New insights in Rett syndrome using pathway analysis for transcriptomics data (Q28530264)

5

0 references

Susan Coort

2

0 references

Leopold M G Curfs

6

Leopold Curfs

0 references

Elisa Cirillo

3

Elisa Cirillo

0 references

Eric E Smeets

4

Eric Smeets

0 references

publication date

September 2016

1 reference

Wiener Medizinische Wochenschrift

PubMed

published in

1 reference

Creative Commons Attribution 4.0 International

PubMed

volume

166

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issue

11-12

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page(s)

346-352

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copyright license

start time

12 August 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

Cytoscape

Cytoscape

2 references

Europe PubMed Central

9 June 2022

https://europepmc.org/search?query=(METHODS:'Cytoscape')

based on heuristic

inferred from PubMed Central ID database lookup

CZ Software Mentions: A large dataset of software mentions in the biomedical literature

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Pathways for ligand activated nuclear receptors to unravel the genomic responses induced by hepatotoxicants

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Metabolic fingerprints of altered brain growth, osmoregulation and neurotransmission in a Rett syndrome model

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

19 March 2017

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Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes

7 April 2017

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Rett syndrome: a complex disorder with simple roots

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A network biology workflow to study transcriptomics data of the diabetic liver

29 September 2017

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Cell-type-specific repression by methyl-CpG-binding protein 2 is biased toward long genes

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Systems-level perspective of sudden infant death syndrome

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Transcriptional regulation by infliximab therapy in Kawasaki disease patients with immunoglobulin resistance

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GluD1 is a common altered player in neuronal differentiation from both MECP2-mutated and CDKL5-mutated iPS cells

29 September 2017

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GO-Elite: a flexible solution for pathway and ontology over-representation

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Rett syndrome in Australia: a review of the epidemiology.

29 September 2017

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On a unusual brain atrophy syndrome in hyperammonemia in childhood

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Integrative network-based analysis of mRNA and microRNA expression in 1,25-dihydroxyvitamin D3-treated cancer cells

29 September 2017

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Effects of Rett syndrome mutations of the methyl-CpG binding domain of the transcriptional repressor MeCP2 on selectivity for association with methylated DNA

2 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27517371

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S10354-016-0488-4

1 reference

Dimensions Publication ID

1032432270

0 references

1 reference

1 reference

PubMed publication ID

27517371

1 reference