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foxg1 (172) 172
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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
Journal Article
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
Journal Article
Shengwu Gongcheng Xuebao/Chinese Journal of Biotechnology, ISSN 1000-3061, 05/2018, Volume 34, Issue 5, pp. 752 - 760
Journal Article
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
Journal Article
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
Journal Article
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
Journal Article
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
Journal Article
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
Journal Article
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
Journal Article
Genetics in Medicine, ISSN 1098-3600, 01/2018, Volume 20, Issue 1, pp. 98 - 108
Journal Article
Journal Article