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Boschann, F.; Moreno, D. A.; Mensah, M. A.; Sczakiel, H. L.; Skipalova , K.; Holtgrewe , M.; Mundlos, S.; Fischer-Zirnsak, B.: Xq27.1 palindrome mediated interchromosomal insertion likely causes familial congenital bilateral laryngeal abductor paralysis (Plott syndrome). Journal of Human Genetics 2022 (2022)
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Pei, Y.; Forstmeier, W.; Ruiz-Ruano, F. J.; Mueller, J. C.; Cabrero, J.; Camacho, J. P. M.; Alché, J. D.; Franke, A.; Hoeppner, M.; Börno, S. et al.; Gessara, I.; Hertel, M.; Teltscher, K.; Knief, U.; Suh, A.; Kempenaers, B.: Occasional paternal inheritance of the germline-restricted chromosome in songbirds. Proceedings of the National Academy of Sciences of the United States of America 119 (4), e2103960119 (2022)
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Pour, M.; Sampath Kumar, A.; Farag, N.; Bolondi, A.; Kretzmer, H.; Walther, M.; Wittler, L.; Meissner, A.; Nachman, I.: Emergence and patterning dynamics of mouse-definitive endoderm. iScience 25 (1), (1):103556 (2022)
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Sivkina, A. L.; Karlova, M. G.; Valieva, M. E.; McCullough, L. L.; Formosa, T.; Shaytan, A. K.; Feofanov, A. V.; Kirpichnikov, M. P.; Sokolova, O. S.; Studitsky, V. M.: Electron microscopy analysis of ATP-independent nucleosome unfolding by FACT. Communications Biology 5 (1), (1):2 (2022)
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Gjaltema, R.; Schwämmle, T.; Kautz, P.; Robson, M.; Schöpflin, R.; Lustig, L. R.; Brandenburg, L.; Dunkel, I.; Vechiatto, C.; Ntini, E. et al.; Mutzel, V.; Schmiedel, V.; Marsico, A.; Mundlos, S.; Schulz, E. G.: Distal and proximal cis-regulatory elements sense X chromosome dosage and developmental state at the Xist locus. Molecular Cell 82, pp. 1 - 19 (2022)
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Zi, Z.; Li, Y.: Optogenetic Control of TGF-β Signaling. In: TGF-Beta Signaling, pp. 113 - 124 (Eds. Zi, Z.; Liu, Xuedong). Humana Press, Totowa. New Jersey (2022)
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Deng, D.; Zi, Z.: Absolute Quantification of TGF-β Signaling Proteins Using Quantitative Western Blot. In: TGF-Beta Signaling, pp. 1 - 12. Humana Press, Totowa, New Jersey (2022)

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Oheim, R.; Tsourdi , E.; Seefried , L.; Beller , G.; Schubach , M.; Vettorazzi , E.; Stürznickel, J.; Rolvien , T.; Ehmke , N.; Delsmann , A. et al.; Genest, F.; Krüger, U.; Zemojtel , T.; Barvencik , F.; Schinke , T.; Jakob, F.; Hofbauer, L. C.; Mundlos, S.; Kornak, U.: Genetic Diagnostics in Routine Osteological Assessment of Adult Low Bone Mass Disorders. Journal of Clinical Endocrinology and Metabolism, dgac147 (2022)

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Ambrozkiewicz, M. C.; Borisova, E.; Newman, A. G.; Kraushar, M.; Schaub, T.; Dannenberg, R.; Brockmann, M.; Rosário, M.; Turko, P.; Jahn, O. et al.; Kaplan, D. R.; Iwawaki, T.; Spahn, C. M. T.; Rosenmund, C.; Tarabykin, V.: Ire1a-Regulated mRNA Translation Rate Controls the Identity and Polarity of Upper Layer Cortical Neurons. (2022)
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Cova, G.; Glaser, J.; Schöpflin, R.; Ali, S.; Prada-Medina, C. A.; Franke, M.; Falcone, R.; Federer, M.; Ponzi, E.; Ficarella, R. et al.; Novara, F.; Wittler, L.; Timmermann, B.; Gentile, M.; Zuffardi, O.; Spielmann, M.; Mundlos, S.: Combinatorial effects on gene expression at the Lbx1/Fgf8 locus resolve Split-Hand/Foot Malformation type 3. (2022)
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