(Q28584738)

31 January 2017

title

Autonomic cardiovascular control in methyl-CpG-binding protein 2 (Mecp2) deficient mice (English)

1 reference

Methyl CpG binding protein 2

31 January 2017

main subject

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GOA release 2020-03-11

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John M. Bissonnette

1

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31 January 2017

Sharon J. Knopp

series ordinal

2

1 reference

31 January 2017

James Maylie

series ordinal

3

1 reference

31 January 2017

Tran Thong

series ordinal

4

1 reference

31 January 2017

publication date

30 October 2007

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Autonomic Neuroscience: Basic and Clinical

31 January 2017

published in

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31 January 2017

volume

136

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31 January 2017

issue

1-2

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31 January 2017

page(s)

82–89

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Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice

31 January 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866300

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

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866300

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

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866300

Heart rate variability: standards of measurement, physiological interpretation and clinical use. Task Force of the European Society of Cardiology and the North American Society of Pacing and Electrophysiology

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866300

Reversal of neurological defects in a mouse model of Rett syndrome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866300

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866300

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866300

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866300

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866300

A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866300

Depressed heart rate variability and arterial baroreflex in conscious transgenic mice with overexpression of cardiac Gsalpha

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866300

A Mathematical Model to Assess Changes in the Baroreceptor Reflex

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866300

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866300

Modulation of the baroreceptor reflex by alpha 2A-adrenoceptors: a study in alpha 2A knockout mice

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866300

Diet‐induced obesity and cardiovascular regulation in C57BL/6J mice

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866300

Impaired parasympathetic heart rate control in mice with a reduction of functional G protein betagamma-subunits

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866300

Short-term and long-term blood pressure and heart rate variability in the mouse.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2866300

Progressive cardiac dysautonomia observed in patients affected by classic Rett syndrome and not in the preserved speech variant

27 November 2018

1 reference

12 December 2020

Decreased heart rate variability in transgenic mice overexpressing atrial beta 1-adrenoceptors

1 reference

12 December 2020

Functional evidence of brain stem immaturity in Rett syndrome

1 reference

12 December 2020

Rett syndrome: analysis of deaths in the British survey

1 reference

12 December 2020

Real-time measurement of cardiac vagal tone in conscious dogs

1 reference

12 December 2020

Neurophysiology of Rett syndrome

1 reference

12 December 2020

Autonomic nervous system dysregulation: breathing and heart rate perturbation during wakefulness in young girls with Rett syndrome

1 reference

12 December 2020

Optimal frequency ranges for extracting information on cardiovascular autonomic control from the blood pressure and pulse interval spectrograms in mice

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1016/J.AUTNEU.2007.04.007

Identifiers

DOI

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31 January 2017

0 references

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