Characterization of Cellular Alterations in a Novel NAGLU Enzyme-Deficient Cellular Model Generated from U-87MG Cell Line
- 24 September 2026
- journal article
- research article
- Published by Springer Nature in Neurochemical Research
- Vol. 51 (5) , 275
Abstract
No abstract availableKeywords
Funding Information
- Pontificia Universidad Javeriana (Master scholarship)
- Pontificia Universidad Javeriana (Doctoral scholarship)
- Pontificia Universidad Javeriana (Investigar PUJ 20646 and 20567)
- Pontificia Universidad Javeriana (Investigar PUJ 20646 and 20567)
This publication has 97 references indexed in Scilit:
- Creation of an in vitro model of GM1 gangliosidosis by CRISPR/Cas9 knocking‐out the GLB1 gene in SH‐SY5Y human neuronal cell lineCell Biochemistry and Function, 2024
- Twenty years of Colombian experience with enzymatic screening in patients with features of mucopolysaccharidosisJIMD Reports, 2022
- Human recombinant lysosomal β‐Hexosaminidases produced in Pichia pastoris efficiently reduced lipid accumulation in Tay‐Sachs fibroblastsAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, 2020
- Novel therapies for mucopolysaccharidosis type IIIJournal of Inherited Metabolic Disease, 2020
- Rapid Quantitative Evaluation of CRISPR Genome Editing by TIDE and TIDER2019
- Trypan Blue Exclusion Test of Cell ViabilityCurrent Protocols in Immunology, 2015
- Oxidative stress is independent of inflammation in the neurodegenerative sanfilippo syndrome type BJournal of Neuroscience Research, 2014
- Thin layer chromatography of gangliosidesGlycoconjugate Journal, 2008
- Cytokines, neurotrophins, and oxidative stress in brain disease from mucopolysaccharidosis IIIBJournal of Neuroscience Research, 2006
- Control of cell division in hepatoma cells by exogenous heparan sulfate proteoglycanJournal of Cellular Physiology, 1989