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...
Yazar: | Platt, F |
---|---|
Materyal Türü: | Journal article |
Baskı/Yayın Bilgisi: |
Springer Nature
2017
|
Benzer Materyaller
-
New therapeutics for the treatment of glycosphingolipid lysosomal storage diseases.
Yazar:: Butters, T, ve diğerleri
Baskı/Yayın Bilgisi: (2003) -
Substrate deprivation: a new therapeutic approach for the glycosphingolipid lysosomal storage diseases.
Yazar:: Platt, F, ve diğerleri
Baskı/Yayın Bilgisi: (2000) -
Therapeutic applications of imino sugars in lysosomal storage disorders.
Yazar:: Butters, T, ve diğerleri
Baskı/Yayın Bilgisi: (2003) -
Lysosomal Ca(2+) homeostasis: role in pathogenesis of lysosomal storage diseases.
Yazar:: Lloyd-Evans, E, ve diğerleri
Baskı/Yayın Bilgisi: (2011) -
Lysosomal storage diseases
Yazar:: Platt, F, ve diğerleri
Baskı/Yayın Bilgisi: (2018)