Control of immune responses by trafficking cell surface proteins, vesicles and lipid rafts to and from the immunological synapse. per Taner, S, Onfelt, B, Pirinen, N, McCann, F, Magee, A, Davis, D

High plasma membrane lipid order imaged at the immunological synapse periphery in live T cells. per Owen, D, Oddos, S, Kumar, S, Davis, D, Neil, M, French, P, Dustin, M, Magee, A, Cebecauer, M

Evidence of a locus for orofacial clefting on human chromosome 6p24 and STS content map of the region. per Davies, A, Stephens, R, Olavesen, MG, Heather, L, Dixon, M, Magee, A, Flinter, F, Ragoussis, I

A compact, multidimensional spectrofluorometer exploiting supercontinuum generation. per Manning, H, Kennedy, G, Owen, D, Grant, D, Magee, A, Neil, M, Itoh, Y, Dunsby, C, French, P

Synthesis and characterisation of 5-acyl-6,7-dihydrothieno[3,2-c]pyridine inhibitors of Hedgehog acyltransferase per Lanyon-Hogg, T, Masumoto, N, Bodakh, G, Konitsiotis, A, Thinon, E, Rodgers, U, Owens, R, Magee, A, Tate, E

Cell surface organization of stress-inducible proteins ULBP and MICA that stimulate human NK cells and T cells via NKG2D. per Eleme, K, Taner, S, Onfelt, B, Collinson, L, McCann, F, Chalupny, N, Cosman, D, Hopkins, C, Magee, A, Davis, D

Acylation-coupled lipophilic induction of polarisation (Acyl-cLIP): a universal assay for lipid transferase and hydrolase enzymes per Lanyon-Hogg, T, Ritzefeld, M, Sefer, L, Bickel, J, Rudolf, A, Panyain, N, Bineva-Todd, G, Ocasio, C, O'Reilly, N, Siebold, C, Magee, A, Tate, E

Photochemical probe identification of a small-molecule inhibitor binding site in Hedgehog acyltransferase (HHAT) per Lanyon-Hogg, T, Ritzefeld, M, Zhang, L, Pogranyi, B, Mondal, M, Andrei, S, Sefer, L, Johnston, C, Coupland, C, Greenfield, J, Newington, J, Fuchter, M, Magee, A, Siebold, C, Tate, E

Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism per Ansari, M, Poke, G, Ferry, Q, Williamson, K, Aldridge, R, Meynert, A, Bengani, H, Chan, C, Kayserili, H, Avci, Ş, Hennekam, R, Lampe, A, Redeker, E, Homfray, T, Ross, A, Smeland, M, Mansour, S, Parker, M, Cook, J, Splitt, M, Fisher, R, Fryer, A, Magee, A, Wilkie, A, Barnicoat, A

De novo mutations in EBF3 cause a neurodevelopmental syndrome per Sleven, H, Welsh, S, Yu, J, Churchill, M, Wright, C, Henderson, A, Horvath, R, Rankin, J, Vogt, J, Magee, A, McConnell, V, Green, A, King, M, Cox, H, Armstrong, L, Lehman, A, Nelson, T, Deciphering Developmental Disorders study, CAUSES study, Williams, J, Clouston, P, Hagman, J, Németh, A

How genetically heterogeneous is Kabuki syndrome: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrum per Banka, S, Veeramachaneni, R, Reardon, W, Howard, E, Bunstone, S, Ragge, N, Parker, M, Crow, Y, Kerr, B, Kingston, H, Metcalfe, K, Chandler, K, Magee, A, Stewart, F, McConnell, V, Donnelly, D, Berland, S, Houge, G, Morton, J, Oley, C, Revencu, N, Park, S, Davies, S, Fry, A, Lynch, SA

Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism. per Ansari, M, Poke, G, Ferry, Q, Williamson, K, Aldridge, R, Meynert, A, Bengani, H, Chan, C, Kayserili, H, Avci, S, Hennekam, R, Lampe, A, Redeker, E, Homfray, T, Ross, A, Falkenberg Smeland, M, Mansour, S, Parker, M, Cook, J, Splitt, M, Fisher, R, Fryer, A, Magee, A, Wilkie, A, Barnicoat, A