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74632 Treffer
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< 2021
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Johannes Gutenberg-Universität Mainz
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Universität Koblenz
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Hochschule Kaiserslautern
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Hochschule Koblenz
- Ritz, Ulrike; Koegler, Peter; Hoefer, Isabel et al.
- Photocrosslinkable polysaccharide hydrogel composites based on dextran or pullulan-amylose blends with cytokines for a human co-culture model of human osteoblasts and endothelial cells
- JOURNAL OF MATERIALS CHEMISTRY B. Bd. 4. H. 40. 2016 S. 6552-6564
- Triantafyllias, Konstantinos; De Blasi, Michele; Hoffmann, Isabell et al.
- The count of tender rather than swollen joints correlates with aortic stiffness in patients with rheumatoid arthritis
- SPRINGERPLUS. Bd. 5. 2016
- Wagner, Daniel; Kamer, Lukas; Sawaguchi, Takeshi et al.
- Sacral Bone Mass Distribution Assessed by Averaged Three-Dimensional CT Models Implications for Pathogenesis and Treatment of Fragility Fractures of the Sacrum
- JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME. Bd. 98. H. 7. 2016 S. 584-590
- Mattyasovszky, Stefan G.; Wollstaedter, Jochen; Martin, Anne et al.
- Inhibition of Contractile Function in Human Joint Capsule Myofibroblasts by Targeting the TGF-beta 1 and PDGF Pathways
- PLOS ONE. Bd. 11. H. 1. 2016
- Montano, Adriana M.; Lock-Hock, Ngu; Steiner, Robert D. et al.
- Clinical course of sly syndrome (mucopolysaccharidosis type VII)
- JOURNAL OF MEDICAL GENETICS. Bd. 53. H. 6. 2016 S. 403-418
- Cassiman, David; Packman, Seymour; Bembi, Bruno et al.
- Cause of death in patients with chronic visceral and chronic neurovisceral acid sphingomyelinase deficiency (Niemann-Pick disease type B and B variant): Literature review and report of new cases
- MOLECULAR GENETICS AND METABOLISM. Bd. 118. H. 3. 2016 S. 206-213
- Imrie, Jackie; Mengel, Karl Eugen; Cassiman, David et al.
- Cause of death in patients with attenuated acid sphingomyelinase deficiency: Comprehensive literature review and report of new cases
- MOLECULAR GENETICS AND METABOLISM. Bd. 117. H. 2. 2016 S. S60-S60
- van Capelle, C. I.; van der Meijden, J. C.; van den Hout, J. M. P. et al.
- Childhood Pompe disease: clinical spectrum and genotype in 31 patients
- ORPHANET JOURNAL OF RARE DISEASES. Bd. 11. 2016
- Fischer, J*; Paret, C*; El Malki, K et al.
- CD19 isoforms lacking the CART-19 epitope are expressed before any therapy
- Journal of Immunotherapy. 2016 S. ff
- Knoll, RL; Forslund, K; Kultima, JR et al.
- Gut microbiota differs between children with Inflammatory Bowel Disease and healthy siblings in taxonomic and functional composition – a metagenomic analysis
- Am J Physiol Gastrointest Liver Physiol. 2016 S. ff