Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Christine Leibiger"'
Autor:
Christine Leibiger, Jana Deisel, Andreas Aufschnaiter, Stefanie Ambros, Maria Tereshchenko, Bert M. Verheijen, Sabrina Büttner, Ralf J. Braun
Publikováno v:
Microbial Cell, Vol 5, Iss 4, Pp 212-214 (2018)
The accumulation of protein aggregates in neurons is a typical pathological hallmark of the motor neuron disease amyotrophic lateral sclerosis (ALS) and of frontotemporal dementia (FTD). In many cases, these aggregates are composed of the 43 kDa TAR
Externí odkaz:
https://doaj.org/article/0fc3323040ed48058962ad0a9d04384b
Autor:
Ralf J. Braun, Cornelia Sommer, Christine Leibiger, Romina J.G. Gentier, Verónica I. Dumit, Katrin Paduch, Tobias Eisenberg, Lukas Habernig, Gert Trausinger, Christoph Magnes, Thomas Pieber, Frank Sinner, Jörn Dengjel, Fred W. van Leeuwen, Guido Kroemer, Frank Madeo
Publikováno v:
Cell Reports, Vol 10, Iss 9, Pp 1557-1571 (2015)
Neuronal accumulation of UBB+1, a frameshift variant of ubiquitin B, is a hallmark of Alzheimer’s disease (AD). How UBB+1 contributes to neuronal dysfunction remains elusive. Here, we show that in brain regions of AD patients with neurofibrillary t
Externí odkaz:
https://doaj.org/article/82827895d6f54a068f30299b67cf92a1
Autor:
Ralf J. Braun, Cornelia Sommer, Christine Leibiger, Romina J.G. Gentier, Verónica I. Dumit, Katrin Paduch, Tobias Eisenberg, Lukas Habernig, Gert Trausinger, Christoph Magnes, Thomas Pieber, Frank Sinner, Jörn Dengjel, Fred W. van Leeuwen, Guido Kroemer, Frank Madeo
Publikováno v:
Microbial Cell, Vol 2, Iss 4, Pp 136-138 (2015)
Impaired protein degradation and mitochondrial dysfunction are believed to contribute to neurodegenerative disorders, including Alzheimer disease (AD). In patients suffering from non-hereditary AD, UBB+1, the frameshift variant of ubiquitin B, accumu
Externí odkaz:
https://doaj.org/article/d3db5e16de364cd0aa782086fbc8062a
Autor:
Maria Tereshchenko, Stefanie Ambros, Bert M. Verheijen, Sabrina Büttner, Christine Leibiger, Ralf J. Braun, Jana Deisel, Andreas Aufschnaiter
Publikováno v:
Microbial Cell
The accumulation of protein aggregates in neurons is a typical pathological hallmark of the motor neuron disease amyotrophic lateral sclerosis (ALS) and of frontotemporal dementia (FTD). In many cases, these aggregates are composed of the 43 kDa TAR
Autor:
Jana Deisel, Sabrina Büttner, Bert M. Verheijen, Andreas Aufschnaiter, Christine Leibiger, Maria Tereshchenko, Ralf J. Braun, Stefanie Ambros
Publikováno v:
Microbial Cell, Vol 5, Iss 4, Pp 212-214 (2018)
The accumulation of protein aggregates in neurons is a typical pathological hallmark of the motor neuron disease amyotrophic lateral sclerosis (ALS) and of frontotemporal dementia (FTD). In many cases, these aggregates are composed of the 43 kDa TAR
Autor:
Katrin Paduch, Verónica I. Dumit, Guido Kroemer, Tobias Eisenberg, Frank Madeo, Fred W. van Leeuwen, Frank Sinner, Gert Trausinger, Lukas Habernig, Thomas R. Pieber, Christine Leibiger, Christoph Magnes, Jörn Dengjel, Cornelia Sommer, Romina J.G. Gentier, Ralf J. Braun
Publikováno v:
Cell Reports
Microbial Cell
Microbial Cell, Vol 2, Iss 4, Pp 136-138 (2015)
Cell Reports, 10(9), 1557-1571. Cell Press
Cell Reports, Vol 10, Iss 9, Pp 1557-1571 (2015)
Microbial Cell
Microbial Cell, Vol 2, Iss 4, Pp 136-138 (2015)
Cell Reports, 10(9), 1557-1571. Cell Press
Cell Reports, Vol 10, Iss 9, Pp 1557-1571 (2015)
Summary Neuronal accumulation of UBB+1, a frameshift variant of ubiquitin B, is a hallmark of Alzheimer’s disease (AD). How UBB+1 contributes to neuronal dysfunction remains elusive. Here, we show that in brain regions of AD patients with neurofibr
Publikováno v:
Mutagenesis. 28:145-151
The comet assay is increasingly used to measure the repair of various types of DNA damage. Modifications of the stand- ard protocol have been introduced to determine the repair capacity of specific DNA repair pathways by the removal of pathway-specif
Autor:
Michael Glei, Hasmik Mkrtchyan, Thomas Liehr, Christine Leibiger, Nadezda Kosyakova, Vladimir A. Trifonov
Publikováno v:
Journal of Histochemistry and Cytochemistry
Since being established in 1963, the murine fibroblast cell line NIH 3T3 has been used in thousands of studies. NIH 3T3 immortalized spontaneously and became tetraploid shortly after its establishment. Here we report the first molecular cytogenetic c