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

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...

Full description

Bibliographic Details
Main Authors: Sari Sugahara, Yuki Ishino, Koki Sawada, Tsumugi Iwata, Yuta Shimanaka, Junken Aoki, Hiroyuki Arai, Nozomu Kono
Format: Article
Language:English
Published: Elsevier 2023-11-01
Series:Journal of Lipid Research
Subjects:
Glycerophospholipids
Phospholipids
Phospholipids/Biosynthesis
Phospholipids/Metabolism
Lipidomics
phosphatidylserine
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227523001165

Internet

http://www.sciencedirect.com/science/article/pii/S0022227523001165

Similar Items