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Christina Mauritz

Researcher at Hannover Medical School

Publications -  9
Citations -  921

Christina Mauritz is an academic researcher from Hannover Medical School. The author has contributed to research in topics: Induced pluripotent stem cell & Embryonic stem cell. The author has an hindex of 8, co-authored 9 publications receiving 894 citations.

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Generation of Functional Murine Cardiac Myocytes From Induced Pluripotent Stem Cells

TL;DR: The aim of this study was to characterize the cardiac differentiation potential of a murine iPS cell clone in comparison to a well-established murine ES cell line, and found that iPS cells differentiate into functional cardiomyocytes.
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Induced pluripotent stem cell (iPSC)-derived Flk-1 progenitor cells engraft, differentiate, and improve heart function in a mouse model of acute myocardial infarction

TL;DR: A first proof of concept study evaluates the potential of a murine iPSC-derived cardiovascular progenitor population, which expresses the surface marker foetal liver kinase-1 (Flk-1), to restore myocardial tissue and improve cardiac function after acuteMyocardial infarction (MI) in mice and paves the way for an autologous i PSC-based therapy of MI.
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Human and rat adult Schwann cell cultures: fast and efficient enrichment and highly effective non-viral transfection protocol.

TL;DR: A fast protocol that can be used to obtain highly purified cultures of proliferating adult human and rat Schwann cells accessible for non-viral transfection methods and results in Schwann cell cultures that are more than 90–95% pure.
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Comparative study of cell culture and purification methods to obtain highly enriched cultures of proliferating adult rat Schwann cells.

TL;DR: A fast protocol is presented that could be used to obtain highly purified cultures of maximal proliferating adult rat Schwann cells, which can be transfected in a nonbiological way using the physical transfection method of electroporation.
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Serum-free differentiation of murine embryonic stem cells into alveolar type II epithelial cells.

TL;DR: The results demonstrate the differentiation of AT2-like cells from mESCs after serum-induction and under serum-free conditions and will facilitate the identification of key differentiation factors leading to a more specific and effective generation of AT1- like cells from ESCs.