Susann Meyer

03.12.2021

The fibres of the cytoskeleton (in blue) and the mitochondria (in yellow) are clearly visible in their structure due to the microscope used and the dyes that are (further) developed in parallel at abberior.
Image: Francesca Bottanelli, FU Berlin, © abberior Instruments GmbH

03.12.2021

Technology transfer award for light microscopes with molecular resolution

For the entrepreneurial implementation of research results in the field of high-resolution light microscopy, abberior Instruments GmbH, the Max Planck Innovation GmbH and the Max Planck Institute for Biophysical Chemistry […]

02.12.2021

Dr. Funsho Fakuade, UMG, receives Dissertation Prize. Photo: MBExC.

02.12.2021

Funsho Fakuade receives Dissertation Prize

The MBExC congratulates Hertha Sponer College member Funsho Fakuade, Institute of Pharmacology and Toxicology at the UMG, for receiving the Dissertation Prize 2020 of the Universitätsbund Göttingen e.V. His excellently […]

01.12.2021

Ann Statist

01.12.2021

Posterior analysis of n in the binomial (n,p) problem with both parameters unknown — with applications to quantitative nanoscopy

Schmidt-Hieber J, Schneider LF, Staudt T, Krajina A, Aspelmeier T, Munk A

24.11.2021

Cell Rep

24.11.2021

The TFAM-to-mtDNA ratio defines inner-cellular nucleoid populations with distinct activity levels

Brüser C, Keller-Findeisen J, Jakobs S

23.11.2021

f.l.: First author, Dr. Luis Daniel Cruz-Zaragoza, scientist at the Department of Cellular Biochemistry, UMG, and senior author, Prof. Dr. Peter Rehling, Director of the Department of Cellular Biochemistry, UMG. Photo: R. Yousefi, UMG.

23.11.2021

Targeting gene expression in mitochondria

Scientists of the Göttingen Cluster of Excellence Multiscale Bioimaging (MBExC) and the Collaborative Research Center 1190 develop novel strategy to investigate gene expression in mitochondria. Published in “Cell”. Mitochondria […]

22.11.2021

Marmosets at the German Primate Center.
Photo: Anton Säckl

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 […]