December 19, 2018Frontiers in GeneticsOpen Access

MECP2 Mutation Interrupts Nucleolin–mTOR–P70S6K Signaling in Rett Syndrome Patients

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Abstract

-mTOR-P70S6K signaling in the human RTT brain. Our results provide important insight toward understanding the molecular properties of human RTT brain.

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Cite This Study

Olson et al. (2018) studied this question.

synapsesocial.com/papers/6a0031e72ff633f36577d6ec https://doi.org/10.3389/fgene.2018.00635

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Abstract

-mTOR-P70S6K signaling in the human RTT brain. Our results provide important insight toward understanding the molecular properties of human RTT brain.

MECP2 Mutation Interrupts Nucleolin–mTOR–P70S6K Signaling in Rett Syndrome Patients

Abstract

Discussion

Cite This Study

MECP2 Mutation Interrupts Nucleolin–mTOR–P70S6K Signaling in Rett Syndrome Patients

Abstract

Discussion

Cite This Study

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