Saxty et al. “Identification of Inhibitors of Protein Kinase B Using Fragment-Based Lead Discovery.” Journal of Medicinal Chemistry 50, no. 10 2007: 2293–2296. DOI: 10.1021/jm070091b.

Saxty et al. “Identification of Inhibitors of Protein Kinase B Using Fragment-Based Lead Discovery.” Journal of Medicinal Chemistry 50, no. 10 2007: 2293–2296. DOI: 10.1021/jm070091b.

Davies Thomas G., et al. “Pyramid: An integrated platform for fragment-based drug discovery.” Fragment-based approaches in drug discovery: Volume 34, Chapter 10, pp 193-214. Edited by W Jahnke and D. A. Erlanson. WILEY-VCG Verlag GmbH & Co. KGaA, Weinheim 2007. ISBN: 978-3-527-31291-7.

Davies Thomas G., et al. “Pyramid: An integrated platform for fragment-based drug discovery.” Fragment-based approaches in drug discovery: Volume 34, Chapter 10, pp 193-214. Edited by W Jahnke and D. A. Erlanson. WILEY-VCG Verlag GmbH & Co. KGaA, Weinheim 2007. ISBN: 978-3-527-31291-7.

Howard, N., et al. “Application of Fragment Screening and Fragment Linking to the Discovery of Novel Thrombin Inhibitors.” Journal of Medicinal Chemistry 49, no. 4 2006: 1346–1355. DOI: 10.1021/jm050850v.

Howard, N., et al. “Application of Fragment Screening and Fragment Linking to the Discovery of Novel Thrombin Inhibitors.” Journal of Medicinal Chemistry 49, no. 4 2006: 1346–1355. DOI: 10.1021/jm050850v.

Mooij W. T. M. et al. “Automated Protein–Ligand Crystallography for Structure-Based Drug Design.” ChemMedChem 1, no. 8 2006: 827–838. DOI: 10.1002/cmdc.200600074.

Mooij W. T. M. et al. “Automated Protein–Ligand Crystallography for Structure-Based Drug Design.” ChemMedChem 1, no. 8 2006: 827–838. DOI: 10.1002/cmdc.200600074.

Murray C. W., Verdonk et al. “Entropic consequences of linking ligands.” Fragment-based approaches in drug discovery: Volume 34, Chapter 3, pp 55-66. Edited by W Jahnke and D. A. Erlanson. WILEY-VCG Verlag GmbH & Co. KGaA, Weinheim 2006. ISBN: 978-3-527-31291-7.

Murray C. W., Verdonk et al. “Entropic consequences of linking ligands.” Fragment-based approaches in drug discovery: Volume 34, Chapter 3, pp 55-66. Edited by W Jahnke and D. A. Erlanson. WILEY-VCG Verlag GmbH & Co. KGaA, Weinheim 2006. ISBN: 978-3-527-31291-7.

Gill, A., et al. “The Discovery of Novel Protein Kinase Inhibitors by Using Fragment-Based High-Throughput X-ray Crystallography.” ChemBioChem 6, no. 3 2005: 506–512. DOI: 10.1002/cbic.200400188.

Gill, A., et al. “The Discovery of Novel Protein Kinase Inhibitors by Using Fragment-Based High-Throughput X-ray Crystallography.” ChemBioChem 6, no. 3 2005: 506–512. DOI: 10.1002/cbic.200400188.

Gill, A.L., et al. “Identification of Novel p38α MAP Kinase Inhibitors Using Fragment-Based Lead Generation.” Journal of Medicinal Chemistry 48, no. 2 2005: 414–426. DOI: 10.1021/jm049575n.

Gill, A.L., et al. “Identification of Novel p38α MAP Kinase Inhibitors Using Fragment-Based Lead Generation.” Journal of Medicinal Chemistry 48, no. 2 2005: 414–426. DOI: 10.1021/jm049575n.

Hartshorn, M.J., et al. “Fragment-Based Lead Discovery Using X-ray Crystallography.” Journal of Medicinal Chemistry 48, no. 2 2005: 403–413. DOI: 10.1021/jm0495778.

Hartshorn, M.J., et al. “Fragment-Based Lead Discovery Using X-ray Crystallography.” Journal of Medicinal Chemistry 48, no. 2 2005: 403–413. DOI: 10.1021/jm0495778.

Kirton, S.B., et al. “Prediction of binding modes for ligands in the cytochromes P450 and other heme-containing proteins.” Proteins: Structure, Function, and Bioinformatics 58, no. 4 2005: 836–844. DOI: 10.1002/prot.20389.

Kirton, S.B., et al. “Prediction of binding modes for ligands in the cytochromes P450 and other heme-containing proteins.” Proteins: Structure, Function, and Bioinformatics 58, no. 4 2005: 836–844. DOI: 10.1002/prot.20389.

Miles Congreve, Christopher W. Murray and Tom L. Blundell. “Keynote review: Structural biology and drug discovery.” Drug Discovery Today 10, no. 13 2005: 895–907. DOI: 10.1016/S1359-6446(05)03484-7.

Miles Congreve, Christopher W. Murray and Tom L. Blundell. “Keynote review: Structural biology and drug discovery.” Drug Discovery Today 10, no. 13 2005: 895–907. DOI: 10.1016/S1359-6446(05)03484-7.