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IFN-alpha disarms human CD4+CD25+FOXP3+regulatory T cells through cAMP repression without alteration of the Treg lineage programEXPERIMENTAL DERMATOLOGY. Bd. 22. H. 3. 2013 S. E24-E24
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Induced Pluripotent Mesenchymal Stromal Cell Clones Retain Donor-derived Differences in DNA Methylation ProfilesMOLECULAR THERAPY. Bd. 21. H. 1. 2013 S. 240-250
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Interferon-alpha Suppresses cAMP to Disarm Human Regulatory T CellsCANCER RESEARCH. Bd. 73. H. 18. 2013 S. 5647-5656
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Metabolic Programming of MEST DNA Methylation by Intrauterine Exposure to Gestational Diabetes MellitusDIABETES. Bd. 62. H. 4. 2013 S. 1320-1328
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Novel VANGL 1 Gene Mutations in 144 Slovakian , Romanian and German Patients with Neural Tube DefectsMolecular syndromology. Bd. 3. H. 2. 2013 S. 76-81
Lehnen, H.; Mosblech, N.; Reineke, T. et al.
Prenatal Clinical Assessment of sFlt-1 (Soluble fms-like Tyrosine Kinase-1)/PlGF (Placental Growth Factor) Ratio as a Diagnostic Tool for Preeclampsia, Pregnancy-induced Hypertension, and ProteinuriaGEBURTSHILFE UND FRAUENHEILKUNDE. Bd. 73. H. 5. 2013 S. 440-445
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Searching for Gene Expression Differences in Primary Fibroblasts Between Patients with One and Two Neoplasms in ChildhoodPEDIATRIC HEMATOLOGY AND ONCOLOGY. Bd. 30. H. 1. 2013 S. 33-45
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Sirtuin-6-Dependent Genetic and Epigenetic Alterations Are Associated With Poor Clinical Outcome in Hepatocellular Carcinoma PatientsHEPATOLOGY. Bd. 58. H. 3. 2013 S. 1054-1064
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Spectrum of novel mutations found in Waardenburg syndrome types 1 and 2: implications for molecular genetic diagnosticsBMJ OPEN. Bd. 3. H. 3. 2013
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Stochastic Loss of Silencing of the Imprinted Ndn/NDN Allele, in a Mouse Model and Humans with Prader-Willi Syndrome, Has Functional ConsequencesPLOS GENETICS. Bd. 9. H. 9. 2013