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1. Full Text Multiple roles for Pax2 in the embryonic mouse eye
by Bosze, Bernadett and Suarez-Navarro, Julissa and Soofi, Abdul and Lauderdale, James D and Dressler, Gregory R and Brown, Nadean L
Developmental biology, ISSN 0012-1606, 04/2021, Volume 472, pp. 18 - 29
RPE | Foxg1 | Coloboma | Retina | Pax6 | Optic stalk | Pax2 | Index Medicus
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2. Full Text Knockdown of Foxg1 in supporting cells increases the trans-differentiation of supporting cells into hair cells in the neonatal mouse cochlea
by Zhang, Shasha and Zhang, Yuan and Dong, Ying and Guo, Lingna and Zhang, Zhong and Shao, Buwei and Qi, Jieyu and Zhou, Han and Zhu, Weijie and Yan, Xiaoqian and Hong, Guodong and Zhang, Liyan and Zhang, Xiaoli and Tang, Mingliang and Zhao, Chunjie and Gao, Xia and Chai, Renjie
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
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3. Full Text RettBASE: Rett syndrome database update
by Krishnaraj, Rahul and Ho, Gladys and Christodoulou, John
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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4. Full Text Transcription and Beyond: Delineating FOXG1 Function in Cortical Development and Disorders
by Hou, Pei-Shan and HAilin, Darren O and Vogel, Tanja and Hanashima, Carina
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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5. Full Text FOXG1 syndrome: Genotype-phenotype association in 83 patients with FOXG1 variants
by Mitter, Diana and Pringsheim, Milka and Kaulisch, Marc and Plümacher, Kim Sarah and Schröder, Simone and Warthemann, Rita and Abou Jamra, Rami and Baethmann, Martina and Bast, Thomas and Büttel, Hans-Martin and Cohen, Julie S and Conover, Elizabeth and Courage, Carolina and Eger, Angelika and Fatemi, Ali and Grebe, Theresa A and Hauser, Natalie S and Heinritz, Wolfram and Helbig, Katherine L and Heruth, Marion and Huhle, Dagmar and Höft, Karen and Karch, Stephanie and Kluger, Gerhard and Korenke, G Christoph and Lemke, Johannes R and Lutz, Richard E and Patzer, Steffi and Prehl, Isabelle and Hoertnagel, Konstanze and Ramsey, Keri and Rating, Tina and Rieß, Angelika and Rohena, Luis and Schimmel, Mareike and Westman, Rachel and Zech, Frank-Martin and Zoll, Barbara and Malzahn, Dörthe and Zirn, Birgit and Brockmann, Knut
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
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6. Full Text Epilepsy in Rett syndrome, and CDKL5‐ and FOXG1‐gene–related encephalopathies
by Guerrini, Renzo and Parrini, Elena
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
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7. Full Text Disruption of Foxg1 impairs neural plasticity leading to social and cognitive behavioral defects
by Yu, Baocong and Liu, Junhua and Su, Mingzhao and Wang, Chunlian and Chen, Huanxin and Zhao, Chunjie
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
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8. Full Text FOXG1 Orchestrates Neocortical Organization and Cortico-Cortical Connections
by Cargnin, Francesca and Kwon, Ji-Sun and Katzman, Sol and Chen, Bin and Lee, Jae W and Lee, Soo-Kyung
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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