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Published in 2020 at "Journal of pharmaceutical and biomedical analysis"
DOI: 10.1016/j.jpba.2020.113253
Abstract: A highly sensitive method for determining urine homogentisic acid (HGA) is required to provide adequate diagnosis and therapy for alkaptonuria in early stages. In this study, we developed a highly sensitive high-performance liquid chromatography with…
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Keywords:
hga;
hplc;
homogentisic acid;
hplc ecd ... See more keywords
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Published in 2025 at "Scientific Reports"
DOI: 10.1038/s41598-025-90953-w
Abstract: A novel deep eutectic solvent (ChCl/HGA-DES) was prepared by a mixture of two moles of choline chloride (ChCl) and one mole of 2,3-dihydroxybenzoic acid (hypogallic acid, HGA). The eutectic point phase diagram showed that the…
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Keywords:
chcl hga;
benzo thiazolo;
hga;
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Published in 2021 at "Journal of Veterinary Internal Medicine"
DOI: 10.1111/jvim.16077
Abstract: Abstract Background Hypoglycin A (HGA) intoxication after ingestion of Acer spp. tree material has never been confirmed in domesticated ruminants despite their similar grazing habitats. Objectives To investigate whether sheep have low HGA bioavailability caused…
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Keywords:
hga;
hypoglycin absorption;
nursing lambs;
disease ... See more keywords
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Published in 2024 at "PLOS Neglected Tropical Diseases"
DOI: 10.1371/journal.pntd.0012313
Abstract: Human granulocytotropic anaplasmosis (HGA) is a zoonotic tick-borne bacterial infection caused by Anaplasma phagocytophilum. While most cases are reported from North America, HGA has been recognized as an emerging disease in several regions of the…
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Keywords:
granulocytotropic anaplasmosis;
human granulocytotropic;
literature;
hga ... See more keywords
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Published in 2020 at "PLoS ONE"
DOI: 10.1371/journal.pone.0232263
Abstract: Gentisic acid (GA), a metabolite of acetylsalicylic acid (ASA), and homogentisic acid (HGA), which is excreted at high levels in alkaptonuria, are divalent phenolic acids with very similar structures. Urine containing HGA is dark brown…
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Keywords:
oxidation reaction;
hga;
oxidation;
acid ... See more keywords
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1
Published in 2022 at "Metabolites"
DOI: 10.3390/metabo12100920
Abstract: Changes in the phenylalanine (PHE)/tyrosine (TYR) pathway metabolites before and during homogentisic acid (HGA)-lowering by nitisinone in the Suitability of Nitisinone in Alkaptonuria (AKU) 2 (SONIA 2) study enabled the magnitude of the flux in…
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Keywords:
tyrosine;
nitisinone treatment;
nitisinone;
ochronotic pathway ... See more keywords
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Published in 2022 at "Metabolites"
DOI: 10.3390/metabo12100990
Abstract: Alkaptonuria (AKU) is a rare autosomal recessive disorder caused by mutations within a gene coding for homogentisate 1,2-dioxygenase (HGD). To date, 251 different variants of this gene have been reported. The metabolic disorder in AKU…
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Keywords:
siblings alkaptonuria;
analysis phenotype;
phenotype differences;
hga ... See more keywords