A New Fluorescent Method to Detect Sulfamidase Activity in Blood, Tissue Extracts and Dried Blood Spots
Author:
Affiliation:
1. Icahn School of Medicine at Mount Sinai, USA
Publisher
FapUNIFESP (SciELO)
Subject
Genetics(clinical),Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health
Link
http://www.scielo.br/pdf/jiems/v9/2326-4594-jiems-9-e20200021.pdf
Reference15 articles.
1. GeneReviews®;Wagner VF,2020
2. Enhancing the therapeutic potential of sulfamidase for the treatment of mucopolysaccharidosis IIIA;Sorrentino NC;Mol Ther Methods Clin Dev,2019
3. Anatomical changes and pathophysiology of the brain in mucopolysaccharidosis disorders;Bigger BW;Mol Genet Metab,2018
4. In vivo gene therapy for mucopolysaccharidosis type III (Sanfilippo Syndrome): A new treatment horizon;Marcó S;Hum Gene Ther,2019
5. Reduction in brain heparan sulfate with systemic administration of an IgG trojan horse-sulfamidase fusion protein in the mucopolysaccharidosis type IIIA mouse;Boado RJ;Mol Pharm,2018
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2. Characterization of a spontaneous cell line from primary mouse fibroblasts as a model to study Sanfilippo syndrome;The International Journal of Biochemistry & Cell Biology;2022-01
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