Cultivation of Human Neural Progenitor Cells in a 3-dimensional Self-assembling Peptide Hydrogel

Por Liedmann, Andrea, Rolfs, Arndt, Frech, Moritz J.
Publicado em 2012

Gene Transfer into Older Chicken Embryos by ex ovo Electroporation

Por Luo, Jiankai, Yan, Xin, Lin, Juntang, Rolfs, Arndt
Publicado em 2012

Idiopathic Small Fiber Neuropathy: Phenotype, Etiologies, and the Search for Fabry Disease

Por Samuelsson, Kristin, Kostulas, Konstantinos, Vrethem, Magnus, Rolfs, Arndt, Press, Rayomand
Publicado em 2014

Elucidating the Sources of β-Catenin Dynamics in Human Neural Progenitor Cells

Por Mazemondet, Orianne, John, Mathias, Leye, Stefan, Rolfs, Arndt, Uhrmacher, Adelinde M.
Publicado em 2012

Cyclodextrin Alters GABAergic Input to CA1 Pyramidal Cells in Wild-Type But Not in NPC1-Deficient Mice

Por Frech, Moritz J., Rabenstein, Michael, Bovensiepen, Katja, Rost, Sebastian, Rolfs, Arndt
Publicado no Biores Open Access (2015)

Dataset in support of the generation of Niemann-Pick disease Type C1 patient-specific iPS cell lines carrying the novel NPC1 mutation c.1180T>C or the prevalent c.3182T>C mutation...

Por Peter, Franziska, Trilck, Michaela, Rabenstein, Michael, Rolfs, Arndt, Frech, Moritz J.
Publicado no Data Brief (2017)

Anatomical expression patterns of delta-protocadherins in developing chicken cochlea

Por Lin, Juntang, Yan, Xin, Wang, Congrui, Guo, Zhikun, Rolfs, Arndt, Luo, Jiankai
Publicado em 2012

Differentiation of Human Neural Progenitor Cells in Functionalized Hydrogel Matrices

Por Liedmann, Andrea, Frech, Stefanie, Morgan, Peter J., Rolfs, Arndt, Frech, Moritz J.
Publicado em 2012

Niemann-Pick type C1 patient-specific induced pluripotent stem cells display disease specific hallmarks

Por Trilck, Michaela, Hübner, Rayk, Seibler, Philip, Klein, Christine, Rolfs, Arndt, Frech, Moritz J
Publicado em 2013

Pharmacologic Treatment Assigned for Niemann Pick Type C1 Disease Partly Changes Behavioral Traits in Wild-Type Mice

Por Schlegel, Victoria, Thieme, Markus, Holzmann, Carsten, Witt, Martin, Grittner, Ulrike, Rolfs, Arndt, Wree, Andreas
Publicado no Int J Mol Sci (2016)

Persistent increase in cardiac troponin I in Fabry disease: a case report

Por Schneider Christian, Wüsten Oliver, Franzen Wolfgang, Feustel Andreas, Tanislav Christian, Reichenberger Frank, Rolfs Arndt, Sieweke Nicole
Publicado em 2011-01-01

Correction: CAG Repeats Determine Brain Atrophy in Spinocerebellar Ataxia 17: A VBM Study

Por Reetz, Kathrin, Kleiman, Alexandra, Klein, Christine, Lencer, Rebekka, Zuehlke, Christine, Brockmann, Kathrin, Rolfs, Arndt, Binkofski, Ferdinand
Publicado em 2011

CAG Repeats Determine Brain Atrophy in Spinocerebellar Ataxia 17: A VBM Study

Por Reetz, Kathrin, Kleiman, Alexandra, Klein, Christine, Lencer, Rebekka, Zuehlke, Christine, Brockmann, Kathrin, Rolfs, Arndt, Binkofski, Ferdinand
Publicado em 2011

Persistent increase in cardiac troponin I in Fabry disease: a case report

Por Tanislav, Christian, Feustel, Andreas, Franzen, Wolfgang, Wüsten, Oliver, Schneider, Christian, Reichenberger, Frank, Rolfs, Arndt, Sieweke, Nicole
Publicado em 2011

Lyso-Gb3 Indicates that the Alpha-Galactosidase A Mutation D313Y is not Clinically Relevant for Fabry Disease

Por Niemann, Markus, Rolfs, Arndt, Giese, Anne, Mascher, Hermann, Breunig, Frank, Ertl, Georg, Wanner, Christoph, Weidemann, Frank
Publicado em 2012

Continuous Cardiac Troponin I Release in Fabry Disease

Por Feustel, Andreas, Hahn, Andreas, Schneider, Christian, Sieweke, Nicole, Franzen, Wolfgang, Gündüz, Dursun, Rolfs, Arndt, Tanislav, Christian
Publicado em 2014

Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability

Por Steinrücke, Sofia, Lohmann, Katja, Domingo, Aloysius, Rolfs, Arndt, Bäumer, Tobias, Spiegler, Juliane, Hartmann, Corinna, Münchau, Alexander
Publicado no Neurol Genet (2016)

A comprehensive global genotype–phenotype database for rare diseases

Por Trujillano, Daniel, Oprea, Gabriela‐Elena, Schmitz, Yvonne, Bertoli‐Avella, Aida M., Abou Jamra, Rami, Rolfs, Arndt
Publicado no Mol Genet Genomic Med (2016)

Multifocal White Matter Lesions Associated with the D313Y Mutation of the α-Galactosidase A Gene

Por Lenders, Malte, Duning, Thomas, Schelleckes, Michael, Schmitz, Boris, Stander, Sonja, Rolfs, Arndt, Brand, Stefan-Martin, Brand, Eva
Publicado em 2013

Diagnosis of Morquio Syndrome in Dried Blood Spots Based on a New MRM-MS Assay

Por Cozma, Claudia, Eichler, Sabrina, Wittmann, Gyula, Flores Bonet, Alba, Kramp, Guido Johannes, Giese, Anne-Katrin, Rolfs, Arndt
Publicado no PLoS One (2015)