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Developmental biology, ISSN 0012-1606, 04/2021, Volume 472, pp. 18 - 29
Journal Article
Cellular and molecular life sciences : CMLS, ISSN 1420-682X, 04/2020, Volume 77, Issue 7, pp. 1401 - 1419
Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Hair Cells, Auditory - cytology | Cell Proliferation | Receptors, G-Protein-Coupled - metabolism | Cell Count | Nerve Tissue Proteins - deficiency | Cochlea - innervation | Stem Cells - metabolism | Gene Knockdown Techniques | Synapses - metabolism | Forkhead Transcription Factors - metabolism | Cell Transdifferentiation | Forkhead Transcription Factors - deficiency | Animals, Newborn | Cell Survival | Gene Expression Regulation | Mice, Transgenic | Cochlea - cytology | Signal Transduction - genetics | Labyrinth Supporting Cells - cytology | Nerve Tissue Proteins - metabolism | Cell Lineage | Hair Cells, Auditory - ultrastructure | Mechanotransduction, Cellular | Animals | Labyrinth Supporting Cells - ultrastructure | Hair | Neonates | Hair cells | Birth | Cell differentiation | Inner ear | Morphogenesis | Regeneration | Foxg1 protein | Cell fate | Cell cycle | Cochlea | Forkhead protein | Mice | Differentiation | Synapses | Index Medicus | Supporting cells | Foxg1 | Trans-differentiation | Progenitors | Proliferation | Original
Journal Article
Human mutation, ISSN 1059-7794, 08/2017, Volume 38, Issue 8, pp. 922 - 931
MECP2 | mutation | database | CDKL5 | FOXG1 | phenotype–genotype correlations | Rett syndrome | locus‐specific database | locus-specific database | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Humans | Methyl-CpG-Binding Protein 2 - metabolism | Protein-Serine-Threonine Kinases - genetics | Forkhead Transcription Factors - genetics | Nerve Tissue Proteins - genetics | Methyl-CpG-Binding Protein 2 - genetics | Nerve Tissue Proteins - metabolism | Rett Syndrome - metabolism | Phenotype | Forkhead Transcription Factors - metabolism | Female | Rett Syndrome - genetics | Protein-Serine-Threonine Kinases - metabolism | Databases, Factual | Databases | Foxg1 protein | Methyl-CpG binding protein | MeCP2 protein | Children | Mutation | Neurodevelopmental disorders | Index Medicus
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Transcription and Beyond: Delineating FOXG1 Function in Cortical Development and Disorders
Frontiers in cellular neuroscience, ISSN 1662-5102, 02/2020, Volume 14, pp. 35 - 35
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Genetic transcription | Brain | Post-transcription | Transcription factors | Cerebral cortex | Intellectual development | Mental disorders | Genes | Epilepsy | Cognitive ability | Schizophrenia | Infants | Genomes | Microcephaly | Neurodevelopmental disorders | Cell adhesion & migration | Foxg1 protein | Cell growth | Cell cycle | Forkhead protein | Children | Seizures | Congenital diseases | Phenotypic variations | Roles | Haploinsufficiency | Neurological diseases | Autism | Vertebrates | Microencephaly | Molecular modelling | Rett syndrome | Stem cells | Mutation | Binding sites | posttranscriptional regulation | transcription factor | cortical development | FOXG1 syndrome | FOXG1 | cellular reprogramming
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Genetics in medicine, ISSN 1098-3600, 01/2018, Volume 20, Issue 1, pp. 98 - 108
FOXG1 variants | genotype-phenotype association | congenital variant of Rett syndrome | FOXG1 phenotypic spectrum | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Association Studies | Rett Syndrome - diagnosis | Humans | Child, Preschool | Genotype | Male | Forkhead Transcription Factors - genetics | Nerve Tissue Proteins - genetics | Genetic Variation | Magnetic Resonance Imaging | Phenotype | DNA Mutational Analysis | Female | Polymorphism, Single Nucleotide | Rett Syndrome - genetics | Child | Genotype & phenotype | Genetic counseling | Index Medicus
Journal Article
Epilepsia (Copenhagen), ISSN 0013-9580, 12/2012, Volume 53, Issue 12, pp. 2067 - 2078
Epileptic encephalopathy | Infantile spasms | Encephalopathy | Rett syndrome | MECP2 gene | CDKL5 gene | FOXG1 gene | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Brain Diseases - epidemiology | Rett Syndrome - epidemiology | Humans | Brain Diseases - genetics | Protein-Serine-Threonine Kinases - genetics | Electroencephalography | Forkhead Transcription Factors - genetics | Mutation - genetics | Nerve Tissue Proteins - genetics | Epilepsy - epidemiology | Mental Retardation, X-Linked - genetics | Animals | Epilepsy - genetics | Mice | Rett Syndrome - genetics | Anopheles | Seizures (Medicine) | Genes | Epilepsy | Movement disorders | Index Medicus | Cognitive ability | X chromosome | Telencephalon | Neurodevelopmental disorders | Hand | Morphogenesis | Autism | Foxg1 protein | Language | MeCP2 protein | genomics | Children | Age | Dendritic branching | Seizures
Journal Article
Molecular brain, ISSN 1756-6606, 06/2019, Volume 12, Issue 1, pp. 63 - 63
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Psychological aspects | Neuroplasticity | Transcription factors | Gene mutations | Genetic aspects | Gene expression | Identification and classification | Potentiation | Cell culture | Brain | Memory | Spatial discrimination learning | Cognitive ability | Schizophrenia | Plasticity (neural) | Dendritic spines | Foxg1 protein | Behavioral plasticity | Clonal deletion | Rodents | Behavior | Immunoglobulins | Neurons | Long-term potentiation | Telencephalon | Tamoxifen | Fear conditioning | Autism | Pyramidal cells | Alzheimers disease | Tonic immobility | Dendritic branching | Hippocampus | Spatial memory | Index Medicus | Neural plasticity | FOXG1 syndrome | Spine | Spatial learning and memory | Dendritic arborization | Foxg1
Journal Article
Neuron (Cambridge, Mass.), ISSN 0896-6273, 12/2018, Volume 100, Issue 5, pp. 1083 - 1096.e5
cortex | transcription factor | Zbtb18 | development | Znf238 | callosal projection | Foxg1 | Rp58 | radial migration | corpus callosum | BF1 | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Nerve Tissue Proteins - physiology | Humans | Male | Mice, Transgenic | Axons - physiology | Forkhead Transcription Factors - physiology | Forkhead Transcription Factors - genetics | Nerve Tissue Proteins - genetics | Animals | Gene Expression Regulation, Developmental | Agenesis of Corpus Callosum - genetics | Pyramidal Cells - physiology | HEK293 Cells | Cerebral Cortex - growth & development | Female | Axon Guidance | Corpus Callosum - growth & development | Brain | Neurons | Developmental biology | Hypoplasia | Transcription factors | Cerebral cortex | Leukocyte migration | Transcription | Intellectual disabilities | Genes | Reelin protein | Corpus callosum | Atrophy | Foxg1 protein | Brain research | Etiology | Pyramidal cells | Alleles | Mutation | Axon guidance | Cell migration
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