Intracerebral transplantation of mesenchymal stem cells into acid sphingomyelinase–deficient mice delays the onset of neurological abnormalities and extends their life span
Author:
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Reference30 articles.
1. Acid sphingomyelinase deficient mice: a model of types A and B Niemann–Pick disease
2. Acid sphingomyelinase-deficient mice mimic the neurovisceral form of human lysosomal storage disease (Niemann-Pick disease)
3. BIOCHEMICAL, PATHOLOGICAL, AND CLINICAL RESPONSE TO TRANSPLANTATION OF NORMAL BONE MARROW CELLS INTO ACID SPHINGOMYELINASE-DEFICIENT MICE1
4. Hematopoietic stem cell gene therapy leads to marked visceral organ improvements and a delayed onset of neurological abnormalities in the acid sphingomyelinase deficient mouse model of Niemann–Pick disease
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3. The Niemann-Pick type diseases – A synopsis of inborn errors in sphingolipid and cholesterol metabolism;Progress in Lipid Research;2023-04
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5. Stem Cell Applications in Lysosomal Storage Disorders: Progress and Ongoing Challenges;Advances in Experimental Medicine and Biology;2021
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