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

Combined Automated Annotation using Multiple IEA Methods

A mechanism for translationally coupled mRNA turnover: interaction between the poly(A) tail and a c-fos RNA coding determinant via a protein complex.

UNR, a new partner of poly(A)-binding protein, plays a key role in translationally coupled mRNA turnover mediated by the c-fos major coding-region determinant.

Internal initiation of translation from the human rhinovirus-2 internal ribosome entry site requires the binding of Unr to two distinct sites on the 5' untranslated region.

Characterization of unr; a gene closely linked to N-ras.

Insights into RNA biology from an atlas of mammalian mRNA-binding proteins.

The mRNA-bound proteome and its global occupancy profile on protein-coding transcripts.

A proteome-scale map of the human interactome network.

The DDX6-4E-T interaction mediates translational repression and P-body assembly.

High-Density Proximity Mapping Reveals the Subcellular Organization of mRNA-Associated Granules and Bodies.

CSDE1 controls gene expression through the miRNA-mediated decay machinery.

N(6) -methyladenosine-modified lncRNA ARHGAP5-AS1 stabilises CSDE1 and coordinates oncogenic RNA regulons in hepatocellular carcinoma.

unr, a cellular cytoplasmic RNA-binding protein with five cold-shock domains, is required for internal initiation of translation of human rhinovirus RNA.

Context-dependent phosphorylation of CSDE1 drives interactions with ribosomes.

4E-T-bound mRNAs are stored in a silenced and deadenylated form.

UNR facilitates the interaction of MLE with the lncRNA roX2 during Drosophila dosage compensation.

CSDE1 source and evidence index