Pages that link to "Q88609435"

The following pages link to Rett syndrome: insights into genetic, molecular and circuit mechanisms (Q88609435):

Displaying 26 items.

• Regenerative glutamate release in the hippocampus of Rett syndrome model mice (Q58696176) (← links)
• VIII World Rett Syndrome Congress & Symposium of rare diseases, Kazan, Russia (Q60935123) (← links)
• Senescence Phenomena and Metabolic Alteration in Mesenchymal Stromal Cells from a Mouse Model of Rett Syndrome (Q64039248) (← links)
• Strong neuron-to-body coupling implies weak neuron-to-neuron coupling in motor cortex (Q64073530) (← links)
• Correlation Between and Malocclusion in Rett Syndrome: A preliminary study (Q64109608) (← links)
• From Basic Visual Science to Neurodevelopmental Disorders: The Voyage of Environmental Enrichment-Like Stimulation. (Q64997864) (← links)
• Insulin-Like Growth Factor-1 Down-Regulates the Phosphorylation of FXYD1 and Rescues Behavioral Deficits in a Mouse Model of Rett Syndrome (Q89736099) (← links)
• Complete Profiling of Methyl-CpG-Binding Domains for Combinations of Cytosine Modifications at CpG Dinucleotides Reveals Differential Read-out in Normal and Rett-Associated States (Q90053376) (← links)
• MeCP2: A Critical Regulator of Chromatin in Neurodevelopment and Adult Brain Function (Q90133350) (← links)
• Variant Profile of MECP2 Gene in Sri Lankan Patients with Rett Syndrome (Q90173981) (← links)
• The distinct methylation landscape of maturing neurons and its role in Rett syndrome pathogenesis (Q90202348) (← links)
• Novel MECP2 Mutation c.1162_1172del; p.Pro388* in Two Patients with Symptoms of Atypical Rett Syndrome (Q90642797) (← links)
• Ten novel insertion/deletion variants in MECP2 identified in Japanese patients with Rett syndrome (Q90912892) (← links)
• Neuronal network dysfunction in a model for Kleefstra syndrome mediated by enhanced NMDAR signaling (Q91011853) (← links)
• KCC2 expression levels are reduced in post mortem brain tissue of Rett syndrome patients (Q91651927) (← links)
• Comprehensive Analysis of GABAA-A1R Developmental Alterations in Rett Syndrome: Setting the Focus for Therapeutic Targets in the Time Frame of the Disease (Q92702523) (← links)
• X chromosome inactivation does not necessarily determine the severity of the phenotype in Rett syndrome patients (Q92710242) (← links)
• The Expanding Therapeutic Potential of Neuronal KCC2 (Q92812803) (← links)
• Modeling genetic epilepsies in a dish (Q93038643) (← links)
• Psychomotor Dysfunction in Rett Syndrome: Insights into the Neurochemical and Circuit Roots (Q93088060) (← links)
• Detection of Rare Methyl-CpG Binding Protein 2 Gene Missense Mutations in Patients With Schizophrenia (Q95841115) (← links)
• Expansion of the phenotypic spectrum of de novo missense variants in kinesin family member 1A (KIF1A) (Q97542587) (← links)
• Scrutinizing the molecular, biochemical, and cytogenetic attributes in subjects with Rett syndrome (RTT) and their mothers (Q97554029) (← links)
• MeCP2 links heterochromatin condensates and neurodevelopmental disease (Q97650823) (← links)
• Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophrenia (Q99563391) (← links)
• Extracellular Vesicles in CNS Developmental Disorders (Q104477474) (← links)