Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Travis M Bridges"'
Autor:
Pablo Sánchez-Martín, Madushi Raththagala, Travis M Bridges, Satrio Husodo, Matthew S Gentry, Pascual Sanz, Carlos Romá-Mateo
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e69523 (2013)
Laforin, encoded by a gene that is mutated in Lafora Disease (LD, OMIM 254780), is a modular protein composed of a carbohydrate-binding module and a dual-specificity phosphatase domain. Laforin is the founding member of the glucan-phosphatase family
Externí odkaz:
https://doaj.org/article/7122f49752f34a8eb9688f8e4986fdbc
Autor:
Bradley C. Paasch, Matthew S. Gentry, Pascual Sanz, Srinivas Chakravarthy, Simon Hsu, Lance M. Hellman, David A. Meekins, Travis M. Bridges, Vikas V. Dukhande, Craig W. Vander Kooi, Satrio Husodo, Matthew W. Parker, Kyle D. Auger, Adam O. Taylor, M. Kathryn Brewer, Benjamin D. Turner, Virgil L. Woods, Amanda R. Sherwood, Brian Wong, Madushi Raththagala, Sheng Li
Publikováno v:
Molecular Cell. 57(2):261-272
Glycogen is the major mammalian glucose storage cache and is critical for energy homeostasis. Glycogen synthesis in neurons must be tightly controlled, due to neuronal sensitivity to perturbations in glycogen metabolism. Lafora disease (LD) is a fata
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::698457e6934dad80262a2aedb89355ad
Autor:
Diana Santelia, Oliver Kötting, Bradley C. Paasch, Matthew S. Gentry, Hou Fu Guo, Travis M. Bridges, Craig W. Vander Kooi, Satrio Husodo, David A. Meekins
Publikováno v:
Plant Cell
Starch is a water-insoluble, Glc-based biopolymer that is used for energy storage and is synthesized and degraded in a diurnal manner in plant leaves. Reversible phosphorylation is the only known natural starch modification and is required for starch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::147ce8c5a2e74aad12d691305535f253
https://pubmed.ncbi.nlm.nih.gov/23898026
https://pubmed.ncbi.nlm.nih.gov/23898026
Autor:
Travis M. Bridges, Satrio Husodo, Pascual Sanz, Pablo Sánchez-Martín, Matthew S. Gentry, Carlos Romá-Mateo, Madushi Raththagala
Publikováno v:
PLoS ONE
Digital.CSIC. Repositorio Institucional del CSIC
instname
PLoS ONE, Vol 8, Iss 7, p e69523 (2013)
Digital.CSIC. Repositorio Institucional del CSIC
instname
PLoS ONE, Vol 8, Iss 7, p e69523 (2013)
11 páginas, 5 figuras.
Laforin, encoded by a gene that is mutated in Lafora Disease (LD, OMIM 254780), is a modular protein composed of a carbohydrate-binding module and a dual-specificity phosphatase domain. Laforin is the founding member of t
Laforin, encoded by a gene that is mutated in Lafora Disease (LD, OMIM 254780), is a modular protein composed of a carbohydrate-binding module and a dual-specificity phosphatase domain. Laforin is the founding member of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5399d097f8c21c2daa29211bdff9cb2
http://europepmc.org/articles/PMC3724922
http://europepmc.org/articles/PMC3724922
Publikováno v:
The FASEB Journal. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ae5867759129ebc836b4e072a758191
https://doi.org/10.1096/fasebj.26.1_supplement.852.14
https://doi.org/10.1096/fasebj.26.1_supplement.852.14
Autor:
Santiago Vernia, Teresa Rubio, Pascual Sanz, Matthew S. Gentry, Daniel Moreno, Travis M. Bridges, Carlos Romá-Mateo
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
BMC Evolutionary Biology
ResearcherID
BMC Evolutionary Biology, Vol 11, Iss 1, p 225 (2011)
instname
BMC Evolutionary Biology
ResearcherID
BMC Evolutionary Biology, Vol 11, Iss 1, p 225 (2011)
Background Malin is an E3-ubiquitin ligase that is mutated in Lafora disease, a fatal form of progressive myoclonus epilepsy. In order to perform its function, malin forms a functional complex with laforin, a glucan phosphatase that facilitates targe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9996286ab396070f9f09d8908d91f0a4
http://hdl.handle.net/10261/39019
http://hdl.handle.net/10261/39019
