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DDAH2 belongs to the dimethylarginine dimethylaminohydrolase (DDAH) gene family. De plus, nous expédions DDAH2 Anticorps (60) et DDAH2 Kits (30) et beaucoup plus de produits pour cette protéine.
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genetic variations in the DDAH2 gene may influence the ADMA concentration and erythropoietin (Montrer EPO Protéines) resistance in MHD patients
The main finding from this study was that it demonstrated that the C-allele of rs3087894 in DDAH1 is a risk factor for hypertension in the Kazakh group but a protective factor in the Uygur group. In addition, we did not find any genotype of DDAH1 and DDAH2 associated with hypertension in the Han group.
Exogenous human DDAH2 gene promotes differentiation of rabbit bone marrow-derived endothelial progenitor cells into mature endothelial cells.
expression of DDAH2 is associated with invasiveness of lung adenocarcinoma via tumor angiogenesis
Inhibiting the expression of DDAH1 (Montrer DDAH1 Protéines), but not DDAH2, resulted in a significant increase in the sensitivity of the EVT cell line SGHPL-4 to tumour necrosis factor (Montrer TNF Protéines) related apoptosis inducing ligand (TRAIL) induced apoptosis
increased ADMA levels in rheumatoid arthritis do not appear to relate to DDAH genetic polymorphisms
The percentage of senescent endothelial progenitor cells increased while the expression of DDAH2 decreased concomitantly with an increase in the plasma levels of asymmetric dimethylarginine in patients with type 2 diabetes mellitus.
DDAH-1 (Montrer DDAH1 Protéines) is a specific molecular target for portal pressure reduction, through actions on ADMA-mediated regulation of eNOS (Montrer NOS3 Protéines) activity.
Our results suggest that the rs805304 C allele of the DDAH gene was associated with decreased risk of myocardial infarction and decreased risk of obesity.
Homocysteine disrupts EPCs function via inducing the hypermethylation of DDAH2 promoter, suggesting a key role of epigenetic mechanism in the progression of atherosclerosis
We conclude that pp60(Src (Montrer SRC Protéines)) can directly inhibit DDAH II and this is involved in the increased ADMA levels that enhance eNOS (Montrer NOS3 Protéines) uncoupling during the development of acute lung injury (ALI).
In mild CKD, dysregulation of the ADMA/DDAH pathway in adipose tissue triggers lipodystrophy-like phenotype changes, including ectopic fat depositions.
The Sirt1 (Montrer SIRT1 Protéines)/DDAH2/secretagogin (Montrer SCGN Protéines) pathway is a novel regulator of glucose-stimulated insulin (Montrer INS Protéines) secretion.
DDAH2/ADMA pathway can be a novel therapeutic target for vasculopathy in the ADMA or angiotensin II-induced pathophysiological conditions
Report tissue-specific downregulation of DDAH2 in hyperhomocysteinemia.
Results show that asymmetric methylarginine increases pulmonary endothelial permeability, and that its effects on permeability, Rac1 activation and VASP (Montrer VASP Protéines) phosphorylation are prevented by overexpression of active DDAHI (Montrer DDAH1 Protéines) and DDAHII.
ADMA and nitrosative stress are related to increased expression of protein-arginine methyltransferase-2 (Montrer PRMT2 Protéines), an ADMA-synthesizing enzyme, and reduced expression of dimethylarginine dimethylaminohydrolase-2, an ADMA-degrading enzyme, in bronchial epithelia
This gene belongs to the dimethylarginine dimethylaminohydrolase (DDAH) gene family. The encoded enzyme plays a role in nitric oxide generation by regulating cellular concentrations of methylarginines, which in turn inhibit nitric oxide synthase activity.
NG,NG-dimethylarginine dimethylaminohydrolase 2
, dimethylarginine dimethylaminohydrolase 2
, N(G),N(G)-dimethylarginine dimethylaminohydrolase 2
, NG-dimethylarginine dimethylamino hydrolase homolog
, S-phase protein
, alternative name: NG30, G6a
, dimethylarginine dimethylaminohydrolase II
, protein G6a
, Clone 7u