Activation of the Medial Prefrontal Cortex Reverses Cognitive and Respiratory Symptoms in a Mouse Model of Rett Syndrome

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Activation of the Medial Prefrontal Cortex Reverses Cognitive and Respiratory Symptoms in a Mouse Model of Rett Syndrome

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Activation of the Medial Prefr ...... a Mouse Model of Rett Syndrome

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Activation of the Medial Prefr ...... a Mouse Model of Rett Syndrome

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Activation of the Medial Prefr ...... a Mouse Model of Rett Syndrome

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Activation of the Medial Prefr ...... a Mouse Model of Rett Syndrome

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Activation of the Medial Prefr ...... a Mouse Model of Rett Syndrome

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Activation of the Medial Prefr ...... a Mouse Model of Rett Syndrome

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P1476

Activation of the Medial Prefr ...... a Mouse Model of Rett Syndrome

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P2093

C James Howell

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David M Katz

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Fatimah E Abouelsoud

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Heping Yu

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Michael P Sceniak

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Wenceslas Krakowiecki

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P2860

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

Evolving the lock to fit the key to create a family of G protein-coupled receptors potently activated by an inert ligand

The Use of DREADDs to Deconstruct Behavior

Rett Syndrome: Crossing the Threshold to Clinical Translation

Basomedial amygdala mediates top-down control of anxiety and fear.

MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number

G*Power 3: a flexible statistical power analysis program for the social, behavioral, and biomedical sciences

Reversal of neurological defects in a mouse model of Rett syndrome

Mechanisms of Functional Hypoconnectivity in the Medial Prefrontal Cortex of Mecp2 Null Mice.

Brain activity mapping in Mecp2 mutant mice reveals functional deficits in forebrain circuits, including key nodes in the default mode network, that are reversed with ketamine treatment.

P304

ENEURO.0277-17.2017

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scholarly article

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10.1523/ENEURO.0277-17.2017

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English

P433

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P478

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P50

Min Lang

Saloni U Lad

P577

2017-11-01T00:00:00Z

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P698

29333487

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P921

Autism spectrum

hypofrontality

P932

5762598

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