Glycogen metabolism in Lafora disease
Indiana University-Purdue University Indianapolis (IUPUI) === Glycogen, a branched polymer of glucose, serves as an osmotically neutral means of storing glucose. Covalent phosphate is a trace component of mammalian glycogen and has been a point of interest with respect to Lafora disease, a fatal...
Main Author: | Contreras, Christopher J. |
---|---|
Other Authors: | Roach, Peter J. |
Language: | en_US |
Published: |
2018
|
Subjects: | |
Online Access: | http://hdl.handle.net/1805/15445 |
Similar Items
-
Pathogenesis of Lafora Disease: Transition of Soluble Glycogen to Insoluble Polyglucosan
by: Mitchell A. Sullivan, et al.
Published: (2017-08-01) -
Lafora disease ubiquitin ligase malin promotes proteasomal degradation of neuronatin and regulates glycogen synthesis
by: Jaiprakash Sharma, et al.
Published: (2011-10-01) -
Suppression of glycogen synthesis as a treatment for Lafora disease: Establishing the window of opportunity
by: Olga Varea, et al.
Published: (2021-01-01) -
Lafora Disease: A Ubiquitination-Related Pathology
by: Maria Adelaida García-Gimeno, et al.
Published: (2018-07-01) -
Genetics of Lafora progressive myoclonic epilepsy: current perspectives
by: Kecmanović M, et al.
Published: (2016-05-01)