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pro vyhledávání: '"Agnes Molnar-Kasza"'
Autor:
Agnes Molnar-Kasza, Barbara Hinteregger, Joerg Neddens, Roland Rabl, Stefanie Flunkert, Birgit Hutter-Paier
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 14 (2021)
Amyotrophic lateral sclerosis (ALS) still depicts an incurable and devastating disease. Drug development efforts are mostly based on superoxide dismutase 1 gene (SOD1)-G93A mice that present a very strong and early phenotype, allowing only a short ti
Externí odkaz:
https://doaj.org/article/6cfbeb8bdd8e4c9fa1a428a29d137ea9
Autor:
Livia Breznik, Spyridon Sideromenos, Agnes Molnar-Kasza, Roland Rabl, Stefanie Flunkert, Manuela Prokesch, Birgit Hutter-Paier
Publikováno v:
Molecular Genetics and Metabolism. 135:S25-S26
Autor:
Roland Rabl, Joerg Neddens, Barbara Hinteregger, Agnes Molnar-Kasza, Stefanie Flunkert, Birgit Hutter-Paier
Publikováno v:
Frontiers in Molecular Neuroscience
Frontiers in Molecular Neuroscience, Vol 14 (2021)
Frontiers in Molecular Neuroscience, Vol 14 (2021)
Amyotrophic lateral sclerosis (ALS) still depicts an incurable and devastating disease. Drug development efforts are mostly based on superoxide dismutase 1 gene (SOD1)-G93A mice that present a very strong and early phenotype, allowing only a short ti
Autor:
Petra Heinrich, Stefanie Flunkert, Birgit Hutter-Paier, Tina Loeffler, Agnes Molnar-Kasza, Stephan Kurat
Publikováno v:
Brain Research. 1761:147396
Huntington’s disease is known to be a purely genetic disease based on an expansion of a CAG base triplet repeat in the coding region of the Huntingtin gene. Some years ago, researchers were able to introduce the extensive full-length gene sequence