Breathing disturbances in a model of Rett syndrome: A potential involvement of the glycine receptor α3 subunit?-Reference-Cited by-同舟云学术

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Breathing disturbances in a model of Rett syndrome: A potential involvement of the glycine receptor α3 subunit?

Published:2018-01 Issue: Volume:248 Page:43-47
ISSN:1569-9048
Container-title:Respiratory Physiology & Neurobiology
language:en
Short-container-title:Respiratory Physiology & Neurobiology

Author:

Mesuret Guillaume,Dannenberg Julia,Arnoldt Mauricio,Grützner Anja-Annett,Niebert Marcus,Hülsmann Swen

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Physiology,General Neuroscience

Reference38 articles.

1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat. Genet.,1999

2. Control of breathing in experimental anemia;Bartlett;Respir. Physiol.,1970

3. Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus;Ben-Shachar;Hum. Mol. Genet.,2009

4. Dynamic modulation of inspiratory drive currents by protein kinase A and protein phosphatases in functionally active motoneurons;Bocchiaro;J. Neurosci.,2003

5. Comparative studies on mammalian Muller (retinal glial) cells;Chao;J. Neurocytol.,1997

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