Generation and characterization of rat and mouse monoclonal antibodies specific for MeCP2 and their use in X-inactivation studies (Q34090951)

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17 January 2020

title

Generation and characterization of rat and mouse monoclonal antibodies specific for MeCP2 and their use in X-inactivation studies (English)

1 reference

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17 January 2020

1 reference

10

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17 January 2020

Juan Sandoval

7

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17 January 2020

Paolo Petazzi

8

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17 January 2020

author name string

K Laurence Jost

1

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17 January 2020

Andrea Rottach

2

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17 January 2020

Manuela Milden

3

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17 January 2020

Bianca Bertulat

4

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17 January 2020

Annette Becker

5

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17 January 2020

Patricia Wolf

6

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17 January 2020

Dori Huertas

9

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17 January 2020

Elisabeth Kremmer

11

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17 January 2020

Heinrich Leonhardt

12

1 reference

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17 January 2020

M Cristina Cardoso

13

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17 January 2020

language of work or name

English

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publication date

28 November 2011

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17 January 2020

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17 January 2020

volume

6

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17 January 2020

issue

11

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17 January 2020

page(s)

e26499

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Creative Commons Attribution 4.0 International

17 January 2020

copyright license

start time

28 November 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

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Generation and characterization of a rat monoclonal antibody specific for PCNA.

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MeCP2 interacts with HP1 and modulates its heterochromatin association during myogenic differentiation

5 July 2018

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5 July 2018

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X chromosome inactivation patterns in brain in Rett syndrome: implications for the disease phenotype

5 July 2018

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

5 July 2018

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Heterogeneity in residual function of MeCP2 carrying missense mutations in the methyl CpG binding domain

5 July 2018

1 reference

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Chromatin compaction by human MeCP2. Assembly of novel secondary chromatin structures in the absence of DNA methylation

5 July 2018

1 reference

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Isolation of the chromocenter fraction from mouse liver nuclei

5 July 2018

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

5 July 2018

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

5 July 2018

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Rett syndrome: methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations

5 July 2018

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Functional consequences of Rett syndrome mutations on human MeCP2.

5 July 2018

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

5 July 2018

1 reference

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

5 July 2018

1 reference

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Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3225355

MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin

5 July 2018

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Reversal of terminal differentiation and control of DNA replication: cyclin A and Cdk2 specifically localize at subnuclear sites of DNA replication

5 July 2018

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

5 July 2018

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On a unusual brain atrophy syndrome in hyperammonemia in childhood

5 July 2018

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5 July 2018

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

5 July 2018

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

5 July 2018

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Serial passaging and differentiation of myogenic cells isolated from dystrophic mouse muscle

5 July 2018

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Tyrosine hydroxylase deficit in the chemoafferent and the sympathoadrenergic pathways of the Mecp2 deficient mouse.

5 July 2018

1 reference

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Characterization of DNA-binding activity in the N-terminal domain of the DNA methyltransferase Dnmt3a

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22140431

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Chromosomal and Nuclear Location of Mouse Satellite DNA in Individual Cells

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22140431

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0026499

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22140431%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

0 references

1 reference

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17 January 2020

PubMed publication ID

22140431

1 reference