Results 91 to 100 of about 10,535 (179)

Fructose-induced synaptic and neuronal adaptations at neuropeptide Y/agouti-related peptide neurons

open access: yesMolecular Metabolism
Fructose is a naturally-occurring sugar, consumed in excess as sweeteners, and is linked to the development of obesity. Fructose is consumed with glucose (dextrose) in added sugars, but while dextrose produces satiety, excessive fructose intake promotes ...
Mikayla A. Payant   +7 more
doaj   +1 more source

Transferrin hypoglycosylation in hereditary fructose intolerance: using the clues and avoiding the pitfalls. [PDF]

open access: yes, 2007
Contains fulltext : 52444.pdf (Publisher’s version ) (Open Access)Hereditary fructose intolerance (HFI) is caused by a deficiency of aldolase B due to mutations of the ALDOB gene.
Morava, E.   +9 more
core  

Fructose malabsorption and fructan malabsorption are associated in patients with irritable bowel syndrome

open access: yesBMC Gastroenterology
Background Food malabsorption and intolerance is implicated in gastrointestinal symptoms among patients with irritable bowel syndrome (IBS). Key triggers include fructose and fructan.
Twan Sia   +18 more
doaj   +1 more source

Inhibition of phosphomannose isomerase by fructose 1-phosphate: an explanation for defective N-glycosylation in hereditary fructose intolerance. [PDF]

open access: yes, 1996
Isoelectrofocusing of serum sialotransferrins from patients with untreated hereditary fructose intolerance (HFI) shows a cathodal shift similar to that in carbohydrate-deficient glycoprotein (CDG) syndrome type I and in untreated galactosemia.
Pirard, M   +9 more
core   +1 more source

Carbohydrate intolerance [PDF]

open access: yes, 2011
Carbohydrates in the diet 128Carbohydrate digestion 129Hypolactasia/lactose intolerance 130Congenital sucrase–isomaltase deficiency 130Glucose–galactose malabsorption 131Confirmation of diagnosis of carbohydrate malabsorption 131Carbohydrates make up at ...
R. Mark Beattie   +2 more
core   +1 more source

Simple method for detection of mutations causing hereditary fructose intolerance [PDF]

open access: yes, 2002
Aldolase B is critical for sugar metabolism, and a catalytic deficiency due to mutations in its gene may result in hereditary fructose intolerance (HFI) syndrome, with hypoglycaemia and severe abdominal symptoms.
Hannoun, Charles,   +2 more
core  

Sustainable Utilization of Coffee Pulp, a By-Product of Coffee Production: Effects on Metabolic Syndrome in Fructose-Fed Rats

open access: yesAntioxidants
Metabolic syndrome (MetS) is a cluster of metabolic abnormalities that include insulin resistance, impaired glucose tolerance, dyslipidemia, hypertension, and abdominal obesity. Coffee production generates large quantities of waste products, which pose a
Nelson Andrade   +17 more
doaj   +1 more source

Effect of administration of the fructose on the glycogenolytic action of glucagon. An investigation of the pathogeny of hereditary fructose intolerance. [PDF]

open access: yes, 1973
1. The mechanism by which the administration of fructose to patients with hereditary fructose intolerance makes them unresponsive to the hyperglycaemic action of glucagon was studied.
Hue, Louis   +2 more
core  

Correction: Vitamin C and folate status in hereditary fructose intolerance. [PDF]

open access: yesEur J Clin Nutr, 2023
Cano A   +21 more
europepmc   +1 more source

Combined PMM2-CDG and hereditary fructose intolerance in a patient with mild clinical presentation. [PDF]

open access: yesMol Genet Metab, 2023
Hong X   +6 more
europepmc   +1 more source

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