Results 161 to 170 of about 2,410 (172)
Some of the next articles are maybe not open access.
2015
Diabetes mellitus affects ~400 million people worldwide. Novel antidiabetic drugs have been developed aiming to lower blood glucose by inhibiting the activity of sodium-D-glucose cotransporter 1 (SGLT1 in humans/Sglt1 in rodents) in the intestine and kidney.
Karaica, Dean +3 more
openaire +3 more sources
Diabetes mellitus affects ~400 million people worldwide. Novel antidiabetic drugs have been developed aiming to lower blood glucose by inhibiting the activity of sodium-D-glucose cotransporter 1 (SGLT1 in humans/Sglt1 in rodents) in the intestine and kidney.
Karaica, Dean +3 more
openaire +3 more sources
2016
Cellular uptake and metabolism of glucose (G) serves as an important energy source. In mammals, SGLT1 (humans)/Sglt1 (rodents) mediates an almost complete absorption of G in small intestine (SI) and a limited (3-15%) reabsorption of G in kidneys (K). Novel antidiabetic drugs were recently developed aiming to lower blood G by inhibiting SGLT1 in SI and ...
Vrhovac Madunić, Ivana +4 more
openaire +2 more sources
Cellular uptake and metabolism of glucose (G) serves as an important energy source. In mammals, SGLT1 (humans)/Sglt1 (rodents) mediates an almost complete absorption of G in small intestine (SI) and a limited (3-15%) reabsorption of G in kidneys (K). Novel antidiabetic drugs were recently developed aiming to lower blood G by inhibiting SGLT1 in SI and ...
Vrhovac Madunić, Ivana +4 more
openaire +2 more sources
Ekspresija prijenosnika natrija i glukoze Sglt1 (Slc5a1) u organima miševa
2015In mice, sodium-glucose cotransporter (mSglt1/Slc5a1) absorbs and reabsorbs the glucose in the brush-border membrane of small intestinal enterocytes and renal proximal tubules, respectively. Due to unknown localization of mSglt1 in other organs/tissues, mSglt1 expression was determined comparing wild type (Sglt1+/+) and Sglt1 knockout mice (Sglt1 ...
openaire +2 more sources
A Case of Congenital Glucose Galactose Malabsorption With a New Mutation in the SLC5A1 Gene
Journal of Pediatric Genetics, 2022Hasan Akduman +2 more
exaly
Novel Mutation in the SLC5A1 Gene Causing... : JPGN Reports
JPGN Reports, 2023Amanda C Fifi, Liz Febo-Rodriguez
exaly
Congenital Glucose–Galactose Malabsorption: A Novel Deletion Within the SLC5A1 Gene
European Journal of Pediatrics, 2013Stephanie Van Biervliet, Bart L Loeys
exaly
Drosophila SLC5A11 Mediates Hunger by Regulating K+ Channel Activity
Current Biology, 2016Bernardo Rudy, Seonil Kim, Monica Dus
exaly