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Our findings suggested that overexpression of Pofut1 and activated Notch1 (show NOTCH1 ELISA Kits) signaling may be associated with a poor prognosis in breast cancer.
POFUT1 gene expression in gastric cancer
POFUT1, POGLUT1 (show POGLUT1 ELISA Kits) and ADAM10 (show ADAM10 ELISA Kits) are processing enzymes that are involved in different steps of Notch (show NOTCH1 ELISA Kits) receptor activation in the epidermis; the roles of these unique enzymes in a single pathway may explain both the overlapping and distinct clinical features of DDD (show KRT5 ELISA Kits) and RAK (show FRK ELISA Kits) patients
High expression of POFUT1 correlates with aggressive clinicopathological characteristics and poor prognosis of hepatocellular carcinoma patients.
The upregulation of poFUT1 by LIF (show LIF ELISA Kits) facilitated trophoblast cell migration and invasion through activating the PI3K (show PIK3CA ELISA Kits)/Akt (show AKT1 ELISA Kits) signaling pathway.
Silencing of Pofut1 expression exerted antiproliferative and antiadhesive effects on hepatocytes.
Only a novel 1-bp deletion (c.246+5delG) in POFUT1 was found in a Chinese family with Dowling-Degos disease (DDD (show KRT5 ELISA Kits)). No other novel mutation or this deletion was detected in POFUT1 in a second DDD (show KRT5 ELISA Kits) family and a sporadic DDD (show KRT5 ELISA Kits) case by Sanger Sequencing.
Identification of six pathogenic POFUT1 mutations in Dowling-Degos disease patients of different ethnic origin.
POFUT1 expression can contribute to cancer progression and that POFUT1 may serve as a diagnostic marker and a therapeutic target for OSCCs.
The protein product of POFUT1 plays a significant and conserved role in melanin synthesis and transport.
POFUT1 inactivation disrupts angiogenic signaling events and results in excessive angiogenic cell proliferation and plexus formation, leading to anomalous coronary arteries, myocardial infarction and heart failure.
both wild-type and mutant Pofut1 proteins were degraded through lysosome dependent machinery. Pofut1 protein loss in the point mutant embryos caused the same phenotypes as those observed in Pofut1 null embryos
The POFUT1 binds EGF (show EGF ELISA Kits)-like domains of the hEGF type and that the highly correlated presence of POFUT1 and fucosylatable hEGFs has accompanied animal evolution.
Loss of Pofut1 expression is associated with Muscle Aging-Related Phenotypes.
results demonstrated that POFUT1-mediated O-fucosylation of NOTCH (show NOTCH1 ELISA Kits) receptors regulates myogenic cell differentiation and affects postnatal muscle growth in mice
results establish the critical role of Pofut1 on Notch (show NOTCH1 ELISA Kits) pathway activation during myogenic differentiation
mDLL1 O-fucosylation by POFUT1 is dispensable for ligand function
Loss of Pofut1 is associated with myeloid hyperplasia and impaired lymphopoiesis.
Pofut1 and O-fucose have roles in mammalian Notch (show NOTCH1 ELISA Kits) signaling
Pofut1 is required for Notch (show NOTCH1 ELISA Kits) signaling upstream of NICD1.
This gene encodes a member of the glycosyltransferase O-Fuc family. This enzyme adds O-fucose through an O-glycosidic linkage to conserved serine or threonine residues in the epidermal growth factor-like repeats of a number of cell surface and secreted proteins. O-fucose glycans are involved in ligand-induced receptor signaling. Alternative splicing of this gene results in two transcript variants encoding different isoforms.
GDP-fucose protein O-fucosyltransferase 1
, putative protein-O-fucosyltransferase
, peptide-O-fucosyltransferase 1
, protein-O-fucosyltransferase 1
, protein O-fucosyltransferase 1
, o-fucosyltransferase protein