Use your antibodies-online credentials, if available.
Keine Produkte auf Ihrer Vergleichsliste.
Ihr Warenkorb ist leer.
The protein encoded by GPD1L catalyzes the conversion of sn-glycerol 3-phosphate to glycerone phosphate. Zusätzlich bieten wir Ihnen GPD1L Antikörper (48) und GPD1L Kits (4) und viele weitere Produktgruppen zu diesem Protein an.
Showing 7 out of 8 products:
Then bioinformatic analysis identified potential target sites of the miR (zeige MLXIP Proteine)-181a located in the 3' untranslated region of GPD1L. Increased GPD1L and decreased miRNA-181a were observed in tissues from osteoarthritis patients. Our results demonstrated that miR (zeige MLXIP Proteine)-181a may play an important role in the pathogenesis of Osteoarthritis through targeting GPD1L and regulating chondrocyte apoptosis.
In a nonreferred nationwide Danish cohort of SIDS (zeige IDS Proteine) cases, up to 5/66 (7.5%) of SIDS (zeige IDS Proteine) cases can be explained by genetic variants in the sodium channel complex genes.
The results of real-time PCR showed that, compared with the paired normal tissues, mRNA levels of GPD1L were decreased significantly in head and neck squamous cell carcinoma.
Common variations in or near CASQ2 (zeige CASQ2 Proteine), GPD1L, and NOS1AP (zeige NOS1AP Proteine) are associated with increased risk of sudden cardiac death in patients with coronary artery disease
hypoxia-induced miR (zeige MLXIP Proteine)-210 represses GPD1L, contributing to suppression of prolyl hydroxylases activity, and increases of HIF-1alpha (zeige HIF1A Proteine) protein levels.
mutations in GPD1-L as a pathogenic cause for a small subset of sudden infant death syndrome via a secondary loss-of-function mechanism
A GPD1-L mutation decreases SCN5A (zeige SCN5A Proteine) surface membrane expression, reduces inward Na+ current, and causes Brugada syndrome
No non-synonymous mutations were found, indicating that GPD1L does not appear to be a major cause of Brugada syndrome in a Japanese population.
GPD1L links redox state to cardiac excitability by PKC (zeige PRRT2 Proteine)-dependent phosphorylation of the sodium channel SCN5A (zeige SCN5A Proteine).
Mutations of GPD1-L may downregulate Na(v)1.5 by altering the oxidized to reduced NAD(H) balance.
The protein encoded by this gene catalyzes the conversion of sn-glycerol 3-phosphate to glycerone phosphate. The encoded protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A). Defects in this gene are a cause of Brugada syndrome type 2 (BRS2) as well as sudden infant death syndrome (SIDS).
glycerol-3-phosphate dehydrogenase 1-like protein
, glycerol-3-phosphate dehydrogenase 1-like
, glycerol-3-phosphate dehydrogenase 1-like protein-like