Results 21 to 30 of about 536 (156)
Analytical Validation of a New Enzymatic and Automatable Method for d-Xylose Measurement in Human Urine Samples. [PDF]
Biomed Res Int, 2017 Hypolactasia, or intestinal lactase deficiency, affects more than half of the world population. Currently, xylose quantification in urine after gaxilose oral administration for the noninvasive diagnosis of hypolactasia is performed with the hand‐operated nonautomatable phloroglucinol reaction.
Sánchez-Moreno I +11 more
europepmc +2 more sources
Nutrition Journal, 2009 Background Adult-type hypolactasia, the physiological decline of lactase some time after weaning, was previously associated with the LCT -13910C>T polymorphism worldwide except in Africa.
Silva Joyce MK +5 more
doaj +1 more source
Arquivos de Gastroenterologia, 2012 CONTEXT: Genotyping of single nucleotide polymorphism (SNP C/T-13910) located upstream of the lactase gene is used to determine adult-type hypolactasia/lactase persistence in North-European Caucasian subjects.
Evelyn Mendoza Torres +3 more
doaj +1 more source
The FASEB Journal, Volume 34, Issue 3, Page 3983-3995, March 2020., 2020 Abstract Background and aims: Intestinal adaptation in short bowel syndrome (SBS) includes morphologic processes and functional mechanisms. This study investigated whether digestive enzyme expression in the duodenum and colon is upregulated in SBS patients. Method: Sucrase‐isomaltase (SI), lactase‐phlorizin hydrolase (LPH), and neutral Aminopeptidase N
Jan de Laffolie +13 more
wiley +1 more source
Several different lactase persistence associated alleles and high diversity of the lactase gene in the admixed Brazilian population. [PDF]
PLoS ONE, 2012 Adult-type hypolactasia is a common phenotype caused by the lactase enzyme deficiency. The -13910 C>T polymorphism, located 14 Kb upstream of the lactase gene (LCT) in the MCM6 gene was associated with lactase persistence (LP) in Europeans.
Deise C Friedrich +3 more
doaj +1 more source
A felnőttkori hypolactasia születésikohorsz-vizsgálata [PDF]
Orvosi Hetilap, 2019 Abstract: Introduction and aim: To assess the prevalence of lactase gene promoter C/T13910 phenotypes in patients with lactose intolerance symptoms and to analyze the birth-cohort phenomenon in lactose-intolerant patients. Method: 1266 patients consulted between 2010 and 2017 were enrolled.
openaire +1 more source
PROSPECTS OF SYNTHETIC POLYMERS APPLICATION AS INERT CARRIERS FOR β-GALACTOSIDASE IMMOBILISATION
Наука. Инновации. Технологии, 2022 The actuality of lactose-reduced and delactosed products manufacturing is founded. Methods of β-galactosidase immobilization and it’s peculiarities, concerned with type of carrier, are considered.
Victoria Evgen'evna Suprunchuk +2 more
doaj
Вавиловский журнал генетики и селекции, 2017 Retention of lactase activity in adulthood (lactase persistence) is one of the most important adaptive traits for human populations that consume fresh milk from domestic animals.
I. V. Pilipenko +4 more
doaj +1 more source
Molecular Nutrition &Food Research, Volume 63, Issue 21, November 2019., 2019 Despite numerous examples of interindividual variability in the processing of food by the human gastrointestinal tract, the knowledge on this topic, as illustrated for polymorphisms in mineral absorption, remains fragmented. The GutSelf review sets the base for motivating future research specifically addressing the issue of the interindividual ...
Barbara Walther +14 more
wiley +1 more source
DIGESTIVE DISORDERS IN PREMATURELY BORN CHILDREN
Вопросы современной педиатрии, 2012 The article contains data on functional digestive disorders in newborns, mainly on the problem of lactase (disaccharidase) insufficiency. The information on the prevalence of this condition, modern classification of hypolactasia, diagnostic techniques ...
I. A. Belyaeva +2 more
doaj +1 more source