Publikationen von S. Mundlos

S. Stricker, A. J. Poustka, U. Wiecha, A. Stiege, J. Hecht, G. Panopoulou, A. Vilcinskas, S. Mundlos, and V. Seitz, "A single amphioxus and sea urchin runt-gene suggests that runt-gene duplications occurred in early chordate evolution," Developmental and Comparative Immunology 27 (8), 673-684 (2003).

Isao Oishi, Hiroaki Suzuki, Nobuyuki Onishi, Ritsuko Takada, Shuichi Kani, Bisei Ohkawara, Ikure Koshida, Kentaro Suzuki, General Yamada, Georg C. Schwabe, Stefan Mundlos, Hiroshi Shibuya, Shinji Takada, and Yasuhiro Minami, "The receptor tyrosine kinase Ror2 is involved in non-canonical Wnt5a/JNK signalling pathway," Genes to Cells 8 (7), 645-654 (2003).

Michael Stock, Henning Schafer, Sigmar Stricker, Gerhard Gross, Stefan Mundlos, and Florian Otto, "Expression of galectin-3 in skeletal tissues is controlled by Runx2," Journal of Biological Chemistry 278 (19), 17360-17367 (2003).

Michael Stock, Henning Schäfer, Sigmar Stricker, Gerhard Gross, Stefan Mundlos, and Florian Otto, "Expression of galectin-3 in skeletal tissues is controlled by Runx2," Journal of Biological Chemistry 278 (19), 17360-17367 (2003).

Susann Schweiger, Rabih Chaoui, Cornelia Tennstedt, Katarina Lehmann, Stefan Mundlos, and Sigrid Tinschert, "Antenatal onset of cortical hyperostosis (Caffey disease): Case report and review," American Journal of Medical Genetics Part A 120A (4), 547-552 (2003).

Éva Morava, Judit Kárteszi, János Weisenbach, Almuth Caliebe, Stefan Mundlos, and Károly Méhes, "Cleidocranial dysplasia with decreased bone density and biochemical findings of hypophosphatasia," European Journal of Pediatrics 161 (11), 619-622 (2002).

Sheila Unger, Etienne Mornet, Stefan Mundlos, Susan Blaser, and David E. Cole, "Severe cleidocranial dysplasia can mimic hypophosphatasia," European Journal of Pediatrics 161 (11), 623-626 (2002).

Thomas Sander, Mohammad Reza Toliat, Armin Heils, Gundula Leschik, Christian Becker, Franz Rüschendorf, Klaus Rohde, Stefan Mundlos, and Peter Nürnberg, "Association of the 867Asp variant of the human anion exchanger 3 gene with common subtypes of idiopathic generalized epilepsy," Epilepsy Research 51 (3), 249-255 (2002).

Sigmar Stricker, Reinald Fundele, Andrea Vortkamp, and Stefan Mundlos, "Role of Runx Genes in Chondrocyte Differentiation," Developmental Biology 245 (1), 95-108 (2002).

Sigmar Stricker, Reinald Fundele, Andrea Vortkamp, and Stefan Mundlos, "Role of Runx Genes in Chondrocyte Differentiation," Developmental Biology 245 (1), 95-108 (2002).

Sigmar Stricker, Reinald Fundele, Andrea Vortkamp, and Stefan Mundlos, "Role of Runx Genes in Chondrocyte Differentiation," Developmental Biology 245 (1), 95-108 (2002).

Karim D. Kalache, Katarina Lehmann, Rabih Chaoui, Dietmar E. Kivelitz, Stefan Mundlos, and Rainer Bollmann, "Prenatal diagnosis of partial agenesis of the corpus callosum in a fetus with thanatophoric dysplasia type 2," Prenatal Diagnosis 22 (5), 404-407 (2002).

Florian Otto, Hirokazu Kanegane, and Stefan Mundlos, "Mutations in the RUNX2 gene in patients with cleidocranial dysplasia," Human Mutation 19 (3), 209-216 (2002).

Andrea N. Albrecht, Georg C. Schwabe, Sigmar Stricker, Annett Böddrich, Erich E. Wanker, and Stefan Mundlos, "The synpolydactyly homolog (spdh) mutation in the mouse – a defect in patterning and growth of limb cartilage eleme," Mechanisms of Development 112 (1-2), 53-67 (2002).

Andrea N. Albrecht, Georg C. Schwabe, Sigmar Stricker, Annett Böddrich, Erich E. Wanker, and Stefan Mundlos, "The synpolydactyly homolog (spdh) mutation in the mouse – a defect in patterning and growth of limb cartilage eleme," Mechanisms of Development 112 (1-2), 53-67 (2002).

Stefan Mundlos and Denise Horn, Limb Malformations – An Atlas of Genetic Disorders of Limb Development. (Springer-Verlag, Berlin, Heidelberg, 2014).

Marius-Konstantin Klever, Eric Sträng, Julius Jungnitsch, Uirá Souto Melo, Sara Hetzel, Anna Dolnik, Robert Schöpflin, Jens F. Schrezenmeier, Olga Blau, Jörg Westermann, Konstanze Döhner, Hubert Schrezenmeier, Malte Spielmann, Alexander Meissner, Stefan Mundlos, and Lars Bullinger, "Integration of Hi-C and Nanopore Sequencing for Structural Variant Analysis in AML with a Complex Karyotype: (Chromothripsis)²", in Blood, (American Society of Hematology, Washington, DC, 2020), Vol. 136.

Robert Schöpflin, Guillaume Andrey, Verena Heinrich, Martin Franke, Daniel Ibrahim, Christina Paliou, Stefan Mundlos, and Martin Vingron, "Identification of potential regulatory elements in Capture-C interaction profiles", in Genome Regulation in 3D, (Weizmann Institute, Rehovot, Israel, 2015).

Juliane Glaser and Stefan Mundlos, "3D or Not 3D: Shaping the Genome during Development", in Cold Spring Harbor Perspectives in Biology, (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, 2021).

Magdalena Schindler, Christian Feregrino, Silvia Aldrovandi, Bai-Wei Lo, Anna A. Monaco, Alessa R. Ringel, Ariadna Morales, Tobias Zehnder, Rose Yinghan Behncke, Juliane Glaser, Alexander Barclay, Guillaume Andrey, Bjørt K. Kragesteen, René Hägerling, Stefan Haas, Martin Vingron, Igor Ulitsky, Marc Marti-Renom, Julio Hechavarria, ProfileNicolas Fasel, Michael Hiller, Darío Lupiáñez, Stefan Mundlos, and Francisca M. Real, "Comparative single-cell analyses reveal evolutionary repurposing of a conserved gene program in bat wing development", in bioRxiv: the preprint server for biology, (2024).