Kosanke, M., Montag, J., Thum, T., Zweigerdt, R., Kraft, T., Iorga, B., and Meissner, J.D. (2023), J Gen Physiol (2023) 155 (11): e202313377, https://doi.org/10.1085/jgp.202313377 , Online ahead of print

Förster R, Bauersachs J, Ola R, Dobreva G, Völkers M, Heineke J. Analysis of myocardial cellular gene expression during pressure overload reveals matrix based functional intercellular communication. iScience [...] 35281736; PMCID: PMC8908217. Rezalotfi A, Fritz L, Förster R, Bošnjak B. Challenges of CRISPR-Based Gene Editing in Primary T Cells. Int J Mol Sci. 2022 Feb 1;23(3):1689. doi: 10.3390/ijms23031689. PMID: [...] Gentner B, Casanova JL, Bustamante J, Schambach A, Kalinke U, Lachmann N. Hematopoietic stem cell gene therapy for IFNγR1 deficiency protects mice from mycobacterial infections. Blood. 2018 Feb 1;131(

Scientific reports. 2017;7:44113. Ghosh CC, David S, Zhang R, Berghelli A, Milam K, Higgins SJ, et al. Gene control of tyrosine kinase TIE2 and vascular manifestations of infections. PNAS 2016;113(9):2472-7

ne Bioproben wie z.B. kernhaltige Blutzellen, lebende Blutzellen, RNA-stabilisiertes Material (PaxGene), Plasma, Serum, Speichel und Bronchioalveoläre Lavage (BAL) gesammelt und in der Hannover Unified

2024 Karin Wisskirchen Head of Research SCG Cell Therapy Germany D-SOLVE "Clinical application of gene-modified HBV-specific T cells for treatment of HBV-induced HCC" 04.11.2024 Alisa Kielkowski AG Taubert

Gottlieb J, Welte T, Braubach P, Laenger F, Hoeper MM, Kuehnel MP, Jonigk DD. Comparative analysis of gene expression in fibroblastic foci in patients with idiopathic pulmonary fibrosis and pulmonary sarcoidosis

Nugraha B, Anwar SL, Gutenbrunner C, Korallus C. Polymorphism of brain-derived neurotrophic factor genes is associated with anxiety and body mass index in fibromyalgia syndrome patients. BMC Res Note 2020;

Bange FC, Wehling C, Kirschfink M, Bergmann C, Pape L. Systemic complement activation and complement gene analysis in enterohaemorrhagic Escherichia coli -associated paediatric haemolytic uraemic syndrome

exon 12, a heterozygous in-frame deletion in exon 3 and a missense mutation in exon 11 of the BMPR2 gene. Stem Cell Res. 2021;55:102488. https://pubmed.ncbi.nlm.nih.gov/34388490/ . Kokeny G, Calvier L, Hansmann

Arbeiten (Bachelor- und Masterarbeiten, Laborpraktika): Screening von relevanten Virusgenomen auf Gene, die für PDE-/Nukleasehomologe kodieren und Produktion/Reinigung der entsprechenden Enzyme Identifizierung