FOXP1 gene

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

Topic mentions per year

Topic mentions per year

2001-2017
0102020012017

Papers overview

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2015
2015
Neurodevelopmental disorders are multi-faceted and can lead to intellectual disability, autism spectrum disorder and language… (More)
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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… (More)
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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… (More)
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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… (More)
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2010
2010
Foxp1 and Foxp2, which belong to the forkhead transcription factor family, are expressed in the developing and adult mouse brain… (More)
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2010
2010
Human FOXP2 deficiency has been identified as a cause of hereditary developmental verbal dyspraxia. Another member of the same… (More)
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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… (More)
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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… (More)
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Highly Cited
2004
Highly Cited
2004
Foxp1, Foxp2, and Foxp4 are large multidomain transcriptional regulators belonging to the family of winged-helix DNA binding… (More)
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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… (More)
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