Publikationen von Manuela Scholze-Wittler

Pavel Tsaytler, Gaby Blaess, Manuela Scholze-Wittler, David Meierhofer, Lars Wittler, Frederic Koch, and Bernhard G. Herrmann, "SRF promotes long-range chromatin loop formation and stem cell pluripotency," Cell Reports 43 (10), 114846 (2024).

Marco Eijken, A. Michaela Krautzberger, Manuela Scholze-Wittler, Bianca Boers-Sijmons, Marijke Koedam, Barbara Kosiol, Heinrich Schrewe, Johannes P. van Leeuwen, and Bram C. van der Eerden, "Vasorin-deficient mice display disturbed vitamin D and mineral homeostasis in combination with a low bone mass phenotype," Bone Reports 22, Article 101792 (2024).

Pavel Tsaytler, Gaby Blaess, Manuela Scholze-Wittler, Frederic Koch, and Bernhard G. Herrmann, "Early neural specification of stem cells is mediated by a set of SOX2-dependent neural-associated enhancers," Stem Cell Reports 19 (5), 618-628 (2024).

Dennis Schifferl, Manuela Scholze-Wittler, Alba Villaronga Luque, Milena Pustet , Lars Wittler, Jesse V. Veenvliet, Frederic Koch, and Bernhard G. Herrmann, "Genome-wide identification of notochord enhancers comprising the regulatory landscape of the Brachyury (T) locus in mouse," Development 150 (22), dev202111 (2023).

Dennis Schifferl, Manuela Scholze-Wittler, Lars Wittler, Jesse V. Veenvliet, Frederic Koch, and Bernhard G. Herrmann, "A 37 kb region upstream of brachyury comprising a notochord enhancer is essential for notochord and tail development," Development 148 (23), dev200059 (2021).

Jesse V. Veenvliet, Adriano Bolondi, Helene Kretzmer, Leah Haut, Manuela Scholze-Wittler, Dennis Schifferl, Frederic Koch, Léo Guignard, Abhishek Sampath Kumar, Milena Pustet, Simon Heimann, Rene Buschow, Lars Wittler, Bernd Timmermann, Alexander Meissner, and Bernhard G. Herrmann, "Mouse embryonic stem cells self-organize into trunk-like structures with neural tube and somites," Science 370 (6522), eaba4937 (2020).

Joanna Segal, Michael Mülleder, Antje Krüger, Thure Adler, Manuela Scholze-Wittler, Lore Becker, Julia Calzada-Wack, Lillian Garrett, Sabine M. Hölter, Birgit Rathkolb, Jan Rozman, Ildiko Racz, Ralf Fischer, Dirk H. Busch, Frauke Neff, Martin Klingenspor, Thomas Klopstock, Nana-Maria Grüning, Steve Michel, Beata Lukaszewska-McGreal, Ingo Voigt, Ludger Hartmann, Bernd Timmermann, Hans Lehrach, Eckhard Wolf, Wolfgang Wurst, Valérie Gailus-Durner, Helmut Fuchs, Martin H. de Angelis, Heinrich Schrewe, Mariia Yuneva, and Markus Ralser, "Low catalytic activity is insufficient to induce disease pathology in triosephosphate isomerase (TPI) deficiency," Journal of Inherited Metabolic Disease 22 (5), 839-849 (2019).

Frederic Koch, Manuela Scholze, Lars Wittler, Dennis Schifferl, Smita Sudheer, Phillip Grote, Bernd Timmermann, Karol Macura, and Bernhard G. Herrmann, "Antagonistic Activities of Sox2 and Brachyury Control the Fate Choice of Neuro-Mesodermal Progenitors," Developmental Cell 42, 514-526 (2017).

Smita Sudheer, Jinhua Liu, Mathias Marks, Frederic Koch, Anna Anurin, Manuela Scholze, Anna Dorothea Senft, Lars Wittler, Karol Macura, Phillip Grote, and Bernhard G. Herrmann, "Different Concentrations of FGF Ligands, FGF2 or FGF8 Determine Distinct States of WNT-Induced Presomitic Mesoderm.," Stem Cells 34 (7), 1790-800 (2016).

Michaela K. Krautzberger, Barbara Kosiol, Manuela Scholze, and Heinrich Schrewe, "Expression of vasorin (Vasn) during embryonic development of the mouse," Gene Expression Patterns 12 (5-6), 167-171 (2012).

Pedro P. Rocha, Manuela Scholze, Wilfried Bleiß, and Heinrich Schrewe, "Med12 is essential for early mouse development and for canonical Wnt and Wnt/PCP signaling.," Development 137, 2723-2731 (2010).

Yorick Gitton, Nadia Dahmane, Sonya Baik, Ariel Ruiz i Altaba, Lorenz Neidhardt, Manuela Scholze, Bernhard G. Herrmann, Pascal Kahlem, Alia Benkhala, Sabine Schrinner, Reha Yildirimman, Ralf Herwig, Hans Lehrach, and Marie-Laure Yaspo, "A gene expression map of human chromosome 21 orthologues in the mouse," Nature 420 (6917), 586-590 (2002).