Pages that link to "Q37406408"

The following pages link to Rescue of behavioral and EEG deficits in male and female Mecp2-deficient mice by delayed Mecp2 gene reactivation (Q37406408):

Displaying 18 items.

• Network science for the identification of novel therapeutic targets in epilepsy (Q26745355) (← links)
• MECP2 disorders: from the clinic to mice and back (Q26799760) (← links)
• Loss of MeCP2 in cholinergic neurons causes part of RTT-like phenotypes via α7 receptor in hippocampus (Q30355025) (← links)
• Twenty-four hour quantitative-EEG and in-vivo glutamate biosensor detects activity and circadian rhythm dependent biomarkers of pathogenesis in Mecp2 null mice (Q30581752) (← links)
• Monogenic mouse models of autism spectrum disorders: Common mechanisms and missing links. (Q36716971) (← links)
• A Role for Diminished GABA Transporter Activity in the Cortical Discharge Phenotype of MeCP2-Deficient Mice. (Q36799043) (← links)
• Cellular and Circuitry Bases of Autism: Lessons Learned from the Temporospatial Manipulation of Autism Genes in the Brain (Q37714596) (← links)
• Neural and behavioral epigenetics; what it is, and what is hype. (Q38262868) (← links)
• Rett syndrome: a complex disorder with simple roots (Q38366899) (← links)
• Clinical and biological progress over 50 years in Rett syndrome. (Q38375116) (← links)
• Genetic and Pharmacological Reversibility of Phenotypes in Mouse Models of Autism Spectrum Disorder (Q38678066) (← links)
• Postsynaptic mechanisms influencing the duration of depolarization discharges in hyperexcitable neuro-glial networks (Q46457856) (← links)
• Maturation, Refinement, and Serotonergic Modulation of Cerebellar Cortical Circuits in Normal Development and in Murine Models of Autism (Q47130036) (← links)
• Lack of Methyl-CpG Binding Protein 2 (MeCP2) Affects Cell Fate Refinement During Embryonic Cortical Development (Q47851474) (← links)
• Disruption of MeCP2 attenuates circadian rhythm in CRISPR/Cas9-based Rett syndrome model mouse (Q47928200) (← links)
• The roles of motor activity and environmental enrichment in intellectual disability. (Q53667436) (← links)
• Gene therapy for Rett syndrome: prospects and challenges (Q57677438) (← links)
• Glial Dysfunction in MeCP2 Deficiency Models: Implications for Rett Syndrome (Q92454378) (← links)