(Q35922196)

English

Methyl CpG-binding protein isoform MeCP2_e2 is dispensable for Rett syndrome phenotypes but essential for embryo viability and placenta development

scientific article published on 28 February 2012

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Methyl CpG-binding protein isoform MeCP2_e2 is dispensable for Rett syndrome phenotypes but essential for embryo viability and placenta development (English)

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

0 references

author name string

Masayuki Itoh

1

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Candice G T Tahimic

2

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Shuhei Ide

3

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Akihiro Otsuki

4

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Toshikuni Sasaoka

5

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Shigeru Noguchi

6

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Mitsuo Oshimura

7

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Yu-ichi Goto

8

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Akihiro Kurimasa

9

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

language of work or name

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publication date

28 February 2012

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Journal of Biological Chemistry

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

287

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

17

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

13859-13867

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Transgenic complementation of MeCP2 deficiency: phenotypic rescue of Mecp2-null mice by isoform-specific transgenes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

Mesoderm-specific transcript is associated with fat mass expansion in response to a positive energy balance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

Mouse models of implantation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

Development of structures and transport functions in the mouse placenta

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

Imprinted genes in the placenta--a review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

Imprinted X inactivation and reprogramming in the preimplantation mouse embryo.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

Brahma links the SWI/SNF chromatin-remodeling complex with MeCP2-dependent transcriptional silencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

Developmental biology of the placenta and the origins of placental insufficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

Mechanisms underlying lack of insulin-like growth factor-binding protein-3 expression in non-small-cell lung cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

The major form of MeCP2 has a novel N-terminus generated by alternative splicing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

X-chromosome inactivation patterns are unbalanced and affect the phenotypic outcome in a mouse model of rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

Reactivation of the paternal X chromosome in early mouse embryos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

Expression of the imprinted genes MEST/Mest in human and murine placenta suggests a role in angiogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

Heterogeneous X inactivation in trophoblastic cells of human full-term female placentas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

Disruption of primary imprinting during oocyte growth leads to the modified expression of imprinted genes during embryogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

On a unusual brain atrophy syndrome in hyperammonemia in childhood

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

Incomplete X chromosome dosage compensation in chorionic villi of human placenta

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

Characterization of MeCP2, a vertebrate DNA binding protein with affinity for methylated DNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

2 October 2017

Methyl CpG-binding protein 2 (a mutation of which causes Rett syndrome) directly regulates insulin-like growth factor binding protein 3 in mouse and human brains

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

24 September 2018

Differential distribution of the MeCP2 splice variants in the postnatal mouse brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

24 September 2018

Delayed maturation of neuronal architecture and synaptogenesis in cerebral cortex of Mecp2-deficient mice.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

24 September 2018

The expression of CXCR4/CXCL12 in first-trimester human trophoblast cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

24 September 2018

MECP2 mutations or polymorphisms in mentally retarded boys: diagnostic implications.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

24 September 2018

Balanced X chromosome inactivation patterns in the Rett syndrome brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

24 September 2018

Peg1/Mest locates distal to the currently defined imprinting region on mouse proximal chromosome 6 and identifies a new imprinting region affecting growth

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

24 September 2018

Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340147

24 September 2018

Epigenetic heterogeneity at imprinted loci in normal populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/22375006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relaxation of imprinting of IGFII gene in juvenile nasopharyngeal angiofibromas

1 reference

https://pubmed.ncbi.nlm.nih.gov/22375006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Preferential paternal X inactivation in extraembryonic tissues of early mouse embryos

1 reference

https://pubmed.ncbi.nlm.nih.gov/22375006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1074/JBC.M111.309864

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

release_mevnanxirrb3hp25lnatt4y2aa

1 reference

https://api.fatcat.wiki/v0/release/mevnanxirrb3hp25lnatt4y2aa

24 November 2022

based on heuristic

mapped directly with Wikidata item

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

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