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The EMBO Journal|February 16, 2002
Role of the ubiquitin-selective CDC48(UFD1/NPL4 )chaperone (segregase) in ERAD of OLE1 and other substratesSigurd Braun, Kai Matuschewski, Michael Rape, et al.Methods in Molecular Biology (Clifton, N.J.)|April 15, 2017
Dual Reporter Systems for the Analysis of Translational Readthrough in MammalsJulia Hofhuis, Severin Dieterle, Rosemol George, et al.Scientific Reports|May 19, 2018
Super-resolution imaging reveals the sub-diffraction phenotype of Zellweger Syndrome ghosts and wild-type peroxisomesKareem Soliman, Fabian Göttfert, Hendrik Rosewich, et al.Eukaryotic Cell|April 12, 2011
The putative Saccharomyces cerevisiae hydrolase Ldh1p is localized to lipid dropletsSven Thoms, Mykhaylo O Debelyy, Melanie Connerth, et al.Eukaryotic Cell|April 12, 2011
Involvement of the Saccharomyces cerevisiae hydrolase Ldh1p in lipid homeostasisMykhaylo O Debelyy, Sven Thoms, Melanie Connerth, et al.Scientific Reports|December 3, 2015
Conserved targeting information in mammalian and fungal peroxisomal tail-anchored proteinsJudith Buentzel, Fabio Vilardi, Amelie Lotz-Havla, et al.Journal of Structural Biology|July 12, 2011
The unusual extended C-terminal helix of the peroxisomal α/β-hydrolase Lpx1 is involved in dimer contacts but dispensable for dimerizationSven Thoms, Julia Hofhuis, Christian Thöing, et al.BMC Medical Genetics|August 18, 2011
Characterization of two common 5' polymorphisms in PEX1 and correlation to survival in PEX1 peroxisome biogenesis disorder patientsSven Thoms, Sabine Grønborg, Jana Rabenau, et al.The FEBS Journal|January 18, 2008
Lpx1p is a peroxisomal lipase required for normal peroxisome morphologySven Thoms, Mykhaylo O Debelyy, Katja Nau, et al.Journal of Molecular Medicine (Berlin, Germany)|March 2, 2024
Systematic and quantitative analysis of stop codon readthrough in Rett syndrome nonsense mutationsDennis Lebeda, Adrian Fierenz, Lina Werfel, et al.Pageof 6