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The last 5 uploaded publications
Global Impairment of Immediate-Early Genes Expression in Rett Syndrome Models and Patients Linked to Myelination Defects
Paolo Petazzi, Olga C. Jorge-Torres, Antonio Gómez, Iolanda Scognamiglio, Jordi Serra-Musach, Angelika Merkel, Daniela Grases, Clara Xiol, Mar O’Callaghan, Judith Armstrong, Manel Esteller, Sònia Guil (2023). Global Impairment of Immediate-Early Genes Expression in Rett Syndrome Models and Patients Linked to Myelination Defects. , 24(2), DOI: https://doi.org/10.3390/ijms24021453.
Article73 days agoInhibition of Gsk3b Reduces Nfkb1 Signaling and Rescues Synaptic Activity to Improve the Rett Syndrome Phenotype in Mecp2-Knockout Mice
Olga C. Jorge-Torres, Karolina Szczęsna, Laura M. Roa, Carmen Casal, Louisa González Somermeyer, Marta Soler, Cecilia D. Velasco, Pablo Martínez San Segundo, Paolo Petazzi, Mauricio A. Sáez, Raúl Delgado‐Morales, Stéphane Fourcade, Aurora Pujol, Dori Huertas, Artur Llobet, Sònia Guil, Manel Esteller (2018). Inhibition of Gsk3b Reduces Nfkb1 Signaling and Rescues Synaptic Activity to Improve the Rett Syndrome Phenotype in Mecp2-Knockout Mice. , 23(6), DOI: https://doi.org/10.1016/j.celrep.2018.04.010.
Article73 days agoInhibition of Gsk3b Reduces Nfkb1 Signaling and Rescues Synaptic Activity to Improve the Rett Syndrome Phenotype in Mecp2-Knockout Mice
Olga C. Jorge-Torres, Karolina Szczęsna, Laura M. Roa, Carmen Casal, Louisa González Somermeyer, Marta Soler, Cecilia D. Velasco, Pablo Martínez San Segundo, Paolo Petazzi, Mauricio A. Sáez, Raúl Delgado‐Morales, Stéphane Fourcade, Aurora Pujol, Dori Huertas, Artur Llobet, Sònia Guil, Manel Esteller (2018). Inhibition of Gsk3b Reduces Nfkb1 Signaling and Rescues Synaptic Activity to Improve the Rett Syndrome Phenotype in Mecp2-Knockout Mice. , 23(6), DOI: https://doi.org/10.1016/j.celrep.2018.04.010.
Article73 days agoProfiling of oxBS-450K 5-hydroxymethylcytosine in human placenta and brain reveals enrichment at imprinted loci
José Ramón Hernández Mora, Marta Sánchez-Delgado, Paolo Petazzi, Sebastián Morán, Manel Esteller, Isabel Iglesias‐Platas, David Monk (2017). Profiling of oxBS-450K 5-hydroxymethylcytosine in human placenta and brain reveals enrichment at imprinted loci. , 13(2), DOI: https://doi.org/10.1080/15592294.2017.1344803.
Article73 days agoMutations in JMJD1C are involved in Rett syndrome and intellectual disability
Mauricio A. Sáez, Juana Fernández‐Rodríguez, Cátia Moutinho, José V. Sánchez‐Mut, Antonio Gómez, Enrique Vidal, Paolo Petazzi, Karolina Szczęsna, Paula López-Serra, Mario Lucariello, Patricia Lorden, Raúl Delgado‐Morales, Olga J. de la Caridad, Dori Huertas, Josep Lluis Gelpí, Modesto Orozco, Adriana López‐Doriga, Montserrat Milà, Luis A. Pérez‐Jurado, Mercédes Pineda, Judith Armstrong, Conxi Lázaro, Manel Esteller (2015). Mutations in JMJD1C are involved in Rett syndrome and intellectual disability. , 18(4), DOI: https://doi.org/10.1038/gim.2015.100.
Article73 days ago