Results 181 to 190 of about 5,504 (241)

Malectin Alleviates Endoplasmic Reticulum Stress in Gestational Diabetes Mellitus via Glycoprotein Quality Control Mechanisms

open access: yesAdvanced Science, Volume 13, Issue 46, 17 August 2026.
Malectin alleviates high glucose‐induced ER stress and damage in placental trophoblasts, a function dependent on its six critical carbohydrate‐binding residues. In a GDM mouse model, administration of TAT‐Malectin ameliorated hyperglycemia and placental ER stress and prevented fetal macrosomia.
Jiahui Zhu   +12 more
wiley   +1 more source

Alpha-glucosidases in human urine

Clinica Chimica Acta, 1967
Abstract Two α-glucosidases from human urine have been separated by means of Sephadex G-200 gel filtration and further purified by DEAE-Sephadex chromatography. Both enzymes hydrolyse maltose and glycogen to free glucose. Indirect evidence has been obtained of the possible occurrence of further α-glucosidases in human urine.
C Franzini
exaly   +3 more sources

ALPHA-GLUCOSIDASE INHIBITORS

Endocrinology and Metabolism Clinics of North America, 1997
Alpha-glucosidase inhibitors are antihyperglycemic agents that lower blood glucose by delaying the digestion and absorption of complex carbohydrates. They are competitive inhibitors of the enzymes in the brush border of enterocytes that cleave eligosaccharides to monosaccharides.
openaire   +2 more sources

Fermentation of Saccharose by Alpha-Glucosidase

Nature, 1962
I HAVE isolated two melibiose-fermenting yeasts, Saccharomyces oleaginosus1 and S. hienipiensis2, which, by means of Wickerham's method3, are capable of fermenting maltose, but which neither ferment nor assimilate saccharose. With the Delft method (Kreger-van Rij, N. J. W., private communication), slow fermentation of the saccharose was obtained.
openaire   +2 more sources

alpha-Glucosidases.

Biochemistry. Biokhimiia, 2001
This review highlights the main properties of mammalian, plant, and microbial alpha-glucosidases. Special attention is given to the classification of these enzymes, possible catalytic mechanisms, their tertiary structure, and the structure of major inhibitors.
V V, Krasikov, D V, Karelov, L M, Firsov
openaire   +1 more source

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