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FOXG1 gene

Known as: HFK1, FORKHEAD BOX G1B, HFK2 
This gene is involved in transcriptional repression and may play a role in the development of the brain and telencephalon.
National Institutes of Health

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FOXG1 wt Allele
FOXG1B protein, humanHomo sapiensTranscriptional RegulationTranscriptional Repression

Papers overview

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Highly Cited
2019
Highly Cited
2019
The nuclear transcription factor FoxG1 affects the sensitivity of mimetic aging hair cells to inflammation by regulating autophagy pathways
Highly Cited
2018
Highly Cited
2018
Predictive Value of Serum Albumin Level for the Prognosis of Severe Sepsis Without Exogenous Human Albumin Administration: A Prospective Cohort Study
Background: The prognostic significance of serum albumin levels in patients with sepsis has previously been reported; however… 
Highly Cited
2011
Highly Cited
2011
CDKL5-Related Disorders: From Clinical Description to Molecular Genetics
Mutations in the cyclin-dependent kinase-like 5 gene (CDKL5) have been described in girls with Rett-like features and early-onset… 
Highly Cited
2011
Highly Cited
2011
FoxG1 Promotes the Survival of Postmitotic Neurons
The transcription factor FoxG1 regulates neurogenesis in the embryonic telencephalon as well as a number of other… 
Highly Cited
2009
Highly Cited
2009
Medium optimization for the production of a novel bioflocculant from Halomonas sp. V3a' using response surface methodology.
Highly Cited
2008
Highly Cited
2008
Foxg1 Is Required for Development of the Vertebrate Olfactory System
Illuminating the molecular identity and regulation of early progenitor cells in the olfactory sensory epithelium represents an… 
Highly Cited
2006
Highly Cited
2006
FoxG1 haploinsufficiency results in impaired neurogenesis in the postnatal hippocampus and contextual memory deficits
FoxG1 (formerly BF‐1) encodes a transcription factor that regulates neurogenesis in the embryonic telencephalon. The current… 
Highly Cited
2006
Highly Cited
2006
Additional chromosomal abnormalities in patients with a previously detected abnormal karyotype, mental retardation, and dysmorphic features
The detection of chromosomal abnormalities in patients with mental retardation (MR) and dysmorphic features increases with… 
Highly Cited
1995
Highly Cited
1995
The mouse homolog of the orphan nuclear receptor tailless is expressed in the developing forebrain.
The Drosophila tailless gene is a member of the orphan nuclear receptor subfamily. In Drosophila, the tailless gene is required… 
Highly Cited
1994
Highly Cited
1994
Human brain factor 1, a new member of the fork head gene family.
Analysis of cDNA clones that cross-hybridized with the fork head domain of the rat HNF-3 gene family revealed 10 cDNAs from human… 
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