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study found that individuals infected with HBV withwith basal core promoter (BCP (show OPN1SW ELISA Kits)) double mutations (A1762T, G1764A)have lower concentrations of serum DLD than those with the wild-type BCP (show OPN1SW ELISA Kits)
Mitochondrial dihydrolipoamide dehydrogenase is upregulated in response to the brain intermittent hypoxic preconditioning.
IgA autoantibody against DLD could be a novel diagnostic marker for endometrial cancer.
Case Report: novel mutation in the DLD interface giving rise to DLD deficiency.
Certain DLD mutations can simultaneously induce the loss of a primary metabolic activity and the gain of a moonlighting proteolytic activity thus contributing to the metabolic derangement associated with DLD deficiency.
This molecular dynamics study proposes the structural changes that may lead to the modulation in reactive oxygen species generation by pathogenic mutants of human dihydrolipoamide dehydrogenase.
the cryptic activities of DLD promote oxidative damage to neighboring molecules and thus contribute to the clinical severity of DLD mutations
Structural and thermodynamic basis for weak interactions between dihydrolipoamide dehydrogenase and subunit-binding domain of the branched-chain alpha-ketoacid dehydrogenase complex.
the E3 binding protein (show PDHX ELISA Kits) component of the pyruvate dehydrogenase (show PDP ELISA Kits) complex appear to be a rare cause of pyruvate dehydrogenase (show PDP ELISA Kits) deficiency
Activity of human dihydrolipoamide dehydrogenase is reduced by mutation at threonine-44 of FAD (show BRCA2 ELISA Kits)-binding region to valine.
DLD, malic acid, and fumaric acid can be used for development of cosmeceuticals and nutraceuticals regulating the change of skin metabolism induced by the UVB overexposure.
Data show that mitochondrial diaphorases (dihydrolipoamide dehydrogenase) in the liver contribute up to 81% to the NAD(+) pool during respiratory inhibition.
Human, mouse, and pig Dld has moonlighting function as a protease in addition to its canonical function as a a dehydrogenase.
Mice that are deficient in dihydrolipoamide dehydrogenase show increased vulnerability to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP (show PTPN2 ELISA Kits)), malonate and 3-nitropropionic acid, which have been used in models of Parkinson disease and Huntington disease (show HTT ELISA Kits)
identification and characterization of human and mouse D-lactate dehydrogenase (NAD) [D-LDH]
forms of DeltaD that have the MID can activate Notch (show NOTCH1 ELISA Kits) in trans and suppress early neurogenesis when mRNA encoding it is ectopically expressed in zebrafish embryos.
Fgfr4 (show FGFR4 ELISA Kits) mediates a signal-transduction pathway between Wnt16 (show WNT16 ELISA Kits) and Dlc, but not Dld, to regulate haematopoietic stem cells specification.
DeltaC and DeltaD interact as Notch (show NOTCH1 ELISA Kits) ligands in the zebrafish segmentation clock.
DeltaA/DeltaD regulate multiple and temporally distinct phases of notch (show NOTCH1 ELISA Kits) signaling during dopaminergic neurogenesis in zebrafish
Notch (show NOTCH1 ELISA Kits) signalling, via DeltaD, brings together ciliary length control and fluid flow hydrodynamics with transcriptional activation of laterality genes.
Several genomic regions that drive transcription in mesodermal and neuroectodermal domains have been identified. Transcription in all the neural expression domains is controlled by two regions, which are regulated by neurogenin 1 and zash1a/b
Results suggest that Delta/D-Notch 1a signaling is required for spinal cord oligodendrocyte specification.
DeltaD-Notch (show NOTCH1 ELISA Kits) signalling has a role in establishing the secretory fate in the zebrafish intestine
Data suggest that delta/notch (show NOTCH1 ELISA Kits)- and integrinalpha5-dependent cell polarization and fibronectin (show FN1 ELISA Kits) matrix assembly occur concomitantly and interdependently during border morphogenesis.
These findings show that the plastidial LIPOAMIDE DEHYDROGENASE, ptLPD, isoforms are critical in vivo determinants of arsenite-mediated arsenic sensitivity in Arabidopsis and possible strategic targets for increasing arsenic tolerance. [ptLPD2]
Lipoamide dehydrogenase significantly accelerates the conversion of a defined subset of NO donors to NO.
This gene encodes the L protein of the mitochondrial glycine cleavage system. The L protein, also named dihydrolipoamide dehydrogenase, is also a component of the pyruvate dehydrogenase complex, the alpha-ketoglutarate dehydrogenase complex, and the branched-chain alpha-keto acide dehydrogenase complex. Mutations in this gene have been identified in patients with E3-deficient maple syrup urine disease and lipoamide dehydrogenase deficiency.
E3 component of pyruvate dehydrogenase complex, 2-oxo-glutarate complex, branched chain keto acid dehydrogenase complex
, dihydrolipoyl dehydrogenase, mitochondrial
, glycine cleavage system L protein
, glycine cleavage system protein L
, lipoamide dehydrogenase
, lipoamide reductase
, lipoyl dehydrogenase
, branched chain alpha-keto acid dehydrogenase complex subunit E3
, dihydrolipoamide dehydrogenase (E3 component of pyruvate dehydrogenase complex, 2-oxo-glutarate complex, branched chain keto acid dehydrogenase complex)
, dihydrolipoamide dehydrogenase
, dihydrolipoyl dehydrogenase
, protein BfmBC
, dihydrolipoamide:NAD oxidoreductase
, glycine cleavage system L-protein
, probable D-lactate dehydrogenase, mitochondrial
, after eight protein
, delta-like protein D
, dihydrolipoamide: NAD+ oxidoreductase
, Dihydrolipoyl dehydrogenase, mitochondrial