Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Rodger, Catherine E."'
Publikováno v:
FEBS Journal. Apr2018, Vol. 285 Issue 7, p1185-1202. 18p.
Akademický článek
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Mechanistic basis of an epistatic interaction reducing age at onset in hereditary spastic paraplegia
Autor:
Newton, Timothy, Allison, Rachel, Schüle, Rebecca, Depienne, Christel, Goldberg, Lisa, Frahm, Christiane, Stevanin, Giovanni, Durr, Alexandra, Schöls, Ludger, Winner, Beate, Beetz, Christian, Reid, Evan, Edgar, James R, Lumb, Jennifer H, Rodger, Catherine E, Manna, Paul T, Rizo, Tania, Kohl, Zacharias, Nygren, Anders O H, Arning, Larissa
Publikováno v:
Brain
Brain 141(5), 1286-1299 (2018). doi:10.1093/brain/awy034
Brain 141(5), 1286-1299 (2018). doi:10.1093/brain/awy034
The mechanisms underlying disease modifier gene effects are rarely understood. Newton et al. report that deletion of DPY30 reduces age at onset in hereditary spastic paraplegia caused by SPAST mutations. They demonstrate that both genes regulate cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d2f58674556c2f1343945f1db8f441f
https://pubmed.ncbi.nlm.nih.gov/29481671
https://pubmed.ncbi.nlm.nih.gov/29481671
Akademický článek
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Autor:
Connell, James W., Allison, Rachel J., Rodger, Catherine E., Pearson, Guy, Zlamalova, Eliska, Reid, Evan
Funder: National Institute for Health Research; doi: http://dx.doi.org/10.13039/501100000272
Funder: Gates Cambridge Trust; doi: http://dx.doi.org/10.13039/501100005370
Mutations in the gene encoding the microtubule severing ATPase spastin
Funder: Gates Cambridge Trust; doi: http://dx.doi.org/10.13039/501100005370
Mutations in the gene encoding the microtubule severing ATPase spastin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::609707afb71d93250b628d9e09b82a35
Autor:
Connell, James W, Allison, Rachel J, Rodger, Catherine E, Pearson, Guy, Zlamalova, Eliska, Reid, Evan
Mutations in the gene encoding the microtubule severing ATPase spastin are the most frequent cause of hereditary spastic paraplegia, a genetic condition characterised by length-dependent axonal degeneration. Here, we show that HeLa cells lacking spas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a56f96a5d632d2d91cbede6ee4bcf05
Autor:
Connell, James W., Allison, Rachel J., Rodger, Catherine E., Pearson, Guy, Zlamalova, Eliska, Reid, Evan
Funder: National Institute for Health Research; doi: http://dx.doi.org/10.13039/501100000272
Funder: Gates Cambridge Trust; doi: http://dx.doi.org/10.13039/501100005370
Mutations in the gene encoding the microtubule severing ATPase spastin
Funder: Gates Cambridge Trust; doi: http://dx.doi.org/10.13039/501100005370
Mutations in the gene encoding the microtubule severing ATPase spastin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0abdd44a6adb9931bbb94b4c3c634f84
Autor:
Rodger, Catherine E1 c.e.rodger@dundee.ac.uk, Allen, George F.G.1, Weidlich, Simone1, Macartney, Thomas1, Ganley, Ian1
Publikováno v:
BBA - Bioenergetics. Aug2016 Supplement, Vol. 1857, pe25-e26. 1p.
Autor:
Zhao JF; MRC Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences, University of Dundee, Dundee, DD1 5EH, UK.; Equal contribution., Rodger CE; MRC Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences, University of Dundee, Dundee, DD1 5EH, UK.; Equal contribution., Allen GFG; MRC Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences, University of Dundee, Dundee, DD1 5EH, UK., Weidlich S; MRC Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences, University of Dundee, Dundee, DD1 5EH, UK., Ganley IG; MRC Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences, University of Dundee, Dundee, DD1 5EH, UK.
Publikováno v:
Cell stress [Cell Stress] 2020 Mar 04; Vol. 4 (5), pp. 99-113. Date of Electronic Publication: 2020 Mar 04.