Results 61 to 70 of about 113,935,104 (175)
Metachromatic Leukodystrophy: Diagnosis, Modeling, and Treatment Approaches
Metachromatic leukodystrophy is a lysosomal storage disease, which is characterized by damage of the myelin sheath that covers most of nerve fibers of the central and peripheral nervous systems.
Alisa A. Shaimardanova +8 more
doaj +1 more source
Leukodystrophy in Tanzania: A Case Study Highlighting Diagnostic Dilemmas and Clinical Implications
ABSTRACT Leukodystrophies are rare inherited neurodegenerative disorders characterized by progressive white matter dysfunction and neurological decline. In low‐resource settings, limited access to advanced neuroimaging, biochemical investigations, and genetic testing often delays diagnosis and complicates differentiation from more common infectious ...
William Nkenguye +2 more
wiley +1 more source
Arylsulfatase G, a novel lysosomal sulfatase
Frese M-A, Schulz S, Dierks T. Arylsulfatase G, a novel lysosomal sulfatase. JOURNAL OF BIOLOGICAL CHEMISTRY. 2008;283(17):11388-11395.The sulfatases constitute a conserved family of enzymes that specifically hydrolyze sulfate esters in a wide variety of
Dierks, Thomas +2 more
core +1 more source
ABSTRACT Gold has been used for centuries in both ornamental and medicinal contexts. More recently, gold compounds, containing ions or nanoparticles, have attracted attention for their anti‐inflammatory, anticancer, and diagnostic applications. Therefore, concerns about systemic toxicity and biodistribution have prompted investigations into the ...
Samira Maghraoui +2 more
wiley +1 more source
Proper myelin formation is crucial for normal neural circuit function, while myelin deficiency can lead to neural circuit dysfunction and cognitive decline, notably in Alzheimer's disease and other central nervous system demyelinating disorders. This review summarizes central myelin's structure and function, demyelination biomarkers and pathological ...
Lihong Huang +5 more
wiley +1 more source
Detection of a rare Wilson disease mutation associated with arylsulfatase A pseudodeficiency
We have studied a patient with Wilson disease (WD), belonging to a family segregating late-onset, dominant cerebellar ataxia, Analysis of the WD gene showed that the patient is a compound heterozygote, carrying the 14His1069Gln mutation from the father ...
Sangiorgi, S. +8 more
core +1 more source
The brain-specific arylsulfatase Bm (aryl-sulfate sulfohydrolase, EC 3.1.6.1) was demonstrable in human and monkey brain. Arylsulfatases A, B and Bm were separated employing DEAE-cellulose chromatography. There was a distinct difference in the proportion
Lakshmi, S., Balasubramanian, A. S.
core +1 more source
Chondroitin sulfate degradation and eicosanoid metabolism pathways are impaired in focal segmental glomerulosclerosis: Experimental confirmation of an in silico prediction [PDF]
Introduction: Focal segmental glomerulosclerosis (FSGS), the most common primary glomerular disease, is a diverse clinical entity that occurs after podocyte injury.
Shiva Kalantari +5 more
doaj +1 more source
ABSTRACT Background Infertility is a pressing global health concern, affecting one in six couples worldwide. The failure rate for assisted reproductive technologies (ART) cycles remains at approximately 78%, with limited improvements often attributed to a lack of technological innovation.
Mehran Dabiri +3 more
wiley +1 more source
Abstract Soil health underpins crop productivity and sustainability, but current soil health assessment frameworks struggle to balance global standardization with regional dynamic ecological realism. Indicators vary widely across soils and climates, often leading to one‐size‐fits‐all thresholds that penalize producers in inherently low‐capacity soils ...
Saurav Das +5 more
wiley +1 more source

