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The Journal of Clinical Investigation|October 25, 2012
A misplaced lncRNA causes brachydactyly in humansPhilipp G Maass, Andreas Rump, Herbert Schulz, et al.Development (Cambridge, England)|September 2, 2024
Mesenchymal Osr1+ cells regulate embryonic lymphatic vessel formationPedro Vallecillo-García, Mira Nicola Kühnlein, Mickael Orgeur, et al.Genes to Cells : Devoted to Molecular & Cellular Mechanisms|December 1, 2004
Modulation of GDF5/BRI-b signalling through interaction with the tyrosine kinase receptor Ror2Marei Sammar, Sigmar Stricker, Georg C Schwabe, et al.Plos Genetics|March 29, 2008
Evolution of a core gene network for skeletogenesis in chordatesJochen Hecht, Sigmar Stricker, Ulrike Wiecha, et al.Human Molecular Genetics|April 12, 2011
Neurofibromin (Nf1) is required for skeletal muscle developmentNadine Kossler, Sigmar Stricker, Christian Rödelsperger, et al.Proceedings of the National Academy of Sciences of the United States of America|October 3, 2003
Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2Katarina Lehmann, Petra Seemann, Sigmar Stricker, et al.Nature|March 3, 2009
A mutation in Ihh that causes digit abnormalities alters its signalling capacity and rangeBo Gao, Jianxin Hu, Sigmar Stricker, et al.Human Molecular Genetics|February 24, 2007
Multiple roles for neurofibromin in skeletal development and growthMateusz Kolanczyk, Nadine Kossler, Jirko Kühnisch, et al.Development (Cambridge, England)|June 5, 2023
Inhibitory SMAD6 interferes with BMP-dependent generation of muscle progenitor cells and perturbs proximodistal pattern of murine limb musclesHasan Asfour, Estelle Hirsinger, Raquel Rouco, et al.The Journal of Clinical Investigation|April 21, 2005
An inversion involving the mouse Shh locus results in brachydactyly through dysregulation of Shh expressionMichael Niedermaier, Georg C Schwabe, Stephan Fees, et al.Pageof 10