FOXP2 drives neuronal differentiation by interacting with retinoic acid signaling pathways

An In Vitro Model for Neuroscience: Differentiation of SH-SY5Y Cells into Cells with Morphological and Biochemical Characteristics of Mature Neurons

(2017) Lotta Agholme et al.   JOURNAL OF ALZHEIMERS DISEASE

Retinoid Acid Specifies Neuronal Identity through Graded Expression of Ascl1

(2013) John Jacob et al.   CURRENT BIOLOGY

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

Vitamin A and retinoid signaling: genomic and nongenomic effects

(2013) Ziad Al Tanoury et al.   JOURNAL OF LIPID RESEARCH

FoxP2 Regulates Neurogenesis during Embryonic Cortical Development

(2013) D. Tsui et al.   JOURNAL OF NEUROSCIENCE

Rapid Suppression of Inhibitory Synaptic Transmission by Retinoic Acid

(2013) F. Sarti et al.   JOURNAL OF NEUROSCIENCE

Diminished FoxP2 Levels Affect Dopaminergic Modulation of Corticostriatal Signaling Important to Song Variability

(2013) Malavika Murugan et al.   NEURON

The Human Language-Associated Gene SRPX2 Regulates Synapse Formation and Vocalization in Mice

(2013) G. M. Sia et al.   SCIENCE

FOXO3 Shares Common Targets with ASCL1 Genome-wide and Inhibits ASCL1-Dependent Neurogenesis

(2013) Ashley E. Webb et al.   Cell Reports

Retinoic acid signalling during development

(2012) M. Rhinn et al.   DEVELOPMENT

The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders

(2012) Claire Bacon et al.   HUMAN GENETICS

Ceramide Levels Regulated by Carnitine Palmitoyltransferase 1C Control Dendritic Spine Maturation and Cognition

(2012) Patricia Carrasco et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Foxp-Mediated Suppression of N-Cadherin Regulates Neuroepithelial Character and Progenitor Maintenance in the CNS

(2012) David L. Rousso et al.   NEURON

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

Molecular Genetics of Neuronal Migration Disorders

(2011) Judy S. Liu   Current Neurology and Neuroscience Reports

RA–RAR-β counteracts myelin-dependent inhibition of neurite outgrowth via Lingo-1 repression

(2011) Radhika Puttagunta et al.   JOURNAL OF CELL BIOLOGY

An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning

(2011) C A French et al.   MOLECULAR PSYCHIATRY

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

(2011) Brian J O'Roak et al.   NATURE GENETICS

Mosaic 7q31 Deletion Involving FOXP2 Gene Associated With Language Impairment

(2011) C. Palka et al.   PEDIATRICS

Factoring neurotrophins into a neurite-based pathophysiological model of schizophrenia

(2011) Alfredo Bellon et al.   PROGRESS IN NEUROBIOLOGY

Foxp2 Regulates Gene Networks Implicated in Neurite Outgrowth in the Developing Brain

(2011) Sonja C. Vernes et al.   PLoS Genetics

The neuropathology of autism: defects of neurogenesis and neuronal migration, and dysplastic changes

(2010) Jerzy Wegiel et al.   ACTA NEUROPATHOLOGICA

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

Comparison between proliferative and neuron-like SH-SY5Y cells as an in vitro model for Parkinson disease studies

(2010) Fernanda Martins Lopes et al.   BRAIN RESEARCH

Knockdown of FoxP2 alters spine density in Area X of the zebra finch

(2010) S. B. Schulz et al.   GENES BRAIN AND BEHAVIOR

Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits

(2010) Denise Horn et al.   HUMAN MUTATION

Nolz1 promotes striatal neurogenesis through the regulation of retinoic acid signaling

(2010) Noelia Urbán et al.   Neural Development

Guiding Neuronal Cell Migrations

(2010) O. Marin et al.   Cold Spring Harbor Perspectives in Biology

Retinoic acid reduces human neuroblastoma cell migration and invasiveness: effects on DCX, LIS1, neurofilaments-68 and vimentin expression

(2008) Elio Messi et al.   BMC CANCER

Impaired Synaptic Plasticity and Motor Learning in Mice with a Point Mutation Implicated in Human Speech Deficits

(2008) Matthias Groszer et al.   CURRENT BIOLOGY

Synaptic Signaling by All-Trans Retinoic Acid in Homeostatic Synaptic Plasticity

(2008) Jason Aoto et al.   NEURON

A Functional Genetic Link between Distinct Developmental Language Disorders

(2008) Sonja C. Vernes et al.   NEW ENGLAND JOURNAL OF MEDICINE

Modular patterning of structure and function of the striatum by retinoid receptor signaling

(2008) W.-L. Liao et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA