SEC18/NSF-independent, protein-sorting pathway from the yeast cortical ER to the plasma membrane

por Jüschke, Christoph, Wächter, Andrea, Schwappach, Blanche, Seedorf, Matthias
Publicado 2005

The Phosphatase PP4c Controls Spindle Orientation to Maintain Proliferative Symmetric Divisions in the Developing Neocortex

por Xie, Yunli, Jüschke, Christoph, Esk, Christopher, Hirotsune, Shinji, Knoblich, Juergen A.
Publicado 2013

In Vivo Efficacy and Safety Evaluations of Therapeutic Splicing Correction Using U1 snRNA in the Mouse Retina

por Swirski, Sebastian, May, Oliver, Ahlers, Malte, Wissinger, Bernd, Greschner, Martin, Jüschke, Christoph, Neidhardt, John
Publicado 2023

Translational Read-Through Therapy of RPGR Nonsense Mutations

por Vössing, Christine, Owczarek-Lipska, Marta, Nagel-Wolfrum, Kerstin, Reiff, Charlotte, Jüschke, Christoph, Neidhardt, John
Publicado 2020

Autosomal dominant optic atrophy: A novel treatment for OPA1 splice defects using U1 snRNA adaption

por Jüschke, Christoph, Klopstock, Thomas, Catarino, Claudia B., Owczarek-Lipska, Marta, Wissinger, Bernd, Neidhardt, John
Publicado 2021

Mouse Inscuteable Induces Apical-Basal Spindle Orientation to Facilitate Intermediate Progenitor Generation in the Developing Neocortex

por Postiglione, Maria Pia, Jüschke, Christoph, Xie, Yunli, Haas, Gerald A., Charalambous, Christoforos, Knoblich, Juergen A.
Publicado 2011

Afadin controls cell polarization and mitotic spindle orientation in developing cortical radial glia

por Rakotomamonjy, Jennifer, Brunner, Molly, Jüschke, Christoph, Zang, Keling, Huang, Eric J., Reichardt, Louis F., Chenn, Anjen
Publicado 2017

Transcriptome and proteome quantification of a tumor model provides novel insights into post‐transcriptional gene regulation

por Jüschke, Christoph, Dohnal, Ilse, Pichler, Peter, Harzer, Heike, Swart, Remco, Ammerer, Gustav, Mechtler, Karl, Knoblich, Juergen A
Publicado 2013

Skewed X-inactivation is associated with retinal dystrophy in female carriers of RPGR mutations

por Usman, Muhammad, Jüschke, Christoph, Song, Fei, Kastrati, Dennis, Owczarek-Lipska, Marta, Eilers, Jannis, Pauleikhoff, Laurenz, Lange, Clemens, Neidhardt, John
Publicado 2023

The mutation p.E113K in the Schiff base counterion of rhodopsin is associated with two distinct retinal phenotypes within the same family

por Reiff, Charlotte, Owczarek-Lipska, Marta, Spital, Georg, Röger, Carsten, Hinz, Hebke, Jüschke, Christoph, Thiele, Holger, Altmüller, Janine, Nürnberg, Peter, Da Costa, Romain, Neidhardt, John
Publicado 2016

Extraction and analysis of signatures from the Gene Expression Omnibus by the crowd

por Wang, Zichen, Monteiro, Caroline D., Jagodnik, Kathleen M., Fernandez, Nicolas F., Gundersen, Gregory W., Rouillard, Andrew D., Jenkins, Sherry L., Feldmann, Axel S., Hu, Kevin S., McDermott, Michael G., Duan, Qiaonan, Clark, Neil R., Jones, Matthew R., Kou, Yan, Goff, Troy, Woodland, Holly, Amaral, Fabio M R., Szeto, Gregory L., Fuchs, Oliver, Schüssler-Fiorenza Rose, Sophia M., Sharma, Shvetank, Schwartz, Uwe, Bausela, Xabier Bengoetxea, Szymkiewicz, Maciej, Maroulis, Vasileios, Salykin, Anton, Barra, Carolina M., Kruth, Candice D., Bongio, Nicholas J., Mathur, Vaibhav, Todoric, Radmila D, Rubin, Udi E., Malatras, Apostolos, Fulp, Carl T., Galindo, John A., Motiejunaite, Ruta, Jüschke, Christoph, Dishuck, Philip C., Lahl, Katharina, Jafari, Mohieddin, Aibar, Sara, Zaravinos, Apostolos, Steenhuizen, Linda H., Allison, Lindsey R., Gamallo, Pablo, de Andres Segura, Fernando, Dae Devlin, Tyler, Pérez-García, Vicente, Ma'ayan, Avi
Publicado 2016