Results 81 to 90 of about 686,065 (200)

Behaviour of some lysosomal enzymes in the plasma of insulin dependent diabetic patients during artificial pancreas treatment

open access: yes, 1987
The plasma levels of three lysosomal enzymes, β-D-N-acetylglucosaminidase, β-D-glucuronidase, and α-L-fucosidase, were fluorimetrically determined in seven insulin-dependent diabetic patients one day before, one day after, and during a two-day treatment ...
BURLINA A   +5 more
core   +1 more source

Pancreatic secretion of lysosomal enzymes stimulated by intraduodenal instillation of a liquid meal in rabbits

open access: yes, 1992
1. Studies have been performed to determine the effect of intraduodenal food on pancreatic secretion of lysosomal enzymes. 2. Intraduodenal instillation of a liquid meal (3 g/kg body weight; 15.3% protein, 19.7% fat, 59.7% carbohydrate) caused ...
Steer, M. L   +3 more
core   +1 more source

KCTD7 mutations impair the trafficking of lysosomal enzymes through CLN5 accumulation to cause neuronal ceroid lipofuscinoses. [PDF]

open access: yesSci Adv, 2022
Wang Y   +10 more
europepmc   +1 more source

Mr 46 000 mannose 6-phosphate specific receptor: its role in targeting of lysosomal enzymes

open access: yes, 1987
Antibodies that block the ligand binding site of the cationdependent mannose 6-phosphate specific receptor (Mr 46 000 MIPR) were used to probe the function of the receptor in transport of lysosomal enzymes.
Stein, Martin   +4 more
core  

Autoantibodies against myeloid lysosomal-enzymes in crescentic glomerulonephritis

open access: yes, 1990
Autoantibodies against myeloid lysosomal enzymes in crescentic glomerulonephritis. To investigate the possible association of crescentic glomerulonephritis (CGN) with autoantibodies to myeloid lysosomal enzymes, we tested sera from 35 consecutive ...
Elema, J. D.   +17 more
core   +1 more source

Glyco-engineering strategies for the development of therapeutic enzymes with improved efficacy for the treatment of lysosomal storage diseases

open access: yes, 2015
Lysosomal storage diseases (LSDs) are a group of inherent diseases characterized by massive accumulation of undigested compounds in lysosomes, which is caused by genetic defects resulting in the deficiency of a lysosomal hydrolase.
Doo-Byoung Oh
core   +1 more source

Diabetes mellitus alters lysosomal enzymes activity in rabbit epididymis

open access: yesCurrent Issues in Pharmacy and Medical Sciences, 2009
Diabetes is a metabolic disease caused by inappropriate secretion and/or function of insulin, which may disturb morphology and function of various internal organs. The aim of the study was to evaluate the activity of selected lysosomal enzymes.
Zbigniew Wójtowicz   +10 more
doaj  

Ancestral lysosomal enzymes with increased activity harbor therapeutic potential for treatment of Hunter syndrome. [PDF]

open access: yesiScience, 2021
Hendrikse NM   +13 more
europepmc   +1 more source

Role of β-glucans in reducing oxidative stress and improving muscle tissue health in European whitefish (Coregonus lavaretus L.)

open access: yesFisheries & Aquatic Life
β-glucans are currently a notable topic in research on enhancing immunity in fishes and their significant role in improving fish health and productivity in aquaculture.
Tkaczenko Halina   +2 more
doaj   +1 more source

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