Oil spill processes and models / by Mackay, D.

Oil spill processes and models/ by Mackay, D.

Oil spill modelling : Oil spill modelling / by Paterson, S., Mackay, D.

Focus on molecules: cytochrome P450 family 4, subfamily V, polypeptide 2 (CYP4V2). by Mackay, D, Halford, S

Focus on Molecules: Cytochrome P450 family 4, subfamily V, polypeptide 2 (CYP4V2) by Mackay, D, Halford, S

QUANTUM AND SEMI-CLASSICAL CALCULATION OF REGGE-POLE POSITIONS AND RESIDUES FOR COMPLEX OPTICAL POTENTIALS by Connor, J, Mackay, D, Sukumar, C

Transforming the Bodleian: Chapter 15 - Reader services during a time of major changes by Mackay, D, Ptak-Danchak, A, Shaw, J

PROPERTIES OF REGGE-POLE POSITIONS AND RESIDUES FOR INTER-ATOMIC POTENTIALS by Connor, J, Jakubetz, W, Mackay, D, Sukumar, C

The application of bioassay techniques to water pollution problems - the United Kingdom experience / by 278217 Mackay, D. W., Holmes, P. J., Redshaw, C. J.

Novel mutations in the CYP4v2 gene associated with Bietti crystalline corneoretinal dystrophy by Halford, S, Ocaka, L, Mackay, D, Peirson, S, Moore, A, Webster, A

Effects of new urban motorway infrastructure on road traffic accidents in the local area: a retrospective longitudinal study in Scotland by Olsen, J, Mitchell, R, Mackay, D, Humphreys, D, Ogilvie, D

Enhancing information support to health and biomedical researchers: A project to support Oxford BRC-funded researchers by Harriss, E, Mackay, D, Coxall, O, Urquhart, C, Yeoman, A

Complete glucokinase deficiency is not a common cause of permanent neonatal diabetes. by Gloyn, A, Ellard, S, Shield, J, Temple, I, Mackay, D, Polak, M, Barrett, T, Hattersley, A

Risk genotypes, allele-specific expression and methylation status in human islets at the KCNQ1 type 2 diabetes-susceptibility locus by Travers, M, Nitert, MD, Mackay, D, Lindgren, C, Groop, L, Gloyn, A, McCarthy, M

Mosaic paternal uniparental isodisomy and an ABCC8 gene mutation in a patient with permanent neonatal diabetes and hemihypertrophy. by Shield, J, Flanagan, SE, Mackay, D, Harries, L, Proks, P, Girard, C, Ashcroft, F, Temple, I, Ellard, S

Site-specific glycosylation of recombinant rat and human soluble CD4 variants expressed in Chinese hamster ovary cells. by Ashford, D, Alafi, C, Gamble, V, Mackay, D, Rademacher, T, Williams, P, Dwek, R, Barclay, A, Davis, S, Somoza, C

Erratum: Mutations in ATP-sensitive K+ cannel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthood (Diabetes (2007) 56 (1930-1937)) by Flanagan, SE, Patch, A, Mackay, D, Edghill, E, Gloyn, A, Robinson, D, Shield, J, Temple, K, Ellard, S, Hattersley, A

Mutations in ATP-sensitive K+ channel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthood (vol 56, pg 1930, 2007) by Flanagan, SE, Patch, A, Mackay, D, Edghill, E, Gloyn, A, Robinson, D, Shield, J, Temple, K, Ellard, S, Hattersley, A

Mutations in ATP-sensitive K+ channel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthood. by Flanagan, SE, Patch, A, Mackay, D, Edghill, E, Gloyn, A, Robinson, D, Shield, J, Temple, K, Ellard, S, Hattersley, A

Assessment of the role of common genetic variation in the transient neonatal diabetes mellitus (TNDM) region in type 2 diabetes: a comparative genomic and tagging single nucleotide... by Gloyn, A, Mackay, D, Weedon, M, McCarthy, M, Walker, M, Hitman, G, Knight, B, Owen, K, Hattersley, A, Frayling, T