Emptying the stores: lysosomal diseases and therapeutic strategies
Lysosomal storage disorders (LSDs) — designated as 'orphan' diseases — are inborn errors of metabolism caused by defects in genes that encode proteins involved in various aspects of lysosomal homeostasis. For many years, LSDs were viewed as unattractive targets for the development of thera...
Hlavní autor: | Platt, F |
---|---|
Médium: | Journal article |
Vydáno: |
Springer Nature
2017
|
Podobné jednotky
-
New therapeutics for the treatment of glycosphingolipid lysosomal storage diseases.
Autor: Butters, T, a další
Vydáno: (2003) -
Substrate deprivation: a new therapeutic approach for the glycosphingolipid lysosomal storage diseases.
Autor: Platt, F, a další
Vydáno: (2000) -
Therapeutic applications of imino sugars in lysosomal storage disorders.
Autor: Butters, T, a další
Vydáno: (2003) -
Lysosomal Ca(2+) homeostasis: role in pathogenesis of lysosomal storage diseases.
Autor: Lloyd-Evans, E, a další
Vydáno: (2011) -
Lysosomal storage diseases
Autor: Platt, F, a další
Vydáno: (2018)