Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Paul Atigbire"'
Autor:
Christine Vössing, Paul Atigbire, Jannis Eilers, Fenja Markus, Knut Stieger, Fei Song, John Neidhardt
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 7, p 3583 (2021)
X-linked retinitis pigmentosa (XLRP) is frequently caused by mutations in the retinitis pigmentosa GTPase regulator (RPGR) gene. A complex splicing process acts on the RPGR gene resulting in three major isoforms: RPGRex1-19, RPGRORF15 and RPGRskip14/
Externí odkaz:
https://doaj.org/article/6b740196e9ab4242a7ea5b0feaa898a6
Autor:
Annika Kannengießer, Patricia Näder, Marta Owczarek-Lipska, Paul Atigbire, Christine Vössing, Fenja Markus, G. Christoph Korenke, Eva Bültmann, John Neidhardt, Alexander Scholten
Publikováno v:
Journal of Human Genetics
Heterotopia is a brain malformation caused by a failed migration of cortical neurons during development. Clinical symptoms of heterotopia vary in severity of intellectual disability and may be associated with epileptic disorders. Abnormal neuronal mi
Autor:
Katja Müller, Hans-Dieter Arndt, Peter Hemmerich, Torsten Kroll, Koret Hirschberg, Christoph Kaether, Paul Atigbire, Olga Shomron, Christian Hoischen, Torben Mentrup, Richard Nohl, Yoji Yonemura, Andreas Krämer, Xiaolin Li, Talitha Feuerhake
Publikováno v:
Journal of Cell Science.
Export out of the endoplasmic reticulum (ER) involves the Sar1 and COPII machinery acting at ER exit sites (ERES). Whether and how cargo proteins are recruited upstream of Sar1 and COPII is unclear. Two models are conceivable, a recruitment model whe