(Q29616328)

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11242118

30 April 2017

1 reference

4

Jaenisch R

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11242118

30 April 2017

author name string

Chen RZ

series ordinal

1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11242118

30 April 2017

Akbarian S

series ordinal

2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11242118

30 April 2017

Tudor M

series ordinal

3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11242118

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11242118

30 April 2017

language of work or name

1 reference

30 April 2017

publication date

March 2001

1 reference

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30 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11242118

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volume

27

1 reference

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page(s)

327-31

1 reference

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issue

3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11242118

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

30 April 2017

cites work

1 reference

7 January 2021

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

1 reference

7 January 2021

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

1 reference

7 January 2021

A complex pattern of evolutionary conservation and alternative polyadenylation within the long 3"-untranslated region of the methyl-CpG-binding protein 2 gene (MeCP2) suggests a regulatory role in gene expression

1 reference

7 January 2021

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

1 reference

7 January 2021

Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots

1 reference

7 January 2021

Methyl-CpG-binding protein 2 mutations in Rett syndrome

1 reference

7 January 2021

Rett syndrome: a surprising result of mutation in MECP2.

1 reference

7 January 2021

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

1 reference

7 January 2021

Review of Rett syndrome.

1 reference

7 January 2021

The methyl-CpG binding protein MeCP2 is essential for embryonic development in the mouse.

1 reference

7 January 2021

Rett syndrome: clinical update and review of recent genetic advances.

1 reference

7 January 2021

Neonatal encephalopathy in two boys in families with recurrent Rett syndrome.

1 reference

7 January 2021

A severely affected male born into a Rett syndrome kindred supports X-linked inheritance and allows extension of the exclusion map.

1 reference

7 January 2021

Two affected boys in a Rett syndrome family: clinical and molecular findings

1 reference

7 January 2021

A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males

1 reference

7 January 2021

Somatic mutation in MECP2 as a non-fatal neurodevelopmental disorder in males

1 reference

7 January 2021

MECP2 mutation in male patients with non-specific X-linked mental retardation.

1 reference

7 January 2021

Cre-mediated gene inactivation demonstrates that FGF8 is required for cell survival and patterning of the first branchial arch

1 reference

7 January 2021

DNA hypomethylation perturbs the function and survival of CNS neurons in postnatal animals.

1 reference

7 January 2021

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

1 reference

7 January 2021

Neuropathology of Rett syndrome

1 reference

7 January 2021

Microscopic Observations of the Brain in Rett Syndrome

1 reference

7 January 2021

Pervasive neuroanatomic abnormalities of the brain in three cases of Rett's syndrome

1 reference

7 January 2021

Essential role for TrkB receptors in hippocampus-mediated learning

1 reference

7 January 2021

Generalized lacZ expression with the ROSA26 Cre reporter strain

1 reference

7 January 2021

CaMKIIalpha-Cre transgene expression and recombination patterns in the mouse brain

1 reference

7 January 2021

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11242118

Identifiers

2 references

30 April 2017

Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

456681

1029028960

0 references

456681

1 reference

Consolidated OpenCitations Corpus – April 2017

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11242118

2 references

30 April 2017

Consolidated OpenCitations Corpus – April 2017