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Global Impairment of Immediate-Early Genes Expression in Rett Syndrome Models and Patients Linked to Myelination Defects.
Petazzi, Paolo; Jorge-Torres, Olga Caridad; Gomez, Antonio; Scognamiglio, Iolanda; Serra-Musach, Jordi; Merkel, Angelika; Grases, Daniela; Xiol, Clara; O'Callaghan, Mar; Armstrong, Judith; Esteller, Manel; Guil, Sonia.
Afiliação
  • Petazzi P; Josep Carreras Leukemia Research Institute, School of Medicine, University of Barcelona, Carrer Casanova 143, 400° floor, 08036 Barcelona, Spain.
  • Jorge-Torres OC; RICORS-TERAV, Instituto de Salud Carlos III, 28029 Madrid, Spain.
  • Gomez A; Josep Carreras Leukaemia Research Institute (IJC), Badalona, 08916 Barcelona, Spain.
  • Scognamiglio I; Biosciences Department, Faculty of Sciences and Technology (FCT), University of Vic-Central University of Catalonia (UVic-UCC), C. de la Laura, 13, 08500 Vic, Spain.
  • Serra-Musach J; Cancer Epigenetics and Biology Program (PEBC), Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, 08908 Barcelona, Spain.
  • Merkel A; Cancer Epigenetics and Biology Program (PEBC), Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, 08908 Barcelona, Spain.
  • Grases D; Josep Carreras Leukaemia Research Institute (IJC), Badalona, 08916 Barcelona, Spain.
  • Xiol C; Josep Carreras Leukaemia Research Institute (IJC), Badalona, 08916 Barcelona, Spain.
  • O'Callaghan M; Fundación San Juan de Dios, 08950 Barcelona, Spain.
  • Armstrong J; Servei de Medicina Genètica i Molecular, Institut de Recerca Pediàtrica, Hospital Sant Joan de Déu, 08950 Barcelona, Spain.
  • Esteller M; Clínica Rett, Neurology Department, Hospital Sant Joan de Déu, 08950 Barcelona, Spain.
  • Guil S; CIBER-ER (Biomedical Network Research Center for Rare Diseases), Instituto de Salud Carlos III, 28029 Madrid, Spain.
Int J Mol Sci ; 24(2)2023 Jan 11.
Article em En | MEDLINE | ID: mdl-36674969

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Rett Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Rett Idioma: En Ano de publicação: 2023 Tipo de documento: Article