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Researchers in Finland and Norway have discovered a gene defect that causes a novel inherited immune deficiency. The same gene, DIAPH1, has been previously shown to cause SCBMS syndrome, a rare genetic disease associated with severe brain development defects.
A new study from FIMM group leader, Johan Lundin, at the University of Helsinki and Karolinska Institutet shows that artificial intelligence-supported digital microscopy at the point-of-care can be used to identify atypical Pap smears in a resource-limited setting.
Congratulations to Himanshu Sharma, a postdoctoral researcher in the Barandun Lab at MIMS & the Department of Molecular Biology, Umeå University on receiving a prestigious Marie Skłodowska-Curie Actions (MSCA) Individual Fellowship.
The EMBL (European Molecular Biology Laboratory) Council helps to guide EMBL's operations, administratively and scientifically.
Blog by NCMM group leader, Dr Sebastian Waszak: Whilst there has been good progress in treating many types of childhood cancer, some remain incurable. New precision medicine approach offers hope for young patients diagnosed with a rare and incurable brain tumour.
Lecture by Richard L. Huganir, Professor at the Department of Neuroscience, Kavli Neuroscience Discovery Institute, Johns Hopkins University School…
Intended for (PhD) students and postdocs, aiming to learn EM, or those who already started an EM project and would like to get an overview.