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pro vyhledávání: '"van Roon, Willeke M. C."'
Frequency of nuclear mutant huntingtin inclusion formation in neurons and glia is cell-type-specific
Autor:
Jansen, Anne H. P., van Hal, Maurik, Op den Kelder, Ilse C., Meier, Romy T., de Ruiter, Anna-Aster, Schut, Menno H., Smith, Donna L., Grit, Corien, Brouwer, Nieske, Kamphuis, Willem, Boddeke, H. W. G. M., den Dunnen, Wilfred F. A., van Roon, Willeke M. C., Bates, Gillian P., Hol, Elly M., Reits, Eric A.
Publikováno v:
GLIA, 65, 50-61. John Wiley and Sons Inc.
Glia, 65(1), 50-61. Wiley
Glia, 65(1), 50-61. John Wiley and Sons Inc.
Glia, 65(1), 50-61. Wiley
Glia, 65(1), 50-61. John Wiley and Sons Inc.
Huntington's disease (HD) is an autosomal dominant inherited neurodegenerative disorder that is caused by a CAG expansion in the Huntingtin (HTT) gene, leading to HTT inclusion formation in the brain. The mutant huntingtin protein (mHTT) is ubiquitou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0387328b88b415234f036c81830e572c
https://pure.knaw.nl/portal/en/publications/80861db7-6e52-4c3d-b34c-c624dc737800
https://pure.knaw.nl/portal/en/publications/80861db7-6e52-4c3d-b34c-c624dc737800
Autor:
Jansen AH; Department of Cell biology & Histology, Academic Medical Center, Amsterdam, The Netherlands., van Hal M; Department of Cell biology & Histology, Academic Medical Center, Amsterdam, The Netherlands., Op den Kelder IC; Department of Cell biology & Histology, Academic Medical Center, Amsterdam, The Netherlands., Meier RT; Department of Cell biology & Histology, Academic Medical Center, Amsterdam, The Netherlands., de Ruiter AA; Department of Cell biology & Histology, Academic Medical Center, Amsterdam, The Netherlands., Schut MH; Center for Human and Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands., Smith DL; Department of Medical and Molecular Genetics, King's College London, London, United Kingdom., Grit C; Department of Neuroscience, Section Medical Physiology, University of Groningen, University Medical Center Groningen, Groningen, AV, 9713, The Netherlands., Brouwer N; Department of Neuroscience, Section Medical Physiology, University of Groningen, University Medical Center Groningen, Groningen, AV, 9713, The Netherlands., Kamphuis W; Netherlands Institute for Neuroscience, an institute of the Royal Netherlands Academy of Arts and Sciences, Amsterdam, The Netherlands., Boddeke HW; Department of Neuroscience, Section Medical Physiology, University of Groningen, University Medical Center Groningen, Groningen, AV, 9713, The Netherlands., den Dunnen WF; Department of Neuroscience, Section Medical Physiology, University of Groningen, University Medical Center Groningen, Groningen, AV, 9713, The Netherlands., van Roon WM; Center for Human and Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands., Bates GP; Department of Medical and Molecular Genetics, King's College London, London, United Kingdom., Hol EM; Netherlands Institute for Neuroscience, an institute of the Royal Netherlands Academy of Arts and Sciences, Amsterdam, The Netherlands.; Department of Translational Neuroscience, Brain Center Rudolf Magnus, University Medical Center Utrecht, The Netherlands.; Swammerdam Institute for Life Sciences, Center for Neuroscience, University of Amsterdam, The Netherlands., Reits EA; Department of Cell biology & Histology, Academic Medical Center, Amsterdam, The Netherlands.
Publikováno v:
Glia [Glia] 2017 Jan; Vol. 65 (1), pp. 50-61. Date of Electronic Publication: 2016 Sep 12.
