| scholarly article | Q13442814 |
| P50 | author | Sonja C Vernes | Q55704484 |
| P2093 | author name string | Jon-Ruben van Rhijn | |
| P2860 | cites work | Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X. | Q21092748 |
| Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain | Q21144946 | ||
| MRI analysis of an inherited speech and language disorder: structural brain abnormalities | Q24292386 | ||
| Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits | Q24530823 | ||
| Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder | Q24562840 | ||
| Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits | Q24594611 | ||
| Group 1 mGluR-dependent synaptic long-term depression: mechanisms and implications for circuitry and disease | Q24620534 | ||
| The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders | Q24629522 | ||
| Stone tools, language and the brain in human evolution | Q24634219 | ||
| Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain | Q24648621 | ||
| High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders | Q24648773 | ||
| Human-specific transcriptional regulation of CNS development genes by FOXP2 | Q24655742 | ||
| The role of the basal ganglia and cerebellum in language processing | Q24657658 | ||
| Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia | Q24672211 | ||
| A forkhead-domain gene is mutated in a severe speech and language disorder | Q28190379 | ||
| Localisation of a gene implicated in a severe speech and language disorder | Q28261550 | ||
| An extended family with a dominantly inherited speech disorder | Q28283400 | ||
| Modular patterning of structure and function of the striatum by retinoid receptor signaling | Q28507367 | ||
| Synaptic signaling by all-trans retinoic acid in homeostatic synaptic plasticity | Q28583711 | ||
| Disrupted motor learning and long-term synaptic plasticity in mice lacking NMDAR1 in the striatum | Q28592654 | ||
| Gene expression regulation by retinoic acid | Q28645746 | ||
| An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning | Q28714759 | ||
| The functional anatomy of basal ganglia disorders | Q29617461 | ||
| A review of brain circuitries involved in stuttering. | Q30423907 | ||
| Area-specific temporal control of corticospinal motor neuron differentiation by COUP-TFI | Q30493742 | ||
| The declarative/procedural model of lexicon and grammar | Q30645694 | ||
| Distinct contribution of the cortico-striatal and cortico-cerebellar systems to motor skill learning | Q30750434 | ||
| BAI1 regulates spatial learning and synaptic plasticity in the hippocampus | Q33112266 | ||
| Progressive nonfluent aphasia and its characteristic motor speech deficits | Q33311113 | ||
| Retinoic acid functions as a key GABAergic differentiation signal in the basal ganglia | Q33885769 | ||
| Differential contributions of motor cortex, basal ganglia, and cerebellum to speech motor control: effects of syllable repetition rate evaluated by fMRI. | Q33929412 | ||
| Vitamin A deprivation results in reversible loss of hippocampal long-term synaptic plasticity | Q33944863 | ||
| Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia. | Q33957708 | ||
| On the nature and evolution of the neural bases of human language | Q34185578 | ||
| Language fMRI abnormalities associated with FOXP2 gene mutation | Q34269471 | ||
| Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2. | Q34540341 | ||
| Phenotypic characterization of retinoic acid differentiated SH-SY5Y cells by transcriptional profiling. | Q34749363 | ||
| Metabotropic glutamate receptors and striatal synaptic plasticity: implications for neurological diseases | Q35974770 | ||
| Striatal plasticity and basal ganglia circuit function | Q37336143 | ||
| Immunohistochemical localization of the D1 dopamine receptor in rat brain reveals its axonal transport, pre- and postsynaptic localization, and prevalence in the basal ganglia, limbic system, and thalamic reticular nucleus | Q37346892 | ||
| Striatal mechanisms underlying movement, reinforcement, and punishment | Q37431197 | ||
| Disruption of glutamate receptor-interacting protein in nucleus accumbens enhances vulnerability to cocaine relapse. | Q37491638 | ||
| Direct and indirect pathways of basal ganglia: a critical reappraisal | Q38234309 | ||
| Role of retinoids in the CNS: differential expression of retinoid binding proteins and receptors and evidence for presence of retinoic acid | Q38327576 | ||
| Cell-specific interaction of retinoic acid receptors with target genes in mouse embryonic fibroblasts and embryonic stem cells | Q38349181 | ||
| Conditional RARα knockout mice reveal acute requirement for retinoic acid and RARα in homeostatic plasticity | Q41128531 | ||
| Hippocampal function is compromised in an animal model of multiple sclerosis | Q41185068 | ||
| FOXP2 drives neuronal differentiation by interacting with retinoic acid signaling pathways | Q41967307 | ||
| Retinoic acid from the meninges regulates cortical neuron generation | Q42120123 | ||
| Humanized Foxp2 specifically affects cortico-basal ganglia circuits | Q42480395 | ||
| Endocannabinoid-mediated rescue of striatal LTD and motor deficits in Parkinson's disease models | Q42508054 | ||
| Dietary retinoic acid affects song maturation and gene expression in the song system of the zebra finch | Q42658848 | ||
| The forkhead transcription factors, Foxp1 and Foxp2, identify different subpopulations of projection neurons in the mouse cerebral cortex | Q43205409 | ||
| Glutamate Receptor Subunit 2 Serine 880 Phosphorylation Modulates Synaptic Transmission and Mediates Plasticity in CA1 Pyramidal Cells | Q44610940 | ||
| FoxP2 regulates neurogenesis during embryonic cortical development. | Q44700299 | ||
| An essential role for retinoid receptors RARbeta and RXRgamma in long-term potentiation and depression | Q46249486 | ||
| Vitamin A deficiency induces motor impairments and striatal cholinergic dysfunction in rats. | Q46986232 | ||
| Characterization of Foxp2-expressing cells in the developing spinal cord | Q47741390 | ||
| FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder | Q47742684 | ||
| Vitamin A supplementation induces a prooxidative state in the striatum and impairs locomotory and exploratory activity of adult rats | Q48087247 | ||
| Differential expression of retinoid receptors in the adult mouse central nervous system. | Q48191389 | ||
| Retinoids are produced by glia in the lateral ganglionic eminence and regulate striatal neuron differentiation | Q48282472 | ||
| Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain. | Q48340477 | ||
| Impaired locomotion and dopamine signaling in retinoid receptor mutant mice | Q48525361 | ||
| Behavioral effects of low-dose gestational day 11-13 retinoic acid exposure | Q48621746 | ||
| Does orbital proprioception contribute to gaze stability during translation? | Q48879884 | ||
| The termination of fibres from the cerebral cortex and thalamus upon dendritic spines in the caudate nucleus: a study with the Golgi method. | Q51120870 | ||
| The pattern of retinoic acid receptor expression and subcellular, anatomic and functional area translocation during the postnatal development of the rat cerebral cortex and white matter. | Q51891160 | ||
| Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: clinical report and review. | Q51906415 | ||
| Tissue-specific expression of retinoic acid receptor isoform transcripts in the mouse embryo. | Q52167825 | ||
| A learning impairment associated with maternal hypervitaminosis-A in rats. | Q52326684 | ||
| Phenotype of FOXP2 haploinsufficiency in a mother and son. | Q52618605 | ||
| Maternally and paternally inherited deletion of 7q31 involving the FOXP2 gene in two families | Q82622734 | ||
| Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment | Q82822297 | ||
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | tretinoin | Q29417 |
| P304 | page(s) | 1816 | |
| P577 | publication date | 2015-11-26 | |
| P1433 | published in | Frontiers in Psychology | Q2794477 |
| P1476 | title | Retinoic Acid Signaling: A New Piece in the Spoken Language Puzzle | |
| P478 | volume | 6 |
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