(Q34657630)

3 August 2017

title

Separate respiratory phenotypes in methyl-CpG-binding protein 2 (Mecp2) deficient mice (English)

1 reference

3 August 2017

John M Bissonnette

1

1 reference

3 August 2017

Sharon J Knopp

series ordinal

2

1 reference

3 August 2017

language of work or name

English

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publication date

1 April 2006

1 reference

3 August 2017

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3 August 2017

volume

59

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3 August 2017

issue

4 Pt 1

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3 August 2017

page(s)

513-518

1 reference

Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice

3 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1473964

Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1473964

DNA methylation and Rett syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1473964

Growth factor signaling in lung morphogenetic centers: automaticity, stereotypy and symmetry

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1473964

Rett syndrome and MeCP2: linking epigenetics and neuronal function

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1473964

Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1473964

Genetic basis of Rett syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1473964

Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1473964

Quantitative localization of heterogeneous methyl-CpG-binding protein 2 (MeCP2) expression phenotypes in normal and Rett syndrome brain by laser scanning cytometry

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1473964

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1473964

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1473964

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1473964

Methyl-CpG-binding protein 2 mutations in Rett syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1473964

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1473964

Molecular mechanisms controlling lung morphogenesis

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1473964

Recent insights into hyperventilation from the study of Rett syndrome.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1473964

Size-dependent morphology of the conductive bronchial tree in four species of myomorph rodents

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1473964

Mice lacking brain-derived neurotrophic factor develop with sensory deficits

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1473964

Rett's syndrome: characterization of respiratory patterns and sleep

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1473964

Hyperventilation in the awake state: potentially treatable component of Rett syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1473964

Polysomnographic characteristics of patients with Rett syndrome.

7 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1203%2F01.PDR.0000203157.31924.4A

Inbred strain variation in lung function.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1203%2F01.PDR.0000203157.31924.4A

On defining total lung capacity in the mouse

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1203%2F01.PDR.0000203157.31924.4A

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000203157.31924.4A

No evidence for long-term facilitation after episodic hypoxia in spontaneously breathing, anesthetized rats.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1473964

Polysomnographic recordings of respiratory disturbances in Rett syndrome.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1473964

Mice lacking brain-derived neurotrophic factor exhibit visceral sensory neuron losses distinct from mice lacking NT4 and display a severe developmental deficit in control of breathing.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1473964

Differential lung mechanics are genetically determined in inbred murine strains

26 October 2018

1 reference

12 December 2020

A lungful of transcription factors

1 reference

12 December 2020

Two-sidearm tracheal cannula for respiratory airflow measurements in small animals

1 reference

12 December 2020

Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes

1 reference

12 December 2020

10.1203/01.PDR.0000203157.31924.4A

Identifiers

DOI

1 reference

Dimensions Publication ID

3 August 2017

0 references

1 reference

3 August 2017

1 reference