Auflistung nach Autor "Nagel, Maike"

Anzeige der Dokumente 1-6 von 6

A combinatorial approach to identify calpain cleavage sites in the Machado-Joseph disease protein ataxin-3

Golla, Matthias; Guaitoli, Giambattista; Hayer, Stefanie Nicole; Hauser, Stefan; Krahl, Ann-Christin; Nagel, Maike; Samer, Sebastian; Schöls, Ludger; Weber, Jonasz Jeremiasz; Rieß, Olaf; Gloeckner, Christian; Nguyen, Huu Phuc; Hübener-Schmid, Jeannette (2017)
Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia

Gehweiler, Ina; Nagel, Maike; Ulmer, Ulrike; Kernstock, Christoph; Reich, Selina; Reichbauer, Jennifer; Hölbling, Benedikt; Schüle-Freyer, Rebecca (2019)
Calpastatin ablation aggravates the molecular phenotype in cell and animal models of Huntington disease

Weber, Jonasz Jeremiasz; Kloock, Simon Johannes; Nagel, Maike; Ortiz-Rios, Midea Malena; Hofmann, Julian; Rieß, Olaf; Nguyen, Huu Phuc (2018)
Generation of the CRISPR/Cas9-mediated KIF1C knock-out human iPSC line HIHRSi003-A-1

Nagel, Maike; Höflinger, Philip; Schöls, Ludger; Hauser, Stefan; Schüle-Freyer, Rebecca (2020)
Generation of two iPSC lines derived from two unrelated patients with Gaucher disease

Nagel, Maike; Reichbauer, Jennifer; Böhringer, Judith; Schelling, Yvonne; Krägeloh-Mann, Ingeborg; Schüle-Freyer, Rebecca; Ulmer, Ulrike (2019)
The role of the kinesin motor KIF1C in hereditary spastic paraplegia

Nagel, Maike (2023)

Anzeige der Dokumente 1-6 von 6

Stöbern