Hypomyelination Leukodystrophy 16 (HLD16)-Associated Mutation p.Asp252Asn of TMEM106B Blunts Cell Morphological Differentiation
Transmembrane protein 106B (TMEM106B), which is a type II transmembrane protein, is believed to be involved in intracellular dynamics and morphogenesis in the lysosome. TMEM106B is known to be a risk factor for frontotemporal lobar degeneration and has been recently identified as the receptor needed...
Autors principals: | Sui Sawaguchi, Miki Ishida, Yuki Miyamoto, Junji Yamauchi |
---|---|
Format: | Article |
Idioma: | English |
Publicat: |
MDPI AG
2024-07-01
|
Col·lecció: | Current Issues in Molecular Biology |
Matèries: | |
Accés en línia: | https://www.mdpi.com/1467-3045/46/8/478 |
Ítems similars
-
Identification of a de novo Mutation in TMEM106B in a Saudi Child Causes Hypomyelination Leukodystrophy
per: Lena Alotaibi, et al.
Publicat: (2023-01-01) -
The major TMEM106B dementia risk allele affects TMEM106B protein levels, fibril formation, and myelin lipid homeostasis in the ageing human hippocampus
per: Jun Yup Lee, et al.
Publicat: (2023-09-01) -
TMEM106B deficiency impairs cerebellar myelination and synaptic integrity with Purkinje cell loss
per: Tuancheng Feng, et al.
Publicat: (2022-03-01) -
TMEM106B aggregation in neurodegenerative diseases: linking genetics to function
per: Hai-Shan Jiao, et al.
Publicat: (2023-08-01) -
TMEM106a is a Novel Tumor Suppressor in Human Renal Cancer
per: Chenglong Wu, et al.
Publicat: (2017-10-01)