Identification of FMR1-regulated molecular networks in human neurodevelopment
Published 2020 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Identification of FMR1-regulated molecular networks in human neurodevelopment
Authors
Keywords
-
Journal
GENOME RESEARCH
Volume 30, Issue 3, Pages 361-374
Publisher
Cold Spring Harbor Laboratory
Online
2020-03-17
DOI
10.1101/gr.251405.119
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Genome-Scale Transcriptional Regulatory Network Models of Psychiatric and Neurodegenerative Disorders
- (2019) Jocelynn R. Pearl et al. Cell Systems
- Impaired Ribosomal Biogenesis by Non-Canonical Degradation of β-catenin during Hyperammonemia
- (2019) Gangarao Davuluri et al. MOLECULAR AND CELLULAR BIOLOGY
- Inferring Regulatory Programs Governing Region Specificity of Neuroepithelial Stem Cells during Early Hindbrain and Spinal Cord Development
- (2019) Deborah Chasman et al. Cell Systems
- The Spatiotemporal Construction of the Axon Initial Segment via KIF3/KAP3/TRIM46 Transport under MARK2 Signaling
- (2019) Sotaro Ichinose et al. Cell Reports
- FMRP has a cell-type-specific role in CA1 pyramidal neurons to regulate autism-related transcripts and circadian memory
- (2019) Kirsty Sawicka et al. eLife
- Cell-Intrinsic Control of Interneuron Migration Drives Cortical Morphogenesis
- (2018) Carla G. Silva et al. CELL
- The COPII cargo adapter SEC24C is essential for neuronal homeostasis
- (2018) Bo Wang et al. JOURNAL OF CLINICAL INVESTIGATION
- Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence
- (2018) Jeanne E. Savage et al. NATURE GENETICS
- HITS-CLIP in various brain areas reveals new targets and new modalities of RNA binding by fragile X mental retardation protein
- (2018) Thomas Maurin et al. NUCLEIC ACIDS RESEARCH
- Reducing histone acetylation rescues cognitive deficits in a mouse model of Fragile X syndrome
- (2018) Yue Li et al. Nature Communications
- Downregulation of ribosome biogenesis during early forebrain development
- (2018) Kevin F Chau et al. eLife
- Ribosomal biogenesis as an emerging target of neurodevelopmental pathologies
- (2018) Michal Hetman et al. JOURNAL OF NEUROCHEMISTRY
- Fragile X mental retardation 1 gene enhances the translation of large autism-related proteins
- (2018) Ethan J. Greenblatt et al. SCIENCE
- Human Models Are Needed for Studying Human Neurodevelopmental Disorders
- (2018) Xinyu Zhao et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Widespread RNA editing dysregulation in brains from autistic individuals
- (2018) Stephen S. Tran et al. NATURE NEUROSCIENCE
- CRISPR/Cas9-mediated integration enables TAG-eCLIP of endogenously tagged RNA binding proteins
- (2017) Eric L. Van Nostrand et al. METHODS
- Autism Spectrum Disorder in Fragile X Syndrome: Cooccurring Conditions and Current Treatment
- (2017) Walter E. Kaufmann et al. PEDIATRICS
- Advances and challenges in the detection of transcriptome-wide protein-RNA interactions
- (2017) Emily C. Wheeler et al. Wiley Interdisciplinary Reviews-RNA
- Elongator controls cortical interneuron migration by regulating actomyosin dynamics
- (2016) Sylvia Tielens et al. CELL RESEARCH
- Network-based approaches for analysis of complex biological systems
- (2016) Deborah Chasman et al. CURRENT OPINION IN BIOTECHNOLOGY
- Assessing similarity to primary tissue and cortical layer identity in induced pluripotent stem cell-derived cortical neurons through single-cell transcriptomics
- (2016) Adam E. Handel et al. HUMAN MOLECULAR GENETICS
- irCLIP platform for efficient characterization of protein–RNA interactions
- (2016) Brian J Zarnegar et al. NATURE METHODS
- Robust transcriptome-wide discovery of RNA-binding protein binding sites with enhanced CLIP (eCLIP)
- (2016) Eric L Van Nostrand et al. NATURE METHODS
- DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants
- (2016) Janet Piñero et al. NUCLEIC ACIDS RESEARCH
- Fragile X Mental Retardation Protein (FMRP) controls diacylglycerol kinase activity in neurons
- (2016) Ricardos Tabet et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- RNA G-quadruplexes are globally unfolded in eukaryotic cells and depleted in bacteria
- (2016) J. U. Guo et al. SCIENCE
- Integrated transcriptome analysis of human iPS cells derived from a fragile X syndrome patient during neuronal differentiation
- (2016) Ping Lu et al. Science China-Life Sciences
- Mavoglurant in fragile X syndrome: Results of two randomized, double-blind, placebo-controlled trials
- (2016) Elizabeth Berry-Kravis et al. Science Translational Medicine
- Depletion of the Fragile X Mental Retardation Protein in Embryonic Stem Cells Alters the Kinetics of Neurogenesis
- (2016) Olfa Khalfallah et al. STEM CELLS
- Establishment of Reporter Lines for Detecting Fragile X Mental Retardation (FMR1) Gene Reactivation in Human Neural Cells
- (2016) Meng Li et al. STEM CELLS
- Integrating Transcriptomic and Proteomic Data Using Predictive Regulatory Network Models of Host Response to Pathogens
- (2016) Deborah Chasman et al. PLoS Computational Biology
- Delayedin vitrodevelopment of Up states but normal network plasticity in Fragile X circuits
- (2015) Helen Motanis et al. EUROPEAN JOURNAL OF NEUROSCIENCE
- Mavoglurant in adolescents with fragile X syndrome: analysis of Clinical Global Impression-Improvement source data from a double-blind therapeutic study followed by an open-label, long-term extension study
- (2015) Donald B. Bailey et al. Journal of Neurodevelopmental Disorders
- Dysregulation and restoration of translational homeostasis in fragile X syndrome
- (2015) Joel D. Richter et al. NATURE REVIEWS NEUROSCIENCE
- Molecular Mechanisms Regulating Impaired Neurogenesis of Fragile X Syndrome Human Embryonic Stem Cells
- (2015) Michael Telias et al. STEM CELLS AND DEVELOPMENT
- Deregulation of protein translation control, a potential game-changing hypothesis for Parkinson's disease pathogenesis
- (2015) Jean-Marc Taymans et al. TRENDS IN MOLECULAR MEDICINE
- Selective Role of the Catalytic PI3K Subunit p110β in Impaired Higher Order Cognition in Fragile X Syndrome
- (2015) Christina Gross et al. Cell Reports
- Molecular Mechanisms Regulating the Defects in Fragile X Syndrome Neurons Derived from Human Pluripotent Stem Cells
- (2015) Tomer Halevy et al. Stem Cell Reports
- Cortical neurogenesis from pluripotent stem cells: complexity emerging from simplicity
- (2014) Stewart Anderson et al. CURRENT OPINION IN NEUROBIOLOGY
- Pan-cancer network analysis identifies combinations of rare somatic mutations across pathways and protein complexes
- (2014) Mark D M Leiserson et al. NATURE GENETICS
- iPSC-Derived Forebrain Neurons from FXS Individuals Show Defects in Initial Neurite Outgrowth
- (2014) Matthew E. Doers et al. STEM CELLS AND DEVELOPMENT
- Optimizing neuronal differentiation from induced pluripotent stem cells to model ASD
- (2014) Dae-Sung Kim et al. Frontiers in Cellular Neuroscience
- The emerging roles of ribosome biogenesis in craniofacial development
- (2014) Adam P. Ross et al. Frontiers in Physiology
- FMR1 Epigenetic Silencing Commonly Occurs in Undifferentiated Fragile X-Affected Embryonic Stem Cells
- (2014) Michal Avitzour et al. Stem Cell Reports
- Directed Differentiation and Functional Maturation of Cortical Interneurons from Human Embryonic Stem Cells
- (2013) Asif M. Maroof et al. Cell Stem Cell
- The translation of translational control by FMRP: therapeutic targets for FXS
- (2013) Jennifer C Darnell et al. NATURE NEUROSCIENCE
- Linking Proteomic and Transcriptional Data through the Interactome and Epigenome Reveals a Map of Oncogene-induced Signaling
- (2013) Shao-shan Carol Huang et al. PLoS Computational Biology
- SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)
- (2013) Brett S Abrahams et al. Molecular Autism
- Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration
- (2012) H. Thorvaldsdottir et al. BRIEFINGS IN BIOINFORMATICS
- Species-Dependent Posttranscriptional Regulation of NOS1 by FMRP in the Developing Cerebral Cortex
- (2012) Kenneth Y. Kwan et al. CELL
- Neural differentiation of fragile X human embryonic stem cells reveals abnormal patterns of development despite successful neurogenesis
- (2012) Michael Telias et al. DEVELOPMENTAL BIOLOGY
- FMRP targets distinct mRNA sequence elements to regulate protein expression
- (2012) Manuel Ascano et al. NATURE
- An experimental investigation of kernels on graphs for collaborative recommendation and semisupervised classification
- (2012) François Fouss et al. NEURAL NETWORKS
- Molecular Mechanisms of Fragile X Syndrome: A Twenty-Year Perspective
- (2011) Michael R. Santoro et al. Annual Review of Pathology-Mechanisms of Disease
- FMRP Stalls Ribosomal Translocation on mRNAs Linked to Synaptic Function and Autism
- (2011) Jennifer C. Darnell et al. CELL
- Algorithms for Detecting Significantly Mutated Pathways in Cancer
- (2011) Fabio Vandin et al. JOURNAL OF COMPUTATIONAL BIOLOGY
- Epigenetic Characterization of the FMR1 Gene and Aberrant Neurodevelopment in Human Induced Pluripotent Stem Cell Models of Fragile X Syndrome
- (2011) Steven D. Sheridan et al. PLoS One
- Excess Phosphoinositide 3-Kinase Subunit Synthesis and Activity as a Novel Therapeutic Target in Fragile X Syndrome
- (2010) C. Gross et al. JOURNAL OF NEUROSCIENCE
- The STRING database in 2011: functional interaction networks of proteins, globally integrated and scored
- (2010) D. Szklarczyk et al. NUCLEIC ACIDS RESEARCH
- Coordination of sonic hedgehog and Wnt signaling determines ventral and dorsal telencephalic neuron types from human embryonic stem cells
- (2009) X.-J. Li et al. DEVELOPMENT
- Highly efficient neural conversion of human ES and iPS cells by dual inhibition of SMAD signaling
- (2009) Stuart M Chambers et al. NATURE BIOTECHNOLOGY
- Bridging high-throughput genetic and transcriptional data reveals cellular responses to alpha-synuclein toxicity
- (2009) Esti Yeger-Lotem et al. NATURE GENETICS
- The State of Synapses in Fragile X Syndrome
- (2009) Brad E. Pfeiffer et al. NEUROSCIENTIST
- Walking the Interactome for Prioritization of Candidate Disease Genes
- (2008) Sebastian Köhler et al. AMERICAN JOURNAL OF HUMAN GENETICS
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started