Loss of BICD2 in muscle drives motor neuron loss in a developmental form of spinal muscular atrophy
Abstract Autosomal dominant missense mutations in BICD2 cause Spinal Muscular Atrophy Lower Extremity Predominant 2 (SMALED2), a developmental disease of motor neurons. BICD2 is a key component of the cytoplasmic dynein/dynactin motor complex, which in axons drives the microtubule-dependent retrogra...
Main Authors: | Alexander M. Rossor, James N. Sleigh, Michael Groves, Francesco Muntoni, Mary M. Reilly, Casper C. Hoogenraad, Giampietro Schiavo |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2020-03-01
|
Series: | Acta Neuropathologica Communications |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s40478-020-00909-6 |
Similar Items
-
Muscle and bone characteristics of a Chinese family with spinal muscular atrophy, lower extremity predominant 1 (SMALED1) caused by a novel missense DYNC1H1 mutation
by: Yazhao Mei, et al.
Published: (2023-03-01) -
Coil-to-α-helix transition at the Nup358-BicD2 interface activates BicD2 for dynein recruitment
by: James M Gibson, et al.
Published: (2022-03-01) -
Identification and functional characterization of BICD2 as a candidate disease gene in an consanguineous family with dilated cardiomyopathy
by: Kai Luo, et al.
Published: (2022-09-01) -
Dominant spinal muscular atrophy is caused by mutations in BICD2, an important golgin protein
by: Brunhilde eWirth, et al.
Published: (2015-11-01) -
BICD Cargo Adaptor 1 (BICD1) Downregulation Correlates with a Decreased Level of PD-L1 and Predicts a Favorable Prognosis in Patients with IDH1-Mutant Lower-Grade Gliomas
by: Shang-Pen Huang, et al.
Published: (2021-07-01)