Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q36387350)
Watch
English
Methyl-CpG Binding Protein 2 (Mecp2) Regulates Sensory Function Through Sema5b and Robo2
scientific article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
4685056
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26733807%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
title
Methyl-CpG Binding Protein 2 (Mecp2) Regulates Sensory Function Through Sema5b and Robo2
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
4685056
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26733807%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
author
Vladimir Korzh
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
4685056
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26733807%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
Thomas Pietri
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
4685056
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26733807%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
author name string
Wan Y Leong
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
4685056
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26733807%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
Zhi H Lim
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
4685056
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26733807%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
Eyleen L K Goh
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMC publication ID
4685056
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26733807%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
language of work or name
English
1 reference
based on heuristic
inferred from title
publication date
21 December 2015
1 reference
stated in
Europe PubMed Central
PMC publication ID
4685056
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26733807%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
published in
Frontiers in Cellular Neuroscience
1 reference
stated in
Europe PubMed Central
PMC publication ID
4685056
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26733807%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
volume
9
1 reference
stated in
Europe PubMed Central
PMC publication ID
4685056
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26733807%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
page(s)
481
1 reference
stated in
Europe PubMed Central
PMC publication ID
4685056
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26733807%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
describes a project that uses
ImageJ
1 reference
stated in
Europe PubMed Central
retrieved
11 June 2022
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4685056/fullTextXML
based on heuristic
inferred from PubMed Central ID database lookup
cites work
Genetic Analysis of the Touch Response in Zebrafish (Danio rerio).
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
Genetic compensation induced by deleterious mutations but not gene knockdowns.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
The methyl-CpG-binding domain (MBD) is crucial for MeCP2's dysfunction-induced defects in adult newborn neurons
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
Rescue of Methyl-CpG Binding Protein 2 Dysfunction-induced Defects in Newborn Neurons by Pentobarbital
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
TALEN-mediated gene mutagenesis in rhesus and cynomolgus monkeys
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
The first mecp2-null zebrafish model shows altered motor behaviors
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
Class 3 semaphorin mediates dendrite growth in adult newborn neurons through Cdk5/FAK pathway
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
MeCP2 binds to 5hmC enriched within active genes and accessible chromatin in the nervous system.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
Female Mecp2(+/-) mice display robust behavioral deficits on two different genetic backgrounds providing a framework for pre-clinical studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
Isoform-specific toxicity of Mecp2 in postmitotic neurons: suppression of neurotoxicity by FoxG1
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
Robo2 determines subtype-specific axonal projections of trigeminal sensory neurons
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
Normal mitral cell dendritic development in the setting of Mecp2 mutation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
TRPM7 is required within zebrafish sensory neurons for the activation of touch-evoked escape behaviors.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
Neuronal maturation defect in induced pluripotent stem cells from patients with Rett syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
The role of MeCP2 in the brain.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
Sensory impairment in mental retardation: a potential role for NGF.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
Rett syndrome: revised diagnostic criteria and nomenclature
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
Neuronal MeCP2 is expressed at near histone-octamer levels and globally alters the chromatin state.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
MeCP2 deficiency disrupts axonal guidance, fasciculation, and targeting by altering Semaphorin 3F function.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
In vivo birthdating by BAPTISM reveals that trigeminal sensory neuron diversity depends on early neurogenesis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
MeCP2, a key contributor to neurological disease, activates and represses transcription
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
Controlling morpholino experiments: don't stop making antisense.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
Role of semaphorins during axon growth and guidance
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
The role of Slit-Robo signaling in the generation, migration and morphological differentiation of cortical interneurons
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
The story of Rett syndrome: from clinic to neurobiology
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
p53 activation by knockdown technologies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
The transcriptional repressor Mecp2 regulates terminal neuronal differentiation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
MECP2 and beyond: phenotype-genotype correlations in Rett syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
Molecular genetics of Rett syndrome and clinical spectrum of MECP2 mutations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
Analysis of upstream elements in the HuC promoter leads to the establishment of transgenic zebrafish with fluorescent neurons
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
Biochemical purification of a mammalian slit protein as a positive regulator of sensory axon elongation and branching
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 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
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
30 September 2017
A case of Rett syndrome with reduced pain sensitivity.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
28 June 2018
Primary neurons that express the L2/HNK-1 carbohydrate during early development in the zebrafish.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
28 June 2018
Widespread changes in dendritic and axonal morphology in Mecp2-mutant mouse models of Rett syndrome: evidence for disruption of neuronal networks
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
21 September 2018
The methyl-CpG-binding protein MeCP2 and neurological disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
21 September 2018
Slit1a inhibits retinal ganglion cell arborization and synaptogenesis via Robo2-dependent and -independent pathways
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
21 September 2018
Dual branch-promoting and branch-repelling actions of Slit/Robo signaling on peripheral and central branches of developing sensory axons.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
21 September 2018
Robo1 and Robo2 cooperate to control the guidance of major axonal tracts in the mammalian forebrain
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
21 September 2018
HuC:Kaede, a useful tool to label neural morphologies in networks in vivo
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
21 September 2018
Repulsive interactions shape the morphologies and functional arrangement of zebrafish peripheral sensory arbors.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
21 September 2018
Differential expression of the methyl-cytosine binding protein 2 gene in embryonic and adult brain of zebrafish
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
21 September 2018
Involvement of Islet-2 in the Slit signaling for axonal branching and defasciculation of the sensory neurons in embryonic zebrafish
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
21 September 2018
Irx4-mediated regulation of Slit1 expression contributes to the definition of early axonal paths inside the retina
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
21 September 2018
Apoptosis in the developing zebrafish embryo.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
21 September 2018
Sensory axon response to substrate-bound Slit2 is modulated by laminin and cyclic GMP.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
21 September 2018
Altered development of glutamate and GABA receptors in the basal ganglia of girls with Rett syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
21 September 2018
Disruption of semaphorin III/D gene causes severe abnormality in peripheral nerve projection.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4685056
retrieved
21 September 2018
Linking MECP2 and pain sensitivity: the example of Rett syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/26733807
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Neuropathology of Rett syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/26733807
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The methyl-CpG binding transcriptional repressor MeCP2 stably associates with nucleosomal DNA
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/26733807
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.3389/FNCEL.2015.00481
1 reference
stated in
Europe PubMed Central
PMC publication ID
4685056
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26733807%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
PMC publication ID
4685056
1 reference
stated in
Europe PubMed Central
PMC publication ID
4685056
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26733807%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
PubMed publication ID
26733807
1 reference
stated in
Europe PubMed Central
PMC publication ID
4685056
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26733807%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
ResearchGate publication ID
289524827
0 references
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit