Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Josefine Sell"'
Autor:
Murat Kirtay, Josefine Sell, Christian Marx, Holger Haselmann, Mihai Ceanga, Zhong-Wei Zhou, Vahid Rahmati, Joanna Kirkpatrick, Katrin Buder, Paulius Grigaravicius, Alessandro Ori, Christian Geis, Zhao-Qi Wang
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-18 (2021)
Ataxia Telangiectasia and Rad3-related (ATR) is a key regulator of replication stress response; yet, mutations within the ATR gene cause human ATR-Seckel Syndrome associated with microcephaly and intellectual disability. Here, the authors show neuron
Externí odkaz:
https://doaj.org/article/2dd9c267ac854fe5bdc2ba175941b03b
Autor:
Josefine Sell, Vahid Rahmati, Marin Kempfer, Sarosh R. Irani, Andreas Ritzau-Jost, Stefan Hallermann, Christian Geis
Publikováno v:
Neurology - Neuroimmunology Neuroinflammation. 10:e200096
Background and ObjectivesAutoantibodies to leucine-rich glioma inactivated protein 1 (LGI1) cause an autoimmune limbic encephalitis with frequent focal seizures and anterograde memory dysfunction. LGI1 is a neuronal secreted linker protein with 2 fun
Autor:
Zhao-Qi Wang, Holger Haselmann, Vahid Rahmati, Paulius Grigaravicius, Joanna Kirkpatrick, Mihai Ceanga, Christian Geis, Zhong-Wei Zhou, Murat Kirtay, Katrin Buder, Josefine Sell, Christian Marx, Alessandro Ori
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-18 (2021)
Nature Communications
Nature Communications
Ataxia Telangiectasia and Rad3-related (ATR) protein, as a key DNA damage response (DDR) regulator, plays an essential function in response to replication stress and controls cell viability. Hypomorphic mutations of ATR cause the human ATR-Seckel syn
Publikováno v:
Expert opinion on therapeutic targets. 25(1)
Antibody-mediated encephalitides (AE) with pathogenic autoantibodies (aAB) against neuronal surface antigens are a growing group of diseases characterized by antineuronal autoimmunity in the brain. AE patients typically present with rapidly progressi
Autor:
Ha-Yeun, Chung, Jonathan, Wickel, Annika, Voss, Mihai, Ceanga, Josefine, Sell, Otto W, Witte, Christian, Geis
Publikováno v:
Medicine
Supplemental Digital Content is available in the text
Rationale: Anti-IgLON5 disease is a complex neurological illness which is characterized by progressive sleep and movement disorders and defined by specific autoantibodies to IgLON5. We here d
Rationale: Anti-IgLON5 disease is a complex neurological illness which is characterized by progressive sleep and movement disorders and defined by specific autoantibodies to IgLON5. We here d