— Maja Lindenmeyer, PhD
©Maja Lindenmeyer, created with BioRender
Our group represents the core facility of the “European Renal cDNA Bank-Kroener Fresenius Biopsy Bank” (ERCB-KFB), a multicenter study for gene expression analysis in different human renal diseases, and the “Hamburg and European Renal Omics Bank” (HERO), a collaborative project for conducting translational research in human renal diseases. Using state of the art omics and non-omics technologies, we aim to
III. Department of Medicine, University Medical Center Hamburg-Eppendorf (UKE)
Martinistr. 52
20246 Hamburg, Germany
since 2024 | Principal Investigator SFB 1192 |
since 2022 | Principal Investigator / Co-Coordinator BMBF STOP-FSGS |
since 2022
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Principal Investigator BMBF UPTAKE |
since 2021
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Project Leader/ Study Coordinator of the Hamburg and European Renal Omics Biobank (HERO) |
since 2018
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Laboratory head, III. Department of Medicine, UKE, Prof. Dr. T. B. Huber |
since 2018 | Coordinator of the ERCB |
1994 – 2000
|
Chemistry, Technical University Karlsruhe, University of Freiburg |
2014 - 2020
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Habilitation in Molecular Nephrology, University of Zurich (Switzerland) |
2004
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PhD, Department of Pharmaceutical Biology and Biotechnology, University of Freiburg |
2000
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Diploma in Chemistry, University of Freiburg |
2015 – 2018
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Junior Group leader, Nephrology Center, IV. Department of Medicine, University Hospital of Munich (LMU) |
2012 – 2018
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Deputy-Coordinator of the European Renal cDNA Bank-Kroener Fresenius |
2010 – 2014
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Laboratory Head of the Nephrology Lab Zurich, University of Zurich (Switzerland) |
2008 – 2010
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Postdoctoral Fellow, Institute of Physiology and Division of Nephrology, University of Zurich (Switzerland), Prof. Dr. C. Cohen |
2006 – 2007
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Postdoctoral Fellow, Nephrology Center, IV. Deparment of Medicine, University Hospital of Munich (LMU), Prof Dr. C. Cohen |
2004 – 2005
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Postdoctoral Fellow, School of Biological Sciences, Queen Mary College, London (UK), Prof. Dr. M. Warren |
2010 - 2020
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Habilitation Scholarship of the Holcim Foundation |
2004 – 2005
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Post-Doc fellowship of the German Academic Exchange Service (DAAD) |
2001 – 2003
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PhD fellowship of the “Landesgraduiertenförderung Baden-Württemberg” |
1. | Molecular consequences of SARS-CoV-2 liver tropism. |
2. | Pro-cachectic factors link experimental and human chronic kidney disease to skeletal muscle wasting. |
3. | Endothelial-Specific Deletion of CD146 Protects Against Experimental Glomerulonephritis in Mice. |
4. | SARS-CoV-2 renal tropism associates with acute kidney injury. |
5. | ADAM10-Mediated Ectodomain Shedding Is an Essential Driver of Podocyte Damage. |
6. | Dysregulated mesenchymal PDGFR-β drives kidney fibrosis |
7. | Multiorgan and Renal Tropism of SARS-CoV-2. |
8. | Tubular NOX4 expression decreases in chronic kidney disease but does not modify fibrosis evolution. |
9. | Metabolic pathways and immunometabolism in rare kidney diseases. |
10. | Transcriptome-based network analysis reveals renal cell type-specific dysregulation of hypoxia-associated transcripts. *contributed equally |
Martinistraße 52
Campus Research N27
20246 Hamburg Germany