Sporadic amyotrophic lateral sclerosis (SALS) – skeletal muscle response to cerebrospinal fluid from SALS patients in a rat model
Skeletal muscle atrophy is the most prominent feature of amyotrophic lateral sclerosis (ALS), an adult-onset neurodegenerative disease of motor neurons. However, the contribution of skeletal muscle to disease progression remains elusive. Our previous studies have shown that intrathecal injection of...
Main Authors: | Shruthi Shanmukha, Gayathri Narayanappa, Atchayaram Nalini, Phalguni Anand Alladi, Trichur R. Raju |
---|---|
Format: | Article |
Language: | English |
Published: |
The Company of Biologists
2018-04-01
|
Series: | Disease Models & Mechanisms |
Subjects: | |
Online Access: | http://dmm.biologists.org/content/11/4/dmm031997 |
Similar Items
-
Fasudil improves survival and promotes skeletal muscle development in a mouse model of spinal muscular atrophy
by: Bowerman Melissa, et al.
Published: (2012-03-01) -
Evidence of endoplasmic reticular stress in the spinal motor neurons exposed to CSF from sporadic amyotrophic lateral sclerosis patients
by: K. Vijayalakshmi, et al.
Published: (2011-03-01) -
Modeling sporadic amyotrophic lateral sclerosis (sals) in zebrafish using environmental stressors
by: Morrice, Jessica Rebecca Marie
Published: (2017) -
Chitotriosidase, a biomarker of amyotrophic lateral sclerosis, accentuates neurodegeneration in spinal motor neurons through neuroinflammation
by: Anu Mary Varghese, et al.
Published: (2020-08-01) -
CD44 is expressed in non-myelinating Schwann cells of the adult rat, and may play a role in neurodegeneration-induced glial plasticity at the neuromuscular junction
by: Adam Gorlewicz, et al.
Published: (2009-05-01)