Use your antibodies-online credentials, if available.
Human DECR1 Protein expressed in Escherichia coli (E. coli) - ABIN2128859
Wunsch, Jabari, Voussen, Enders, Srinivasan, Cossais, Wedel, Boettner, Schwarz, Weyer, Göcer, Schroeter, Maeurer, Woenckhaus, Pollok, Radbruch, Klotz, Scholz, Nickel, Friebe, Addicks, Ergün, Lehmann et al.: The enteric nervous system is a potential autoimmune target in multiple sclerosis. ... in Acta neuropathologica 2018
Human DECR1 Protein expressed in Wheat germ - ABIN1351392
Rong, Zhong, Lleo, Leung, Bowlus, Yang, Yang, Coppel, Ansari, Cuebas, Worman, Invernizzi, Gores, Norman, He, Gershwin: Epithelial cell specificity and apotope recognition by serum autoantibodies in primary biliary cirrhosis. in Hepatology (Baltimore, Md.) 2011
Expression levels of ADSL, GARS-AIRS-GART, and DGAT1 were higher in longissimus lumborum muscle than in heart or liver tissues
This lack of consistency across families, combined with the fact that the ME1 mutation is synonymous and that the two DECR1 polymorphisms are conservative, suggests that the associations found are not causative.
We characterized the nearly complete coding sequence of the pig 2,4-dienoyl CoA reductase 1 (DECR1) gene, and found differences among genotypes for isocitrate dehydrogenase activity, longissimus thoracis pH, lightness, and redness.
These results suggest that polymorphisms discovered in DECR1, CBFA2T1, and FGF8 may play a role in the lipid metabolism pathway affecting carcass quality traits in beef cattle.
Our study is the first to demonstrate the novel function of UA in NET formation and may provide insight into the management of patients with hyperuricemia.
A protein encoded by this locus was found to be differentially expressed in postmortem brains from patients with atypical frontotemporal lobar degeneration.
Structure and reactivity of human mitochondrial 2,4-dienoyl-CoA reductase
Sequence alignment indicates that there are five highly conserved acidic residues, one of which (E276) might act as a proton donor.
mutational defects cause chronic granulomatous disease in humans
The luminal NADPH pool is an important antiapoptotic factor in neutrophil granulocytes.
The TT genotype of C677T polymorphism in the MTHFR gene contributes to genetic susceptibility of acute ischemic stroke in a Singapore population.
Fasted Decr(-/-) mice displayed increased serum acylcarnitines and unimpaired ketogenesis.
This gene encodes an accessory enzyme which participates in the beta-oxidation and metabolism of unsaturated fatty enoyl-CoA esters.
2,4-dienoyl-CoA reductase 1, mitochondrial
, 2,4-dienoyl-CoA reductase, mitochondrial
, 2,4-dienoyl-CoA reductase, NADPH
, 4-enoyl-CoA reductase, NADPH
, 4-enoyl-CoA reductase
, short chain dehydrogenase/reductase family 18C, member 1
, 2,4-dienoyl CoA reductase 1, mitochondrial
, putative 24-dienoyl CoA reductase 1 mitochondrial