Journal Article (402)

401.
Journal Article
Albrecht, A. N.; Schwabe, G. C.; Stricker, S.; Böddrich, A.; Wanker, E. E.; Mundlos, S.: The synpolydactyly homolog (spdh) mutation in the mouse – a defect in patterning and growth of limb cartilage eleme. Mechanisms of Development 112 (1-2), pp. 53 - 67 (2002)
402.
Journal Article
Albrecht, A. N.; Schwabe, G. C.; Stricker, S.; Böddrich, A.; Wanker, E. E.; Mundlos, S.: The synpolydactyly homolog (spdh) mutation in the mouse – a defect in patterning and growth of limb cartilage eleme. Mechanisms of Development 112 (1-2), pp. 53 - 67 (2002)

Book (1)

403.
Book
Mundlos, S.; Horn, D.: Limb Malformations – An Atlas of Genetic Disorders of Limb Development. Springer-Verlag, Berlin, Heidelberg (2014), 767 pp.

Book Chapter (1)

404.
Book Chapter
Schulz, M. H.; Köhler, S.; Bauer, S.; Vingron, M.; Robinson, P. N.: Exact Score Distribution Computation for Similarity Searches in Ontologies. In: Algorithms in Bioinformatics, pp. 298 - 309 (Eds. Salzberg, S. L.; Warnow, T.). Springer, New York [et al] (2009)

Conference Paper (1)

405.
Conference Paper
Schöpflin, R.; Andrey, G.; Heinrich, V.; Franke, M.; Ibrahim, D.; Paliou, C.; Mundlos, S.; Vingron, M.: Identification of potential regulatory elements in Capture-C interaction profiles. In: Genome Regulation in 3D, Vol. 2015. Genome Regulation in 3D, Rehovot, Israel, June 28, 2015 - June 30, 2015. Weizmann Institute, Rehovot, Israel (2015)

Thesis (2)

406.
Thesis
Viebig, J.: Sequenzierung des LoxP flankierten Exon 6 des Gens Piga im Mausmodell. Humboldt Universität zu Berlin, (2015)
407.
Thesis
Wiegmann Rollet, R.: Analyse von Mutationen monogener Erkrankungen bezüglich evolutionärer Konservierung und Transkriptionsfaktorbindungsstellen. Freie Universität Berlin (2015)

Thesis - PhD (13)

408.
Thesis - PhD
Grünhagen, J.: Nicht kodierende RNAs in der Knochenentwicklung. Dissertation, Medizinische Fakultät Charité - Universitätsmedizin Berlin (2015)
409.
Thesis - PhD
Bosquillon de Jarcy, L.: Brachydaktylie Typ E und ZNF521. Dissertation, Charité Berlin, Berlin (2014)
410.
Thesis - PhD
Grohmann, J.: The role of the tumour suppressor Nf1 in growth and metabolism of skeletal muscle cells. Dissertation, TU Berlin, Fakultät III - Prozesswissenschaften, Berlin (2014)
411.
Thesis - PhD
Ibrahim, D.: ChIP-seq Reveals Mutation-Specific Pathomechanismus of HOXD13 Missense Mutations. Dissertation, Humboldt University, FB Mathemathik, Berlin (2014)
412.
Thesis - PhD
Sprenger, S.: The role of Pycr1 in the Pathomechanism of Autosomal recessive Cutis Laxa. Dissertation, TU Berlin, FB Biotechnol., Berlin (2014)
413.
Thesis - PhD
Zimmer, J.: From Skeletal Diseases to Bone Regeneration: Analysis of Agonist-Antagonist Interactions for Design of tailored bone Morphogenetic Protein2 Variants with improved biological activity. Dissertation (2012)
414.
Thesis - PhD
Köhler, S.: Penotype informatics: Network approaches towards understanding the diseasome. Dissertation (2012)
415.
Thesis - PhD
Chan, W. L.: Molecular basis of Gerodermia Osteodysplastica, apremature ageing disorder. Dissertation (2012)
416.
Thesis - PhD
Forler, S.: Effekte von Polymorphysmen auf die geschlechtsspezifische Proteinexpression in gesunden und hüpertrophierten Herzen. Dissertation (2011)
417.
Thesis - PhD
Rödelsperger, C.: Computational Characterization of Genome-wide DNA-binding Pro les. Dissertation, Freie Universität Berlin, Berlin (2011)
418.
Thesis - PhD
Bauer, S.: Algorithms for Knoledge Integration in Biomedical Sciences. Dissertation (2011)
419.
Thesis - PhD
Schwarzer, W.: Phenotypic variability in monogenic disorders involving skeletal malformations. Dissertation, Freie Universität Berlin, Berlin (2010)
420.
Thesis - PhD
Hecht, J.: Gene-Expression analysis in bone development and fracture healing Genexpressionsanalysen zum besseren Verständnis von Knochenheilung und -entwicklung. Dissertation, Freie Universität Berlin, Berlin (2007)
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