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ProteomicsNucleolin is a cell surface receptor of C1QTNF4
C1QTNF4 is a secreted protein that is structurally unique within the C1QTNF family, a family of proteins that have structural homology with both complement C1q and the tumor necrosis factor superfamily. The role of C1QTNF4 in immunity and inflammation remains poorly defined and a cell surface recept...
ORGANISM(S): Homo sapiens (Human) 
2021-03-21 | PXD023088 | Pride
Innate immunity Nucleolin Cell surface receptor Inflammation Ctrp4 C1qtnf4 Monocyte Autoimmune disease Systemic lupus erythematosus 
UnknownInhibition of estrogen signaling in myeloid cells increases tumor immunity in melanoma.
Not available
S-EPMC8631601 | biostudies-literature
UnknownA New Chemotype of Chemically Tractable Nonsteroidal Estrogens Based on a Thieno[2,3-d]pyrimidine Core.
Not available
S-EPMC9290010 | biostudies-literature
UnknownThe prognostic effects of somatic mutations in ER-positive breast cancer.
Not available
S-EPMC6123466 | biostudies-literature
UnknownThe EstroGene2.0 database for endocrine therapy response and resistance in breast cancer.
Not available
S-EPMC11659402 | biostudies-literature
UnknownNew Sequencing technologies help revealing unexpected mutations in Autosomal Dominant Hypercholesterolemia.
Not available
S-EPMC5792649 | biostudies-literature
UnknownInhibition of ERRα Prevents Mitochondrial Pyruvate Uptake Exposing NADPH-Generating Pathways as Targetable Vulnerabilities in Breast Cancer.
Not available
S-EPMC6604861 | biostudies-literature
UnknownBreast Cancer Neoantigens Can Induce CD8+ T-Cell Responses and Antitumor Immunity.
Not available
S-EPMC5647648 | biostudies-literature
UnknownProteomic Resistance Biomarkers for PI3K Inhibitor in Triple Negative Breast Cancer Patient-Derived Xenograft Models.
Not available
S-EPMC7765949 | biostudies-literature
GenomicCCDG-Cardiovascular: University of Pennsylvania Cohort

The National Human Genome Research Institute (NHGRI) has funded the Centers for Common Disease Genomics (CCDG), a collaborative large-scale genome sequencing effort to comprehensively identify rare risk and protective variants contributing to multiple common disease phenotypes and to better under...

phs001502 | dbGaP
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