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GenomicsSERPINC1
Sequence of the SERPINC1 gene on patients from Centro Regional de Hemodonacion
PRJEB12779 | ENA
ProteomicsSerpinc1 acts as a tumor suppressor in hepatocellular carcinoma through inducing apoptosis and blocking macrophage polarization in an ubiquitin-proteasome manner
Serpinc1 is a serine protease inhibitor in the coagulation cascade, but its role in tumor biology remains obscure. Here, we report an unexpected role of serpinc1 in suppression of hepatocellular carcinoma (HCC). In HCC patients, the mRNA and protein expression of serpinc1 is up-regulated, which is n...
ORGANISM(S): Homo sapiens (Human) 
2022-02-17 | PXD026782 | Pride
Serpinc1  apoptosis  liver cancer  macrophage  ubiquitination 
UnknownSERPINC1 c.1247dupC: a novel SERPINC1 gene mutation associated with familial thrombosis results in a secretion defect and quantitative antithrombin deficiency.
Not available
S-EPMC10860291 | biostudies-literature
UnknownUtility of the SERPINC1 Gene Test in Ischemic Stroke Patients With Antithrombin Deficiency.
Not available
S-EPMC9203840 | biostudies-literature
UnknownUrine SERPINC1/ORM1 as biomarkers for early detection of lupus nephritis in MRL-lpr mice.
Not available
S-EPMC10515280 | biostudies-literature
UnknownCirculating exosomal protein EFEMP1 and SERPINC1 as diagnostic biomarkers for epithelial ovarian cancer.
Not available
S-EPMC11462355 | biostudies-literature
UnknownSerpinc1 Acts as a Tumor Suppressor in Hepatocellular Carcinoma Through Inducing Apoptosis and Blocking Macrophage Polarization in an Ubiquitin-Proteasome Manner.
Not available
S-EPMC8645897 | biostudies-literature
UnknownIdentification and characterization of two SERPINC1 mutations causing congenital antithrombin deficiency.
Not available
S-EPMC9830717 | biostudies-literature
UnknownIdentification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency.
Not available
S-EPMC4803246 | biostudies-literature
UnknownNew genetic variant in the SERPINC1 gene: hereditary Antithrombin deficiency case report, familial thrombosis and considerations on genetic counseling.
Not available
S-EPMC7137186 | biostudies-literature
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