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FUS Mislocalization and Vulnerability to DNA Damage in ALS Patients Derived hiPSCs and Aging Motoneurons
Higelin, Julia et al. (2016)
Wissenschaftlicher Artikel
Stepwise acquirement of hallmark neuropathology in FUS-ALS iPSC models depends on mutation type and neuronal aging
Japtok, Julia et al. (2015)
Wissenschaftlicher Artikel
Actin-Dependent Alterations of Dendritic Spine Morphology in Shankopathies
Sarowar, Tasnuva; Grabrucker, Andreas M. (2016)
Wissenschaftlicher Artikel
Neuroectodermally converted human mesenchymal stromal cells provide cytoprotective effects on neural stem cells and inhibit their glial differentiation
Habisch, Hans-Joerg et al. (2010)
Wissenschaftlicher Artikel
Reduced dendritic arborization and hyperexcitability of pyramidal neurons in a Scn1b-based model of Dravet syndrome
Reid, Christopher A. et al. (2014)
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Axon initial segment dysfunction in a mouse model of genetic epilepsy with febrile seizures plus
Wimmer, Verena C. et al. (2010)
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Water-soluble allyl sulfones for dual site-specific labelling of proteins and cyclic peptides
Wang, Tao et al. (2016)
Wissenschaftlicher Artikel
Molecular correlates of age-dependent seizures in an inherited neonatal-infantile epilepsy
Liao, Yunxiang et al. (2010)
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Implementation of a population-based epidemiological rare disease registry: study protocol of the amyotrophic lateral sclerosis (ALS) - registry Swabia
Nagel, Gabriele et al. (2013)
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A novel optineurin truncating mutation and three glaucoma-associated missense variants in patients with familial amyotrophic lateral sclerosis in Germany
Weishaupt, Jochen H. et al. (2013)
Wissenschaftlicher Artikel