Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Adrian Schelling"'
Autor:
Marius Costel Alupei, Pallab Maity, Philipp Ralf Esser, Ioanna Krikki, Francesca Tuorto, Rosanna Parlato, Marianna Penzo, Adrian Schelling, Vincent Laugel, Lorenzo Montanaro, Karin Scharffetter-Kochanek, Sebastian Iben
Publikováno v:
Cell Reports, Vol 23, Iss 6, Pp 1612-1619 (2018)
Summary: Retarded growth and neurodegeneration are hallmarks of the premature aging disease Cockayne syndrome (CS). Cockayne syndrome proteins take part in the key step of ribosomal biogenesis, transcription of RNA polymerase I. Here, we identify a m
Externí odkaz:
https://doaj.org/article/98f1ad7eb84b485e8b920342542da1cf
Autor:
Robin Assfalg, Marius Costel Alupei, Maximilian Wagner, Sylvia Koch, Omar Garcia Gonzalez, Adrian Schelling, Karin Scharffetter-Kochanek, Sebastian Iben
Publikováno v:
PLoS ONE, Vol 12, Iss 6, p e0179843 (2017)
The nucleolus has long been considered to be a pure ribosome factory. However, over the last two decades it became clear that the nucleolus is involved in numerous other functions besides ribosome biogenesis. Our experiments indicate that the activit
Externí odkaz:
https://doaj.org/article/591eb3bbe4ea4ff1a21513df0458c341
Autor:
Marius Costel Alupei, Maximilian Wagner, Omar Garcia Gonzalez, Robin Assfalg, Adrian Schelling, Sebastian Iben, Sylvia Koch, Karin Scharffetter-Kochanek
Publikováno v:
PLoS ONE, Vol 12, Iss 6, p e0179843 (2017)
PLoS ONE
PLoS ONE
The nucleolus has long been considered to be a pure ribosome factory. However, over the last two decades it became clear that the nucleolus is involved in numerous other functions besides ribosome biogenesis. Our experiments indicate that the activit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c41e36f17f96176f85ee537b8344335
http://europepmc.org/articles/PMC5479586?pdf=render
http://europepmc.org/articles/PMC5479586?pdf=render
Autor:
Adrian Schelling, Sebastian Iben, Patrick Schäfer, Robin Assfalg, Sylvia Koch, Omar Garcia Gonzalez, Karin Scharffetter-Kochanek
Publikováno v:
Cell Cycle
Mutations in the Cockayne syndrome A (CSA) protein account for 20% of Cockayne syndrome (CS) cases, a childhood disorder of premature aging and early death. Hitherto, CSA has exclusively been described as DNA repair factor of the transcription-couple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d60b5cc9dca88fcdd54d5c765ac1054f
http://europepmc.org/articles/PMC4111694
http://europepmc.org/articles/PMC4111694
Autor:
Omar Garcia Gonzalez, Sylvia Koch, Anton Lebedev, Sebastian Iben, Robin Assfalg, Adrian Schelling
Publikováno v:
Nucleic Acids Research
TFIIH is a multisubunit factor essential for transcription initiation and promoter escape of RNA polymerase II and for the opening of damaged DNA double strands in nucleotide excision repair (NER). In this study, we have analyzed at which step of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd67d88d20a0e24337f88f91a21567eb
http://europepmc.org/articles/PMC3258137
http://europepmc.org/articles/PMC3258137
Autor:
Lorenzo Montanaro, Francesca Tuorto, Philipp Ralf EBer, Sebastian Iben, Rosanna Parlato, Adrian Schelling, Ioanna Krikki, Vincent Laugel, Marius Costel Alupei, Marianna Penzo, Pallab Maity, Karin Scharffetter-Kochanek
Publikováno v:
Journal of Investigative Dermatology. 138:S137
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1342cf2538f27da3fc5be1a2ae5d07f8
https://doi.org/10.1016/j.jid.2018.03.816
https://doi.org/10.1016/j.jid.2018.03.816
Publikováno v:
Technical University of Denmark Orbit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::040b3a0c1749cc010cc30c9e5e7322e6
https://orbit.dtu.dk/en/publications/48157b16-d132-4e15-a1eb-335c660a3f1d
https://orbit.dtu.dk/en/publications/48157b16-d132-4e15-a1eb-335c660a3f1d
