson, M. Tomlinson, 2007 .

Synthesis and evaluation of arylaminoethyl amides as noncovalent inhibitors of cathepsin S. Part 3: heterocyclic P3.

Jun Li, Glen Spraggon, Tove Tuntland, 2006, Bioorganic & medicinal chemistry letters.

Functional Profiling of Recombinant NS3 Proteases from All Four Serotypes of Dengue Virus Using Tetrapeptide and Octapeptide Substrate Libraries*[boxs]

Jennifer L. Harris, D. Wen, S. Vasudevan, 2005, Journal of Biological Chemistry.

Discovery of inhibitors of the channel-activating protease prostasin (CAP1/PRSS8) utilizing structure-based design.

H. M. Petrassi, Aaron Shipway, Jennifer L. Harris, 2008, Bioorganic & Medicinal Chemistry Letters.

Synthesis and SAR of arylaminoethyl amides as noncovalent inhibitors of cathepsin S: P3 cyclic ethers.

Jun Li, Glen Spraggon, Tove Tuntland, 2006, Bioorganic & medicinal chemistry letters.

Arylaminoethyl carbamates as a novel series of potent and selective cathepsin S inhibitors.

Jun Li, Tove Tuntland, Jennifer L. Harris, 2006, Bioorganic & medicinal chemistry letters.