Comprehensive analysis of two Shank3 and the Cacna1c mouse models of autism spectrum disorder von Kabitzke, P.A., Brunner, D., He, D., Fazio, P.A., Cox, K., Sutphen, J., Thiede, L., Sabath, E., Hanania, T., Alexandrov, V., Rasmusson, R., Spooren, W., Ghosh, A., Feliciano, P., Biemans, B., Benedetti, M., Clayton, A.L.

Volltext

Genome degeneration and adaptation in a nascent stage of symbiosis von Oakeson, Kelly F, Gil, Rosario, Clayton, Adam L, Dunn, Diane M, von Niederhausern, Andrew C, Hamil, Cindy, Aoyagi, Alex, Duval, Brett, Baca, Amanda, Silva, Francisco J, Vallier, Agnès, Jackson, D Grant, Latorre, Amparo, Weiss, Robert B, Heddi, Abdelaziz, Moya, Andrés, Dale, Colin

Volltext

Core histone hyperacetylation co‐maps with generalized DNase I sensitivity in the chicken beta‐globin chromosomal domain von Hebbes, T.R., Clayton, A.L., Thorne, A.W., Crane‐Robinson, C.

Volltext

Oxidation of sulphite in a caramel-containing system von Wedzicha, B.L., Clayton, A.L.

Volltext

A nonlinear anisotropic elastic–inelastic constitutive model for polycrystalline ceramics and minerals with application to boron carbide von Clayton, J.D., Tonge, A.L.

Volltext

634P Real-world (RW) health-related quality of life (QoL) in patients (pts) with follicular lymphoma (FL): Comparisons by line of therapy (LOT) and region (Europe vs United States... von Johnson, P.C., Bailey, A.L., Milloy, N., Clayton, E., Quek, R., Ma, Q.

Volltext

P16 Digestibility did not differ between Composite, Dorper and Merino ewes von Bates, A.L., Clayton, E., McGrath, S.R.

Volltext

Regional magma plumbing and emplacement mechanisms of the Faroe‐Shetland Sill Complex: implications for magma transport and petroleum systems within sedimentary basins von Schofield, Nick, Holford, Simon, Millett, John, Brown, David, Jolley, David, Passey, Simon R., Muirhead, Dave, Grove, Clayton, Magee, Craig, Murray, Joanne, Hole, Malcolm, Jackson, Christopher A.‐L., Stevenson, Carl

Volltext

Effects of the mu-opioid receptor antagonist GSK1521498 on hedonic and consummatory eating behaviour: a proof of mechanism study in binge-eating obese subjects von Ziauddeen, H, Chamberlain, S R, Nathan, P J, Koch, A, Maltby, K, Bush, M, Tao, W X, Napolitano, A, Skeggs, A L, Brooke, A C, Cheke, L, Clayton, N S, Sadaf Farooqi, I, O'Rahilly, S, Waterworth, D, Song, K, Hosking, L, Richards, D B, Fletcher, P C, Bullmore, E T

Volltext

Synoptic assessment of coastal total alkalinity through community science von Rheuban, J E, Gassett, P R, McCorkle, D C, Hunt, C W, Liebman, M, Bastidas, C, O'Brien-Clayton, K, Pimenta, A R, Silva, E, Vlahos, P, Woosley, R J, Ries, J, Liberti, C M, Grear, J, Salisbury, J, Brady, D C, Guay, K, LaVigne, M, Strong, A L, Stancioff, E, Turner, E

Volltext

Five new pedigrees with inherited RUNX1 mutations causing familial platelet disorder with propensity to myeloid malignancy von Owen, Carolyn J., Toze, Cynthia L., Koochin, Anna, Forrest, Donna L., Smith, Clayton A., Stevens, Jane M., Jackson, Shannon C., Poon, Man-Chiu, Sinclair, Gary D., Leber, Brian, Johnson, Peter R.E., Macheta, Anthony, Yin, John A.L., Barnett, Michael J., Lister, T. Andrew, Fitzgibbon, Jude

Volltext

"A good death but there was all this tension around"- perspectives of residential managers on the experience of delivering end of life care for people living with dementia von Borbasi, Jessica A. L., Tong, Allison, Ritchie, Alison, Poulos, Christopher J., Clayton, Josephine M.

Volltext

Experimental aspects of copy number variant assays at CCL3L1 von Todd, John A, Field, Sarah F, Howson, Joanna M M, Maier, Lisa M, Walker, Susan, Walker, Neil M, Smyth, Deborah J, Armour, John A L, Clayton, David G

Volltext

Prevalence of Deleterious Variants in MC3R in Patients With Constitutional Delay of Growth and Puberty von Duckett, Katie, Williamson, Alice, Kincaid, John W R, Rainbow, Kara, Corbin, Laura J, Martin, Hilary C, Eberhardt, Ruth Y, Huang, Qin Qin, Hurles, Matthew E, He, Wen, Brauner, Raja, Delaney, Angela, Dunkel, Leo, Grinspon, Romina P, Hall, Janet E, Hirschhorn, Joel N, Howard, Sasha R, Latronico, Ana C, Jorge, Alexander A L, McElreavey, Ken, Mericq, Verónica, Merino, Paulina M, Palmert, Mark R, Plummer, Lacey, Rey, Rodolfo A, Rezende, Raíssa C, Seminara, Stephanie B, Salnikov, Kathryn, Banerjee, Indraneel, Lam, Brian Y H, Perry, John R B, Timpson, Nicholas J, Clayton, Peter, Chan, Yee-Ming, Ong, Ken K, O’Rahilly, Stephen

Volltext

De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder von Reijnders, Margot R.F., Miller, Kerry A., Alvi, Mohsan, Goos, Jacqueline A.C., Lees, Melissa M., de Burca, Anna, Henderson, Alex, Kraus, Alison, Mikat, Barbara, de Vries, Bert B.A., Isidor, Bertrand, Kerr, Bronwyn, Marcelis, Carlo, Schluth-Bolard, Caroline, Deshpande, Charu, Ruivenkamp, Claudia A.L., Wieczorek, Dagmar, Baralle, Diana, Blair, Edward M., Engels, Hartmut, Lüdecke, Hermann-Josef, Eason, Jacqueline, Santen, Gijs W.E., Clayton-Smith, Jill, Chandler, Kate, Tatton-Brown, Katrina, Payne, Katelyn, Helbig, Katherine, Radtke, Kelly, Nugent, Kimberly M., Cremer, Kirsten, Strom, Tim M., Bird, Lynne M., Sinnema, Margje, Bitner-Glindzicz, Maria, van Dooren, Marieke F., Alders, Marielle, Koopmans, Marije, Brick, Lauren, Kozenko, Mariya, Harline, Megan L., Klaassens, Merel, Steinraths, Michelle, Cooper, Nicola S., Edery, Patrick, Yap, Patrick, Terhal, Paulien A., van der Spek, Peter J., Lakeman, Phillis, Taylor, Rachel L., Littlejohn, Rebecca O., Pfundt, Rolph, Mercimek-Andrews, Saadet, Stegmann, Alexander P.A., Kant, Sarina G., McLean, Scott, Joss, Shelagh, Swagemakers, Sigrid M.A., Douzgou, Sofia, Wall, Steven A., Küry, Sébastien, Calpena, Eduardo, Koelling, Nils, McGowan, Simon J., Twigg, Stephen R.F., Mathijssen, Irene M.J., Nellaker, Christoffer, Brunner, Han G., Wilkie, Andrew O.M.

Volltext

ZnSe:Mn aqueous colloidal quantum dots for optical and biomedical applications von Silva, Thiago G., Moura, Igor M. R., Filho, Paulo E. Cabral, Pereira, Maria I. A., Filho, Clayton A. Azevedo, Pereira, Goreti, Pereira, Giovannia A. L., Fontes, Adriana, Santos, Beate S.

Volltext

Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14 von Lin, Sheng-Jia, Orr, David, Holden, Simon, Harrison, Mike, Burrows, Nigel, Petree, Cassidy, Donnelly, Deirdre, Ambrose, J.C., Arumugam, P., Boardman-Pretty, F., Chan, G.C., Henderson, S., Kasperaviciute, D., Kayikci, M., Kousathanas, A., Lahnstein, L., Lakey, A., Lopez, F.J., Maleady-Crowe, F., O‘Donovan, P., Patch, C., Pereira, M.B., Rahim, T., Savage, K., Sieghart, A., Taylor Tavares, A.L., Thomas, E.R.A., Tucci, A., Welland, M.J., Williams, E., Zurek, Birte, Demidov, German, Schulze-Hentrich, Julia M., Kessler, Christoph, Traschütz, Andreas, Schöls, Ludger, Scheffer, Hans, Steyaert, Wouter, Sablauskas, Karolis, van Os, Nienke, Janssen, Erik, Yaldiz, Burcu, Kleefstra, Tjitske, Brookes, Anthony J., Mehtarizadeh, Mehdi, Töpf, Ana, Banka, Siddharth, Faivre, Laurence, Bruel, Ange-Line, Peyron, Christine, Pélissier, Aurore, Laurie, Steven, Matalonga, Leslie, Paramonov, Ida, Lochmüller, Hanns, Gumus, Gulcin, Hanauer, Marc, Havrylenko, Svitlana, Izem, Katia, Nelson, Isabelle, Eymard, Bruno, Macek, Milan, Turnovec, Marek, Thomasová, Dana, Kremlik, Vlastimil, Parkinson, Helen, Robinson, Peter, Hanna, Mike, Houlden, Henry, Vandrovcova, Jana, Muntoni, Francesco, Sarkozy, Anna, Van de Vondel, Liedewei, Banfi, Sandro, Aretz, Stefan, Spier, Isabel, José, Celina São, Ferreira, Marta, Carneiro, Fátima, Johansson, Lennart, van der Vries, Gerben, Roelofs-Prins, Dieuwke, Castello, Raffaele, Morleo, Manuela, De la Paz, Manuel Posada, Sánchez, Eva Bermejo, Alonso García de la Rosa, F. Javier, Ciolfi, Andrea, Renieri, Alessandra, Benetti, Elisa, Lohmann, Katja, Macaya, Alfons, Marcé-Grau, Anna, Polavarapu, Kiran, Beeson, David, Udd, Bjarne, Holinski-Feder, Elke, Steinke-Lange, Verena, Schröck, Evelin, Varshney, Gaurav K.

Volltext

Biophysical Effects and Ground Force of the Baldree Traffic Simulator von Kowalewski, A.R., Schwartz, B.M., Grimshaw, A.L., Sullivan, D.G., Peake, J.B., Green, T.O., Rogers, J.N., Kaiser, L.J., Clayton, H.M.

Volltext

Deletions in the VPS13B (COH1) gene as a cause of Cohen syndrome von Balikova, I, Lehesjoki, A.E, de Ravel, T.J.L, Thienpont, B, Chandler, K.E, Clayton-Smith, J, Träskelin, A.L, Fryns, J.P, Vermeesch, J.R

Volltext

Effects of the mu-opioid receptor antagonist GSK1521498 on hedonic and consummatory eating behaviour: a proof of mechanism study in binge-eating obese subjects von Ziauddeen, H, Chamberlain, S.R, Nathan, P.J, Koch, A, Maltby, K, Bush, M, Tao, W.X, Napolitano, A, Skeggs, A.L, Brooke, A.C, Cheke, L, Clayton, N.S, Farooqi, I. Sadaf, O'Rahilly, S, Waterworth, D, Song, K, Hosking, L, Richards, D.B, Fletcher, P.C, Bullmore, E.T

Volltext