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Thiamine, gastrointestinal beriberi and acetylcholine signaling [PDF]
Research has highlighted numerous detrimental consequences of thiamine deficiency on digestive function. These range from impaired gastric and intestinal motility to aberrant changes in pancreatic exocrine function, gastric acidity and disturbances in ...
Elliot Overton+4 more
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Substrate transport and drug interaction of human thiamine transporters SLC19A2/A3 [PDF]
Thiamine and pyridoxine are essential B vitamins that serve as enzymatic cofactors in energy metabolism, protein and nucleic acid biosynthesis, and neurotransmitter production.
Peipei Li+13 more
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Thiamin, sometimes called vitamin B1, is essential in carbohydrate metabolism and neural function. It is widely distributed in foods, although cereal grains contribute the greatest levels to most human diets. It is water soluble and is absorbed through both active transport and passive diffusion.
Jennifer C, Kerns, Jean L, Gutierrez
openaire +4 more sources
Thiamine helps transketolase in removing toxic metabolites, counteracting high glucose-induced damage in microvascular cells, and progression of diabetic retinopathy/nephropathy in diabetic animals.
Aurora Mazzeo+6 more
doaj +1 more source
Early rearing of steelhead (Oncorhynchus mykiss) in Oregon hatcheries is often problematic; fry can become emaciated and die during the period between hatch and first feed. Thiamine (vitamin B1) deficiency has caused early mortality in salmonids; however,
Aimee N. Reed+3 more
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Thiamine diphosphate in whole blood, thiamine and thiamine monophosphate in breast-milk in a refugee population. [PDF]
The provision of high doses of thiamine may prevent thiamine deficiency in the post-partum period of displaced persons.The study aimed to evaluate a supplementation regimen of thiamine mononitrate (100 mg daily) at the antenatal clinics in Maela refugee ...
Wolfgang Stuetz+5 more
doaj +1 more source
High-dose thiamine prevents brain lesions and prolongs survival of Slc19a3-deficient mice. [PDF]
SLC19A3 deficiency, also called thiamine metabolism dysfunction syndrome-2 (THMD2; OMIM 607483), is an autosomal recessive neurodegenerative disorder caused by mutations in SLC19A3, the gene encoding thiamine transporter 2.
Kaoru Suzuki+5 more
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Thiamine (vitamin B1) is an essential micronutrient in the human diet, found both naturally and as a fortification ingredient in many foods and supplements.
Adrienne L. Voelker+2 more
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Application of Fe3O4/thiamine Magnetic Particles in the Removal of Methylene Blue
Fe3O4/thiamine particles were prepared in this work via precipitation method. The synthesis method is based on the principle of precipitation of Fe3O4 particles in the presence of thiamine coating agent.
Lan Tran-Nguyen+8 more
doaj +1 more source
The Thiamine Transporter 2 (THTR2) encoded by SLC19A3 plays an ill-defined role in the maintenance of tissue thiamine, thiamine monophosphate, and thiamine diphosphate (TDP) levels. To evaluate the impact of THTR2 on tissue thiamine status and metabolism,
Anita Wen+6 more
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