A Prospective Treatment Option for Lysosomal Storage Diseases: CRISPR/Cas9 Gene Editing Technology for Mutation Correction in Induced Pluripotent Stem Cells-Reference-Cited by-同舟云学术

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A Prospective Treatment Option for Lysosomal Storage Diseases: CRISPR/Cas9 Gene Editing Technology for Mutation Correction in Induced Pluripotent Stem Cells

Published:2017-02-24 Issue:1 Volume:5 Page:6
ISSN:2079-9721
Container-title:Diseases
language:en
Short-container-title:Diseases

Author:

Christensen Chloe,Choy Francis

Publisher

MDPI AG

Link

http://www.mdpi.com/2079-9721/5/1/6/pdf

Reference113 articles.

1. Fluorogenic Substrates for Visualizing Acidic Organelle Enzyme Activities

2. Prevalence of Lysosomal Storage Disorders

3. Epidemiology of lysosomal storage diseases: An overview;Fuller,2006

4. Lysosomal storage diseases as differential diagnosis of hepatosplenomegaly

5. Fabry Disease: Recognition, Diagnosis, and Treatment of Neurological Features

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1. Lysosomal storage disorders: Clinical and therapeutic aspects;Handbook of Clinical Neurology;2023

2. Advance in strategies to build efficient vaccines against tuberculosis;Frontiers in Veterinary Science;2022-11-24

3. Oligosaccharidoses and Sialic Acid Disorders;Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases;2022

4. Modeling Sialidosis with Neural Precursor Cells Derived from Patient-Derived Induced Pluripotent Stem Cells;International Journal of Molecular Sciences;2021-04-22

5. Genome editing in mucopolysaccharidoses and mucolipidoses;Progress in Molecular Biology and Translational Science;2021

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