1. A mutation-led search for novel functional domains in MeCP2. (27th April 2018) Authors: Guy, Jacky; Alexander-Howden, Beatrice; FitzPatrick, Laura; DeSousa, Dina; Koerner, Martha V; Selfridge, Jim; Bird, Adrian Journal: Human molecular genetics Issue: Volume 27:Number 14(2018:Jul. 15) Page Start: 2531 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Abnormal N-glycosylation pattern for brain nucleotide pyrophosphatase-5 (NPP-5) in Mecp2-mutant murine models of Rett syndrome. (April 2016) Authors: Cortelazzo, Alessio; De Felice, Claudio; Guerranti, Roberto; Signorini, Cinzia; Leoncini, Silvia; Pecorelli, Alessandra; Scalabrì, Francesco; Madonna, Michele; Filosa, Stefania; Della Giovampaola, Cinzia; Capone, Antonietta; Durand, Thierry; Mirasole, Cristiana; Zolla, Lello; Valacchi, Giuseppe; ... Journal: Neuroscience research Issue: Volume 105(2016:Apr.) Page Start: 28 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Disease Modeling Using Embryonic Stem Cells: MeCP2 Regulates Nuclear Size and RNA Synthesis in Neurons123. (20th September 2012) Authors: Yazdani, Morteza; Deogracias, RubÉn; Guy, Jacky; Poot, Raymond A.; Bird, Adrian; Barde, Yves‐Alain Journal: Stem cells Issue: Volume 30:Number 10(2012) Page Start: 2128 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Reversibility of functional deficits in experimental models of Rett syndrome. (22nd March 2010) Authors: Cobb, Stuart; Guy, Jacky; Bird, Adrian Journal: Biochemical Society transactions Issue: Volume 38:Number 2(2010) Page Start: 498 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗