Results 101 to 110 of about 326,261 (230)
Evolutionary GEM: Evolution of Lactase Persistence
Though humans are known to lose lactase ability post-weaning, some people maintain lactase production into adulthood, a condition known as lactase persistence. Global distribution patterns of lactase persistency are inconsistent; the condition is much more prevalent in some populations than others.
Patricia M. Gray, Xinghan Du
openaire +3 more sources
Background/Aims: Polymorphisms in the enhancer of the lactase gene (LCT) are strongly associated with lactase persistence, but not always predictive of the phenotype.
Luana Caroline Oliveira +3 more
doaj +1 more source
Late Pleistocene human genome suggests a local origin for the first farmers of central Anatolia [PDF]
Anatolia was home to some of the earliest farming communities. It has been long debated whether a migration of farming groups introduced agriculture to central Anatolia.
Baird, Douglas +9 more
core +1 more source
Targeting the potential sources and risk factors for antibiotic resistance transmittance and development of antibiotic resistant‐free probiotics. ABSTRACT Antibiotic resistance (AR) in lactic acid bacteria (LAB) has become an emerging concern in the probiotic and food industries. LAB, a key component of the human microbiota and widely used in probiotic
Salma Sherif Refaat +4 more
wiley +1 more source
Background Domestication and introduction of dairy animals facilitated the permanent human occupation of the Tibetan Plateau. Yet the history of dairy pastoralism in the Tibetan Plateau remains poorly understood.
Min-Sheng Peng +25 more
doaj +1 more source
Population genomics on the origin of lactase persistence in Europe and South Asia
The C to T mutation at rs4988235 located upstream of the lactase (LCT) gene is the primary determinant for lactase persistence (LP) that is prevalent among Europeans and South Asians. Here, we review evolutionary studies of this mutation based on ancient
Y. Satta, N. Takahata
semanticscholar +1 more source
Abstract We present a case of a young female patient with persistent and severe fat‐soluble vitamin deficiency since infancy. Despite extensive investigations during childhood, the underlying cause remained elusive. The patient was generally asymptomatic while receiving continuous vitamin subsidy.
Christine Rungoe +4 more
wiley +1 more source
Excellent agreement between genetic and hydrogen breath tests for lactase deficiency and the role of extended symptom assessment [PDF]
Clinical manifestations of lactase (LCT) deficiency include intestinal and extra-intestinal symptoms. Lactose hydrogen breath test (H2-BT) is considered the gold standard to evaluate LCT deficiency (LD).
Behlis, Z. +8 more
core
Структурно-функциональное состояние костной ткани у лиц молодого возраста с остеоартрозом в зависимости от уровня плазматического апелина и полиморфизма гена лактазы [PDF]
В исследовании проведено детальное изучение влияния уровня содержания плазматического апелина-13 на развитие нарушений структурно-функционального состояния костной ткани у пациентов с остеоартрозом в зависимости от разных вариантов полиморфизма гена ...
Терешкин, К. И. +1 more
core +2 more sources
ABSTRACT Peroxisome proliferator‐activated receptors (PPARs), functioning as nuclear receptors, regulate the expression of genes associated with inflammation, lipid metabolism, and glucose metabolism. The primary isotypes of PPARs are PPARα, PPARβ, and PPARγ. PPARγ is mostly expressed in adipose tissue and the colon.
Aya A. Touny +9 more
wiley +1 more source

