Buscar
Mostrando ítems 1-10 de 14
Rett’s Syndrome and full inclusionSíndrome de Rett e inclusão
(Universidade Federal de Santa Maria, 2008)
Un caso de síndrome de RettA case of Rett syndrome
(SABER ULA, 2005)
WDR45 mutations in Rett (-like) syndrome and developmental delay: Case report and an appraisal of the literature
(Academic Press Ltd - Elsevier Science Ltd, 2016-02)
Mutations in the WDR45 gene have been identified as causative for the only X-linked type of neurodegeneration with brain iron accumulation (NBIA), clinically characterized by global developmental delay in childhood, followed ...
Unconventional transcriptional response to environmental enrichment in a mouse model of rett syndromePLOS ONEPLOS ONE
(PUBLIC LIBRARY SCIENCE, 2016)
Unconventional transcriptional response to environmental enrichment in a mouse model of rett syndromePLOS ONEPLOS ONE
(PUBLIC LIBRARY SCIENCE, 2016)
Unconventional transcriptional response to environmental enrichment in a mouse model of rett syndromePLOS ONEPLOS ONE
(PUBLIC LIBRAY OF SCIENCE, 2016)
Unconventional transcriptional response to environmental enrichment in a mouse model of rett syndromePLOS ONEPLOS ONE
(PUBLIC LIBRARY SCIENCE, 2016)
Normal mitral cell dendritic development in the setting of Mecp2 mutation
(Pergamon-Elsevier Science Ltd, 2012-01)
Rett syndrome (RTT) is an autism spectrum disorder caused by mutation in the gene encoding methyl CpG binding protein 2 (MECP2). Evidence to date suggests that these disorders display defects in synaptic organization and ...
MeCP2 Regulates the Synaptic Expression of a Dysbindin-BLOC-1 Network Component in Mouse Brain and Human Induced Pluripotent Stem Cell-Derived Neurons
(Public Library of Science, 2013-06-04)
Clinical, epidemiological, and genetic evidence suggest overlapping pathogenic mechanisms between autism spectrum disorder (ASD) and schizophrenia. We tested this hypothesis by asking if mutations in the ASD gene MECP2 ...
FOXG1 Regulates PRKAR2B Transcriptionally and Posttranscriptionally via miR200 in the Adult Hippocampus
(Humana Press, 2019-07)
Rett syndrome is a complex neurodevelopmental disorder that is mainly caused by mutations in MECP2. However, mutations in FOXG1 cause a less frequent form of atypical Rett syndrome, called FOXG1 syndrome. FOXG1 is a key ...