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foxg1 (172) 172
index medicus (143) 143
humans (94) 94
nerve tissue proteins - genetics (85) 85
animals (82) 82
forkhead transcription factors - genetics (79) 79
foxg1 protein (70) 70
genetics & heredity (65) 65
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rett syndrome (59) 59
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nerve tissue proteins - metabolism (36) 36
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developmental biology (34) 34
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mecp2 (32) 32
neurogenesis (32) 32
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rett-syndrome (30) 30
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forebrain (27) 27
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transcription factors (25) 25
genetics (24) 24
14q12 (23) 23
clinical neurology (23) 23
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stem cells (20) 20
autism (19) 19
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progenitor cells (19) 19
research article (19) 19
deletion (18) 18
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microcephaly (18) 18
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gene expression regulation, developmental (17) 17
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methyl-cpg binding protein (15) 15
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chromosomes, human, pair 14 - genetics (14) 14
forkhead protein (14) 14
haploinsufficiency (14) 14
infantile spasms (14) 14
microcephaly - genetics (14) 14
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1. Full Text Epilepsy in Rett syndrome, and CDKL5‐ and FOXG1‐gene–related encephalopathies
by Guerrini, Renzo and Parrini, Elena
Epilepsia, ISSN 0013-9580, 12/2012, Volume 53, Issue 12, pp. 2067 - 2078
Summary Rett syndrome is an X‐linked neurodevelopmental disorder that manifests in early childhood with developmental stagnation, and loss of spoken language... 
Epileptic encephalopathy | Infantile spasms | Encephalopathy | Rett syndrome | MECP2 gene | CDKL5 gene | FOXG1 gene | SEVERE MENTAL-RETARDATION | FOXG1 MUTATIONS | HELIX TRANSCRIPTION FACTOR | CPG-BINDING PROTEIN-2 | CLINICAL NEUROLOGY | INTERSTITIAL DELETION | ONSET SEIZURE VARIANT | MECP2 DUPLICATION SYNDROME | COPY NUMBER | CONGENITAL VARIANT | 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 | 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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2. Full Text Baicalin exerts antidepressant effects through Akt/FOXG1 pathway promoting neuronal differentiation and survival
by Zhang, Ruyi and Ma, Shiping and Ma, Zhanqiang and Ma, Zhongxuan and Liu, Kaili and Liu, Dongni and Li, Yawei and Xu, Lixing and Deng, Xueyang and Qu, Rong
Life Sciences, ISSN 0024-3205, 03/2019, Volume 221, pp. 241 - 248
Impaired neurogenesis in hippocampus may contribute to a variety of neurological diseases, such as Alzheimer's disease and depression. Baicalin (BA), which is... 
Akt/FOXG1 | Depression | Neurogenesis | Baicalin | MEDICINE, RESEARCH & EXPERIMENTAL | CELLS | BDNF | FOXG1 | BEHAVIOR | MEMORY IMPAIRMENT | MODEL | CHRONIC STRESS | PHARMACOLOGY & PHARMACY | Nervous system diseases | Neurons | Antidepressants | Analysis | Depression, Mental | Stem cells | Fibroblast growth factors | Genetic transcription | Alzheimer's disease | Fibroblast growth factor 2 | Transformation | Cell survival | Sucrose | Neurodegenerative diseases | Telencephalon | AKT protein | Survival | Neurological diseases | Herbal medicine | Foxg1 protein | Molecular modelling | Doublecortin protein | Alzheimers disease | Differentiation | Dendritic structure | Sugars | Elongation
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3. Full Text Chromosome 14q11.2‐q21.1 duplication: a rare cause of West syndrome
by Çetin, Özdem Ertürk and Yalçınkaya, Cengiz and Karaman, Birsen and Demirbilek, Veysi and Tüysüz, Beyhan
Epileptic Disorders, ISSN 1294-9361, 06/2018, Volume 20, Issue 3, pp. 219 - 224
ABSTRACT Proximal duplication of chromosome 14q, including the FOXG1 gene located on 14q12, is a rare condition characterised by developmental delay,... 
West syndrome | neurodevelopmental encephalopathy | chromosome 14q duplication | FOXG1‐related disorders | epileptic spasms | FOXG1-related disorders | 14Q12 | HARBORING FOXG1 | EPILEPSY | CLINICAL NEUROLOGY | IMPAIRMENT | Firing pattern | Foxg1 protein | EEG | Epilepsy | Speech | Gene duplication | Chromosome 14 | Chromosomes | Speech disorders | Seizures
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4. Full Text Collagen-derived dipeptide prolyl hydroxyproline directly binds to Foxg1 to change its conformation and inhibit the interaction with Runx2
by Nomura, Kaho and Kimira, Yoshifumi and Osawa, Yoshihiro and Shimizu, Jun and Kataoka-Matsushita, Aya and Mano, Hiroshi
Bioscience, Biotechnology, and Biochemistry, ISSN 0916-8451, 11/2019, Volume 83, Issue 11, pp. 2027 - 2033
Collagen-derived dipeptide prolyl hydroxyproline (Pro-Hyp) is involved in the proliferation and differentiation of various types of cultured cells. To... 
osteoblast | Prolyl-hydroxyproline | collagen-derived peptide | Foxg1 | Runx2
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5. Full Text A New Approach to Rare Diseases of Children: The Undiagnosed Diseases Network
by Reuter, Chloe M and Brimble, Elise and DeFilippo, Colette and Dries, Annika M and Enns, Gregory M and Ashley, Euan A and Bernstein, Jonathan A and Fisher, Paul Graham and Wheeler, Matthew T and Undiagnosed Dis Network and Undiagnosed Diseases Network
The Journal of Pediatrics, ISSN 0022-3476, 05/2018, Volume 196, pp. 291 - 297.e2
diagnostic dilemma | clinical research | FOXG1 | genetic testing | diagnostic odyssey | secondary finding | whole exome sequencing | SEVERE DEVELOPMENTAL DELAY | MICRODELETION | RETT-SYNDROME | 14Q12 | SEVERE MENTAL-RETARDATION | FOXG1 MUTATIONS | CORPUS-CALLOSUM | CONGENITAL VARIANT | PEDIATRICS | EPILEPSY | PREVALENCE
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6. Role and mechanism of FOXG1 in invasion and metastasis of colorectal cancer
by Wu, Haixia and Qian, Cheng and Liu, Chungang and Xiang, Junyu and Ye, Di and Zhang, Zhenfang and Zhang, Xianquan
Shengwu Gongcheng Xuebao/Chinese Journal of Biotechnology, ISSN 1000-3061, 05/2018, Volume 34, Issue 5, pp. 752 - 760
FOXG1 | Colorectal cancer | Metastasis | EMT
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7. Full Text FOXG1 -Related Syndrome: From Clinical to Molecular Genetics and Pathogenic Mechanisms
by Wong, Lee-Chin and Singh, Shekhar and Wang, Hsin-Pei and Hsu, Chia-Jui and Hu, Su-Ching and Lee, Wang-Tso
International journal of molecular sciences, ISSN 1422-0067, 08/2019, Volume 20, Issue 17, p. 4176
Individuals with mutations in forkhead box G1 ( ) belong to a distinct clinical entity, termed " -related encephalopathy". There are two clinical... 
telencephalon | hyperkinetic movements | transcriptional factor | FOXG1 | Rett syndrome
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8. Full Text Hierarchical genetic interactions between FOXG1 and LHX2 regulate the formation of the cortical hem in the developing telencephalon
by Godbole, Geeta and Shetty, Ashwin S and Roy, Achira and D’Souza, Leora and Chen, Bin and Miyoshi, Goichi and Fishell, Gordon and Tole, Shubha
Development (Cambridge), ISSN 0950-1991, 01/2018, Volume 145, Issue 1, pp. dev154583 - dev154583
During forebrain development, a telencephalic organizer called the cortical hem is crucial for inducing hippocampal fate in adjacent cortical neuroepithelium.... 
Hem | Patterning | Mouse | LHX2 | FOXG1 | Telencephalon | Hippocampus | PAX6 | DEVELOPMENTAL BIOLOGY | FATE | CEREBRAL-CORTEX | IDENTITY | NEOCORTEX | ROLES | BF-1 | GSH2 | MICE | EXPRESSION | Forebrain | Transformation | Foxg1 protein | Cortex | 205 | Research Report
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9. Full Text Disruption of Foxg1 impairs neural plasticity leading to social and cognitive behavioral defects
by Yu, BC and Liu, JH and Su, MZ and Wang, CL and Chen, HX and Zhao, CJ
MOLECULAR BRAIN, ISSN 1756-6606, 06/2019, Volume 12, Issue 1, pp. 63 - 12
The transcription factor Foxg1 is known to be continuously expressed at a high level in mature neurons in the telencephalon, but little is known about its role... 
Neural plasticity | AMPA RATIO | Spine | SEVERE MENTAL-RETARDATION | Dendritic arborization | LTP | FOXG1 syndrome | Spatial learning and memory | NEUROSCIENCES | HAPLOINSUFFICIENCY | MEMORY | Foxg1 | MOUSE MODEL | TELENCEPHALON | NMDA | CONGENITAL VARIANT | LONG-TERM POTENTIATION | EXPRESSION | Tamoxifen | Neurons | Potentiation | Cell culture | Brain | Memory | Spatial discrimination learning | Cognitive ability | Schizophrenia | Plasticity (neural) | Learning | Plasticity (behavioral) | Dendritic spines | Foxg1 protein | Clonal deletion | Rodents | Behavior | Immunoglobulins | Long-term potentiation | Telencephalon | Fear conditioning | Fear | Autism | Pyramidal cells | Alzheimers disease | Tonic immobility | Dendritic branching | Hippocampus | Spatial memory
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10. Full Text A triheptanoin-supplemented diet rescues hippocampal hyperexcitability and seizure susceptibility in FoxG1+/− mice
by Testa, Giovanna and Mainardi, Marco and Olimpico, Francesco and Pancrazi, Laura and Cattaneo, Antonino and Caleo, Matteo and Costa, Mario
Neuropharmacology, ISSN 0028-3908, 04/2019, Volume 148, pp. 305 - 310
The ( ) gene encodes a transcription factor with an essential role in mammalian telencephalon development. -related disorders, caused by deletions, intragenic... 
vGAT | Anaplerotic diet | KCC2 | Kainic acid | Hippocampus | FoxG1 | PHARMACOLOGY & PHARMACY | EPILEPSY | EXPRESSION | NEUROSCIENCES
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11. 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
Rett syndrome (RTT) is an X‐linked progressive neurodevelopmental disorder that primarily affects females. Mutations in the MECP2 gene have been attributed as... 
MECP2 | mutation | database | CDKL5 | FOXG1 | phenotype–genotype correlations | Rett syndrome | locus‐specific database | locus-specific database | MECP2 MUTATION TYPE | PROTEIN | MENTAL-RETARDATION | DISEASE SEVERITY | VARIANT | CDKL5 MUTATIONS | NOMENCLATURE | SYNDROME PHENOTYPE | GENETICS & HEREDITY | phenotype-genotype correlations | DISORDER | X-CHROMOSOME INACTIVATION | 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 | Data bases
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12. Full Text Foxg1 Regulates the Postnatal Development of Cortical Interneurons
by Shen, Wei and Ba, Ru and Su, Yan and Ni, Yang and Chen, Dongsheng and Xie, Wei and Pleasure, Samuel J and Zhao, Chunjie
Cerebral Cortex, ISSN 1047-3211, 04/2019, Volume 29, Issue 4, pp. 1547 - 1560
Abstract Abnormalities in cortical interneurons are closely associated with neurological diseases. Most patients with Foxg1 syndrome experience seizures,... 
migration | Dlx1 | CXCR4 | interneuron | Foxg1 | INHIBITORY INTERNEURONS | TANGENTIAL MIGRATION | FATE | CALRETININ | NEUROSCIENCES | SOMATOSTATIN | GABAERGIC INTERNEURONS | NEURONS | GENERATION | PRECURSORS
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13. Full Text 14q12 and severe Rett-like phenotypes: New clinical insights and physical mapping of FOXG1-regulatory elements
by Allou, Lila and Lambert, Laetitia and Amsallem, Daniel and Bieth, Eric and Edery, Patrick and Destrée, Anne and Rivier, François and Amor, David and Thompson, Elizabeth and Nicholl, Julian and Harbord, Michael and Nemos, Christophe and Saunier, Aline and Moustaïne, Aissa and Vigouroux, Adeline and Jonveaux, Philippe and Philippe, Christophe
European Journal of Human Genetics, ISSN 1018-4813, 12/2012, Volume 20, Issue 12, pp. 1216 - 1223
The Forkhead box G1 (FOXG1) gene has been implicated in severe Rett-like phenotypes. It encodes the Forkhead box protein G1, a winged-helix transcriptional... 
cis-acting regulatory element | CNV | 14q12 | FOXG1 | Rett syndrome | DUPLICATIONS | SEVERE MENTAL-RETARDATION | FOXG1 MUTATIONS | BIOCHEMISTRY & MOLECULAR BIOLOGY | QUESTIONABLE PATHOGENICITY | DELETION | GENETICS & HEREDITY | CONGENITAL VARIANT | PATIENT | EPILEPSY | Agenesis of Corpus Callosum - diagnosis | Protein Kinase C - genetics | Microcephaly - genetics | Humans | Child, Preschool | Male | DNA Copy Number Variations | Intellectual Disability - genetics | Forkhead Transcription Factors - metabolism | Agenesis of Corpus Callosum - genetics | Gene Deletion | Female | Transcription, Genetic | Child | Dyskinesias - genetics | Cell Line | Rett Syndrome - diagnosis | Physical Chromosome Mapping | Silencer Elements, Transcriptional - genetics | Microcephaly - diagnosis | Forkhead Transcription Factors - genetics | Nerve Tissue Proteins - genetics | Syndrome | Nerve Tissue Proteins - metabolism | Point Mutation | Phenotype | Dyskinesias - diagnosis | Intellectual Disability - diagnosis | Rett Syndrome - genetics | Chromosomes, Human, Pair 14 - genetics | Phenotypes | Congenital diseases | Transcription | Intellectual disabilities | Genes | Forebrain | Regulatory sequences | Microcephaly | Neurodevelopmental disorders | Kinases | Corpus callosum | Proteins | Genotype & phenotype | Foxg1 protein | Microencephaly | Language | Genetics | Forkhead protein | Speech | Mutation | Gene mapping | Physical mapping | Dyskinesia | Data processing | Gene deletion | Mental retardation | speech | DNA | Encephalopathy | Point mutation | Fibroblasts
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14. Full Text The hyperkinetic movement disorder of FOXG1‐related epileptic–dyskinetic encephalopathy
by Cellini, Elena and Vignoli, Aglaia and Pisano, Tiziana and Falchi, Melania and Molinaro, Anna and Accorsi, Patrizia and Bontacchio, Alessia and Pinelli, Lorenzo and Giordano, Lucio and Guerrini, Renzo and Fusco, Carlo and Bertani, Gianna and FOXG1 Syndrome Study Grp and FOXG1 Syndrome Study Group
Developmental Medicine & Child Neurology, ISSN 0012-1622, 01/2016, Volume 58, Issue 1, pp. 93 - 97
Aim Forkhead Box G1 (FOXG1) syndrome is a developmental encephalopathy characterized by postnatal microcephaly, structural brain abnormalities, facial... 
PEDIATRICS | INFANTILE SPASMS | RETT-SYNDROME | FOXG1 | CLINICAL NEUROLOGY | Hyperkinesis - genetics | Humans | Adolescent | Child, Preschool | Epilepsy - genetics | Female | Male | Movement Disorders - genetics | Forkhead Transcription Factors - genetics | Child | Nerve Tissue Proteins - genetics | Syndrome
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15. 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
Purpose: The study aimed at widening the clinical and genetic spectrum and assessing genotype-phenotype associations in FOXG1 syndrome due to FOXG1 variants.... 
FOXG1 variants | genotype-phenotype association | congenital variant of Rett syndrome | FOXG1 phenotypic spectrum | RETT-SYNDROME | 14Q12 | SEVERE MENTAL-RETARDATION | HAPLOINSUFFICIENCY | DELETION | GENE | GENETICS & HEREDITY | DISORDER | CONGENITAL VARIANT | MUTATIONS | EPILEPSY | 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
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16. 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, ISSN 0896-6273, 12/2018, Volume 100, Issue 5, pp. 1083 - 1096.e5
The hallmarks of FOXG1 syndrome, which results from mutations in a single allele, include cortical atrophy and corpus callosum agenesis. However, the etiology... 
cortex | transcription factor | Zbtb18 | development | Znf238 | callosal projection | Foxg1 | Rp58 | radial migration | corpus callosum | BF1 | PROGENITOR CELLS | TRANSCRIPTION FACTORS | PYRAMIDAL NEURONS | MENTAL-RETARDATION | CORTICAL NEURON MIGRATION | CORPUS-CALLOSUM | TELENCEPHALON | NEUROGENESIS | DIFFERENTIATION | NEUROSCIENCES | HAPLOINSUFFICIENCY | 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 | Leukocyte migration | Transcription | Intellectual disabilities | Genes | Cortex | Reelin protein | Corpus callosum | Atrophy | Foxg1 protein | Brain research | Etiology | Pyramidal cells | Alleles | Mutation | Axon guidance | Cell migration
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