Chapter 3: Small molecules and disease. by David S Wishart

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In defence of consideration by Chen-Wishart, M

LEGAL TRANSPLANT AND UNDUE INFLUENCE: LOST IN TRANSLATION OR A WORKING MISUNDERSTANDING? by Chen-Wishart, M

Performance-based measures of transparency in locally-balanced motions by Wishart, K, Braddick, O

Performance-based measures of motion transparency by Wishart, K, Braddick, O

Directional performance in motion transparency. by Braddick, O, Wishart, K, Curran, W

Responsible Artificial Intelligence Hyper-Automation with Generative AI Agents for Sustainable Cities of the Future by Daswin De Silva, Nishan Mills, Harsha Moraliyage, Prabod Rathnayaka, Sam Wishart, Andrew Jennings

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SMN deficiency disrupts brain development in a mouse model of severe spinal muscular atrophy. by Wishart, T, Huang, J, Murray, L, Lamont, D, Mutsaers, C, Ross, J, Geldsetzer, P, Ansorge, O, Talbot, K, Parson, S, Gillingwater, T

Reversible molecular pathology of skeletal muscle in spinal muscular atrophy. by Mutsaers, C, Wishart, T, Lamont, D, Riessland, M, Schreml, J, Comley, L, Murray, L, Parson, S, Lochmüller, H, Wirth, B, Talbot, K, Gillingwater, T

Combining comparative proteomics and molecular genetics uncovers regulators of synaptic and axonal stability and degeneration in vivo. by Thomas M Wishart, Timothy M Rooney, Douglas J Lamont, Ann K Wright, A Jennifer Morton, Mandy Jackson, Marc R Freeman, Thomas H Gillingwater

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Human genetic variation and its impact on public health and medicine by Hill, A, Sanchez-Mazas, A, Barbujani, G, Dunston, G, Excoffier, L, Hancock, J, Klein, J, Meyer, U, Motulsky, A, Presciuttini, S, Wishart, W, Langaney, A

Systemic inflammation and metabolic disturbances underlie inpatient mortality among ill children with severe malnutrition by Wen, B, Njunge, JM, Bourdon, C, Bryan Gonzales, G, Gichuki, BM, Lee, D, Wishart, DS, Ngari, M, Chimwezi, E, Thitiri, J, Mwalekwa, L, Voskuijl, W, Berkley, JA, Bandsma, RHJ

Linkage analysis in the Diabetes (UK) Warren 2 sibpair repository supports localisation of a type 2 diabetes susceptibility gene to chromosome 1q21-24. by McCarthy, M, Hattersley, A, Walker, M, Hitman, G, Levy, J, O'Rahilly, S, Lathrop, G, Simecek, N, Wishart, M, Dhillon, R, Fletcher, C, Frayling, T, Bennett, A, Groves, C, Smedley, D, Menzel, S, Wiltshire, S

The BDA Warren Type 2 Diabetes Sibpair Repository: Susceptibility regions identified by genome scan of 439 European families by McCarthy, M, Hattersley, A, Walker, M, Hitman, G, Levy, J, O'Rahilly, S, Lathrop, G, Simecek, N, Wishart, M, Dhillon, R, Prestwich, P, Fletcher, C, Jones, E, Frayling, T, Rao, P, Bennett, A, Menzel, S

A genome scan reveals heterogeneity among European families with maturity onset diabetes of the young by Frayling, T, Menzel, S, Wishart, M, Vaxillaire, M, Lindgren, C, Tuomi, T, Wang, Y, Brown, A, Bulman, M, Ellard, S, Evans, J, Rao, P, Mills, J, Tack, C, Dina, C, Froguel, P, Groop, L, Mahtani, M, Hattersley, A

Year-Long Stability of Nucleic Acid Bases in Concentrated Sulfuric Acid: Implications for the Persistence of Organic Chemistry in Venus’ Clouds by Seager, Sara, Petkowski, Janusz J., Seager, Maxwell D., Grimes, John H., Zinsli, Zachary, Vollmer-Snarr, Heidi R., Abd El-Rahman, Mohamed K., Wishart, David S., Lee, Brian L., Gautam, Vasuk, Herrington, Lauren, Bains, William, Darrow, Charles

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A genome-wide scan in families with maturity-onset diabetes of the young: evidence for further genetic heterogeneity. by Frayling, T, Lindgren, C, Chevre, J, Menzel, S, Wishart, M, Benmezroua, Y, Brown, A, Evans, J, Rao, P, Dina, C, Lecoeur, C, Kanninen, T, Almgren, P, Bulman, M, Wang, Y, Mills, J, Wright-Pascoe, R, Mahtani, M, Prisco, F, Costa, A, Cognet, I, Hansen, T, Pedersen, O, Ellard, S, Tuomi, T

The discovery of novel 8-azabicyclo[3.2.1]octan-3-yl)-3-(4-chlorophenyl) propanamides as vasopressin V1A receptor antagonists. by Napier, S, Wishart, G, Arbuckle, W, Baker, J, Barn, D, Bingham, M, Brown, A, Byford, A, Claxton, C, Craighead, M, Buchanan, K, Fielding, L, Gibson, L, Goodwin, R, Goutcher, S, Irving, N, MacSweeney, C, Milne, R, Mort, C, Presland, J, Sloan, H, Thomson, F, Turnbull, Z, Young, T

Studies of association between the gene for calpain-10 and type 2 diabetes mellitus in the United Kingdom. by Evans, J, Frayling, T, Cassell, P, Saker, P, Hitman, G, Walker, M, Levy, J, O'Rahilly, S, Rao, P, Bennett, A, Jones, E, Menzel, S, Prestwich, P, Simecek, N, Wishart, M, Dhillon, R, Fletcher, C, Millward, A, Demaine, A, Wilkin, T, Horikawa, Y, Cox, N, Bell, G, Ellard, S, McCarthy, M

A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of... by Wiltshire, S, Hattersley, A, Hitman, G, Walker, M, Levy, J, Sampson, M, O'Rahilly, S, Frayling, T, Bell, J, Lathrop, G, Bennett, A, Dhillon, R, Fletcher, C, Groves, C, Jones, E, Prestwich, P, Simecek, N, Rao, P, Wishart, M, Bottazzo, G, Foxon, R, Howell, S, Smedley, D, Cardon, L, Menzel, S