Millard H. Lambert

CSAR 2014: A Benchmark Exercise Using Unpublished Data from Pharma

Richard D. Smith, Heather A. Carlson, Aqeel Ahmed, 2016, J. Chem. Inf. Model..

D3R Grand Challenge 3: blind prediction of protein–ligand poses and affinity rankings

Huanwang Yang, Stephen K. Burley, W. Patrick Walters, 2018, Journal of Computer-Aided Molecular Design.

Identification of a series of PPARγ/δ dual agonists via solid-phase parallel synthesis

Millard H. Lambert, Timothy M. Willson, T. Willson, 2001 .

Pattern recognition in the prediction of protein structure. III. An importance‐sampling minimization procedure

Harold A. Scheraga, Millard H. Lambert, H. Scheraga, 1989 .

CRYSTAL STRUCTURES OF THE CATALYTIC DOMAIN OF PHOSPHODIESTERASE 4B2B COMPLEXED WITH 8-Br-AMP

Millard H. Lambert, Dana E. Vanderwall, Robert X. Xu, 2004 .

PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR ∞ AND METABOLIC DISEASE

Millard H. Lambert, Timothy M. Willson, T. Willson, 2001 .

Structural basis for antagonist-mediated recruitment of nuclear co-repressors by PPARα

Millard H. Lambert, Timothy M. Willson, T. Willson, 2002, Nature.

Pattern recognition in the prediction of protein structure. II. Chain conformation from a probability‐directed search procedure

Harold A. Scheraga, Millard H. Lambert, H. Scheraga, 1989 .

Asymmetry in the PPARγ/RXRα Crystal Structure Reveals the Molecular Basis of Heterodimerization among Nuclear Receptors

Millard H. Lambert, Timothy M. Willson, T. Willson, 2000 .