Results 141 to 150 of about 5,907 (191)
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Acid Alpha-Glucosidase from Human Heart

Enzyme, 1983
An alpha-glucosidase maximally active at acid pH has been purified from human heart some 2,600-fold and its properties compared to a purified alpha-glucosidase from human liver. Molecular weight was evaluated using three different analytical procedures. The effect of various cations was determined.
J P, Chambers, J C, Williams
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Identity of alpha-glucosidase of human kidney with urine F-1 alpha-glucosidase.

Journal of biochemistry, 1982
alpha-Glucosidase was extracted from a homogenate of human kidney, initially with 0.02 M Tris-HCl buffer, pH 7.6, and subsequently with a mixture of 0.5% cholate and 0.5% Triton X-100 in the same buffer, pH 7.6. The enzyme in each of these two fractions was purified to the electrophoretically pure state by fractional precipitation with ammonium sulfate,
N, Minamiura   +3 more
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Human acid alpha-glucosidase

Drugs of the Future, 2003
Pompe's disease or glycogen storage disease type II is an inherited progressive skeletal muscle disorder caused by deficiency of the lysosomal enzyme α-glucosidase. The most severe form of the disease affects infants and results in feeding difficulties, respiratory and cardiac problems and motor delay.
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[alpha-Glucosidase inhibitor].

Nihon rinsho. Japanese journal of clinical medicine, 1999
Oral anti-diabetic agents with hypoglycemic action via mechanisms distinct from the sulfonylureas have recently been developed. One of these, alpha-glucosidase inhibitor slows the absorption rate of carbohydrate from the small intestine. Effects of voglibose on glycemic control and on the function of pancreatic islets were evaluated using Goto-Kakizaki
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[Alpha-glucosidase inhibitor].

Nihon rinsho. Japanese journal of clinical medicine, 2015
Alpha-glucosidase inhibitors (α-GI) have abdominal signs which are generally regarded as side-reaction. The abdominal signs are caused by generation of intestinal gas which contains hydrogen gas. The hydrogen gas absorbed in the body eliminates oxidant stress and consequently the abdominal signs may have beneficial effects preventing onset and ...
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alpha-Glucosidase deficiency (Pompe's disease).

Enzyme, 1987
alpha-Glucosidase is deficient (less than 30% of control) in Pompe's disease, but the extent of the deficiency does not always correlate with the severity of the clinical symptoms. The defects that lead to a deficiency of alpha-glucosidase include synthesis of catalytically inactive protein, absence of mRNA for the enzyme, decreased synthesis of the ...
Tager, J. M.   +6 more
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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.
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Les inhibiteurs des alpha-glucosidases

Actualités Pharmaceutiques, 2017
Resume L’arsenal therapeutique permettant la prise en charge du diabete evolue regulierement. Cependant, d’anciennes classes sont toujours sur le marche, meme si elles sont parfois caracterisees par une efficacite modeste comme les inhibiteurs des alpha-glucosidases.
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alpha-glucosidase (CHO) (Genzyme).

Current opinion in investigational drugs (London, England : 2000), 2005
Genzyme General is developing recombinant human alpha-glucosidase, produced in mammalian cell culture, as a potential treatment for Pompe disease. By July 2004, enrollment was completed in two clinical trials and an observational study in adults. Genzyme was planning to file for regulatory approval in Europe during 2004, followed by filings in the US ...
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Alpha-glucosidase

1991
Dietmar Schomburg, Margit Salzmann
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