General Assembly and gave their input and advice during the session "Bioprocessing technologies for hiPSC: current status". During the subsequent Steering Committee Meeting upcoming events geared towards

Fischer, Dr. M. Klein, Dr. J. de la Roche, Dr. M. Schänzler Physiology of native cardiac cells and hiPSC derived cardiomyocytes Cardiovascular diseases (CVDs) are the number one cause of death worldwide

attended the GA and gave their input and advice during the session "Bioprocessing technologies for hiPSC: current status". _______________________________________________________________________________

Ricke-Hoch Klinik für Kardiologie und Angiologie Teilprojekt 6 Ex vivo Zelltherapie der PAH mittels hiPSC abgeleiteter Endothelzellen im SuNx-Rattenmodell und Etablierung eines organspezifischen BMPR2-Kn

wollen wir respiratorische Epithelzellen abgeleitet aus humanen induzierten pluripotenten Stammzellen (hiPSC) für die Verwendung als innovatives organotypisches in-vitro-Infektionsmodell weiterentwickeln. Durch

mittels MyoCam (IonOptix) Genomeditierung, knock-in einer Punktmutation (CRISPR/Cas9) Zellkultur (hiPSC) Lehre Praktikum „Physiologie und physikalische Grundlagen der Medizin“ für Studierende der HM, ZM

cells Complex protocols have been developed to differentiate human induced pluripotent stem cells (hiPSC) via endoderm, foregut and NKX2.1pos early respiratory progenitor cells towards mature respiratory

human induced pluripotent stem cell (hiPSC) line, which enables modulation of telomerase activity and telomere length at will. Furthermore utilizing the power of hiPSC differentiation protocols, these cells [...] tracking of human cardiomyocyte proliferation We have developed a human induced pluripotent stem cell (hiPSC) fluorescent reporter line to track and sort replicating cardiomyocytes, overcoming the limitations

Primary Immunodeficiencies Volume 11 - 2020 https://doi.org/10.3389/fimmu.2020.608802 Generation of two hiPSC lines (MHHi016-A, MHHi016-B) from a primary ciliary dyskinesia patient carrying a homozygous 5 bp

Lachmann, N., Ringshausen, F. C., Welte, T., Martin, U. , and Olmer, R. 2020. Generation of two hiPSC lines (MHHi016-A, MHHi016-B) from a primary ciliary dyskinesia patient carrying a homozygous 5 bp [...] A., Göhring, G., Welte, T., Martin, U., Ringshausen, F. C., and Olmer, R. 2020. Generation of two hiPSC clones (MHHi019-A, MHHi019-B) from a primary ciliary dyskinesia patient carrying a homozygous deletion