Beyond Pathway Analysis: Identification of Active Subnetworks in Rett Syndrome-Reference-Cited by-同舟云学术

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Beyond Pathway Analysis: Identification of Active Subnetworks in Rett Syndrome

Published:2019-02-21 Issue: Volume:10 Page:
ISSN:1664-8021
Container-title:Frontiers in Genetics
language:
Short-container-title:Front. Genet.

Author:

Miller Ryan A.,Ehrhart Friederike,Eijssen Lars M. T.,Slenter Denise N.,Curfs Leopold M. G.,Evelo Chris T.,Willighagen Egon L.,Kutmon Martina

Publisher

Frontiers Media SA

Subject

Genetics(clinical),Genetics,Molecular Medicine

Reference35 articles.

1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat. Genet.,1999

2. Rett syndrome and the urge of novel approaches to study MeCP2 functions and mechanisms of action;Bedogni;Neurosci. Biobehav. Rev.,2014

3. MeCP2, a key contributor to neurological disease, activates and represses transcription;Chahrour;Science,2008

4. A patient with classic Rett syndrome with a novel mutation in MECP2 exon 1;Chunshu;Clin. Genet.,2006

5. Gene expression profiling in postmortem Rett syndrome brain: differential gene expression and patient classification;Colantuoni;Neurobiol. Dis.,2001

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1. Identification of molecular signatures and pathways involved in Rett syndrome using a multi-omics approach;2023-01-20

2. Understanding signaling and metabolic paths using semantified and harmonized information about biological interactions;PLOS ONE;2022-04-18

3. Target-agnostic discovery of Rett Syndrome therapeutics by coupling computational network analysis and CRISPR-enabled in vivo disease modeling;2022-03-21

4. A resource to explore the discovery of rare diseases and their causative genes;Scientific Data;2021-05-04

5. Rett syndrome in Russia and abroad: a scientific historical review;Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics);2020-07-08

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