Items where Author is "Helferich, Anika M."

Article

Freischmidt, Axel and Goswami, Anand and Limm, Katharina and Zimyanin, Vitaly L. and Demestre, Maria and Glass, Hannes and Holzmann, Karlheinz and Helferich, Anika M. and Brockmann, Sarah J. and Tripathi, Priyanka and Yamoah, Alfred and Poser, Ina and Oefner, Peter J. and Boeckers, Tobias M. and Aronica, Eleonora and Ludolph, Albert C. and Andersen, Peter M. and Hermann, Andreas and Weis, Joachim and Reinders, Joerg and Danzer, Karin M. and Weishaupt, Jochen H. (2021) A serum microRNA sequence reveals fragile X protein pathology in amyotrophic lateral sclerosis. BRAIN, 144. pp. 1214-1229. ISSN 0006-8950, 1460-2156

Brockmann, Sarah J. and Freischmidt, Axel and Oeckl, Patrick and Mueller, Kathrin and Ponna, Srinivas K. and Helferich, Anika M. and Paone, Christoph and Reinders, Joerg and Kojer, Kerstin and Orth, Michael and Jokela, Manu and Auranen, Mari and Udd, Bjarne and Hermann, Andreas and Danzer, Karin M. and Lichtner, Peter and Walther, Paul and Ludolph, Albert C. and Andersen, Peter M. and Otto, Markus and Kursula, Petri and 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. ISSN 0964-6906, 1460-2083

Helferich, Anika M. and Brockmann, Sarah J. and Reinders, Joerg and Deshpande, Dhruva and Holzmann, Karlheinz and Brenner, David and Andersen, Peter M. and Petri, Susanne and Thal, Dietmar R. and Michaelis, Jens and Otto, Markus and Just, Steffen and Ludolph, Albert C. and Danzer, Karin M. and 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. ISSN 1420-682X, 1420-9071