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FOXP1 gene

Known as: Forkhead Box P1 Gene, GLUTAMINE-RICH FACTOR 1, hFKH1B 
This gene is involved in transcriptional modulation.
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2012
Review
2012
Rare disruptions of FOXP2 have been strongly implicated in deficits in language development. Research over the past decade has… Expand
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Highly Cited
2010
Highly Cited
2010
Heterozygous mutations in FOXP2, which encodes a forkhead transcription factor, have been shown to cause developmental verbal… Expand
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Highly Cited
2010
Highly Cited
2010
MicroRNAs (miRNAs) can influence lineage choice or affect critical developmental checkpoints during hematopoiesis. We examined… Expand
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Highly Cited
2010
Highly Cited
2010
Mental retardation affects 2-3% of the population and shows a high heritability. Neurodevelopmental disorders that include… Expand
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Highly Cited
2007
Highly Cited
2007
The airways of the lung develop through a reiterative process of branching morphogenesis that gives rise to the intricate and… Expand
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Review
2007
Review
2007
Forkhead Box P1 (FOXP1) is a member of the FOX family of transcription factors which have a broad range of functions. Foxp1 is… Expand
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Highly Cited
2004
Highly Cited
2004
Humans and songbirds are two of the rare animal groups that modify their innate vocalizations. The identification of FOXP2 as the… Expand
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Highly Cited
2004
Highly Cited
2004
ABSTRACT Foxp1, Foxp2, and Foxp4 are large multidomain transcriptional regulators belonging to the family of winged-helix DNA… Expand
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Highly Cited
2003
Highly Cited
2003
Foxp2 and Foxp1 are recently identified members of the Fox family of winged-helix/forkhead transcription factor genes. A recent… Expand
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Highly Cited
2001
Highly Cited
2001
The JC12 monoclonal antibody recognizes a previously unknown nuclear protein that showed a restricted distribution in normal… Expand
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