Search Results - "Weise, Stefan C."

FOXG1 Regulates PRKAR2B Transcriptionally and Posttranscriptionally via miR200 in the Adult Hippocampus by Weise, Stefan C., Arumugam, Ganeshkumar, Villarreal, Alejandro, Videm, Pavankumar, Heidrich, Stefanie, Nebel, Nils, Dumit, Verónica I., Sananbenesi, Farahnaz, Reimann, Viktoria, Craske, Madeline, Schilling, Oliver, Hess, Wolfgang R., Fischer, Andre, Backofen, Rolf, Vogel, Tanja

“…Rett syndrome is a complex neurodevelopmental disorder that is mainly caused by mutations in MECP2 . However, mutations in FOXG1 cause a less frequent form of…”
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Neural deletion of Tgfbr2 impairs angiogenesis through an altered secretome by Hellbach, Nicole, Weise, Stefan C, Vezzali, Riccardo, Wahane, Shalaka D, Heidrich, Stefanie, Roidl, Deborah, Pruszak, Jan, Esser, Jennifer S, Vogel, Tanja

“…Simultaneous generation of neural cells and that of the nutrient-supplying vasculature during brain development is called neurovascular coupling. We report on…”
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DGCR8 Promotes Neural Progenitor Expansion and Represses Neurogenesis in the Mouse Embryonic Neocortex by Hoffmann, Nadin, Weise, Stefan C, Marinaro, Federica, Vogel, Tanja, De Pietri Tonelli, Davide

“…DGCR8 and DROSHA are the minimal functional core of the Microprocessor complex essential for biogenesis of canonical microRNAs and for the processing of other…”
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Ultra-Thin Porous PDLLA Films Promote Generation, Maintenance, and Viability of Stem Cell Spheroids by Tsai, Ya An, Li, Tianshu, Torres-Fernández, Lucia A., Weise, Stefan C., Kolanus, Waldemar, Takeoka, Shinji

“…Three-dimensional (3D) culture bridges and minimizes the gap between in vitro and in vivo states of cells and various 3D culture systems have been developed…”
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Impaired neurogenesis alters brain biomechanics in a neuroprogenitor-based genetic subtype of congenital hydrocephalus by Duy, Phan Q., Weise, Stefan C., Marini, Claudia, Li, Xiao-Jun, Liang, Dan, Dahl, Peter J., Ma, Shaojie, Spajic, Ana, Dong, Weilai, Juusola, Jane, Kiziltug, Emre, Kundishora, Adam J., Koundal, Sunil, Pedram, Maysam Z., Torres-Fernández, Lucia A., Händler, Kristian, De Domenico, Elena, Becker, Matthias, Ulas, Thomas, Juranek, Stefan A., Cuevas, Elisa, Hao, Le Thi, Jux, Bettina, Sousa, André M. M., Liu, Fuchen, Kim, Suel-Kee, Li, Mingfeng, Yang, Yiying, Takeo, Yutaka, Duque, Alvaro, Nelson-Williams, Carol, Ha, Yonghyun, Selvaganesan, Kartiga, Robert, Stephanie M., Singh, Amrita K., Allington, Garrett, Furey, Charuta G., Timberlake, Andrew T., Reeves, Benjamin C., Smith, Hannah, Dunbar, Ashley, DeSpenza, Tyrone, Goto, June, Marlier, Arnaud, Moreno-De-Luca, Andres, Yu, Xin, Butler, William E., Carter, Bob S., Lake, Evelyn M. R., Constable, R. Todd, Rakic, Pasko, Lin, Haifan, Deniz, Engin, Benveniste, Helene, Malvankar, Nikhil S., Estrada-Veras, Juvianee I., Walsh, Christopher A., Alper, Seth L., Schultze, Joachim L., Paeschke, Katrin, Doetzlhofer, Angelika, Wulczyn, F. Gregory, Jin, Sheng Chih, Lifton, Richard P., Sestan, Nenad, Kolanus, Waldemar, Kahle, Kristopher T.

“…Hydrocephalus, characterized by cerebral ventricular dilatation, is routinely attributed to primary defects in cerebrospinal fluid (CSF) homeostasis. This…”
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