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Results 1-10 of 22 (Search time: 0.005 seconds).
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PreviewIssue DateTitleAuthor(s)
2014Aberrant GDF9 expression and activation are associated with common human ovarian disordersSimpson, C.; Robertson, D.; Al-Musawi, S.; Heath, D.; McNatty, K.; Ritter, L.; Mottershead, D.; Gilchrist, R.; Harrison, C.; Stanton, P.
2013Phl p 1-Specific Human Monoclonal IgE and Design of a Hypoallergenic Group 1 Grass Pollen Allergen FragmentLevin, M.; Rydnert, F.; Kallstrom, E.; Tan, L.; Wormald, P.; Lindstedt, M.; Greiff, L.; Ohlin, M.
2015p84 forms a negative regulatory complex with p110γ to control PI3Kγ signalling during cell migrationTurvey, M.; Klingler-Hoffmann, M.; Hoffmann, P.; McColl, S.
2013The genomic landscape of hypodiploid acute lymphoblastic leukemiaTo, L.
2013Yunis-Varón Syndrome is caused by mutations in FIG4, encoding a phosphoinositide phosphataseCampeau, P.; Lenk, G.; Lu, J.; Bae, Y.; Burrage, L.; Turnpenny, P.; Corona-Rivera, J.; Morandi, L.; Mora, M.; Reutter, H.; Vulto-van Silfhout, A.; Faivre, L.; Haan, E.; Gibbs, R.; Meisler, M.; Lee, B.
2011An MD2 hot-spot-mimicking peptide that suppresses TLR4-mediated inflammatory response in vitro and in vivoLiu, L.; Ghosh, N.; Slivka, P.; Fiorini, Z.; Hutchinson, M.; Watkins, L.; Yin, H.
2012A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disabilityHuang, L.; Jolly, L.; Willis-Owen, S.; Gardner, A.; Sharma, R.; Douglas, E.; Shoubridge, C.; Wieczorek, D.; Tzschach, A.; Cohen, M.; Hackett, A.; Field, M.; Froyen, G.; Hu, H.; Haas, S.; Ropers, H.; Kalscheuer, V.; Corbett, M.; Gecz, J.
2014Differential, dominant activation and inhibition of Notch signalling and APP cleavage by truncations of PSEN1 in human diseaseNewman, M.; Wilson, L.; Verdile, G.; Lim, A.; Khan, I.; Nik, S.; Pursglove, S.; Chapman, G.; Martins, R.; Lardelli, M.
2015LRGUK-1 is required for basal body and manchette function during spermatogenesis and male fertilityLiu, Y.; DeBoer, K.; de Kretser, D.; O Donnell, L.; O Connor, A.; Merriner, D.; Okuda, H.; Whittle, B.; Jans, D.; Efthymiadis, A.; McLachlan, R.; Ormandy, C.; Goodnow, C.; Jamsai, D.; O Bryan, M.; Yan, W.
2012PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndromeHeron, S.; Grinton, B.; Kivity, S.; Afawi, Z.; Zuberi, S.; Hughes, J.; Pridmore, C.; Hodgson, B.; Iona, X.; Sadleir, L.; Pelekanos, J.; Herlenius, E.; Goldberg-Stern, H.; Bassan, H.; Haan, E.; Korczyn, A.; Gardner, A.; Corbett, M.; Gecz, J.; Thomas, P.; et al.

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