Publications by Just, Steffen

Brockmann, Sarah J., Freischmidt, Axel, Oeckl, Patrick , Müller, Kathrin, Ponna, Srinivas K., Helferich, Anika M., Paone, Christoph, Reinders, Jörg, Kojer, Kerstin, Orth, Michael, Jokela, Manu, Auranen, Mari, Udd, Bjarne, Hermann, Andreas, Danzer, Karin M., Lichtner, Peter, Walther, Paul, Ludolph, Albert C., Andersen, Peter M., Otto, Markus , Kursula, Petri , Just, Steffen and Weishaupt, Jochen H. (2018) CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency. Human Molecular Genetics 27 (4), pp. 706-715. Fulltext not available.

Helferich, Anika M., Brockmann, Sarah J., Reinders, Jörg, Deshpande, Dhruva, Holzmann, Karlheinz, Brenner, David, Andersen, Peter M., Petri, Susanne, Thal, Dietmar R. , Michaelis, Jens, Otto, Markus , Just, Steffen, Ludolph, Albert C., Danzer, Karin M., Freischmidt, Axel and Weishaupt, Jochen H. (2018) Dysregulation of a novel miR-1825/TBCB/TUBA4A pathway in sporadic and familial ALS. Cellular and Molecular Life Sciences 75 (23), pp. 4301-4319. Fulltext not available.