The following publications were published exclusively under the affiliation of the Max Planck Society. For publications by the principal investigator outside of the Max Planck Society, see the links on the lower left.

Thesis - PhD (14)

Thesis - PhD
Grünhagen, J.: Nicht kodierende RNAs in der Knochenentwicklung. Dissertation, Medizinische Fakultät Charité - Universitätsmedizin Berlin (2015)
Thesis - PhD
Ibrahim, D.: ChIP-seq Reveals Mutation-Specific Pathomechanismus of HOXD13 Missense Mutations. Dissertation, Humboldt University, FB Mathemathik, Berlin (2014)
Thesis - PhD
Bosquillon de Jarcy, L.: Brachydaktylie Typ E und ZNF521. Dissertation, Charité Berlin, Berlin (2014)
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)
Thesis - PhD
Sprenger, S.: The role of Pycr1 in the Pathomechanism of Autosomal recessive Cutis Laxa. Dissertation, TU Berlin, FB Biotechnol., Berlin (2014)
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)
Thesis - PhD
Köhler, S.: Penotype informatics: Network approaches towards understanding the diseasome. Dissertation (2012)
Thesis - PhD
Chan, W. L.: Molecular basis of Gerodermia Osteodysplastica, apremature ageing disorder. Dissertation (2012)
Thesis - PhD
Forler, S.: Effekte von Polymorphysmen auf die geschlechtsspezifische Proteinexpression in gesunden und hüpertrophierten Herzen. Dissertation (2011)
Thesis - PhD
Rödelsperger, C.: Computational Characterization of Genome-wide DNA-binding Pro les. Dissertation, Freie Universität Berlin, Berlin (2011)
Thesis - PhD
Bauer, S.: Algorithms for Knoledge Integration in Biomedical Sciences. Dissertation (2011)
Thesis - PhD
Schwarzer, W.: Phenotypic variability in monogenic disorders involving skeletal malformations. Dissertation, Freie Universität Berlin, Berlin (2010)
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)

Thesis - Habilitation (2)

Thesis - Habilitation
Stricker, S.: Molekulargenetik und funktionelle Analyse embryonaler Extremitätenfehlbildungen. Habilitation, Charité- Univeristätsmedizin Berlin, Berlin (2010)
Thesis - Habilitation
Robinson, P. N.: Molekulare und klinische Untersuchungen beim Marfan-Syndrom und verwandten Erkrankungen. Habilitation, Charité- Univeristätsmedizin Berlin, Berlin (2009)

Thesis - Diploma (3)

Thesis - Diploma
Borschiwer, M.: Anwendung des CRISPR/Cas9-Systems im Epha4-Lokus von embryonalen Stammzellen. Diploma, FU Berlin, FB Biologie, Berlin (2014)
Thesis - Diploma
Kraft, K.: Polarität von Chondrozyten in den Extremitäten der Hoxd13 Mausmutante synpolydactyly homolog (spdh). Diploma, Technische Universität, Berlin (2011)
Thesis - Diploma
Wiegand, S.: In vivo Analyse des Fingerphänotyps der Noggin Mausmutante. Diploma, Freie Universität, Berlin ()

Thesis - Master (3)

Thesis - Master
Di Tommaso, J.: RNA-seq Data Analysis of Mouse RNA-seq Data Analysis of Mouse Osteoblasts in Differentiation. Master, Univ. Bologna, FB Biologie, Bologna (2014)
Thesis - Master
Brzezinka, K.: Potential downstream targets regulated by OSR I in the chicken connective tissue. Master (2012)
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