Fetal akinesia: review of the genetics of the neuromuscular causes von Ravenscroft, Gianina, Sollis, Elliot, Charles, Adrian K, North, Kathryn N, Baynam, Gareth, Laing, Nigel G

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Variants in ACTG2 underlie a substantial number of Australasian patients with primary chronic intestinal pseudo‐obstruction von Ravenscroft, G., Pannell, S., O'Grady, G., Ong, R., Ee, H. C., Faiz, F., Marns, L., Goel, H., Kumarasinghe, P., Sollis, E., Sivadorai, P., Wilson, M., Magoffin, A., Nightingale, S., Freckmann, M.‐L., Kirk, E. P., Sachdev, R., Lemberg, D. A., Delatycki, M. B., Kamm, M. A., Basnayake, C., Lamont, P. J., Amor, D. J., Jones, K., Schilperoort, J., Davis, M. R., Laing, N. G.

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P3.32 The molecular genetics of monogenic neuromuscular disorders characterised by reduced foetal movement von Ravenscroft, G, Sollis, E, Charles, A.K, Fabian, V.A, North, K.N, Baynam, G, Laing, N.G

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D.P.6 Whole exome sequencing applied to foetal akinesia von Ravenscroft, G, Todd, E, Yau, K.S, Kresoje, N, Sivadorai, P, Sollis, E, Friend, K, Riley, K, Thompson, E, Manton, N, Blumbergs, P, Kiraly-Borri, C, Haliloglu, G, Orhan, D, Kale, G, Charles, A.K, Fabian, V, Davis, M.R, Allcock, R.J, Laing, N.G

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Variants in ACTG 2 underlie a substantial number of Australasian patients with primary chronic intestinal pseudo‐obstruction von Ravenscroft, G., Pannell, S., O'Grady, G., Ong, R., Ee, H. C., Faiz, F., Marns, L., Goel, H., Kumarasinghe, P., Sollis, E., Sivadorai, P., Wilson, M., Magoffin, A., Nightingale, S., Freckmann, M.‐L., Kirk, E. P., Sachdev, R., Lemberg, D. A., Delatycki, M. B., Kamm, M. A., Basnayake, C., Lamont, P. J., Amor, D. J., Jones, K., Schilperoort, J., Davis, M. R., Laing, N. G.

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Dihydropyrancarboxamides Related to Zanamivir:  A New Series of Inhibitors of Influenza Virus Sialidases. 1. Discovery, Synthesis, Biological Activity, and Structure−Activity Relat... von Smith, Paul W, Sollis, Steven L, Howes, Peter D, Cherry, Peter C, Starkey, Ian D, Cobley, Kevin N, Weston, Helen, Scicinski, Jan, Merritt, Andrew, Whittington, Andrew, Wyatt, Paul, Taylor, Neil, Green, Darren, Bethell, Richard, Madar, Safia, Fenton, Robert J, Morley, Peter J, Pateman, Tony, Beresford, Alan

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Discovery and Development of Highly Potent and Orally Bioavailable Nonpeptidic αvβ6 Integrin Inhibitors von Procopiou, Panayiotis A., Barrett, John, Crawford, Matthew H. J., Hatley, Richard J. D., Hancock, Ashley P., Pritchard, John M., Rowedder, James E., Copley, Royston C. B., Slack, Robert J., Sollis, Steven L., Thorp, Lee R., Lippa, Rhys A., Macdonald, Simon J. F., Barrett, Tim N.

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Discovery and Development of Highly Potent and Orally Bioavailable Nonpeptidic α v β 6 Integrin Inhibitors von Procopiou, Panayiotis A, Barrett, John, Crawford, Matthew H J, Hatley, Richard J D, Hancock, Ashley P, Pritchard, John M, Rowedder, James E, Copley, Royston C B, Slack, Robert J, Sollis, Steven L, Thorp, Lee R, Lippa, Rhys A, Macdonald, Simon J F, Barrett, Tim N

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Erratum to: Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders von Estruch, Sara B, Graham, Sarah A, Quevedo, Martí, Vino, Arianna, Dekkers, Dick H W, Deriziotis, Pelagia, Sollis, Elliot, Demmers, Jeroen, Poot, Raymond A, Fisher, Simon E

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Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder von Sollis, Elliot, Graham, Sarah A, Vino, Arianna, Froehlich, Henning, Vreeburg, Maaike, Dimitropoulou, Danai, Gilissen, Christian, Pfundt, Rolph, Rappold, Gudrun A, Brunner, Han G, Deriziotis, Pelagia, Fisher, Simon E

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Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders von Estruch, Sara B, Graham, Sarah A, Quevedo, Martí, Vino, Arianna, Dekkers, Dick H W, Deriziotis, Pelagia, Sollis, Elliot, Demmers, Jeroen, Poot, Raymond A, Fisher, Simon E

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Functional characterization of TBR1 variants in neurodevelopmental disorder von den Hoed, Joery, Sollis, Elliot, Venselaar, Hanka, Estruch, Sara B., Deriziotis, Pelagia, Fisher, Simon E.

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Characterization of the TBR1 interactome: variants associated with neurodevelopmental disorders disrupt novel protein interactions von Sollis, Elliot, den Hoed, Joery, Quevedo, Marti, Estruch, Sara B, Vino, Arianna, Dekkers, Dick H W, Demmers, Jeroen A A, Poot, Raymond, Deriziotis, Pelagia, Fisher, Simon E

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Discovery of (S)‑3-(3-(3,5-Dimethyl‑1H‑pyrazol-1-yl)phenyl)-4-((R)‑3-(2-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)ethyl)pyrrolidin-1-yl)butanoic Acid, a Nonpeptidic αvβ6 Integrin I... von Procopiou, Panayiotis A, Anderson, Niall A, Barrett, John, Barrett, Tim N, Crawford, Matthew H. J, Fallon, Brendan J, Hancock, Ashley P, Le, Joelle, Lemma, Seble, Marshall, Richard P, Morrell, Josie, Pritchard, John M, Rowedder, James E, Saklatvala, Paula, Slack, Robert J, Sollis, Steven L, Suckling, Colin J, Thorp, Lee R, Vitulli, Giovanni, Macdonald, Simon J. F

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Pyridyl-2,5-Diketopiperazines as Potent, Selective, and Orally Bioavailable Oxytocin Antagonists: Synthesis, Pharmacokinetics, and In Vivo Potency von Borthwick, Alan D, Liddle, John, Davies, Dave E, Exall, Anne M, Hamlett, Christopher, Hickey, Deirdre M, Mason, Andrew M, Smith, Ian E. D, Nerozzi, Fabrizio, Peace, Simon, Pollard, Derek, Sollis, Steve L, Allen, Michael J, Woollard, Patrick M, Pullen, Mark A, Westfall, Timothy D, Stanislaus, Dinesh J

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Discovery of ( S)-3-(3-(3,5-Dimethyl-1 H-pyrazol-1-yl)phenyl)-4-(( R)-3-(2-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)ethyl)pyrrolidin-1-yl)butanoic Acid, a Nonpeptidic α v β 6 Inte... von Procopiou, Panayiotis A, Anderson, Niall A, Barrett, John, Barrett, Tim N, Crawford, Matthew H J, Fallon, Brendan J, Hancock, Ashley P, Le, Joelle, Lemma, Seble, Marshall, Richard P, Morrell, Josie, Pritchard, John M, Rowedder, James E, Saklatvala, Paula, Slack, Robert J, Sollis, Steven L, Suckling, Colin J, Thorp, Lee R, Vitulli, Giovanni, Macdonald, Simon J F

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The discovery of GSK221149A: A potent and selective oxytocin antagonist von Liddle, John, Allen, Michael J., Borthwick, Alan D., Brooks, David P., Davies, David E., Edwards, Richard M., Exall, Anne M., Hamlett, Chris, Irving, Wendy R., Mason, Andrew M., McCafferty, Gerald P., Nerozzi, Fabrizio, Peace, Simon, Philp, Joanne, Pollard, Derek, Pullen, Mark A., Shabbir, Shaila S., Sollis, Steve L., Westfall, Timothy D., Woollard, Pat M., Wu, Charlene, Hickey, Deirdre M.B.

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The Ontology of Biological Attributes (OBA)—computational traits for the life sciences von Stefancsik, Ray, Balhoff, James P., Balk, Meghan A., Ball, Robyn L., Bello, Susan M., Caron, Anita R., Chesler, Elissa J., de Souza, Vinicius, Gehrke, Sarah, Haendel, Melissa, Harris, Laura W., Harris, Nomi L., Ibrahim, Arwa, Koehler, Sebastian, Matentzoglu, Nicolas, McMurry, Julie A., Mungall, Christopher J., Munoz-Torres, Monica C., Putman, Tim, Robinson, Peter, Smedley, Damian, Sollis, Elliot, Thessen, Anne E., Vasilevsky, Nicole, Walton, David O., Osumi-Sutherland, David

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Synthesis and Structure–Activity Relationships of Indazole Arylsulfonamides as Allosteric CC-Chemokine Receptor 4 (CCR4) Antagonists von Procopiou, Panayiotis A, Barrett, John W, Barton, Nicholas P, Begg, Malcolm, Clapham, David, Copley, Royston C. B, Ford, Alison J, Graves, Rebecca H, Hall, David A, Hancock, Ashley P, Hill, Alan P, Hobbs, Heather, Hodgson, Simon T, Jumeaux, Coline, Lacroix, Yannick M. L, Miah, Afjal H, Morriss, Karen M. L, Needham, Deborah, Sheriff, Emma B, Slack, Robert J, Smith, Claire E, Sollis, Steven L, Staton, Hugo

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Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders von Sollis, Elliot, Deriziotis, Pelagia, Saitsu, Hirotomo, Miyake, Noriko, Matsumoto, Naomichi, Hoffer, Mariëtte J.V., Ruivenkamp, Claudia A.L., Alders, Mariëlle, Okamoto, Nobuhiko, Bijlsma, Emilia K., Plomp, Astrid S., Fisher, Simon E.

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