Gene Ontology annotation through association of InterPro records with GO terms

Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity

Annotation inferences using phylogenetic trees

Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt

Gene Ontology annotation based on curation of immunofluorescence data

Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara

Automatic assignment of GO terms using logical inference, based on on inter-ontology links

Gene Ontology annotation of human sequence-specific DNA binding transcription factors (DbTFs) based on the TFClass database

Electronic Gene Ontology annotations created by ARBA machine learning models

Integrin engagement regulates monocyte differentiation through the forkhead transcription factor Foxp1.

Cooperative regulation in development by SMRT and FOXP1.

FOXP1 is an androgen-responsive transcription factor that negatively regulates androgen receptor signaling in prostate cancer cells.

Down-regulation of the forkhead transcription factor Foxp1 is required for monocyte differentiation and macrophage function.

Human-specific transcriptional regulation of CNS development genes by FOXP2.

De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment.

FoxP1 stimulates angiogenesis by repressing the inhibitory guidance protein semaphorin 5B in endothelial cells.

Investigating protein-protein interactions in live cells using bioluminescence resonance energy transfer.

Transcriptional regulation by FOXP1, FOXP2, and FOXP4 dimerization.

FOXP1 directly represses transcription of proapoptotic genes and cooperates with NF-κB to promote survival of human B cells.

Proteomic analyses reveal distinct chromatin-associated and soluble transcription factor complexes.

A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment.

Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder.

Aurora kinase A regulates Survivin stability through targeting FBXL7 in gastric cancer drug resistance and prognosis.

Impact of cytosine methylation on DNA binding specificities of human transcription factors.

MicroRNA miR-34a downregulates FOXP1 during DNA damage response to limit BCR signalling in chronic lymphocytic leukaemia B cells.

Functional characterization of TBR1 variants in neurodevelopmental disorder.

Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.

POU5F1 (OCT4), SOX2, NANOG, ZSCAN10, PRDM14, SMAD2, FOXP1-ES bind the POU5F1 (OCT4) promoter

POU5F1 (OCT4), SOX2, NANOG, KLF4, PBX1, SMAD2 bind the NANOG promoter

An alternative splicing switch regulates embryonic stem cell pluripotency and reprogramming.

The transcription factor Foxp1 is a critical negative regulator of the differentiation of follicular helper T cells.

Expression of Foxp2, a gene involved in speech and language, in the developing and adult striatum.

Expression of Foxp4 in the developing and adult rat forebrain.

Androgen modulation of Foxp1 and Foxp2 in the developing rat brain: impact on sex specific vocalization.

miR-206 Mediates YAP-Induced Cardiac Hypertrophy and Survival.

A Nuclear Attack on Traumatic Brain Injury: Sequestration of Cell Death in the Nucleus.

Brain-specific Foxp1 deletion impairs neuronal development and causes autistic-like behaviour.

Foxp1 regulation of neonatal vocalizations via cortical development.