关注
Diego Alejandro Suarez Garcia
Diego Alejandro Suarez Garcia
Investigator
在 unal.edu.co 的电子邮件经过验证
标题
引用次数
引用次数
年份
Therapeutic options for mucopolysaccharidoses: current and emerging treatments
K Sawamoto, M Stapleton, CJ Alméciga-Díaz, AJ Espejo-Mojica, ...
Drugs 79 (10), 1103-1134, 2019
862019
GM2 gangliosidoses: clinical features, pathophysiological aspects, and current therapies
AF Leal, E Benincore-Flórez, D Solano-Galarza, RG Garzón Jaramillo, ...
International journal of molecular sciences 21 (17), 6213, 2020
832020
A perspective on research, diagnosis, and management of lysosomal storage disorders in Colombia
MA Puentes-Tellez, PA Lerma-Barbosa, RG Garzón-Jaramillo, DA Suarez, ...
Heliyon 6 (3), 2020
92020
Delivery and assessment of a CRISPR/nCas9-based genome editing system on in vitro models of mucopolysaccharidoses IVA assisted by magnetite-based nanoparticles
AF Leal, J Cifuentes, CE Torres, D Suárez, V Quezada, SC Gómez, ...
Scientific Reports 12 (1), 15045, 2022
82022
Sphingolipids and their role in health and disease in the central nervous system
AF Leal, DA Suarez, OY Echeverri-Peña, SL Albarracín, ...
Advances in Biological Regulation 85, 100900, 2022
62022
Evaluation of lentiviral vectors in Morquio syndrome type A patients' fibroblasts
A Puentes-Tellez, F Rojas-Rodríguez, D Suarez, OA Hidalgo, ...
Molecular Genetics and Metabolism 126 (2), S120, 2019
22019
Molecular Trojan Horses for treating lysosomal storage diseases
AF Leal, OK Inci, V Seyrantepe, E Rintz, B Celik, Y Ago, D León, ...
Molecular Genetics and Metabolism, 107648, 2023
12023
GM2 gangliosidosis insights: Tay-Sachs models via CRISPR-Cas9
D Suarez, AJ Espejo, CJ Alméciga-Díaz
Molecular Genetics and Metabolism 141 (2), 108052, 2024
2024
Treatment with recombinant human lysosomal β-hexosaminidase reduces GM2 accumulation in Tay-Sachs disease cells
OK Inci, AF Leal, N Ates, D Suarez, AJ Espejo, CJ Alméciga-Díaz, ...
Molecular Genetics and Metabolism 141 (2), 107896, 2024
2024
Initial characterization of cellular models for mucopolysaccharidosis type IIIB generated by CRISPR/Cas9
K Niño, D Suarez, AJ Espejo, CJ Alméciga-Díaz
Molecular Genetics and Metabolism 141 (2), 107982, 2024
2024
Genome Editing Tools for Lysosomal Storage Disorders
EA Gonzalez, H Nader, M Siebert, DA Suarez, CJ Alméciga-Díaz, G Baldo
Genome Editing in Biomedical Sciences, 127-155, 2023
2023
Pharmacological chaperones as an alternative to increase GALNS activity in mucopolysaccharidosis type IVA
L Prada, DA Suárez, CJ Alméciga-Díaz
Molecular Genetics and Metabolism 138 (2), 107276, 2023
2023
Magnetoliposomes as Carriers for CRISPR/nCas9-Based Gene Therapy on In Vitro Models of Mucopolysaccharidoses IVA and GM2 Gangliosidoses: Proof-of-Concept Experiments
AF Leal, D Suarez, V Quezada, CE Torres, SC Gomez, J Espejo-Mojica, ...
MOLECULAR THERAPY 30 (4), 475-476, 2022
2022
Genome editing in mucopolysaccharidosis type IVA fibroblasts using CRISPR/Cas9
DA Suarez, CJ Almeciga
Molecular Genetics and Metabolism 135 (2), S117, 2022
2022
Sphingolipids and cell signaling: Relationship between health and disease in the central nervous system
AF Leal, DA Suarez, OY Echeverri-Peña, SL Albarracín, ...
Preprints, 2021
2021
A perspective on research, diagnosis, and management of lysosomal disorders in Colombia: An update
MA Puentes-Tellez, PA Lerma-Barbosa, RG Garzón-Jaramillo, D Suarez, ...
Molecular Genetics and Metabolism 132 (2), S88, 2021
2021
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