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Heinrich-Heine University Duesseldorf


Incurable Leigh Syndrome: German scientists create first human model for rare disease

Researchers developed a human model of Leigh syndrome caused by SURF1 mutations, discovering that energy deficits in neural precursors lead to neuronal defects and brain function impairment. This breakthrough provides potential therapeutic strategies, including gene replacement therapy and the use of Bezafibrate, for treating children ...

SourceHeinrich-Heine University Duesseldorf·JournalNature Communications·DateMar 26, 2021

Evolution of cereal spikes

Scientists have identified a gene responsible for varying cereal spike forms, offering a possible solution to increasing grain yields. The research focuses on the INT-M/DUB1 gene's ability to regulate meristem activity and determine lateral spikelet formation.

SourceHeinrich-Heine University Duesseldorf·JournalProceedings of the National Academy of Sciences·DateFeb 15, 2021

Hydrogen energy at the root of life

A new study by Dr. Martina Preiner and colleagues simulates the emergence of life in a lab environment using hydrogen gas and carbon dioxide as starting materials. The team found that these simple chemical reactions can produce the same building blocks used by early cells, providing insight into the origins of life.

SourceHeinrich-Heine University Duesseldorf·JournalNature Ecology & Evolution·DateMar 2, 2020

Human iPSC-derived MSCs from aged individuals acquire a rejuvenation signature

Researchers have discovered that human iPSC-derived MSCs (iMSCs) from aged individuals acquire a rejuvenation-associated 50-gene signature, which is also expressed in pluripotent stem cells. This finding highlights the potential of iMSCs to act via paracrine signalling and circumvent drawbacks associated with adult MSCs.

SourceHeinrich-Heine University Duesseldorf·JournalStem Cell Research & Therapy·DateApr 10, 2019