Klopocki, E., S. Lohan, F. Brancati, R. Koll, A. Brehm, P. Seemann, K. Dathe, S. Stricker, J. Hecht, K. Bosse, R. C. Betz, F. G. Garaci, B. Dallapiccola, M. Jain, M. Muenke, V. C. Ng, W. Chan, D. Chan and S. Mundlos: Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis.. In: American Journal of Human Genetics 88, 1, 70-75 (2011).
url: http://www.ncbi.nlm.nih.gov/pubmed/21167467
doi: i:10.1016/j.ajhg.2010.11.006
Brancati, F., P. Fortugno, I. Bottillo, M. Lopez, E. Josselin, O. Boudghene-Stambouli, E. Agolini, L. Bernardini, E. Bellacchio, M. Iannicelli, A. Rossi, A. Dib-Lachachi, L. Stuppia, G. Palka, S. Mundlos, S. Stricker, U. Kornak, G. Zambruno and B. Dallapiccola: Mutations in PVRL4, encoding cell adhesion molecule nectin-4, cause ectodermal dysplasia-syndactyly syndrome. In: American Journal of Human Genetics 87, 2, 265-273 (2010).
url: http://www.ncbi.nlm.nih.gov/pubmed/20691405
doi: 10.1016/j.ajhg.2010.07.003.
Witte, F., D. Chan, A. N. Economides, S. Mundlos and S. Stricker: Receptor tyrosine kinase-like orphan receptor 2 (ROR2) and Indian hedgehog regulate digit outgrowth mediated by the phalanx-forming region. In: Proceedings of the National Academy of Sciences U S A 107, 32, 14211-14216 (2010).
url: http://www.ncbi.nlm.nih.gov/pubmed/20660756
doi: 10.1073/pnas.1009314107
Clayton, P., B. Fischer, A. Mann, S. Mansour, E. Rossier, M. Veen, C. Lang, S. Baasanjav, M. Kieslich, K. Brossuleit, S. Gravemann, N. Schnipper, M. Karbasyian, I. Demuth, M. Zwerger, A. Vaya, G. Utermann, S. Mundlos, S. Stricker, K. Sperling and K. Hoffmann: Mutations causing Greenberg dysplasia but not Pelger anomaly uncouple enzymatic from structural functions of a nuclear membrane protein.. In: Nucleus 1, 4, 354-366 (2010).
url: http://www.ncbi.nlm.nih.gov/pubmed/21327084
doi: 10.4161/nucl.1.4.12435
Witte, F., O. Bernatik, K. Kirchner, J. Masek, A. Mahl, P. Krejci, S. Mundlos, A. Schambony, V. Bryja and S. Stricker: Negative regulation of Wnt signaling mediated by CK1-phosphorylated Dishevelled via Ror2.. In: The FASEB Journal 24, 7, 2417-2426 (2010).
url: http://www.ncbi.nlm.nih.gov/pubmed/20215527
doi: 10.1096/fj.09-150615
Liska, F., P. Snajdr, S. Stricker, C. Gosele, D. Krenova, S. Mundlos and N. Hubner: Impairment of Sox9 expression in limb buds of rats homozygous for hypodactyly mutation.. In: Folia Biologica 56, 2, 58-65 (2010).
url: http://www.ncbi.nlm.nih.gov/pubmed/20492757
Kolanczyk, M., N. Kossler, J. Kuhnisch, L. Lavitas, S. Stricker, U. Wilkening, I. Manjubala, P. Fratzl, R. Sporle, B. G. Herrmann, L. F. Parada, U. Kornak and S. Mundlos: Multiple roles for neurofibromin in skeletal development and growth. In: Human Molecular Genetics 16, 8, 874-886 (2007).
Woods, C. G., S. Stricker, P. Seemann, R. Stern, J. Cox, E. Sherridan, E. Roberts, K. Springell, S. Scott, G. Karbani, S. M. Sharif, C. Toomes, J. Bond, D. Kumar, L. Al-Gazali and S. Mundlos: Mutations in WNT7A Cause a Range of Limb Malformations, Including Fuhrmann Syndrome and Al-Awadi/Raas-Rothschild/Schinzel Phocomelia Syndrome. In: American Journal of Human Genetics (Chicago, IL) 79, 2, 402-408 (2006).
Stricker, S., 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. In: Developmental and Comparative Immunology 27, 8, 673-684 (2003).
doi: 10.1016/S0145-305X(03)00037-5
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