Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Manja von Hahn"'
Autor:
Christine Unsicker, Flavia-Bianca Cristian, Manja von Hahn, Volker Eckstein, Gudrun A. Rappold, Simone Berkel
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-15 (2021)
Abstract SHANK2 mutations have been identified in individuals with neurodevelopmental disorders, including intellectual disability and autism spectrum disorders (ASD). Using CRISPR/Cas9 genome editing, we obtained SH-SY5Y cell lines with frameshift m
Externí odkaz:
https://doaj.org/article/e4089156251d45adb3fc38da76c6052a
Autor:
Katja Baur, Carmen Carrillo García, Şeydanur Şan, Manja von Hahn, Jens Strelau, Gabriele Hölzl-Wenig, Claudia Mandl, Francesca Ciccolini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8bce100ae2413e24401ace6cb1b1549
https://doi.org/10.15252/rc.2023698029
https://doi.org/10.15252/rc.2023698029
Autor:
Katja Baur, Carmen Carrillo-García, Şeydanur Şan, Manja von Hahn, Jens Strelau, Gabriele Hölzl-Wenig, Claudia Mandl, Francesca Ciccolini
Late in neural development, the expression of growth/differentiation factor (GDF) 15 increases in the germinal epithelium of the murine ganglionic eminence (GE) especially in progenitors with characteristics of neural stem cells (NSCs) and expressing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf9a358b355c02061f71937c989a83f9
https://doi.org/10.1101/2022.12.02.518869
https://doi.org/10.1101/2022.12.02.518869
Autor:
Gudrun A. Rappold, Volker Eckstein, Simone Berkel, Flavia-Bianca Cristian, Manja von Hahn, Christine Unsicker
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-15 (2021)
Scientific Reports
Scientific Reports
SHANK2 mutations have been identified in individuals with neurodevelopmental disorders, including intellectual disability and autism spectrum disorders (ASD). Using CRISPR/Cas9 genome editing, we obtained SH-SY5Y cell lines with frameshift mutations