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Sven Thoms (born 1970 in Geldern) is a German biochemist.
Thoms's research areas are peroxisomes, translational readthrough, dysferlin,[1] and rare diseases caused by defective cell organelles. Thoms and colleagues discovered a new isoform of lactate dehydrogenase that arises from translational readthrough.[2]
References
edit- ^ Hofhuis, Julia; Bersch, Kristina; Büssenschütt, Ronja; Drzymalski, Marzena; Liebetanz, David; Nikolaev, Viacheslav O.; Wagner, Stefan; Maier, Lars S.; Gärtner, Jutta; Klinge, Lars; Thoms, Sven (2017-01-01). "Dysferlin mediates membrane tubulation and links T-tubule biogenesis to muscular dystrophy". Journal of Cell Science. 130 (5): 841–852. doi:10.1242/jcs.198861. ISSN 1477-9137. PMID 28104817. S2CID 6644085.
- ^ Schueren, Fabian; Lingner, Thomas; George, Rosemol; Hofhuis, Julia; Dickel, Corinna; Gärtner, Jutta; Thoms, Sven (2014-09-23). Sonenberg, Nahum (ed.). "Peroxisomal lactate dehydrogenase is generated by translational readthrough in mammals". eLife. 3: e03640. doi:10.7554/eLife.03640. ISSN 2050-084X. PMC 4359377. PMID 25247702.
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