Zobrazeno 1 - 10
of 122
pro vyhledávání: '"Martin Steup"'
Autor:
Felix Nitschke, Mitchell A Sullivan, Peixiang Wang, Xiaochu Zhao, Erin E Chown, Ami M Perri, Lori Israelian, Lucia Juana‐López, Paola Bovolenta, Santiago Rodríguez de Córdoba, Martin Steup, Berge A Minassian
Publikováno v:
EMBO Molecular Medicine, Vol 9, Iss 7, Pp 906-917 (2017)
Abstract Lafora disease (LD) is a fatal progressive epilepsy essentially caused by loss‐of‐function mutations in the glycogen phosphatase laforin or the ubiquitin E3 ligase malin. Glycogen in LD is hyperphosphorylated and poorly hydrosoluble. It
Externí odkaz:
https://doaj.org/article/a2b1331cf25e4a71adbb2ac75bba0a1b
Publikováno v:
International Journal of Molecular Sciences, Vol 18, Iss 8, p 1743 (2017)
Lafora disease (LD, OMIM #254780) is a rare, recessively inherited neurodegenerative disease with adolescent onset, resulting in progressive myoclonus epilepsy which is fatal usually within ten years of symptom onset. The disease is caused by loss-of
Externí odkaz:
https://doaj.org/article/527b3db891a141faa67d3a08b7a4372f
Autor:
Yasunori Nakamura, Martin Steup, Christophe Colleoni, Alberto A. Iglesias, Jinsong Bao, Naoko Fujita, Ian Tetlow
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffc98915d400900922efe7df298c3cec
https://publishup.uni-potsdam.de/frontdoor/index/index/docId/59487
https://publishup.uni-potsdam.de/frontdoor/index/index/docId/59487
Autor:
Xiaochu Zhao, Martin Steup, Lori Israelian, Mitchell A. Sullivan, Santiago Rodríguez de Córdoba, Ami M. Perri, Peixiang Wang, Erin E. Chown, Berge A. Minassian, Lucía Juana-López, Paola Bovolenta, Felix Nitschke
Publikováno v:
EMBO Molecular Medicine
Digital.CSIC. Repositorio Institucional del CSIC
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Digital.CSIC. Repositorio Institucional del CSIC
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12 p.-7 fig. Nitschke, Felix et al.
Lafora disease (LD) is a fatal progressive epilepsy essentially caused by loss-of-function mutations in the glycogen phosphatase laforin or the ubiquitin E3 ligase malin. Glycogen in LD is hyperphosphorylated
Lafora disease (LD) is a fatal progressive epilepsy essentially caused by loss-of-function mutations in the glycogen phosphatase laforin or the ubiquitin E3 ligase malin. Glycogen in LD is hyperphosphorylated
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 18, Iss 8, p 1743 (2017)
International Journal of Molecular Sciences, Vol 18, Iss 8, p 1743 (2017)
Lafora disease (LD, OMIM #254780) is a rare, recessively inherited neurodegenerative disease with adolescent onset, resulting in progressive myoclonus epilepsy which is fatal usually within ten years of symptom onset. The disease is caused by loss-of
Maltose frequently occurs as intermediate of the central carbon metabolism of prokaryotic and eukaryotic cells. Various mutants possess elevated maltose levels. Maltose exists as two anomers, (alpha- and beta-form) which are rapidly interconverted wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c457de38c6aa5ee40fbbfd4aac2e35e6
https://publishup.uni-potsdam.de/frontdoor/index/index/docId/46412
https://publishup.uni-potsdam.de/frontdoor/index/index/docId/46412
Publikováno v:
Plant science : an international journal of experimental plant biology. 264
Functional interactions of plastidial phosphorylase (Phol) and starch branching enzymes (BEs) from the developing rice endosperm are the focus of this study. In the presence of both Phol and BE, the same branched primer molecule is elongated and furt
Publikováno v:
Magnetic Resonance in Chemistry. 51:655-661
Phosphorylation and dephosphorylation of starch and glycogen are important for their physicochemical properties and also their physiological functions. It is therefore desirable to reliably determine the phosphorylation sites. Heteronuclear multidime
Autor:
Julia Smirnova, Darrell Cockburn, Martin Steup, Oliver Ebenhöh, William G.T. Willats, Alison M. Smith, Robert A. Field, Henriette L. Pedersen, Birte Svensson, Martin Rejzek, Christian Ruzanski, Marilyn J. Pike
Publikováno v:
The Journal of Biological Chemistry
Ruzanski, C, Smirnova, J, Rejzek, M, Cockburn, D, Pedersen, H L, Pike, M, Willats, W G T, Svensson, B, Steup, M, Ebenhöh, O, Smith, A M & Field, R A 2013, ' A Bacterial Glucanotransferase Can Replace the Complex Maltose Metabolism Required for Starch to Sucrose Conversion in Leaves at Night ', Journal of Biological Chemistry, vol. 288, no. 40, pp. 2028581-28598 . https://doi.org/10.1074/jbc.M113.497867
Ruzanski, C, Smirnova, J, Rejzek, M, Cockburn, D, Pedersen, H L, Pike, M, Willats, W G T, Svensson, B, Steup, M, Ebenhöh, O, Smith, A M & Field, R A 2013, ' A Bacterial Glucanotransferase Can Replace the Complex Maltose Metabolism Required for Starch to Sucrose Conversion in Leaves at Night ', Journal of Biological Chemistry, vol. 288, no. 40, pp. 2028581-28598 . https://doi.org/10.1074/jbc.M113.497867
Background: Maltose metabolism during leaf starch degradation requires a multidomain glucanotransferase and a complex polysaccharide. Results: A conventional bacterial glucanotransferase rescues an Arabidopsis mutant lacking the multidomain glucanotr
Publikováno v:
Journal of Applied Glycoscience. 60:3-20