Biofabrication of an in-vitro bone model for Gaucher disease

Gaucher disease (GD), the most prevalent lysosomal disorder, is caused by GBA1 gene mutations, leading to deficiency of glucocerebrosidase, and accumulation of glycosphingolipids in cells of the mononuclear phagocyte system. While skeletal diseases are the leading cause of morbidity and reduced qual...

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Detalles Bibliográficos
Autores principales: Banerjee, Dishary, Ivanova, Margarita M, Celik, Nazmiye, Kim, Myoung Hwan, Derman, Irem Deniz, Limgala, Renuka Pudi, Ozbolat, Ibrahim T, Goker-Alpan, Ozlem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOP Publishing 2023
Materias:
Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10515412/
https://www.ncbi.nlm.nih.gov/pubmed/37703870
http://dx.doi.org/10.1088/1758-5090/acf95a

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10515412/
https://www.ncbi.nlm.nih.gov/pubmed/37703870
http://dx.doi.org/10.1088/1758-5090/acf95a

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