Author Dickmanns, Achim
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2008 | Journal Article
Disease-causing missense mutations affect enzymatic activity, stability and oligomerization of glutaryl-CoA dehydrogenase (GCDH)
Keyser, B.; Muehlhausen, C.; Dickmanns, A.; Christensen, E.; Muschol, N.; Ullrich, K. & Braulke, T. (2008)
Human Molecular Genetics, 17(24) pp. 3854-3863. DOI: https://doi.org/10.1093/hmg/ddn284
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2010 | Journal Article
Crystal structure of a homodimeric 4-thiouridine synthetase-RNA complex
Neumann, P.; Lakomek, K.; Naumann, P.-T.; Dickmanns, A.; Lauhon, C. T. & Ficner, R. (2010)
Acta Crystallographica Section A Foundations of Crystallography, 66(a1) pp. s22-s22. DOI: https://doi.org/10.1107/S0108767310099514
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2010 | Journal Article
Structure of an intramolecular chaperone mediating triple-β-helix folding
Schulz, E. C.; Dickmanns, A.; Urlaub, H.; Schmitt, A.; Mühlenhoff, M.; Stummeyer, K. & Schwarzer, D. et al. (2010)
Acta Crystallographica Section A Foundations of Crystallography, 66(a1) pp. s25-s25. DOI: https://doi.org/10.1107/S0108767310099460
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2018 | Journal Article
Validating Resolution Revolution
Neumann, P.; Dickmanns, A. & Ficner, R. (2018)
Structure, 26(12) pp. 1678. DOI: https://doi.org/10.1016/j.str.2018.10.028
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2018 | Journal Article |
Biallelic mutations in nucleoporin NUP88 cause lethal fetal akinesia deformation sequence
Bonnin, E.; Cabochette, P.; Filosa, A.; Jühlen, R.; Komatsuzaki, S.; Hezwani, M. & Dickmanns, A. et al. (2018)
PLOS Genetics, 14(12) art. e1007845. DOI: https://doi.org/10.1371/journal.pgen.1007845
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2021 | Journal Article | Research Paper |
Bucky Ball Is a Novel Zebrafish Vasa ATPase Activator
Perera, R. P.; Shaikhqasem, A.; Rostam, N.; Dickmanns, A.; Ficner, R. ; Tittmann, K. & Dosch, R. (2021)
Biomolecules, 11(10) pp. 1507. DOI: https://doi.org/10.3390/biom11101507
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2021 | Journal Article | Research Paper |
A meet-up of two second messengers: the c-di-AMP receptor DarB controls (p)ppGpp synthesis in Bacillus subtilis
Krüger, L.; Herzberg, C.; Wicke, D.; Bähre, H.; Heidemann, J. L.; Dickmanns, A. & Schmitt, K. et al. (2021)
Nature Communications, 12(1). DOI: https://doi.org/10.1038/s41467-021-21306-0
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2021 | Journal Article
Expanding the phenotype of NUP85 mutations beyond nephrotic syndrome to primary autosomal recessive microcephaly and Seckel syndrome spectrum disorders
Ravindran, E.; Jühlen, R.; Vieira-Vieira, C. H; Ha, T.; Salzberg, Y.; Fichtman, B. & Luise-Becker, L. et al. (2021)
Human Molecular Genetics, 30(22) pp. 2068-2081. DOI: https://doi.org/10.1093/hmg/ddab160
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2022 | Journal Article
Structural basis for c-di-AMP-dependent regulation of the bacterial stringent response by receptor protein DarB
Heidemann, J. L.; Neumann, P.; Krüger, L.; Wicke, D.; Vinhoven, L.; Linden, A. & Dickmanns, A. et al. (2022)
Journal of Biological Chemistry, art. 102144. DOI: https://doi.org/10.1016/j.jbc.2022.102144
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2023 | Journal Article
Interaction of nucleoporins with nuclear transport receptors: a structural perspective
Kehlenbach, R. H.; Neumann, P.; Ficner, R. & Dickmanns, A. (2023)
Biological Chemistry,. DOI: https://doi.org/10.1515/hsz-2023-0155
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2023 | Journal Article
Structure and function of spliceosomal DEAH-box ATPases
Enders, M.; Neumann, P.; Dickmanns, A. & Ficner, R. (2023)
Biological Chemistry,. DOI: https://doi.org/10.1515/hsz-2023-0157
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2023 | Journal Article |
Case report: Compound heterozygous NUP85 variants cause autosomal recessive primary microcephaly
Ravindran, E.; Lesca, G.; Januel, L.; Goldgruber, L.; Dickmanns, A.; Margot, H. & Kaindl, A. M. (2023)
Frontiers in Neurology, 14. DOI: https://doi.org/10.3389/fneur.2023.1124886
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