Publications

Publications marked with an * were directly funded through the KFO 329

*Rive, C., …, Rieckher, M. & Schumacher, B. Improved Biocompatibility of Amino-Functionalized Graphene Oxide in Caenorhabditis elegans. Small e1902699 (2019). doi:10.1002/smll.201902699

*Bayersdorf, R. & Schumacher, B. Recent advances in understanding the mechanisms determining longevity. F1000Research 8, 1403 (2019).

*Ou, H.-L., Kim, C. S., Uszkoreit, S., Wickström, S. A. & Schumacher, B. Somatic Niche Cells Regulate the CEP-1/p53-Mediated DNA Damage Response in Primordial Germ Cells. Dev. Cell 50, 167-183.e8 (2019)

*Doll, M. A., Soltanmohammadi, N. & Schumacher, B. ALG-2/AGO-Dependent mir-35 Family Regulates DNA Damage-Induced Apoptosis Through MPK-1/ERK MAPK Signaling Downstream of the Core Apoptotic Machinery in Caenorhabditis elegans. Genetics 213, 173-194 (2019).

*Brinkkoetter, P. T., …, Schermer, B., Benzing, T., … & Huber, T. B. Anaerobic Glycolysis Maintains the Glomerular Filtration Barrier Independent of Mitochondrial Metabolism and Dynamics. Cell Rep. 27, 1551-1566.e5 (2019).

*Hagmann, H. & Brinkkoetter, P. T. Experimental Models to Study Podocyte Biology: Stock-Taking the Toolbox of Glomerular Research. Front. Pediatr. 6, 193 (2018).

* Hoefele, J., Beck, B., Weber, L. Brinkkoetter, P. Steroid-resistent nephrotic syndrome. Med. Genet. 30, 410–421 (2018).

*Karaiskos, N., Rahmatollahi, M., …, Hoehne, M., Rinschen, M. M., Schermer, B., Benzing, T., Rajewsky, N., Kocks, C., Kann, M., Müller, R.-U. A Single-Cell Transcriptome Atlas of the Mouse Glomerulus. J. Am. Soc. Nephrol. 29, 2060-2068 (2018).

Rinschen, M. M., …, Schermer, B., …, Benzing, T., Huber, T. B. A Multi-layered Quantitative In Vivo Expression Atlas of the Podocyte Unravels Kidney Disease Candidate Genes. Cell Rep. 23, 2495–2508 (2018).

Koehler, S., …, Höhne, M., Wunderlich, F. T., Schermer, B., Benzing, T., Brinkkoetter, P. T. Construction of a viral T2A-peptide based knock-in mouse model for enhanced Cre recombinase activity and fluorescent labeling of podocytes. Kidney Int. 91, 1510–1517 (2017).

Kuczkowski, A., Brinkkoetter, P. Metabolism and homeostasis in the kidney: metabolic regulation through insulin signaling in the kidney. Cell Tissue Res. 369, 199–210 (2017).

Burst, V., Grundmann, F., …, Verbalis, J. Thiazide-Associated Hyponatremia, Report of the Hyponatremia Registry: An Observational Multicenter International Study. Am. J. Nephrol. 45, 420–430 (2017).

Rinschen, M., …, Höhne, M., …, Brinkkoetter, P., Huber, T., Kann, M., Wickström, S., Benzing, T., Schermer, B. YAP-mediated mechanotransduction determines the podocyte’s response to damage. Sci. Signal. 10, (2017).

Ising, C., Brinkkoetter, P. T. Prohibitin Signaling at the Kidney Filtration Barrier. Adv. Exp. Med. Biol. 982, 563–575 (2017).

Siede, D., …, Altmüller, J., …, Dieterich, C. Identification of circular RNAs with host gene-independent expression in human model systems for cardiac differentiation and disease. J. Mol. Cell. Cardiol. 109, 48–56 (2017).

Rajman, M., …, Dieterich, C., Schratt, G. A microRNA-129-5p/Rbfox crosstalk coordinates homeostatic downscaling of excitatory synapses. EMBO J. 36, 1770–1787 (2017).

Altmüller, J., …, Molderings, G. J. Mutational profiling in the peripheral blood leukocytes of patients with systemic mast cell activation syndrome using next-generation sequencing. Immunogenetics 69, 359–369 (2017).

Reynolds, J. J., …, Altmüller, J., …, Stewart, G. S. Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism. Nat. Genet. 49, 537–549 (2017).

Gordon, C. T., …, Altmüller, J., …, Reversade, B. De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development. Nat. Genet. 49, 249–255 (2017).

Rinschen, M. M., …, Schermer, B., Höhne, M., …, Müller, R.-U., Krüger, M., Benzing, T. The ubiquitin ligase Ubr4 controls stability of podocin/MEC-2 supercomplexes. Hum. Mol. Genet. 25, 1328–1344 (2016).

Bartram, M. P., Habbig, S., Pahmeyer, C., Höhne, M., Weber, L. T., Thiele, H., Altmüller, J., …, Schermer, B., Benzing, T., Rinschen, M. M., Beck, B. B. Three-layered proteomic characterization of a novel ACTN4 mutation unravels its pathogenic potential in FSGS. Hum. Mol. Genet. 25, 1152–1164 (2016).

Bartram, M. P., Amendola, E., Benzing, T., Schermer, B., de Vita, G., Muller, R.-U. Mice lacking microRNAs in Pax8-expressing cells develop hypothyroidism and end-stage renal failure. BMC Mol. Biol. 17, 11 (2016).

Laghmani, K., Beck, B. B., …, Benzing, T., …, Komhoff, M. Polyhydramnios, Transient Antenatal Bartter’s Syndrome, and MAGED2 Mutations. N. Engl. J. Med. 374, 1853–1863 (2016).

Rinschen, M. M., …, Schermer, B., Kann, M., Benzing, T., Brinkkoetter, P. T. Quantitative deep-mapping of the cultured podocyte proteome uncovers shifts in proteostatic mechanisms during differentiation. Am. J. Physiol. Cell. Physiol. 311, C404-417 (2016).