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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...

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Principais autores: Margarita M. Ivanova, Julia Dao, Neala Loynab, Sohailla Noor, Neil Kasaci, Andrew Friedman, Ozlem Goker-Alpan
Formato: Artigo
Idioma:Inglês
Publicado: MDPI AG 2024-04-01
Series:Cells
Assuntos:
Gaucher disease
osteoporosis
TRAP
macrophages
Gaucher cells
bone
Acceso en liña:https://www.mdpi.com/2073-4409/13/8/716
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