The Expression and Secretion Profile of TRAP5 Isoforms in Gaucher Disease
Background: Gaucher disease (GD) is caused by glucocerebrosidase (GCase) enzyme deficiency, leading to glycosylceramide (Gb-1) and glucosylsphingosine (Lyso-Gb-1) accumulation. The pathological hallmark for GD is an accumulation of large macrophages called Gaucher cells (GCs) in the liver, spleen, a...
Shranjeno v:
| Principais autores: | , , , , , , |
|---|---|
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
MDPI AG
2024-04-01
|
| Serija: | Cells |
| Teme: | |
| Online dostop: | https://www.mdpi.com/2073-4409/13/8/716 |
| Oznake: |
Brez oznak, prvi označite!
|