D. Danger

发表

Identification of diarylsulfonamides as agonists of the free fatty acid receptor 4 (FFA4/GPR120).

J. Collins, J. Way, C. Laudeman, 2014, Bioorganic & medicinal chemistry letters.

High-Affinity Monoclonal Antibodies to PED/PEA-15 Generated Using 5 μg of DNA

K. Kilpatrick, D. Danger, W. Dallas, 2000 .

Synthesis and SAR of Benzisothiazole- and Indolizine-β-d-glucopyranoside Inhibitors of SGLT2.

Chari D Smith, S. Roller, D. Danger, 2010, ACS medicinal chemistry letters.

Rapid and parallel formation of Fe3+ multimers, including a trimer, during H-type subunit ferritin mineralization.

Elizabeth C. Theil, D. Edmondson, B. Huynh, 1997, Biochemistry.

Photoaffinity labelling of steroid-hormone-binding glutathione S-transferases with [3H]methyltrienolone. Inhibition of steroid-binding activity by the anticarcinogen indole-3-carbinol.

G. LeBlanc, W. S. Baldwin, D. Danger, 1992, The Biochemical journal.

The influence of conserved tyrosine 30 and tissue-dependent differences in sequence on ferritin function: use of blue and purple Fe(III) species as reporters of ferroxidation

Elizabeth C. Theil, J. Sanders-Loehr, D. Danger, 1997, JBIC Journal of Biological Inorganic Chemistry.

The ferritin iron entry and exit problem

Elizabeth C. Theil, D. Danger, G. Small, 2000 .

Development of Highly Selective Pyrimidine-Based Aldosterone Synthase (CYP11B2) Inhibitors.

C. M. Yates, R. Schotzinger, S. M. Sparks, 2019, ACS medicinal chemistry letters.

Effectors of HIV-1 protease peptidolytic activity.

M. Hanlon, E. Furfine, D. Danger, 2001, Biochemistry.

Inhibition of wild-type and mutant human immunodeficiency virus type 1 proteases by GW0385 and other arylsulfonamides.

M. Hanlon, E. Furfine, A. Shu, 2004, Biochemistry.