Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
Human Molecular Genetics|October 27, 2005
An animal model for Charcot-Marie-Tooth disease type 4B1Sonja Bonneick, Matthias Boentert, Philipp Berger, et al.
Human Molecular Genetics|March 6, 2012
Efficacy of enzyme replacement therapy in an aggravated mouse model of metachromatic leukodystrophy declines with ageFrank Matthes, Stijn Stroobants, Debora Gerlach, et al.
Human Molecular Genetics|March 18, 2005
Enzyme replacement improves nervous system pathology and function in a mouse model for metachromatic leukodystrophyUlrich Matzner, Eva Herbst, Kerstin Khalaj Hedayati, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 31, 2007
Increasing sulfatide synthesis in myelin-forming cells of arylsulfatase A-deficient mice causes demyelination and neurological symptoms reminiscent of human metachromatic leukodystrophyHariharasubramanian Ramakrishnan, Kerstin Khalaj Hedayati, Renate Lüllmann-Rauch, et al.
Nature Neuroscience|January 26, 2010
Axonal prion protein is required for peripheral myelin maintenanceJuliane Bremer, Frank Baumann, Cinzia Tiberi, et al.
Plos One|October 7, 2014
FoxP3+ regulatory T cells determine disease severity in rodent models of inflammatory neuropathiesGerd Meyer zu Hörste, Steffen Cordes, Anne K Mausberg, et al.
Glia|January 26, 2006
Expression pattern and functional characterization of connexin29 in transgenic miceJürgen Eiberger, Mark Kibschull, Nicola Strenzke, et al.
Brain : a Journal of Neurology|November 23, 2012
Myelin is dependent on the Charcot-Marie-Tooth Type 4H disease culprit protein FRABIN/FGD4 in Schwann cellsMichael Horn, Reto Baumann, Jorge A Pereira, et al.
Elife|January 17, 2019
Schwann cells, but not Oligodendrocytes, Depend Strictly on Dynamin 2 FunctionDaniel Gerber, Monica Ghidinelli, Elisa Tinelli, et al.
Pageof 5