The Qinghai–Tibet Plateau (QTP) wild boar is an excellent model for investigating high-altitude adaptation. In this study, we analyzed genome-wide data from 93 wild boars compiled from various studies worldwide, including the QTP, southern and northern ...
Shiyong Fang +9 more
doaj +2 more sources
Polymorphism analysis of AMY1, AMY2, SLC5A1, SLC2A2 and SLC2A5 genes in Italian horse breeds
The dietary demand of modern competition horse relies on high-cereal feeding daily interspersed by limited forage and it is frequently characterized by marked changes in carbohydrate fractions, above all starch, compared to natural grazing conditions.
B. Coizet +5 more
openaire +3 more sources
A new link between insulinoma and congenital glucose-galactose malabsorption
Congenital glucose-galactose malabsorption (CGGM) is a rare autosomal recessive disorder caused by a biallelic mutation of solute carrier family 5 member 1 (SLC5A1), encoding the sodium-dependent glucose transport-1 (SGLT-1) protein.
Antonio Prinzi +7 more
doaj +2 more sources
Differential changes in anatomical, molecular and functional determinants of intestinal glucose absorption during murine pregnancy [PDF]
Pregnancy demands increased food intake and nutrient delivery to support the growing conceptus. The timing and regional specificity of adaptations in small intestinal (SI) anatomy and transport, and their functional consequences, remain unclear.
T. Sebastian Overduin +5 more
doaj +2 more sources
10 Pre-clinical studies of sotagliflozin in hypertrophic cardiomyopathy
OBJECTIVES/GOALS: Study the regulatory role of sodium glucose co-transporter 1 (SGLT1) in cardiomyocytes and the therapeutic potential of sotagliflozin in hypertrophic cardiomyopathy (HCM) by (a) quantifying SGLT1 expression in HCM and (b) examining the ...
Rebecca Taichman +3 more
doaj +2 more sources
The Na+/glucose cotransporters: from genes to therapy
Glucose enters eukaryotic cells via two types of membrane-associated carrier proteins, the Na+/glucose cotransporters (SGLT) and the facilitative glucose transporters (GLUT). The SGLT family consists of six members.
R. Sabino-Silva +5 more
doaj +1 more source
A Rare Case of Congenital Glucose Galactose Malabsorption Due to SLC5A1 Mutation. [PDF]
Protracted neonatal diarrhea is severe and potentially life-threatening if not promptly diagnosed and treated. Causes include congenital defects in sodium, chloride, glucose/galactose, bile acid transport, enterokinase deficiency, and villous atrophy.
Muralidharan H +5 more
europepmc +3 more sources
Congenital Glucose-Galactose Malabsorption: A Case With a Novel SLC5A1 Mutation in a Saudi Infant [PDF]
While only a few hundred cases have been reported in pediatrics, congenital glucose-galactose malabsorption (GGM) is an extremely rare autosomal-recessive metabolic disorder that is characterized by intractable diarrhea and severe dehydration, which can be life-threatening if not treated appropriately.
Alamoudi, Loujen O +4 more
openaire +2 more sources
Identification of Candidate Causal Polymorphisms in <i>GGT1</i> and <i>SLC5A1</i> Associated with Fat Area Ratio on BTA17 in Japanese Black Cattle. [PDF]
Background/Objectives: Intramuscular fat deposition is a key determinant of beef quality in Japanese Black cattle, and the fat area ratio of the rib eye (FAR) is highly correlated with Beef Marbling Standard scores. Methods: To identify genetic variants underlying variation in the FAR, we conducted a genome-wide association study (GWAS) followed by ...
Sasazaki S +7 more
europepmc +2 more sources
Co-segregation analysis and functional trial in vivo of candidate genes for monogenic diabetes
Introduction The aim of this study was to perform familial co-segregation analysis and functional trial in vivo during mixed meal tolerance test (MMTT) of novel variants in diabetes candidate genes.Research design and methods It is a continuation of the ...
Jean-Louis Blouin +4 more
doaj +1 more source

