DFG Research Unit FOR2722
Novel molecular determinants for musculoskeletal extracellular matrix homeostasis - a systemic approach
At a glance
Projekte
Organisation
Publikationen
Events
Jobs
Kontakt
Highlights
New publication by project D1
The research unit FOR2722 congratulates Prof. Brunhilde Wirth for her outstanding detective work in science.
VWA1 identified as a new disease gene for neuromyopathy: An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy
New publication by projects B1 and D2
New publication by project D2
New publication by project D2
New specific HSP47 functions in collagen subfamily chaperoning
New publication by project B1

Novel structure-function relationships of myopathy patient mutations in collagen VI identified by Mats Paulsson and Raimund Wagner of the Research Unit. Results shed light on possible myopathy mechanisms.
New publication by project D2:
New publication by project D1:
The University of Oulu will confer an honorary doctorate to FOR2722 member Prof. Mats Paulsson
The research unit FOR2722 congratulates Prof. Mats Paulsson for receiving the honorary degree of the University of Oulu.
New publications by project D2:
Autosomal-Recessive Mutations in MESD Cause Osteogenesis Imperfecta
New publication by project B1:

This article has been recommended in F1000Prime as being of special significance in its field by F1000 Faculty Member Peter Torzilli.
FOR2722 member Prof Dr. Brunhilde Wirth receives the NRW-Innovation prize 2019

The state government of North Rhine-Westphalia awarded the NRW-Innovation prize 2019 to Prof. Dr. Brunhilde Wirth for her groundbreaking research on spinal muscular dystrophy.
The research unit FOR2722 congratulates Prof. Dr. Brunhilde Wirth and wishes her every success for her future research.