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FOXP2


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FOXP2

FOXP2

FoxP2

FOXP2: Linking Language and Autism

The Timing of Selection at the Human FOXP2 Gene

Linkage Disequilibrium Extends Across Putative Selected Sites in FOXP2

The DISC1 promoter: characterization and regulation by FOXP2

The Medaka FoxP2, a Homologue of Human Language Gene FOXP2, has a Diverged Structure and Function

FoxP2 in Song-Learning Birds and Vocal-Learning Mammals

A Recent Evolutionary Change Affects a Regulatory Element in the Human FOXP2 Gene

FoxP2 and deep homology in the evolution of birdsong and human language*

Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex

LPS-activated monocytes suppress T-cell immune responses and induce FOXP3+ T cells through a COX-2–PGE2-dependent mechanism

O2–050PD-1 AND FOXP3 PREDICTING THE RESPONSE TO NEOADJUVANT-CHEMOTHERAPY_(NAC) OF BREAST CANCER

FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder

FoxP2 is a Parvocellular-Specific Transcription Factor in the Visual Thalamus of Monkeys and Ferrets

P297 - Local fuelling of IL-2 determines the tissue localisation of CD4+Foxp3+ regulatory T cells – proliferating cells signal inflammation and provide IL-2

T-bet, GATA-3, and Foxp3 Expression and Th1/Th2 Cytokine Production in the Clinical Outcome of Human Infection with Leishmania (Viannia) Species

Microfluidic affinity and ChIP-seq analyses converge on a conserved FOXP2-binding motif in chimp and human, which enables the detection of evolutionarily novel targets

 

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A gene required for the proper development of speech in children. See speech-language disorder 1 (SPCH1).

Subjects: Genetics and Genomics.


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