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UBIAD1 encodes a protein thought to be involved in cholesterol and phospholipid metabolism. De plus, nous expédions UBIAD1 Anticorps (30) et UBIAD1 Kits (5) et beaucoup plus de produits pour cette protéine.
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Study identified a gene with important antioxidant features by analyzing a null allele of zebrafish ubiad1, called barolo (bar). bar mutants sh (Montrer NOS3 Protéines)ow specific cardiovascular failure due to oxidative stress and reactive oxygen species-mediated cellular damage.
Although de novo occurrence of mutations in UBIAD1 is extremely rare, SCD should be considered in the differential diagnosis of bilateral corneal haze and/or crystal deposition, especially in children
Silencing UBIAD1 further aggravates the deleterious effects rendered by Ang II (Montrer AGT Protéines), indicating that a normal or increased level of UBIAD1 may offer protection against the Ang (Montrer ANG Protéines) IIinduced hypertrophic response and apoptosis.
these findings disclose a novel sensing mechanism that allows for stringent metabolic control of intracellular trafficking of UBIAD1, which directly modulates reductase degradation and becomes disrupted in Schnyder corneal dystrophy (SCD (Montrer SCD Protéines)).
UBIAD1 or menaquinone-4 could decrease vascular cell differentiation and calcification, probably via its potent role of inversely modulating cellular cholesterol.
Data show that sterols stimulate binding of prenyltransferase (Montrer FDPS Protéines) UBIAD1 to HMG CoA reductase (Montrer HMGCR Protéines), which is subject to sterol-accelerated, endoplasmic reticulum (ER)-associated degradation augmented by the nonsterol isoprenoid geranylgeraniol.
results suggest that YY1 (Montrer YY1 Protéines) up-regulates UBIAD1 expression and UBIAD1 conversion activity through the UBIAD1 promoter
Golgi localization of UBIAD1 influences its tumor suppressant activity.
Loss of TERE1 may contribute to the altered lipid metabolic phenotype associated with progression in renal clear cell carcinoma via an uncoupling of reactive oxygen species/nitric oxide and SXR (Montrer NR1I2 Protéines) signaling from apoptosis by elevation of cholesterol.
A TERE1-TBL2 (Montrer TBL2 Protéines) complex likely functions in oxidative/nitrosative stress, lipid metabolism, and SXR (Montrer NR1I2 Protéines) signaling pathways in its role as a tumor suppressor.
Physical association of UBIAD1 with enzymes involved in cholesterol synthesis and storage, providing direct links between UBIAD1 and cholesterol metabolism that are likely relevant to Schnyder corneal dystrophy disease pathology.
UBIAD1 is responsible for vitamin K2 synthesis but may not be responsible for CoQ9 synthesis in mice.
This gene encodes a protein thought to be involved in cholesterol and phospholipid metabolism. Mutations in this gene are associated with Schnyder crystalline corneal dystrophy.
UbiA prenyltransferase domain containing 1
, transitional epithelia response protein
, ubiA prenyltransferase domain-containing protein 1
, protein barolo
, protein reddish
, unm t31131
, UbiA prenyltransferase domain-containing protein 1
, transitional epithelial response protein 1