Genome-wide DNA Methylation and RNAseq Analyses Identify Aberrant Signalling Pathways in Focal Cortical Dysplasia (FCD) Type II
Published 2018 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Genome-wide DNA Methylation and RNAseq Analyses Identify Aberrant Signalling Pathways in Focal Cortical Dysplasia (FCD) Type II
Authors
Keywords
-
Journal
Scientific Reports
Volume 8, Issue 1, Pages -
Publisher
Springer Nature
Online
2018-12-14
DOI
10.1038/s41598-018-35892-5
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Altered glutamatergic tone reveals two distinct resting state networks at the cellular level in hippocampal sclerosis
- (2017) Jyotirmoy Banerjee et al. Scientific Reports
- Alterations in BRAF gene, and enhanced mTOR and MAPK signaling in dysembryoplastic neuroepithelial tumors (DNTs)
- (2016) Aanchal Kakkar et al. EPILEPSY RESEARCH
- RNA-seq analysis of hippocampal tissues reveals novel candidate genes for drug refractory epilepsy in patients with MTLE-HS
- (2016) Aparna Banerjee Dixit et al. GENOMICS
- DNA Methylation Profiling Reveals Correlation of Differential Methylation Patterns with Gene Expression in Human Epilepsy
- (2016) Liang Wang et al. JOURNAL OF MOLECULAR NEUROSCIENCE
- Familial cortical dysplasia caused by mutation in the mammalian target of rapamycin regulatorNPRL3
- (2015) Joe C. Sim et al. ANNALS OF NEUROLOGY
- Somatic Mutations in theMTORgene cause focal cortical dysplasia type IIb
- (2015) Mitsuko Nakashima et al. ANNALS OF NEUROLOGY
- Familial focal epilepsy with focal cortical dysplasia due toDEPDC5mutations
- (2015) Stéphanie Baulac et al. ANNALS OF NEUROLOGY
- Diagnostic methods and treatment options for focal cortical dysplasia
- (2015) Renzo Guerrini et al. EPILEPSIA
- Brain somatic mutations in MTOR cause focal cortical dysplasia type II leading to intractable epilepsy
- (2015) Jae Seok Lim et al. NATURE MEDICINE
- Activation of extracellular regulated kinase and mechanistic target of rapamycin pathway in focal cortical dysplasia
- (2015) Vinit V. Patil et al. NEUROPATHOLOGY
- Common Variants of KCNJ10 Are Associated with Susceptibility and Anti-Epileptic Drug Resistance in Chinese Genetic Generalized Epilepsies
- (2015) Yong Guo et al. PLoS One
- Differential DNA methylation profiles of coding and non-coding genes define hippocampal sclerosis in human temporal lobe epilepsy
- (2015) Suzanne F.C. Miller-Delaney et al. BRAIN
- Gene Body Methylation Can Alter Gene Expression and Is a Therapeutic Target in Cancer
- (2014) Xiaojing Yang et al. CANCER CELL
- Basic Mechanisms of Epileptogenesis in Pediatric Cortical Dysplasia
- (2014) Sara Abdijadid et al. CNS Neuroscience & Therapeutics
- Role of BRCA1 in brain development
- (2014) Gerald M. Pao et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Evidence for mTOR pathway activation in a spectrum of epilepsy-associated pathologies
- (2014) Joan Liu et al. Acta Neuropathologica Communications
- Long-duration epilepsy affects cell morphology and glutamatergic synapses in type IIB focal cortical dysplasia
- (2013) Adele Finardi et al. ACTA NEUROPATHOLOGICA
- Deep sequencing reveals increased DNA methylation in chronic rat epilepsy
- (2013) Katja Kobow et al. ACTA NEUROPATHOLOGICA
- Neuroligin1 Drives Synaptic and Behavioral Maturation through Intracellular Interactions
- (2013) J. L. Hoy et al. JOURNAL OF NEUROSCIENCE
- Directed Migration of Cortical Interneurons Depends on the Cell-Autonomous Action of Sip1
- (2013) Veronique van den Berghe et al. NEURON
- The emerging role of DNA methylation in epileptogenesis
- (2012) Katja Kobow et al. EPILEPSIA
- Differential DNA Methylation Patterns Define Status Epilepticus and Epileptic Tolerance
- (2012) S. F. C. Miller-Delaney et al. JOURNAL OF NEUROSCIENCE
- A comparison between different reference genes for expression studies in human hippocampal tissue
- (2012) Claudia V. Maurer-Morelli et al. JOURNAL OF NEUROSCIENCE METHODS
- De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly
- (2012) Jeong Ho Lee et al. NATURE GENETICS
- BCL6 controls neurogenesis through Sirt1-dependent epigenetic repression of selective Notch targets
- (2012) Luca Tiberi et al. NATURE NEUROSCIENCE
- Role of a Neural Cell Adhesion Molecule Found in Cerebrospinal Fluid as a Potential Biomarker for Epilepsy
- (2012) Wei Wang et al. NEUROCHEMICAL RESEARCH
- NGS QC Toolkit: A Toolkit for Quality Control of Next Generation Sequencing Data
- (2012) Ravi K. Patel et al. PLoS One
- Enhanced Epidermal Growth Factor, Hepatocyte Growth Factor, and Vascular Endothelial Growth Factor Expression in Tuberous Sclerosis Complex
- (2011) Whitney E. Parker et al. AMERICAN JOURNAL OF PATHOLOGY
- Ect2, an Ortholog of Drosophila’s Pebble, Negatively Regulates Neurite Outgrowth in Neuroblastoma × Glioma Hybrid NG108-15 Cells
- (2011) Takahiro Tsuji et al. CELLULAR AND MOLECULAR NEUROBIOLOGY
- Frontier of Epilepsy Research - mTOR signaling pathway
- (2011) Chang-Hoon Cho EXPERIMENTAL AND MOLECULAR MEDICINE
- Increased Expression of DNA methyltransferase 1 and 3a in Human Temporal Lobe Epilepsy
- (2011) Qiong Zhu et al. JOURNAL OF MOLECULAR NEUROSCIENCE
- Prospective collection of tissue samples at autopsy in children with diffuse intrinsic pontine glioma
- (2010) Alberto Broniscer et al. CANCER
- Immunohistochemical analysis of developmental neural antigen expression in the balloon cells of focal cortical dysplasia
- (2010) Chang-Woo Han et al. JOURNAL OF CLINICAL NEUROSCIENCE
- Focal cortical dysplasia type II: biological features and clinical perspectives
- (2009) Sanjay M Sisodiya et al. LANCET NEUROLOGY
- Analyzing real-time PCR data by the comparative CT method
- (2008) Thomas D Schmittgen et al. Nature Protocols
- Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists
- (2008) Da Wei Huang et al. NUCLEIC ACIDS RESEARCH
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now