Lysosomal Storage Disease Mouse Models

Lysosomal storage disorders (LSDs) are rare genetic conditions that cause a buildup of toxic materials in the cells of various organs.  As part of our rare disease models platform, WuXi AppTec offers an extensive panel of LSD mouse models, including Gaucher disease, Pompe disease, Fabry disease, and Hurler syndrome (MPS I).  Our service platform supports efficacy, toxicity, and PK/PD studies for all of these models.

Learn more about our Rare Disease Platform by clicking here.

 



Lysosome Storage Disease Mouse Models

Download

← Return to Resources

Related Content

KRAS G12D inhibitors continue to advance, but treatment resistance remains an important challenge. Understanding how that resistance develops is critical...

VIEW RESOURCE

Metabolic dysfunction-associated steatohepatitis (MASH) remains a significant global health challenge, driven by a complex interplay of lipid dysregulation, inflammation, and...

VIEW RESOURCE
← View all in vivo Pharmacology Resources
× peptide, amino acid

Contact An Expert Today!