ALS Related Molecules
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease, pathologically characterized by loss of motor neurons. The mechanism underlying motor neuron degeneration remains incompletely understood. However, mutations have been identified in superoxide dismutase (SOD), suggesting free radical damage may be responsible.
- alpha-Internexin
- Aldehyde Oxidase 1/AOX1
- Ataxin-3
- C9orf72
- CHMP2B
- Cytochrome c
- Dynactin Subunit 1/DCTN1
- Dynactin Subunit 2/DCTN2
- EAAT1/GLAST-1
- EAAT2/GLT1
- G-CSF
- GDNF
- HSP70/HSPA1A
- IGF-I/IGF-1
- NFIL3/E4BP4
- p38
- Ret
- Sirtuin 1/SIRT1
- Sirtuin 3/SIRT3
- SOD (Superoxide Dismutase)
- SOD1/Cu-Zn SOD
- SOD2/Mn-SOD
- alpha-Synuclein
- beta-Synuclein
- gamma-Synuclein
- TDP-43/TARDBP
- UBE2K/E2-25K
- UCP1
- VAP-B
- VCP
- VEGF
- VGF