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Haplotype G-C-A of CYP4A11 was associated with increased risk of coronary artery disease.
Gene-gene interaction between rs1126742 and rs3890011 and gene-environment interaction between rs1126742 and smoking were associated with increased EH risk.
The DEGs, such as AGTR1, CYP3A4 and CYP4A11 may play critical roles in the development of HTN likely via the regulation by hsa-miR-26b-5p and taking part in some pathways.
Heme-thiolate sulfenylation of human cytochrome P450 4A11 functions as a redox switch for catalytic inhibition.
These results point to a potential 20-HETE dependence of intrarenal angiotensinogen production and ANGII receptor type 1 activation that are associated with increases in NCC and SGK1 and identify elevated P450 4A11 activity and 20-HETE as potential risk factors for salt-sensitive human hypertension by perturbation of the renal renin-angiotensin axis.
CYP4A11 Variants are associated with Ischemic Stroke.
The results suggest that individuals carrying the alleles, K276T and S353G, might exhibit higher catalysis of CYP4A11
CYP4A1l rs9333025 GG and CYP4F2 rs2108622 GG two-loci interaction significantly increases the risk for IS and an elevated 20-HETE level.
Single nucleotide polymorphism of CYP4A11 gene is associated with Plaque in Patients with Ischemic Stroke.
Interaction among CYP2C8, EPHX2, and CYP4A11 Gene Variants Significantly Increases the Risk for Ischemic Stroke.
The present study focused on 10 CYP4A11 variant alleles and evaluated their functional characteristics using arachidonic acid as the substrate in a COS-7 cell-based expression system.
To evaluate the associations between four single-nucleotide polymorphisms (SNPs) in CYP4A11 and CYP4F2 and ischemic stroke (IS)
The CC genotype and C allele of the CYP4A11 gene were associated with essential hypertension in the male western Chinese Han population.
individuals homozygous for the CYP4A11 rs3890011 C allele, blood pressure is resistant to mineralocorticoid receptor antagonism, but sensitive to ENaC inhibition, consistent with ENaC activation.
Results indicate that both the transfer of an electron to the ferrous.O2 complex and C-H bond-breaking limit the rate of CYP4A11 ( cytochrome P450 4A11) omega-oxidation.
This meta-analysis suggests the CYP4A11 T8590C polymorphism may be a risk factor for hypertension.
suggests there is a significant association between the CYP4A11 T8590C variant and essential hypertension, especially in Caucasians. The case-control study did not find a significant association among the Han Chinese population
The results suggest that the CYP4A11 GG genotype was a high risk factor for hypertension.
This meta-analysis revealed that the RGS2 1891-1892del TC polymorphism and CYP4A11 T8590C polymorphism were associated with hypertension risk.
The CYP4A11 8590C allele was also associated with low HDL-C in women.
This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and hydroxylates medium-chain fatty acids such as laurate and myristate.
, 20-hydroxyeicosatetraenoic acid synthase
, alkane-1 monooxygenase
, cytochrome P-450HK-omega
, cytochrome P450 4A11
, cytochrome P450, subfamily IVA, polypeptide 11
, cytochrome P450HL-omega
, fatty acid omega-hydroxylase
, lauric acid omega-hydroxylase
, cytochrome P450 family 4 subfamily A
, cytochrome P450, family 4, subfamily A, polypeptide 11