Restricted expression of mutant SOD1 in spinal motor neurons and interneurons induces motor neuron pathology
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by the selective loss of motor neurons (MNs). Approximately 10% of ALS cases are familial (known as FALS), and ∼20% of FALS cases are caused by mutations in Cu/Zn superoxide dismutase type 1 (SOD1). Mutant (MT) SOD1 ind...
Main Authors: | Lijun Wang, Kamal Sharma, Han-Xiang Deng, Teepu Siddique, Gabriella Grisotti, Erdong Liu, Raymond P. Roos |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2008-03-01
|
Series: | Neurobiology of Disease |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S0969996107002367 |
Similar Items
-
Copper delivery to the CNS by CuATSM effectively treats motor neuron disease in SODG93A mice co-expressing the Copper-Chaperone-for-SOD
by: Jared R. Williams, et al.
Published: (2016-05-01) -
The effect of mutant SOD1 dismutase activity on non-cell autonomous degeneration in familial amyotrophic lateral sclerosis
by: Lijun Wang, et al.
Published: (2009-08-01) -
Tryptophan 32 mediates SOD1 toxicity in a in vivo motor neuron model of ALS and is a promising target for small molecule therapeutics
by: Michèle G. DuVal, et al.
Published: (2019-04-01) -
A New Method for the Purification of Cu-Zn Superoxide Dismutase from Human Erythrocytes
by: M Djalali, et al.
Published: (2005-09-01) -
A New Method for the Purification of Cu-Zn Superoxide Dismutase from Human Erythrocytes
by: M Djalali, et al.
Published: (2005-12-01)