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Small Molecule Effectors of Myosin Function.

Manstein DJ, Preller M. Manstein DJ, et al. Among authors: preller m. Adv Exp Med Biol. 2020;1239:61-84. doi: 10.1007/978-3-030-38062-5_5. Adv Exp Med Biol. 2020. PMID: 32451856 Review.

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Myosin structure, allostery, and mechano-chemistry.

Preller M, Manstein DJ. Preller M, et al. Structure. 2013 Nov 5;21(11):1911-22. doi: 10.1016/j.str.2013.09.015. Structure. 2013. PMID: 24210227 Free article. Review.

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Calcium Sensor for Photoacoustic Imaging.

Roberts S, Seeger M, Jiang Y, Mishra A, Sigmund F, Stelzl A, Lauri A, Symvoulidis P, Rolbieski H, Preller M, Deán-Ben XL, Razansky D, Orschmann T, Desbordes SC, Vetschera P, Bach T, Ntziachristos V, Westmeyer GG. Roberts S, et al. Among authors: preller m. J Am Chem Soc. 2018 Feb 28;140(8):2718-2721. doi: 10.1021/jacs.7b03064. Epub 2017 Oct 16. J Am Chem Soc. 2018. PMID: 28945084

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C-mannosylation supports folding and enhances stability of thrombospondin repeats.

Shcherbakova A, Preller M, Taft MH, Pujols J, Ventura S, Tiemann B, Buettner FF, Bakker H. Shcherbakova A, et al. Among authors: preller m. Elife. 2019 Dec 23;8:e52978. doi: 10.7554/eLife.52978. Elife. 2019. PMID: 31868591 Free PMC article.

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A role for actin flexibility in thin filament-mediated contractile regulation and myopathy.

Viswanathan MC, Schmidt W, Franz P, Rynkiewicz MJ, Newhard CS, Madan A, Lehman W, Swank DM, Preller M, Cammarato A. Viswanathan MC, et al. Among authors: preller m. Nat Commun. 2020 May 15;11(1):2417. doi: 10.1038/s41467-020-15922-5. Nat Commun. 2020. PMID: 32415060 Free PMC article.

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Rare germline variants in the E-cadherin gene CDH1 are associated with the risk of brain tumors of neuroepithelial and epithelial origin.

Förster A, Brand F, Banan R, Hüneburg R, Weber CAM, Ewert W, Kronenberg J, Previti C, Elyan N, Beyer U, Martens H, Hong B, Bräsen JH, Erbersdobler A, Krauss JK, Stangel M, Samii A, Wolf S, Preller M, Aretz S, Wiese B, Hartmann C, Weber RG. Förster A, et al. Among authors: preller m. Acta Neuropathol. 2021 Jul;142(1):191-210. doi: 10.1007/s00401-021-02307-1. Epub 2021 Apr 30. Acta Neuropathol. 2021. PMID: 33929593 Free PMC article.

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SPG7 mutations in amyotrophic lateral sclerosis: a genetic link to hereditary spastic paraplegia.

Osmanovic A, Widjaja M, Förster A, Weder J, Wattjes MP, Lange I, Sarikidi A, Auber B, Raab P, Christians A, Preller M, Petri S, Weber RG. Osmanovic A, et al. Among authors: preller m. J Neurol. 2020 Sep;267(9):2732-2743. doi: 10.1007/s00415-020-09861-w. Epub 2020 May 23. J Neurol. 2020. PMID: 32447552 Free PMC article.

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In vivo efficacy of mutant IDH1 inhibitor HMS-101 and structural resolution of distinct binding site.

Chaturvedi A, Goparaju R, Gupta C, Weder J, Klünemann T, Araujo Cruz MM, Kloos A, Goerlich K, Schottmann R, Othman B, Struys EA, Bähre H, Grote-Koska D, Brand K, Ganser A, Preller M, Heuser M. Chaturvedi A, et al. Among authors: preller m. Leukemia. 2020 Feb;34(2):416-426. doi: 10.1038/s41375-019-0582-x. Epub 2019 Oct 4. Leukemia. 2020. PMID: 31586149 Free PMC article.

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Unraveling a Force-Generating Allosteric Pathway of Actomyosin Communication Associated with ADP and P_i Release.

Franz P, Ewert W, Preller M, Tsiavaliaris G. Franz P, et al. Among authors: preller m. Int J Mol Sci. 2020 Dec 24;22(1):104. doi: 10.3390/ijms22010104. Int J Mol Sci. 2020. PMID: 33374308 Free PMC article.

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Structural and Computational Insights into a Blebbistatin-Bound Myosin•ADP Complex with Characteristics of an ADP-Release Conformation along the Two-Step Myosin Power Stoke.

Ewert W, Franz P, Tsiavaliaris G, Preller M. Ewert W, et al. Among authors: preller m. Int J Mol Sci. 2020 Oct 8;21(19):7417. doi: 10.3390/ijms21197417. Int J Mol Sci. 2020. PMID: 33049993 Free PMC article.

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