| scholarly article | Q13442814 |
| P50 | author | Svante Pääbo | Q170342 |
| Ann Graybiel | Q4766422 | ||
| Cheng-Ting Chien | Q61090009 | ||
| Wolfgang Enard | Q61128341 | ||
| Wulf Hevers | Q110965689 | ||
| P2093 | author name string | Hiroshi Takahashi | |
| Fu-Chin Liu | |||
| Ulrich Bornschein | |||
| Yi-Hsin Lee | |||
| Sin-Jhong Cheng | |||
| Yi-Chuan Chen | |||
| Shih-Yun Chen | |||
| Yun-Chia Chou | |||
| Kuan-Ming Lu | |||
| Hao-Yu Yang | |||
| Hsiao-Ying Kuo | |||
| Gui-May Chen | |||
| Jing-Ruei Lin | |||
| P2860 | cites work | Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X. | Q21092748 |
| Advances in autism genetics: on the threshold of a new neurobiology | Q22251023 | ||
| MRI analysis of an inherited speech and language disorder: structural brain abnormalities | Q24292386 | ||
| Postnatal Loss of Mef2c Results in Dissociation of Effects on Synapse Number and Learning and Memory | Q39999607 | ||
| MEF-2 regulates activity-dependent spine loss in striatopallidal medium spiny neurons. | Q40817289 | ||
| Three-dimensional structure of dendritic spines and synapses in rat hippocampus (CA1) at postnatal day 15 and adult ages: implications for the maturation of synaptic physiology and long-term potentiation | Q43699789 | ||
| Dopamine receptor activation is required for corticostriatal spike-timing-dependent plasticity. | Q46717148 | ||
| Refining the phenotype associated with MEF2C haploinsufficiency. | Q48227906 | ||
| Molecular characterization of the intercalated cell masses of the amygdala: implications for the relationship with the striatum | Q48381573 | ||
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| The sequence of formation and development of corticostriate connections in mice | Q48417758 | ||
| DARPP-32, a dopamine- and adenosine 3':5'-monophosphate-regulated phosphoprotein enriched in dopamine-innervated brain regions. III. Immunocytochemical localization. | Q48691508 | ||
| Striatal volume on magnetic resonance imaging and repetitive behaviors in autism | Q48866759 | ||
| Autistic phenotype from MEF2C knockout cells | Q50344028 | ||
| Multiple autism-linked genes mediate synapse elimination via proteasomal degradation of a synaptic scaffold PSD-95 | Q24306675 | ||
| A functional genetic link between distinct developmental language disorders | Q24312638 | ||
| The human language-associated gene SRPX2 regulates synapse formation and vocalization in mice | Q24339037 | ||
| Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene | Q24530590 | ||
| Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits | Q24594611 | ||
| Transcriptional and DNA binding activity of the Foxp1/2/4 family is modulated by heterotypic and homotypic protein interactions | Q24603791 | ||
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| Transcription factor MEF2C influences neural stem/progenitor cell differentiation and maturation in vivo | Q24644531 | ||
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| Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain | Q24648621 | ||
| Identifying autism loci and genes by tracing recent shared ancestry | Q24655308 | ||
| Patterns and rates of exonic de novo mutations in autism spectrum disorders | Q28264242 | ||
| Activity-dependent regulation of MEF2 transcription factors suppresses excitatory synapse number | Q28297899 | ||
| MEF2C, a transcription factor that facilitates learning and memory by negative regulation of synapse numbers and function | Q28507026 | ||
| In vivo analysis of MEF2 transcription factors in synapse regulation and neuronal survival | Q28508411 | ||
| Disruption of the glucocorticoid receptor gene in the nervous system results in reduced anxiety | Q29615160 | ||
| A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice | Q29616201 | ||
| Knockdown of FoxP2 alters spine density in Area X of the zebra finch. | Q30010959 | ||
| Aberrant striatal functional connectivity in children with autism | Q30467954 | ||
| MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations | Q33766816 | ||
| VGLUTs define subsets of excitatory neurons and suggest novel roles for glutamate | Q34315492 | ||
| Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex | Q34341154 | ||
| Cocaine regulates MEF2 to control synaptic and behavioral plasticity | Q34818266 | ||
| Ectopic expression of nolz-1 in neural progenitors promotes cell cycle exit/premature neuronal differentiation accompanying with abnormal apoptosis in the developing mouse telencephalon | Q35000746 | ||
| Basal Ganglia disorders associated with imbalances in the striatal striosome and matrix compartments | Q35208420 | ||
| Synaptic dysfunction in neurodevelopmental disorders associated with autism and intellectual disabilities | Q35765423 | ||
| Monosynaptic cortical input and local axon collaterals of identified striatonigral neurons. A light and electron microscopic study using the golgi-peroxidase transport-degeneration procedure | Q36589530 | ||
| Regulation of MET by FOXP2, genes implicated in higher cognitive dysfunction and autism risk | Q36886944 | ||
| Speech and Language Impairments in Autism: Insights from Behavior and Neuroimaging | Q37389766 | ||
| Dual role for Islet-1 in promoting striatonigral and repressing striatopallidal genetic programs to specify striatonigral cell identity | Q37474815 | ||
| Decoding the genetics of speech and language | Q38066309 | ||
| Activity-dependent neuronal signalling and autism spectrum disorder | Q38074584 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 11 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1513-1522 | |
| P577 | publication date | 2016-09-05 | |
| P1433 | published in | Nature Neuroscience | Q1535359 |
| P1476 | title | Foxp2 controls synaptic wiring of corticostriatal circuits and vocal communication by opposing Mef2c | |
| P478 | volume | 19 |
| Q58568494 | Active intermixing of indirect and direct neurons builds the striatal mosaic |
| Q58122132 | Alpha2-Containing Glycine Receptors Promote Neonatal Spontaneous Activity of Striatal Medium Spiny Neurons and Support Maturation of Glutamatergic Inputs |
| Q57797154 | Altered social behavior in mice carrying a cortical Foxp2 deletion |
| Q64113209 | Beyond Critical Period Learning: Striatal FoxP2 Affects the Active Maintenance of Learned Vocalizations in Adulthood |
| Q47950665 | Brain correlates of constituent structure in sign language comprehension |
| Q42743849 | CD8 T cells contribute to lacrimal gland pathology in the nonobese diabetic mouse model of Sjögren syndrome |
| Q91855017 | Chromatin Decondensation by FOXP2 Promotes Human Neuron Maturation and Expression of Neurodevelopmental Disease Genes |
| Q90372839 | Dynamic FoxP2 levels in male zebra finches are linked to morphology of adult-born Area X medium spiny neurons |
| Q83232400 | FOXP2 exhibits projection neuron class specific expression, but is not required for multiple aspects of cortical histogenesis |
| Q64083815 | Foxp2 loss of function increases striatal direct pathway inhibition via increased GABA release |
| Q64083825 | Foxp2 regulates anatomical features that may be relevant for vocal behaviors and bipedal locomotion |
| Q90442613 | Genes regulated by SATB2 during neurodevelopment contribute to schizophrenia and educational attainment |
| Q64097689 | Humanising the mouse genome piece by piece |
| Q39005713 | Layer-specific chromatin accessibility landscapes reveal regulatory networks in adult mouse visual cortex. |
| Q64120396 | MEF-2 isoforms' (A-D) roles in development and tumorigenesis |
| Q47661198 | Mice lacking cyclin-dependent kinase-like 5 manifest autistic and ADHD-like behaviors |
| Q95840004 | Nectin-2α is localized at cholinergic neuron dendrites and regulates synapse formation in the medial habenula |
| Q90597210 | Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity |
| Q89602927 | Nuclear receptor corepressors in intellectual disability and autism |
| Q55287009 | Sociability and synapse subtype-specific defects in mice lacking SRPX2, a language-associated gene. |
| Q59355730 | Stereotaxic Surgery for Genetic Manipulation in Striatal Cells of Neonatal Mouse Brains |
| Q92089986 | Synaptic Wiring of Corticostriatal Circuits in Basal Ganglia: Insights into the Pathogenesis of Neuropsychiatric Disorders |
| Q42031176 | Talking Convergence: Growing Evidence Links FOXP2 and Retinoic Acid in Shaping Speech-Related Motor Circuitry |
| Q46305191 | Tangential migration of corridor guidepost neurons contributes to anxiety circuits |
| Q51730963 | The Role of ADHD Associated Genes in Neurodevelopment. |
| Q39430418 | The epigenomics of schizophrenia, in the mouse. |
| Q58772354 | is essential for normal mushroom body and wing development |
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