Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Birgit Rau"'
Autor:
Andrea Christ, Öznur Yilmaz, Roger Sandhoff, Henning Kleinert, Birgit Rau, Benjamin Odermatt, Britta Eiberger, Matthias Eckhardt, Anna Sophia Japp, Alexander Harder, Felix Häberlein, Angelika Zoons, Ulrich Kubitscheck, Bhuvaneswari Nagarajan, Dieter Hartmann, Enrico Mingardo
Publikováno v:
Glia. 68:509-527
In contrast to humans and other mammals, zebrafish can successfully regenerate and remyelinate central nervous system (CNS) axons following injury. In addition to common myelin proteins found in mammalian myelin, 36K protein is a major component of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a835468599c88bdaa69f5201f783d36
https://doi.org/10.1002/glia.23732
https://doi.org/10.1002/glia.23732
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-12 (2023)
Abstract Seminal studies suggest that being mimicked increases experienced social closeness and prosocial behavior to a mimicking confederate (i.e., interaction partner). Here we reexamine these results by considering the role of empathy-related trai
Externí odkaz:
https://doaj.org/article/cce9f91d6dc94a168802c59b7ac0706b
Autor:
Karsten Haug, Maike Warnstedt, Alexi K. Alekov, Thomas Sander, Alfredo Ramírez, Barbara Poser, Snezana Maljevic, Simon Hebeisen, Christian Kubisch, Johannes Rebstock, Steve Horvath, Kerstin Hallmann, Joern S. Dullinger, Birgit Rau, Fritz Haverkamp, Stefan Beyenburg, Herbert Schulz, Dieter Janz, Bernd Giese, Gerhard Müller-Newen, Peter Propping, Christian E. Elger, Christoph Fahlke, Holger Lerche, Armin Heils
Publikováno v:
Nature Genetics. 33:527-532
Idiopathic generalized epilepsy (IGE) is an inherited neurological disorder affecting about 0.4% of the world's population. Mutations in ten genes causing distinct forms of idiopathic epilepsy have been identified so far, but the genetic basis of man
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::326f481096221815c6d7b5f4e4358ff7
https://doi.org/10.1038/ng1121
https://doi.org/10.1038/ng1121
Autor:
Stefan Beyenburg, Karsten Haug, Christian E. Elger, Steve Horvath, Peter Propping, Joern S. Dullinger, Christian Kubisch, Kerstin Hallmann, Thomas Sander, Birgit Rau, Armin Heils
Publikováno v:
Epilepsy Research. 42:57-62
Idiopathic generalized epilepsy (IGE) comprises a heterogeneous group of disorders, in which a high genetic predisposition and a complex mode of inheritance have been suggested. Recent identification of ion channel gene mutations in Mendelian epilept
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9298fe5c91ef0b09c348fcb835ce033
https://doi.org/10.1016/s0920-1211(00)00164-9
https://doi.org/10.1016/s0920-1211(00)00164-9
Autor:
Peter Propping, Birgit Rau, Armin Heils, A Barnekow, Joern S. Dullinger, Christian E. Elger, Thomas Sander, Karsten Haug, Kerstin Hallmann, Stefan Beyenburg, M.J Lentze, J Kremerskothen
Publikováno v:
Molecular and Cellular Probes. 14:255-260
Idiopathic generalized epilepsy (IGE) comprises a heterogeneous group of disorders, in which a high genetic predisposition and a complex mode of inheritance have been suggested. However, genes, which confer liability to common IGE subtypes including
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dc9d30c2cdc28fddc7f461310fc8ac4
https://doi.org/10.1006/mcpr.2000.0314
https://doi.org/10.1006/mcpr.2000.0314
Autor:
Steve Horvath, Peter Propping, Christian E. Elger, Armin Heils, Heike Pfeiffer, Birgit Rau, Joana Cobilanschi, Nikola Tilgen
Publikováno v:
Neuroscience Letters. 334:68-70
Recently, an association between a regulatory polymorphism in the gene encoding the pro-inflammatory cytokine interleukin (IL)-1β and febrile convulsions (FC) has been reported. In this study we attempted to confirm these findings in a sample consis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5d9808ac6d83e334df45dcadcf0107a
https://doi.org/10.1016/s0304-3940(02)01069-8
https://doi.org/10.1016/s0304-3940(02)01069-8
Autor:
Karsten Haug, Joern S. Dullinger, Thomas Sander, Peter Propping, Kerstin Hallmann, Christian E. Elger, Armin Heils, Birgit Rau
Publikováno v:
NeuroReport. 11:2687-2689
Recent identification of ion channel gene mutations in Mendelian epilepsies suggests that genetically driven neuronal hyperexcitability plays an important role in epileptogenesis. In this study, we tested the hypothesis that genetic variation in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c2028f281cdd0178725c26fd1ad6932
https://doi.org/10.1097/00001756-200008210-00016
https://doi.org/10.1097/00001756-200008210-00016
Autor:
Dieter Janz, Peter Propping, Gerhard Müller-Newen, Alexi K. Alekov, Stefan Beyenburg, Fritz Haverkamp, JS Dullinger, Maike Warnstedt, Ailing A. Kleefuss-Lie, Holger Lerche, Birgit Rau, Christian Kubisch, Johannes Rebstock, Karsten Haug, Waltraut Friedl, Steve Horvath, Christoph Fahlke, Kerstin Hallmann, Thomas Sander, Bernd Giese, Simon Hebeisen, Barbara Poser, Snezana Maljevic, Alfredo Ramirez, Christian E. Elger, Sven Cichon, Herbert Schulz
Publikováno v:
Nature genetics. 41(9)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65e88432c94562022735fbd9b7d30719
https://pubmed.ncbi.nlm.nih.gov/20037607
https://pubmed.ncbi.nlm.nih.gov/20037607
Autor:
Joern S. Dullinger, Karsten Haug, Sabine Muth, Johannes Rebstock, Armin Heils, Christian E. Elger, Birgit Rau, Fritz Haverkamp, Peter Propping, Heike Pfeiffer, Kerstin Hallmann
Publikováno v:
Epilepsy research. 47(3)
We tested the hypothesis that genetic variation in the human sodium channel gene SCN2A confers liability to idiopathic generalized epilepsy (IGE). We performed a systematic search for mutations in 46 familial IGE cases and detected three novel polymo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6afe5e7e2cd59fe9ca4db06c3af8829b
https://pubmed.ncbi.nlm.nih.gov/11738931
https://pubmed.ncbi.nlm.nih.gov/11738931
Autor:
Maike Warnstedt, Bernd Giese, Joern S. Dullinger, Barbara Poser, Simon Hebeisen, Karsten Haug, Thomas Sander, Gerhard Müller-Newen, Alexi K. Alekov, Christian E. Elger, Herbert Schulz, Christoph Fahlke, Fritz Haverkamp, Birgit Rau, Peter Propping, Stefan Beyenburg, Holger Lerche, Alfredo Ramirez, Johannes Rebstock, Christian Kubisch, Snezana Maljevic, Dieter Janz, Steve Horvath, Kerstin Hallmann, Armin Heils
Publikováno v:
Nature Genetics. 41:1043-1043
Idiopathic generalized epilepsy (IGE) is an inherited neurological disorder affecting about 0.4% of the world's population. Mutations in ten genes causing distinct forms of idiopathic epilepsy have been identified so far, but the genetic basis of man
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb60369d8f52476c69b7f3930c9db903
https://doi.org/10.1038/ng0909-1043
https://doi.org/10.1038/ng0909-1043