Reduced AKT/mTOR signaling and protein synthesis dysregulation in a Rett syndrome animal model. (Q51820369)

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19 January 2020

title

Reduced AKT/mTOR signaling and protein synthesis dysregulation in a Rett syndrome animal model (English)

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19 January 2020

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11

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19 January 2020

Maurizio Giustetto

12

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19 January 2020

Sara Ricciardi

1

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19 January 2020

Stefano Grosso

3

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19 January 2020

Greta Forlani

5

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19 January 2020

Nicoletta Landsberger

9

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19 January 2020

Stefano Biffo

10

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19 January 2020

Vania Broccoli

13

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19 January 2020

author name string

Elena M Boggio

2

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19 January 2020

Giuseppina Lonetti

4

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19 January 2020

Gilda Stefanelli

6

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19 January 2020

Eleonora Calcagno

7

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19 January 2020

Noemi Morello

8

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19 January 2020

publication date

6 January 2011

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19 January 2020

published in

Human Molecular Genetics

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19 January 2020

volume

20

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19 January 2020

page(s)

1182-1196

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19 January 2020

issue

6

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Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized

19 January 2020

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Evolving role of MeCP2 in Rett syndrome and autism

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Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

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A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

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Reduced cortical activity due to a shift in the balance between excitation and inhibition in a mouse model of Rett syndrome

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Intranasal insulin to improve developmental delay in children with 22q13 deletion syndrome: an exploratory clinical trial.

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RAS/ERK signaling promotes site-specific ribosomal protein S6 phosphorylation via RSK and stimulates cap-dependent translation

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NMDA receptor activation results in PKA- and ERK-dependent Mnk1 activation and increased eIF4E phosphorylation in hippocampal area CA1.

21 January 2018

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