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Cellular and Molecular Life Sciences : CMLS|June 26, 2015
Selective cell targeting and lineage tracing of human induced pluripotent stem cells using recombinant avian retrovirusesLaura Hildebrand, Petra Seemann, Andreas Kurtz, et al.
European Journal of Human Genetics : EJHG|September 8, 2006
A novel R486Q mutation in BMPR1B resulting in either a brachydactyly type C/symphalangism-like phenotype or brachydactyly type A2Katarina Lehmann, Petra Seemann, Jan Boergermann, et al.
The FEBS Journal|September 2, 2014
Biophysical and structural characterization of a folded core domain within the proregion of growth and differentiation factor-5Tino Thieme, Rica Patzschke, Florian Job, et al.
Stem Cell Research|June 28, 2016
Generation of integration free induced pluripotent stem cells from fibrodysplasia ossificans progressiva (FOP) patients from urine samplesLaura Hildebrand, Bella Rossbach, Peter Kühnen, et al.
Methods in Enzymology|November 2, 2010
Investigations of activated ACVR1/ALK2, a bone morphogenetic protein type I receptor, that causes fibrodysplasia ossificans progressivaFrederick S Kaplan, Petra Seemann, Julia Haupt, et al.
The Journal of Nutritional Biochemistry|October 10, 2024
Serum selenium, selenoprotein P and glutathione peroxidase 3 in rheumatoid, psoriatic, juvenile idiopathic arthritis, and osteoarthritisLukas Wahl, Thilo Samson Chillon, Petra Seemann, et al.
The Journal of Clinical Endocrinology and Metabolism|March 4, 2023
A Novel In Vitro Assay Correlates Insulin Receptor Autoantibodies With Fasting Insulin in Type B Insulin ResistanceWaldemar B Minich, Brent S Abel, Christian Schwiebert, et al.
Plos One|April 25, 2012
Functional analysis of alleged NOGGIN mutation G92E disproves its pathogenic relevanceJulia Zimmer, Sandra C Doelken, Denise Horn, et al.
Journal of Human Genetics|May 22, 2015
Brachydactyly Type C patient with compound heterozygosity for p.Gly319Val and p.Ile358Thr variants in the GDF5 proregion: benign variants or mutations?Katja Stange, Claus-Eric Ott, Mareen Schmidt-von Kegler, et al.
The Journal of Clinical Investigation|December 17, 2008
Mutant Hoxd13 induces extra digits in a mouse model of synpolydactyly directly and by decreasing retinoic acid synthesisPia Kuss, Pablo Villavicencio-Lorini, Florian Witte, et al.
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