Main Content Research Groups A-Z Jan Pieter Abrahams Uncovering the fundamental shapes of life Markus Affolter Development of blood vessels and complex organs Silvia Arber Motor circuit function Marek Basler Unraveling the…
The Biozentrum organizes a symposium for its employees and students annually. This provides an insight into other areas of research, as well as an overview of the many projects being carried out. Furthermore, the symposium…
This event brings together researchers from the Biozentrum and the Roche Division “Pharmaceutical Research and Early Development” (pRED) and provides them with a platform for scientific exchange, to explore new collaboration…
CV of Prof. Dr. Alex Schier ORCID 0000-0001-7645-5325 Google Scholar Google Scholar Nationality : Swiss/US Positions: Since 2018 Director of the Biozentrum, University of Basel 2014 – 2017 Chair of the Department of…
Press release of the cantons of Basel-Stadt and Basel-Landschaft The governments of the cantons of Basel-Stadt and Basel-Landschaft, represented by Conradin Cramer, Hans-Peter Wessels, Monica Gschwind and Isaac Reber, handed…
How does a complex organism with a large number of different cells develop from a single cell? What are the common ancestors of the individual cells and how are they related to each other? What are the signals that drive the…
The Biozentrum is celebrating its 50th anniversary in 2021. To properly mark the occasion, the 73-meter-high new building was dedicated on Tuesday. Eight years after breaking ground and right on time for the beginning of the…
2023 was a year of significant scientific discoveries and exciting community activities. A major highlight was our first World Alumni Day, celebrating our global community and renewing as well as fostering connections. More…
A farewell event will be held on June 4, 2021, at 4 p.m. in honor of Martin Spiess, who has been Professor of Biochemistry at the Biozentrum since 1986. The program includes a welcome speech as well as words of thanks by the…
Congenital muscular dystrophy is a rare hereditary disease which cannot be cured. The more than 30 known forms of this neuromuscular disease differ in the type of genetic defect and in the severity of disease progression.…
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