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au.\*:("NICHOLLS, Anthony")

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Conformer Generation with OMEGA: Learning from the Data Set and the Analysis of FailuresHAWKINS, Paul C. D; NICHOLLS, Anthony.Journal of chemical information and modeling. 2012, Vol 52, Num 11, pp 2919-2936, issn 1549-9596, 18 p.Article

Predicting Small-Molecule Solvation Free Energies : An Informal Blind Test for Computational ChemistryNICHOLLS, Anthony; MOBLEY, David L; GUTHRIE, J. Peter et al.Journal of medicinal chemistry (Print). 2008, Vol 51, Num 4, pp 769-779, issn 0022-2623, 11 p.Article

Essential considerations for using protein-ligand structures in drug discoveryWARREN, Gregory L; DO, Thanh D; KELLEY, Brian P et al.Drug discovery today. 2012, Vol 17, Num 23-24, pp 1270-1281, issn 1359-6446, 12 p.Article

Comparison of shape-matching and docking as virtual screening toolsHAWKINS, Paul C. D; SKILLMAN, A. Geoffrey; NICHOLLS, Anthony et al.Journal of medicinal chemistry (Print). 2007, Vol 50, Num 1, pp 74-82, issn 0022-2623, 9 p.Article

A shape-based 3-D scaffold hopping method and its application to a bacterial protein-protein interactionRUSH, Thomas S; GRANT, J. Andrew; MOSYAK, Lidia et al.Journal of medicinal chemistry (Print). 2005, Vol 48, Num 5, pp 1489-1495, issn 0022-2623, 7 p.Article

Mesangiocapillary glomerulonephritis type 2 associated with familial partial lipodystrophy (Dunnigan-Kobberling syndrome)OWEN, Katharine R; DONOHOE, Mollie; ELLARD, Sian et al.Nephron. 2004, Vol 96, Num 2, pp c35-c38, issn 0028-2766Article

The generalized aminoaciduria seen in patients with hepatocyte nuclear factor-1α mutations is a feature of all patients with diabetes and is associated with glucosuriaBINGHAM, Coralie; ELLARD, Sian; NICHOLLS, Anthony J et al.Diabetes (New York, NY). 2001, Vol 50, Num 9, pp 2047-2052, issn 0012-1797Article

Atypical familial juvenile hyperuricemic nephropathy associated with a hepatocyte nuclear factor-1β gene mutationBINGHAM, Coralie; ELLARD, Sian; OWEN, Katharine R et al.Kidney international. 2003, Vol 63, Num 5, pp 1645-1651, issn 0085-2538, 7 p.Article

Mutations in the hepatocyte nuclear factor-1β gene are associated with familial hypoplastic glomerulocystic kidney diseaseBINGHAM, Coralie; BULMAN, Michael P; HATTERSLEY, Andrew T et al.American journal of human genetics. 2001, Vol 68, Num 1, pp 219-224, issn 0002-9297Conference Paper

Solitary functioning kidney and diverse genital tract malformations associated with hepatocyte nuclear factor-1β mutationsBINGHAM, Coralie; ELLARD, Sian; NICHOLLS, Anthony J et al.Kidney international. 2002, Vol 61, Num 4, pp 1243-1251, issn 0085-2538Article

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