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
Electronic Gene Ontology annotations created by ARBA machine learning models
Decay accelerating activity of complement receptor type 1 (CD35). Two active sites are required for dissociating C5 convertases.
The role of complement receptors type 1 (CR1, CD35) and 2 (CR2, CD21) in promoting C3 fragment deposition and membrane attack complex formation on normal peripheral human B cells.
Expression and localization of proteins of the complement system in human skin.
The complement receptor 1, CR1 (CD35), mediates inhibitory signals in human T-lymphocytes.
Ligation of erythrocyte CR1 induces its clustering in complex with scaffolding protein FAP-1.
Large-scale proteomics and phosphoproteomics of urinary exosomes.
Abnormal immune complex processing and spontaneous glomerulonephritis in complement factor H-deficient mice with human complement receptor 1 on erythrocytes.
Complement receptor type 1 (CR1, CD35) is a potent inhibitor of B-cell functions in rheumatoid arthritis patients.
Deciphering complement receptor type 1 interactions with recognition proteins of the lectin complement pathway.
In-depth proteomic analyses of exosomes isolated from expressed prostatic secretions in urine.
CR1-mediated ATP release by human red blood cells promotes CR1 clustering and modulates the immune transfer process.
Complement receptor type 1 (CR1/CD35) expressed on activated human CD4+ T cells contributes to generation of regulatory T cells.
C1q and Mannose-Binding Lectin Interact with CR1 in the Same Region on CCP24-25 Modules.
Identification of distinct C3b and C4b recognition sites in the human C3b/C4b receptor (CR1, CD35) by deletion mutagenesis.
Complement Receptor 1 (CR1/CD35)-expressing retinal pigment epithelial cells as a potential therapy for age-related macular degeneration.
Complement receptor is an inhibitor of the complement cascade.
Complement receptor (CR1) deficiency in erythrocytes from patients with systemic lupus erythematosus.
Exocytosis of secretory granule membrane proteins
Exocytosis of ficolin-rich granule membrane proteins
CR1 gene expression is stimulated by RUNX1
Complement factor I binds to MCP, CR1:C4b, C3b
Factor I inactivates MCP/CR1-bound C4b/C3b
Displacement of C2a/Bb by CR1