Disease-related PSS1 mutant impedes the formation and function of osteoclasts

Phosphatidylserine (PS) is an acidic phospholipid that is involved in various cellular events. Heterologous dominant mutations have been identified in the gene encoding PS synthase 1 (PSS1) in patients with a congenital disease called Lenz-Majewski syndrome (LMS). Patients with LMS show various symp...

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Detalles Bibliográficos
Autores principales: Sugahara, Sari, Ishino, Yuki, Sawada, Koki, Iwata, Tsumugi, Shimanaka, Yuta, Aoki, Junken, Arai, Hiroyuki, Kono, Nozomu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2023
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10641532/
https://www.ncbi.nlm.nih.gov/pubmed/37714410
http://dx.doi.org/10.1016/j.jlr.2023.100443

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10641532/
https://www.ncbi.nlm.nih.gov/pubmed/37714410
http://dx.doi.org/10.1016/j.jlr.2023.100443

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