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Moosa, Shahida; Yamamoto, Guilherme L; Garbes, Lutz; Keupp, Katharina; Beleza-Meireles, Ana; Moreno, Carolina Araujo; Valadares, Eugenia Ribeiro; de Sousa, Sérgio B; Maia, Sofia; Saraiva, Jorge; Honjo, Rachel S; Kim, Chong Ae; Cabral de Menezes, Hamilton; Lausch, Ekkehart; Lorini, Pablo Villavicencio; Lamounier, Arsonval; Carniero, Tulio Canella Bezerra; Giunta, Cecilia; Rohrbach, Marianne; Janner, Marco; ... (2019). Autosomal-Recessive Mutations in MESD Cause Osteogenesis Imperfecta. American journal of human genetics, 105(4), pp. 836-843. Cell Press 10.1016/j.ajhg.2019.08.008
Hausherr, Carolin K; Schiffer, Ilka B; Gebhard, Susanne; Banic, Andreas; Tanner, Berno; Kolbl, Heinz; Thoenes, Eric; Beckers, Thomas; Spangenberg, Christian; Prawitt, Dirk; Trost, Tatjana; Zabel, Bernhard; Oesch, Franz; Hermes, Matthias; Hengstler, Jan G (2006). Dephosphorylation of p-ERK1/2 in relation to tumor remission after HER-2 and Raf1 blocking therapy in a conditional mouse tumor model. Molecular carcinogenesis, 45(5), pp. 302-8. Hoboken, N.J.: Wiley 10.1002/mc.20157
