OCRL deficiency impairs endolysosomal function in a humanized mouse model for Lowe syndrome and Dent disease
OCRL 缺乏会损害 Lowe 综合征和 Dent 病人源化小鼠模型中的内溶酶体功能
期刊:Human Molecular Genetics
影响因子:3.1
doi:10.1093/hmg/ddy449
Beatrice Paola Festa, Marine Berquez, Alkaly Gassama, Irmgard Amrein, Hesham M Ismail, Marijana Samardzija, Leopoldo Staiano, Alessandro Luciani, Christian Grimm, Robert L Nussbaum, Maria Antonietta De Matteis, Olivier M Dorchies, Leonardo Scapozza, David Paul Wolfer, Olivier Devuyst
信号转导
FCM
IF
IHC-P
WB
Mouse
LAMP1