Results 1 to 10 of about 88 (85)
Although some 3-D lanthanide glutarates have been reported, they exhibit a very robust structural type, whose structure is not changed by different Ln3+ions, but compound3shows a new structural type.
Jian Zhou, Lianshe Fu, Jian Zhou
exaly +4 more sources
Abstract Using slow diffusion methods at room temperature (RT), we obtained four isomorphous lanthanide glutarate chlorides, accommodating interstitial THF and water molecules, [Ln2(Glut)2Cl2(H2O)8]·2H2O·THF (1–4), with Ln = La (1), Ce (2), Pr (3), Nd (4).
Matthias Zeller
exaly +4 more sources
Glutaric Acidemia, Pathogenesis and Nutritional Therapy [PDF]
Glutaric acidemia (GA) are heterogeneous, genetic diseases that present with specific catabolic deficiencies of amino acid or fatty acid metabolism. The disorders can be divided into type I and type II by the occurrence of different types of recessive mutations of autosomal, metabolically important genes.
Qian Li+10 more
openaire +3 more sources
Increased liver content of DHA‐derived small lipid autacoids (i.e resolvin D1 and maresin 1) associates with enhanced mitochondrial oxidative phosphorylation, fatty acid β‐oxidation and bioenergetic metabolic flux. These features provide hepatic protection from steatotic, pro‐inflammatory and fibrogenic insults.
Cristina López‐Vicario+12 more
wiley +1 more source
Glutaric acidemia type 1 [PDF]
AbstractGlutaric acidemias comprise different disorders resulting in an increased urinary excretion of glutaric acid. Glutaric acidemia type 1 (GA‐1) is an autosomal recessive disorder of lysine, hydroxylysine, and tryptophan metabolism caused by deficiency of glutaryl‐CoA dehydrogenase.
Nicola Longo+2 more
openaire +3 more sources
GLUTARIC ACIDURIA ‘TYPE II’ [PDF]
A new fetal metabolic disorder is described, mainly characterised by severe acidosis and hypoglycaemia, a' sweaty-feet' like odour, and massive glutaric aciduria and acidaemia. In addition, urinary excretion of isobutyric and isovaleric acid was increased, as well as that of some dicarboxylic acids.
Sybe K. Wadman+3 more
openaire +3 more sources
Significance of bound glutarate in the diagnosis of glutaric aciduria type I
Glutaric aciduria type I (GA-I) (McKusick 231670) is an autosomal recessive disorder caused by glutaryl-CoA dehydro genase (GD) deficiency. The diagnosis of GA-I is determined by organic acid analysis of urine and is confirmed by measuring the enzyme activity in cultured skin fibroblasts or leukocytes.
Jaime Campistol+5 more
openaire +4 more sources
Mammalian Metabolism of Glutaric Acid
Abstract Rat liver mitochondria metabolize glutarate at a very slow rate as compared with glutaryl coenzyme A. The stimulatory effect of citric acid cycle intermediates, NAD, and coenzyme A on glutarate metabolism was interpreted as a manifestation of their involvement in the activation of glutarate by a thiol transferase with succinyl-CoA as the ...
Carl E. Polan+2 more
openaire +3 more sources
Deliquescence and crystallization of ammonium sulfate‐glutaric acid and sodium chloride‐glutaric acid particles [PDF]
In the following, we report the deliquescence relative humidities (DRH) and crystallization relative humidities (CRH) of mixed inorganic‐organic particles, specifically ammonium sulfate‐glutaric acid and sodium chloride‐glutaric acid particles. Knowledge of the DRH and CRH of mixed inorganic‐organic particles is crucial for predicting the role of ...
Parsons, Matthew T.+4 more
openaire +3 more sources
Characterization of the Cubamyces Menziesii Terpenome
The genome of Cubamyces menziesii reveals 18 putative sesquiterpene cyclase genes. These genes are cloned and expressed in Escherichia coli, yielding 10 active enzymes. Using farnesyl diphosphate as substrate, the enzymes are analyzed, and the products characterized after bioconversion, uncovering diverse sesquiterpene structures. This study highlights
Létitia Leydet+10 more
wiley +1 more source