Protein-Protein Interaction Among the FoxP Family Members and their Regulation of Two Target Genes, VLDLR and CNTNAP2 in the Zebra Finch Song System
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Title
Protein-Protein Interaction Among the FoxP Family Members and their Regulation of Two Target Genes, VLDLR and CNTNAP2 in the Zebra Finch Song System
Authors
Keywords
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Journal
Frontiers in Molecular Neuroscience
Volume 10, Issue -, Pages -
Publisher
Frontiers Media SA
Online
2017-05-01
DOI
10.3389/fnmol.2017.00112
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Note: Only part of the references are listed.- Foxp1 expression is essential for sex-specific murine neonatal ultrasonic vocalization
- (2017) Henning Fröhlich et al. HUMAN MOLECULAR GENETICS
- Three-Dimensional Domain Swapping Changes the Folding Mechanism of the Forkhead Domain of FoxP1
- (2016) Exequiel Medina et al. BIOPHYSICAL JOURNAL
- Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rate
- (2016) Wu-Lin Charng et al. BMC Medical Genomics
- Genesis of the vertebrate FoxP subfamily member genes occurred during two ancestral whole genome duplication events
- (2016) Xiaowei Song et al. GENE
- FoxP2 directly regulates the reelin receptor VLDLR developmentally and by singing
- (2016) Iris Adam et al. MOLECULAR AND CELLULAR NEUROSCIENCE
- The evolutionary history of genes involved in spoken and written language: beyond FOXP2
- (2016) Alessandra Mozzi et al. Scientific Reports
- Knockout of Foxp2 disrupts vocal development in mice
- (2016) Gregg A. Castellucci et al. Scientific Reports
- A Foxp2 Mutation Implicated in Human Speech Deficits Alters Sequencing of Ultrasonic Vocalizations in Adult Male Mice
- (2016) Jonathan Chabout et al. Frontiers in Behavioral Neuroscience
- Very low density lipoprotein receptor regulates dendritic spine formation in a RasGRF1/CaMKII dependent manner
- (2015) Amanda Marie DiBattista et al. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH
- The FOXP1, FOXP2 and FOXP4 transcription factors are required for islet alpha cell proliferation and function in mice
- (2015) Jason M. Spaeth et al. DIABETOLOGIA
- Differential coexpression of FoxP1, FoxP2, and FoxP4 in the Zebra Finch (Taeniopygia guttata) song system
- (2015) Ezequiel Mendoza et al. JOURNAL OF COMPARATIVE NEUROLOGY
- Behavior-Linked FoxP2 Regulation Enables Zebra Finch Vocal Learning
- (2015) J. B. Heston et al. JOURNAL OF NEUROSCIENCE
- A Single Amino Acid in the Hinge Loop Region of the FOXP Forkhead Domain is Significant for Dimerisation
- (2015) Kershia Perumal et al. PROTEIN JOURNAL
- Conserved role of Drosophila melanogaster FoxP in motor coordination and courtship song
- (2014) Kristy J. Lawton et al. BEHAVIOURAL BRAIN RESEARCH
- What can mice tell us about Foxp2 function?
- (2014) Catherine A French et al. CURRENT OPINION IN NEUROBIOLOGY
- DifferentialFoxP2andFoxP1expression in a vocal learning nucleus of the developing budgerigar
- (2014) Osceola Whitney et al. Developmental Neurobiology
- Androgen Modulation of Foxp1 and Foxp2 in the Developing Rat Brain: Impact on Sex Specific Vocalization
- (2014) J. Michael Bowers et al. ENDOCRINOLOGY
- Transcriptional Regulation by FOXP1, FOXP2, and FOXP4 Dimerization
- (2014) Cora Sin et al. JOURNAL OF MOLECULAR NEUROSCIENCE
- Reference Genes for Quantitative Gene Expression Studies in Multiple Avian Species
- (2014) Philipp Olias et al. PLoS One
- Drosophila FoxP Mutants Are Deficient in Operant Self-Learning
- (2014) Ezequiel Mendoza et al. PLoS One
- Convergent transcriptional specializations in the brains of humans and song-learning birds
- (2014) A. R. Pfenning et al. SCIENCE
- FoxP influences the speed and accuracy of a perceptual decision in Drosophila
- (2014) S. DasGupta et al. SCIENCE
- FOXP1mutations cause intellectual disability and a recognizable phenotype
- (2013) Anna K. Le Fevre et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Shining a light on CNTNAP2: complex functions to complex disorders
- (2013) Pedro Rodenas-Cuadrado et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- 3p14.1 de novo microdeletion involving the FOXP1 gene in an adult patient with autism, severe speech delay and deficit of motor coordination
- (2013) Orazio Palumbo et al. GENE
- Distribution of language-related Cntnap2 protein in neural circuits critical for vocal learning
- (2013) Michael C. Condro et al. JOURNAL OF COMPARATIVE NEUROLOGY
- Expression analysis of the speech-related genes FoxP1 and FoxP2 and their relation to singing behavior in two songbird species
- (2013) Q. Chen et al. JOURNAL OF EXPERIMENTAL BIOLOGY
- Diminished FoxP2 Levels Affect Dopaminergic Modulation of Corticostriatal Signaling Important to Song Variability
- (2013) Malavika Murugan et al. NEURON
- Microfluidic affinity and ChIP-seq analyses converge on a conserved FOXP2-binding motif in chimp and human, which enables the detection of evolutionarily novel targets
- (2013) Christopher S. Nelson et al. NUCLEIC ACIDS RESEARCH
- Young and intense: FoxP2 immunoreactivity in Area X varies with age, song stereotypy, and singing in male zebra finches
- (2013) Christopher K. Thompson et al. Frontiers in Neural Circuits
- Increased gene expression of FOXP1 in patients with autism spectrum disorders
- (2013) Wei-Hsien Chien et al. Molecular Autism
- The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders
- (2012) Claire Bacon et al. HUMAN GENETICS
- Molecular Microcircuitry Underlies Functional Specification in a Basal Ganglia Circuit Dedicated to Vocal Learning
- (2012) Austin T. Hilliard et al. NEURON
- Foxp-Mediated Suppression of N-Cadherin Regulates Neuroepithelial Character and Progenitor Maintenance in the CNS
- (2012) David L. Rousso et al. NEURON
- Analysis of two language-related genes in autism
- (2012) Claudio Toma et al. PSYCHIATRIC GENETICS
- Structural and Biological Features of FOXP3 Dimerization Relevant to Regulatory T Cell Function
- (2012) Xiaomin Song et al. Cell Reports
- Maternally and paternally inherited deletion of 7q31 involving the FOXP2 gene in two families
- (2011) O. Žilina et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Phenotype of FOXP2 haploinsufficiency in a mother and son
- (2011) Gregory M. Rice et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Structure of a Domain-Swapped FOXP3 Dimer on DNA and Its Function in Regulatory T Cells
- (2011) Hozefa S. Bandukwala et al. IMMUNITY
- Zebra finch cell lines from naturally occurring tumors
- (2011) Yuichiro Itoh et al. IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-ANIMAL
- Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
- (2011) Brian J O'Roak et al. NATURE GENETICS
- Solution structure and backbone dynamics of the DNA-binding domain of FOXP1: Insight into its domain swapping and DNA binding
- (2011) Yuan-Ping Chu et al. PROTEIN SCIENCE
- Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes
- (2011) Santhosh Girirajan et al. PLoS Genetics
- Foxp2 Regulates Gene Networks Implicated in Neurite Outgrowth in the Developing Brain
- (2011) Sonja C. Vernes et al. PLoS Genetics
- De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment
- (2010) Fadi F. Hamdan et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Chiari I malformation, delayed gross motor skills, severe speech delay and epileptiform discharges in a child with FOXP1 haploinsufficiency
- (2010) Christopher W Carr et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Knockdown of FoxP2 alters spine density in Area X of the zebra finch
- (2010) S. B. Schulz et al. GENES BRAIN AND BEHAVIOR
- Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex
- (2010) Patrice Roll et al. HUMAN MOLECULAR GENETICS
- Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits
- (2010) Denise Horn et al. HUMAN MUTATION
- Language-relatedCntnap2gene is differentially expressed in sexually dimorphic song nuclei essential for vocal learning in songbirds
- (2010) S. Carmen Panaitof et al. JOURNAL OF COMPARATIVE NEUROLOGY
- Alternative Splicing and Gene Duplication in the Evolution of the FoxP Gene Subfamily
- (2010) M. E. Santos et al. MOLECULAR BIOLOGY AND EVOLUTION
- Twitter evolution: converging mechanisms in birdsong and human speech
- (2010) Johan J. Bolhuis et al. NATURE REVIEWS NEUROSCIENCE
- A Humanized Version of Foxp2 Affects Cortico-Basal Ganglia Circuits in Mice
- (2009) Wolfgang Enard et al. CELL
- Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia
- (2009) Sonja C Vernes et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- A 785kb deletion of 3p14.1p13, including the FOXP1 gene, associated with speech delay, contractures, hypertonia and blepharophimosis
- (2009) Mitchel J. Pariani et al. European Journal of Medical Genetics
- The evolution of Fox genes and their role in development and disease
- (2009) Sridhar Hannenhalli et al. NATURE REVIEWS GENETICS
- Impaired Synaptic Plasticity and Motor Learning in Mice with a Point Mutation Implicated in Human Speech Deficits
- (2008) Matthias Groszer et al. CURRENT BIOLOGY
- Expression ofFOXP2in the developing monkey forebrain: Comparison with the expression of the genesFOXP1,PBX3, andMEIS2
- (2008) Kaoru Takahashi et al. JOURNAL OF COMPARATIVE NEUROLOGY
- Birdsong Decreases Protein Levels of FoxP2, a Molecule Required for Human Speech
- (2008) Julie E. Miller et al. JOURNAL OF NEUROPHYSIOLOGY
- The Reelin Signaling Pathway Promotes Dendritic Spine Development in Hippocampal Neurons
- (2008) S. Niu et al. JOURNAL OF NEUROSCIENCE
- Expression of reelin, its receptors and its intracellular signaling protein, Disabled1 in the canary brain: Relationships with the song control system
- (2008) J. Balthazart et al. NEUROSCIENCE
- A Functional Genetic Link between Distinct Developmental Language Disorders
- (2008) Sonja C. Vernes et al. NEW ENGLAND JOURNAL OF MEDICINE
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