Sven Thoms

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 14

Top Topics

Saccharomyces Cerevisiae

Congenital Heart Disease

Crystal Structure

Top Venues

Journal of molecular medicine (Berlin, Germany)

Journal of cell science

Scientific reports

This page only lists publications with an associated author ORCID identifier.

Publications

Dennis Lebeda, Adrian Fierenz, Lina Werfel, Rina Rosin-Arbesfeld, Julia Hofhuis, Sven Thoms
Systematic and quantitative analysis of stop codon readthrough in Rett syndrome nonsense mutations. Journal of molecular medicine (Berlin, Germany) 102 (5) (2024)
Dennis Lebeda, Adrian Fierenz, Lina Werfel, Rina Rosin-Arbesfeld, Julia Hofhuis, Sven Thoms
Systematic and quantitative analysis of stop codon readthrough in Rett syndrome nonsense mutations. Journal of molecular medicine (Berlin, Germany) 102 (5) (2024)
Dennis Lebeda, Adrian Fierenz, Lina Werfel, Rina Rosin-Arbesfeld, Julia Hofhuis, Sven Thoms
Systematic and quantitative analysis of stop codon readthrough in Rett syndrome nonsense mutations. Journal of molecular medicine (Berlin, Germany) 102 (5) (2024)
Dennis Lebeda, Adrian Fierenz, Lina Werfel, Rina Rosin-Arbesfeld, Julia Hofhuis, Sven Thoms
Systematic and quantitative analysis of stop codon readthrough in Rett syndrome nonsense mutations. Journal of molecular medicine (Berlin, Germany) 102 (5) (2024)
Dennis Lebeda, Adrian Fierenz, Lina Werfel, Rina Rosin-Arbesfeld, Julia Hofhuis, Sven Thoms
Systematic and quantitative analysis of stop codon readthrough in Rett syndrome nonsense mutations. Journal of molecular medicine (Berlin, Germany) (2024)
Dennis Lebeda, Adrian Fierenz, Lina Werfel, Rina Rosin-Arbesfeld, Julia Hofhuis, Sven Thoms
Systematic and quantitative analysis of stop codon readthrough in Rett syndrome nonsense mutations. Journal of molecular medicine (Berlin, Germany) 102 (5) (2024)
Esmeralda Nava, Britta Hartmann, Larissa Boxheimer, Andrea Capone Mori, Jean-Marc Nuoffer, Yelena Sargsyan, Sven Thoms, Hendrik Rosewich, Eugen Boltshauser
How to Detect Isolated PEX10-Related Cerebellar Ataxia? Neuropediatrics 53 (3) (2022)
Yelena Sargsyan, Uta Bickmeyer, Christine S Gibhardt, Katrin Streckfuss-Bömeke, Ivan Bogeski, Sven Thoms
Peroxisomes contribute to intracellular calcium dynamics in cardiomyocytes and non-excitable cells. Life science alliance 4 (9) (2021)
Mirco Schilff, Yelena Sargsyan, Julia Hofhuis, Sven Thoms
Stop Codon Context-Specific Induction of Translational Readthrough. Biomolecules 11 (7) (2021)
Kareem Soliman, Fabian Göttfert, Hendrik Rosewich, Sven Thoms, Jutta Gärtner
Super-resolution imaging reveals the sub-diffraction phenotype of Zellweger Syndrome ghosts and wild-type peroxisomes. Scientific reports 8 (1) (2018)
Julia Hofhuis, Fabian Schueren, Christopher Nötzel, Thomas Lingner, Jutta Gärtner, Olaf Jahn, Sven Thoms
The functional readthrough extension of malate dehydrogenase reveals a modification of the genetic code. Open biology 6 (11) (2017)
Ido Yofe, Kareem Soliman, Silvia G Chuartzman, Bruce Morgan, Uri Weill, Eden Yifrach, Tobias P Dick, Sara J Cooper, Christer S Ejsing, Maya Schuldiner, Einat Zalckvar, Sven Thoms
Pex35 is a regulator of peroxisome abundance. Journal of cell science 130 (4) (2017)
Julia Hofhuis, Kristina Bersch, Ronja Büssenschütt, Marzena Drzymalski, David Liebetanz, Viacheslav O Nikolaev, Stefan Wagner, Lars S Maier, Jutta Gärtner, Lars Klinge, Sven Thoms
Dysferlin mediates membrane tubulation and links T-tubule biogenesis to muscular dystrophy. Journal of cell science 130 (5) (2017)
Fabian Schueren, Sven Thoms
Functional Translational Readthrough: A Systems Biology Perspective. PLoS genetics 12 (8) (2016)