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22.11.2021

Gene therapy against deafness

One in 500 children is born with hearing impairment, and in 50 to 70 percent of cases a genetic defect is the cause. In a joint research project, a team led by Rüdiger Behr (German Primate Center) and MBExC spokesperson Tobias Moser (University Medical Center Göttingen) in cooperation with scientists
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22.11.2021

Postnatal expression of the lysine methyltransferase SETD1B is essential for learning and the regulation of neuron-enriched genes

Authors Michurina A, Sakib MS, Kerimoglu C, Krüger DM, Kaurani L, Islam MR, Devesh JP, Schröder S, Centeno TP, Zhou J, Pradhan R, Cha J, Xu X, Eichele G, Zeisberg EM, Kranz A, Stewart AF, Fischer A Journal Embo Journal Citation EMBO J (2021)e106459. Abstract In mammals, histone 3 lysine
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