(Q48318692)

10 February 2018

title

Breathing dysfunctions associated with impaired control of postinspiratory activity in Mecp2-/y knockout mice. (English)

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10 February 2018

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6

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author name string

Georg M Stettner

1

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10 February 2018

Peter Huppke

2

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10 February 2018

Cornelia Brendel

3

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10 February 2018

Diethelm W Richter

4

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10 February 2018

Jutta Gärtner

5

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language of work or name

English

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publication date

4 January 2007

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10 February 2018

published in

Journal of Physiology

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10 February 2018

volume

579

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10 February 2018

issue

Pt 3

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10 February 2018

page(s)

863-876

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

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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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21 January 2018

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Characterisation of breathing and associated central autonomic dysfunction in the Rett disorder

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Assessment of the maturity-related brainstem functions reveals the heterogeneous phenotypes and facilitates clinical management of Rett syndrome

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Modeling the ponto-medullary respiratory network.

21 January 2018

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Role of pontile mechanisms in the neurogenesis of eupnea

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Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.

21 January 2018

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Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Reduced expression of neuropeptides can be related to respiratory disturbances in Rett syndrome

2 November 2018

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Distribution of N-methyl-D-aspartate-sensitive L-[3H]glutamate-binding sites in rat brain.

2 November 2018

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12 December 2020

Excitatory and inhibitory synaptic inputs shape the discharge pattern of pump neurons of the nucleus tractus solitarii in the rat

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12 December 2020

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10.1113/JPHYSIOL.2006.119966

Identifiers

DOI

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10 February 2018

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10 February 2018