Results 41 to 50 of about 15,724 (296)
The Lysosomal Protein Arylsulfatase B Is a Key Enzyme Involved in Skeletal Turnover
Journal of Bone and Mineral Research, 2018 Skeletal pathologies are frequently observed in lysosomal storage disorders, yet the relevance of specific lysosomal enzymes in bone remodeling cell types is poorly defined.
S. Pohl +27 more
semanticscholar +1 more source
Microbiological characterization of land set-aside before and after Roundup desiccation
Plant, Soil and Environment, 2011 Luvic chernozem (set-aside from 1996) was evaluated. The first period, before Roundup desiccation (2002-2003), was characterized by black, spontaneous and controlled fallows (mowed with the removal of plant biomass or mulched); the following period (2003-
M. Růžková +4 more
doaj +1 more source
Characterization of iodothyronine sulfatase activities in human and rat liver and placenta [PDF]
, 2002 In conditions associated with high serum iodothyronine sulfate concentrations, e.g. during fetal development, desulfation of these conjugates may be important in the regulation of thyroid hormone homeostasis. However, little is known
Coughtrie, M.W. +6 more
core +2 more sources
Mucopolysaccharidosis type VI phenotypes-genotypes and antibody response to galsulfase [PDF]
, 2013 Background: Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome; MPS VI) is an autosomal recessive lysosomal storage disorder in which deficiency of N-acetylgalactosamine 4-sulfatase (arylsulfatase B; ARSB) leads to the storage of glycosaminoglycans ...
Brands, M.M.M.G. (Marion) +11 more
core +4 more sources
Glycosylation and phosphorylation of arylsulfatase A.
Journal of Biological Chemistry, 1994 The glycosylation and phosphorylation of the lysosomal enzyme arylsulfatase A was analyzed by a combination of metabolic labeling, tryptic fragmentation, mass spectrometry, and radiosequencing. The results demonstrate that all three potential N-glycosylation sites at Asn residues 158, 184, and 350 are utilized in arylsufatase A and carry high mannose ...
Volkmar Gieselmann +6 more
openaire +3 more sources
Human Mutation, 2017 Metachromatic leukodystrophy (MLD) is an autosomal‐recessive lysosomal storage disease caused by mutations in the ARSA gene leading to arylsulfatase A (ARSA) deficiency and causing sulfatide accumulation.
J. Böhringer +11 more
semanticscholar +1 more source
Radioimmunoassay for arylsulfatase A in urine.
Clinical Chemistry, 1985 Abstract Purified arylsulfatase A (EC 3.1.6.1) from human urine was radioiodinated under conditions that caused no significant loss of antigenic activity. We used this labeled arylsulfatase A (specific radioactivity 4-7.5 Ci/g) together with nonlabeled enzyme and rabbit antiserum produced against homogeneous enzyme to develop a ...
R L Van Etten +4 more
openaire +3 more sources
Acta Scientiarum: Biological Sciences, 2023 Soil microbiota has a key role in the dynamics of natural and agro-ecosystems and is sensitive to changes in these environments. This study evaluated changes in the microbiological properties of soils under an organic production system of banana ‘BRS ...
Luana Silva Cerqueira +3 more
doaj +1 more source
Annals of Clinical and Translational Neurology, 2023 Objective Metachromatic leukodystrophy is a lysosomal storage disease caused by deficient arylsulfatase A. It is characterized by progressive demyelination and thus mainly affects the white matter.
Murtadha Al‐Saady +13 more
doaj +1 more source
Биопрепараты: Профилактика, диагностика, лечение, 2022 Maroteaux—Lamy syndrome (mucopolysaccharidosis type VI) is an orphan genetic disease caused by mutations in the arylsulfatase B gene (ARSB), which encodes the lysosomal enzyme arylsulfatase B (ASB).
S. S. Timonova +7 more
doaj +1 more source