RT Dissertation/Thesis
T1 Unravelling the Pathogenesis of Celia’s Encephalopathy (PELD): The Role of Seipin in Neurodegeneration, Lipodystrophy, and other Tissue Damage in a Humanized Murine Model
A1 Cobelo Gómez, Silvia
K1 BSCL2
K1 Seipin
K1 Neurodegeneration
K1 PELD
K1 Celia’s encephalopathy
AB Lipodystrophies are rare disorders, with Celia’s encephalopathy, identified by our research group in 2013, being exceptionally rare with only 33 cases to date. Over the years, our research group has unravelled key pathogenic mechanisms of this disease. However, its rarity, severity, and predominant brain involvement pose significant challenges for human studies. Therefore, in this study, we developed a knock-in mouse model expressing the aberrant human BSCL2 transcript, alongside a Bscl2 knock out model, to compare the effects of BSCL2 deficiency and overexpression. These models replicate aspects of Celia’s encephalopathy and congenital generalized lipodystrophy, offering valuable preclinical tools for studying these conditions and exploring potential therapies.
YR 2025
FD 2025
LK https://hdl.handle.net/10347/40233
UL https://hdl.handle.net/10347/40233
LA eng
DS Minerva
RD 3 may 2026