Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Zoe Dobler"'
Autor:
Jasmin Morandell, Lena A. Schwarz, Bernadette Basilico, Saren Tasciyan, Georgi Dimchev, Armel Nicolas, Christoph Sommer, Caroline Kreuzinger, Christoph P. Dotter, Lisa S. Knaus, Zoe Dobler, Emanuele Cacci, Florian K. M. Schur, Johann G. Danzl, Gaia Novarino
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-22 (2021)
De novo loss of function mutations in the ubiquitin ligase-encoding gene Cullin3 (CUL3) lead to autism spectrum disorder (ASD). Here, the authors show that Cul3 is essential to regulate neuronal migration by tightly regulating Plastin3 (Pls3). Pls3 c
Externí odkaz:
https://doaj.org/article/876fc6b3ec944da69828b7d04ddbbfcd
Autor:
Lena A. Schwarz, Saren Tasciyan, Jasmin Morandell, Florian K. M. Schur, Bernadette Basilico, Caroline Kreuzinger, Christoph P. Dotter, Johann G. Danzl, Armel Nicolas, Georgi Dimchev, Lisa S. Knaus, Christoph Sommer, Emanuele Cacci, Gaia Novarino, Zoe Dobler
Publikováno v:
bioRxiv
Nature Communications, Vol 12, Iss 1, Pp 1-22 (2021)
Nature Communications
Nature Communications, Vol 12, Iss 1, Pp 1-22 (2021)
Nature Communications
De novo loss of function mutations in the ubiquitin ligase-encoding gene Cullin3 (CUL3) lead to autism spectrum disorder (ASD). In mouse, constitutive Cul3 haploinsufficiency leads to motor coordination deficits as well as ASD-relevant social and cog
Autor:
Florian K. M. Schur, Jasmin Morandell, Gaia Novarino, Christoph P. Dotter, Caroline Kreuzinger, Christoph Sommer, Johann G. Danzl, Saren Tasciyan, Lena A. Schwarz, Bernadette Basilico, Georgi Dimchev, Emanuele Cacci, Armel Nicolas, Zoe Dobler, Lisa S. Knaus
Publikováno v:
SSRN Electronic Journal.
De novo loss of function mutations in the ubiquitin ligase-encoding gene Cullin3 (CUL3) lead to autism spectrum disorder (ASD). Here, we used Cul3 mouse models to evaluate the consequences of Cul3 mutations in vivo. Our results show that Cul3 haploin