Results 141 to 150 of about 2,410 (172)

Exploring genes associated with metabolic dysfunction as therapeutic targets for head and neck cancers: a novel strategy. [PDF]

Int J Surg
Yin SY, Liu YC, Yang YP, Liang BY, Fu ZY, Fan M, Zhang YC, Xie ZH, Han K, Wang JP, Zhang L, Zhang L, Tong BS, Han YX, Zhang CJ.   +14 more
europepmc   +1 more source

SLC Transporter-Mediated Functional Imaging in Cancer Diagnosis. [PDF]

Biomolecules
Zhang L, He J.
europepmc   +1 more source

Dietary supplementation of lysolecithin improves growth performance of piglets fed a low-nutrient density diet by modulating nutrient utilization and metabolism. [PDF]

Anim Nutr
Song H, Zhang Z, Yao R, Zhou Q, Liu Y, Jin J, Jin J, Luo Z, Tang J, Feng B, Xu S, Lin Y, Hua L, Zhuo Y, Wu, Che L.   +15 more
europepmc   +1 more source

Carbohydrate malabsorption mimicking immune dysregulation: A histological challenge. [PDF]

JPGN Rep
Eroglu S, Nandolia S, Zhang Y, Voltaggio L, Guerrerio AL.   +4 more
europepmc   +1 more source

Differential Regulation of Intestinal Glucose Transporters SGLT1 and GLUT2 by Lactobacillaceae-Derived Heat-Killed Probiotics and Cell-Free Probiotic Supernatants. [PDF]

Nutrients
Kozmos M, Hribernik T, Kozmos M, Langerholc T, Gorenjak M.   +4 more
europepmc   +1 more source

High-Fat Diet-Induced Obesity Enhances Small Intestinal Glucose and NaCl Absorption Through Selective Transporter Reprogramming. [PDF]

Int J Mol Sci
Palaniappan B, Nepal N, Crutchley J, Arthur S.   +3 more
europepmc   +1 more source

Glucose and Inositol Transporters, SLC5A1 and SLC5A3, in Glioblastoma Cell Migration [PDF]

Cancers, 2022
(1) Background: The recurrence of glioblastoma multiforme (GBM) is mainly due to invasion of the surrounding brain tissue, where organic solutes, including glucose and inositol, are abundant. Invasive cell migration has been linked to the aberrant expression of transmembrane solute-linked carriers (SLC).
Markus Sauer, Philipp Kreisz, Patrick Eiring   +2 more
exaly   +4 more sources

SLC5A1 Variants in Turkish Patients With Congenital Glucose-Galactose Malabsorption

Genes, 2023
Congenital glucose-galactose malabsorption is a rare autosomal recessive disorder caused by mutations in SLC5A1 encoding the apical sodium/glucose cotransporter SGLT1. We present clinical and molecular data from eleven affected individuals with congenital glucose-galactose malabsorption from four unrelated, consanguineous Turkish families.
Andreas Janecke, Naz Güleray Lafcı
exaly   +5 more sources

Long-Term Dietary Changes in Subjects With Glucose Galactose Malabsorption Secondary to Biallelic Mutations of SLC5A1 [PDF]

Digestive Diseases and Sciences, 2021
Glucose galactose malabsorption (GGM) is a congenital diarrheal disorder of intestinal Na+/glucose cotransport (SGLT1/SLC5A1). The required glucose and galactose-restricted diet has been well described in infancy, but long-term nutrition follow-up is limited.To perform a comprehensive nutritional assessment on a cohort of patients with GGM to gain ...
Shweta S. Namjoshi, Martín G Martín, Alvin P Chan   +2 more
exaly   +7 more sources