GO_REF:0000033
Annotation inferences using phylogenetic trees
GO_REF:0000043
Gene Ontology annotation based on UniProtKB/Swiss-Prot keyword mapping
GO_REF:0000044
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping
GO_REF:0000052
Gene Ontology annotation based on curation of immunofluorescence data
GO_REF:0000120
Combined Automated Annotation using Multiple IEA Methods
PMID:10567391
The role of human MBF1 as a transcriptional coactivator.
PMID:12040021
Multiprotein bridging factor-1 (MBF-1) is a cofactor for nuclear receptors that regulate lipid metabolism.
PMID:21217774
RAC3 is a pro-migratory co-activator of ERα.
PMID:22658674
Insights into RNA biology from an atlas of mammalian mRNA-binding proteins.
PMID:22681889
The mRNA-bound proteome and its global occupancy profile on protein-coding transcripts.
PMID:24008843
Structure homology and interaction redundancy for discovering virus-host protein interactions.
PMID:25416956
A proteome-scale map of the human interactome network.
PMID:31527615
The RNA-mediated estrogen receptor α interactome of hormone-dependent human breast cancer cell nuclei.
PMID:32814053
Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains.
PMID:35156780
CFTR interactome mapping using the mammalian membrane two-hybrid high-throughput screening system.
PMID:36012204
Differential CFTR-Interactome Proximity Labeling Procedures Identify Enrichment in Multiple SLC Transporters.
PMID:8164657
Mediators of activation of fushi tarazu gene transcription by BmFTZ-F1.
file:human/EDF1/EDF1-deep-research-openai.md
Deep research on EDF1 function
file:human/EDF1/EDF1-deep-research-falcon.md
Deep research on EDF1 function (falcon provider, Edison Scientific Literature)
PMID:32744497
EDF1 coordinates cellular responses to ribosome collisions.
PMID:39566505
Multiprotein bridging factor 1 is required for robust activation of the integrated stress response on collided ribosomes.
PMID:38966981
HBS1L deficiency causes retinal dystrophy in a child and in a mouse model associated with defective development of photoreceptor cells.
PMID:38891865
Long Noncoding RNAs in Diet-Induced Metabolic Diseases.