Transcriptional regulation of the lactase-phlorizin hydrolase gene by polymorphisms associated with adult-type hypolactasia - Wikidata - wikimedia - TriplyDB

Transcriptional regulation of the lactase-phlorizin hydrolase gene by polymorphisms associated with adult-type hypolactasia

Transcriptional regulation of the lactase-phlorizin hydrolase gene by polymorphisms associated with adult-type hypolactasia

http://www.wikidata.org/entity/Q24669722

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A worldwide correlation of lactase persistence phenotype and genotypes Genome-wide detection and characterization of positive selection in human populations Lactase persistence-related genetic variant: population substructure and health outcomes Convergent adaptation of human lactase persistence in Africa and Europe Evidence of still-ongoing convergence evolution of the lactase persistence T-13910 alleles in humans The Diverse Forms of Lactose Intolerance and the Putative Linkage to Several Cancers Infantile onset spinocerebellar ataxia is caused by recessive mutations in mitochondrial proteins Twinkle and Twinky Prevalence and trends in adult-type hypolactasia in different age cohorts in Central Sweden diagnosed by genotyping for the adult-type hypolactasia-linked LCT -13910C > T mutation Predicting Carriers of Ongoing Selective Sweeps without Knowledge of the Favored Allele Changing genes; losing lactase Association of lactase persistence genotype with milk consumption, obesity and blood pressure: a Mendelian randomization study in the 1982 Pelotas (Brazil) Birth Cohort, with a systematic review and meta-analysis Impact of lactose containing foods and the genetics of lactase on diseases: an analytical review of population data.Effects of the lactase 13910 C/T and calcium-sensor receptor A986S G/T gene polymorphisms on the incidence and recurrence of colorectal cancer in Hungarian population.Screening of variants for lactase persistence/non-persistence in populations from South Africa and Ghana.Excellent agreement between genetic and hydrogen breath tests for lactase deficiency and the role of extended symptom assessment.Lactase non-persistence and milk consumption in Estonia Molecularly defined adult-type hypolactasia in school-aged children with a previous history of cow's milk allergy.Differential impact of lactose/lactase phenotype on colonic microflora Correlation of intestinal disaccharidase activities with the C/T-13910 variant and age Molecularly defined adult-type hypolactasia among working age people with reference to milk consumption and gastrointestinal symptoms.The T allele of a single-nucleotide polymorphism 13.9 kb upstream of the lactase gene (LCT) (C-13.9kbT) does not predict or cause the lactase-persistence phenotype in Africans Mutations in the translated region of the lactase gene (LCT) underlie congenital lactase deficiency Several different lactase persistence associated alleles and high diversity of the lactase gene in the admixed Brazilian population.Distinguishing between selective sweeps from standing variation and from a de novo mutation.The T/G 13915 variant upstream of the lactase gene (LCT) is the founder allele of lactase persistence in an urban Saudi population.Correlation between lactose absorption and the C/T-13910 and G/A-22018 mutations of the lactase-phlorizin hydrolase (LCT) gene in adult-type hypolactasia.Molecular genetics of human lactase deficiencies.Functional significance of single nucleotide polymorphisms in the lactase gene in diverse US patients and evidence for a novel lactase persistence allele at -13909 in those of European ancestry.A comparative study on the metabolism of Epimedium koreanum Nakai-prenylated flavonoids in rats by an intestinal enzyme (lactase phlorizin hydrolase) and intestinal flora.Mild CFTR mutations and genetic predisposition to lactase persistence in cystic fibrosis.The European lactase persistence genotype determines the lactase persistence state and correlates with gastrointestinal symptoms in the Hispanic and Amerindian Chilean population: a case-control and population-based study.A genetic test which can be used to diagnose adult-type hypolactasia in children.The C/C-13910 genotype of adult-type hypolactasia is associated with an increased risk of colorectal cancer in the Finnish population.Molecular genetics of adult-type hypolactasia.Molecular diagnosis of adult-type hypolactasia (lactase non-persistence).Genetic variation in the lactase gene, dairy product intake and risk for prostate cancer in the European prospective investigation into cancer and nutrition.Evaluation of a genetic test for diagnose of primary hypolactasia in northeast of iran (khorasan)Dynamic variation in allele-specific gene expression of Paraoxonase-1 in murine and human tissues.Lack of effect of lactose digestion status on baseline fecal micoflora.The -14010*C variant associated with lactase persistence is located between an Oct-1 and HNF1α binding site and increases lactase promoter activity.

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P2860

Regulation of intestinal lactase in adult hypolactasia

Identification of a variant associated with adult-type hypolactasia

The genetically programmed down-regulation of lactase in children

Characterisation of a human homologue of a yeast cell division cycle gene, MCM6, located adjacent to the 5' end of the lactase gene on chromosome 2q21

Relative levels of SCCA2 and SCCA1 mRNA in primary tumors predicts recurrent disease in squamous cell cancer of the head and neck.

DNA sequences required for regulated expression of beta-globin genes in murine erythroleukemia cells.

The human beta-globin gene contains a downstream developmental specific enhancer

Molecular basis of lactase levels in adult humans.

Rat intestinal crypt-cell replication factor with homology to early S-phase proteins required for cell division.

Control of lactase in human adult-type hypolactasia and in weaning rabbits and rats.

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