未登录 Eosinophilic phenotype classification of patients with asthma and/or COPD in NOVELTY Price, David; Pavord, Ian D.; Da Costa, Keith Peres; Agusti, Alvar; Anderson, Gary P.; Bansal, Aruna T.; Bel, Elisabeth H.; Fageras, Malin; Hughes, Rod; Inoue, Hiromasa; Lassi, Glenda; Olaguibel, Jose Maria; Papi, Alberto; Rabahi, Marcelo; Reddel, Helen K.; Rendon, Adrian; Van Den Berge, Maarten; Mullerova, Hana 分享 收藏
Identification of a missense variant in SPDL1 associated with idiopathic pulmonary fibrosis 与特发性肺纤维化相关的SPDL1错义变体的鉴定 Dhindsa, Ryan S.; Mattsson, Johan; Nag, Abhishek; Wang, Quanli; Wain, Louise, V; Allen, Richard; Wigmore, Eleanor M.; Ibanez, Kristina; Vitsios, Dimitrios; Deevi, Sri V. V.; Wasilewski, Sebastian; Karlsson, Maria; Lassi, Glenda; Olsson, Henric; Muthas, Daniel; Monkley, Susan; Mackay, Alex; Murray, Lynne; Young, Simon; Haefliger, Carolina; Maher, Toby M.; Belvisi, Maria G.; Jenkins, Gisli; Molyneaux, Philip L.; Platt, Adam; Petrovski, Slave 分享 收藏
Dlk1 dosage regulates hippocampal neurogenesis and cognition Dlk1剂量调节海马神经发生和认知 Montalban-Loro, Raquel; Lassi, Glenda; Lozano-Urena, Anna; Perez-Villalba, Ana; Jimenez-Villalba, Esteban; Charalambous, Marika; Vallortigara, Giorgio; Horner, Alexa E.; Saksida, Lisa M.; Bussey, Timothy J.; Trejo, Jose Luis; Tucci, Valter; Ferguson-Smith, Anne C.; Ferron, Sacri R. 分享 收藏
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The after-hours circadian mutant has reduced phenotypic plasticity in behaviors at multiple timescales and in sleep homeostasis 小时后昼夜节律突变体在多个时间尺度和睡眠稳态下的行为中降低了表型可塑性 Maggi, Silvia; Balzani, Edoardo; Lassi, Glenda; Garcia-Garcia, Celina; Plano, Andrea; Espinoza, Stefano; Mus, Liudmila; Tinarelli, Federico; Nolan, Patrick M.; Gainetdinov, Raul R.; Balci, Fuat; Nieus, Thierry; Tucci, Valter 分享 收藏
A missense mutation in Katnal1 underlies behavioural, neurological and ciliary anomalies Banks, G.; Lassi, G.; Hoerder-Suabedissen, A.; Tinarelli, F.; Simon, M. M.; Wilcox, A.; Lau, P.; Lawson, T. N.; Johnson, S.; Rutman, A.; Sweeting, M.; Chesham, J. E.; Barnard, A. R.; Horner, N.; Westerberg, H.; Smith, L. B.; Molnar, Z.; Hastings, M. H.; Hirst, R. A.; Tucci, V.; Nolan, P. M. 分享 收藏
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Deletion of the Snord116/SNORD116 Alters Sleep in Mice and Patients with Prader-Willi Syndrome Snord116/SNORD116的缺失会改变prader-willi综合征小鼠和患者的睡眠 Lassi, Glenda; Priano, Lorenzo; Maggi, Silvia; Garcia-Garcia, Celina; Balzani, Edoardo; El-Assawy, Nadia; Pagani, Marco; Tinarelli, Federico; Giardino, Daniela; Mauro, Alessandro; Peters, Jo; Gozzi, Alessandro; Grugni, Graziano; Tucci, Valter 分享 收藏
Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis 人类和小鼠SCN4A的新突变暗示AMPK参与肌强直和周期性麻痹 Corrochano, Silvia; Maennikkoe, Roope; Joyce, Peter I.; McGoldrick, Philip; Wettstein, Jessica; Lassi, Glenda; Rayan, Dipa L. Raja; Blanco, Gonzalo; Quinn, Colin; Liavas, Andrianos; Lionikas, Arimantas; Amior, Neta; Dick, James; Healy, Estelle G.; Stewart, Michelle; Carter, Sarah; Hutchinson, Marie; Bentley, Liz; Fratta, Pietro; Cortese, Andrea; Cox, Roger; Brown, Steve D. M.; Tucci, Valter; Wackerhage, Henning; Amato, Anthony A.; Greensmith, Linda; Koltzenburg, Martin; Hanna, Michael G.; Acevedo-Arozena, Abraham 分享 收藏
Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features Tucci, Valter; Kleefstra, Tjitske; Hardy, Andrea; Heise, Ines; Maggi, Silvia; Willemsen, Marjolein H.; Hilton, Helen; Esapa, Chris; Simon, Michelle; Buenavista, Maria-Teresa; McGuffin, Liam J.; Vizor, Lucie; Dodero, Luca; Tsafitaris, Sotirios; Romero, Rosario; Nillesen, Willy N.; Vissers, Lisenka E. L. M.; Kempers, Marlies J.; Vulto-van Silfhout, Anneke T.; Iqbal, Zafar; Orlando, Marta; Maccione, Alessandro; Lassi, Glenda; Farisello, Pasqualina; Contestabile, Andrea; Tinarelli, Federico; Nieus, Thierry; Raimondi, Andrea; Greco, Barbara; Cantatore, Daniela; Gasparini, Laura; Berdondini, Luca; Bifone, Angelo; Gozzi, Alessandro; Wells, Sara; Nolan, Patrick M. 分享 收藏
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