Hubert Becker
Affiliations: | Génétique Moléculaire, Génomique et Microbiologie | Université de Strasbourg |
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"Hubert Becker"Parents
Sign in to add mentorDaniel Kern | grad student | Université de Strasbourg | |
Dieter Söll | post-doc | Yale (Chemistry Tree) |
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Publications
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Filée J, Becker HF, Mellottee L, et al. (2023) Bacterial origins of thymidylate metabolism in Asgard archaea and Eukarya. Nature Communications. 14: 838 |
Verdura E, Senger B, Raspall-Chaure M, et al. (2022) Loss of seryl-tRNA synthetase () causes complex spastic paraplegia and cellular senescence. Journal of Medical Genetics |
Kabala AM, Binko K, Godard F, et al. (2022) Assembly-dependent translation of subunits 6 (Atp6) and 9 (Atp9) of ATP synthase in yeast mitochondria. Genetics |
Enkler L, Rinaldi B, de Craene JO, et al. (2021) Cex1 is a component of the COPI intracellular trafficking machinery. Biology Open. 10 |
Hemmerle M, Wendenbaum M, Grob G, et al. (2020) Noncanonical inputs and outputs of tRNA aminoacylation. The Enzymes. 48: 117-147 |
Manole A, Efthymiou S, O'Connor E, et al. (2020) De Novo and Bi-allelic Pathogenic Variants in NARS1 Cause Neurodevelopmental Delay Due to Toxic Gain-of-Function and Partial Loss-of-Function Effects. American Journal of Human Genetics |
Bader G, Enkler L, Araiso Y, et al. (2020) Assigning mitochondrial localization of dual localized proteins using a yeast Bi-Genomic Mitochondrial-Split-GFP. Elife. 9 |
Yakobov N, Fischer F, Mahmoudi N, et al. (2020) RNA-dependent sterol aspartylation in fungi. Proceedings of the National Academy of Sciences of the United States of America |
Scheidecker S, Bär S, Stoetzel C, et al. (2019) Mutations in KARS cause a severe neurological and neurosensory disease with optic neuropathy. Human Mutation |
Yakobov N, Debard S, Fischer F, et al. (2017) Cytosolic aminoacyl-tRNA synthetases: unanticipated relocations for unexpected functions. Biochimica Et Biophysica Acta |