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Mutations in HSPB5, HSPB7 and BAG3 lead to juvenile DCM

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Title: Mutations in HSPB5, HSPB7 and BAG3 lead to juvenile DCM.
Investigators:  post-doc (vacancy)
Promoter: HH Kampinga (PI)
Co-promoter:  BJJM Brundel (Co-PI)
Summary:   Mutations in specific heat shock proteins lead to juvenile DCM. We hypothesize that such mutations in these chaperones impairs the maintenance of protein homeostasis and thus lead to alterations in cardiomyocyte structure and contractile function. Insight in why these mutants cause DCM will help to understand how DCM arises in general. Also, it will allow testing how loss of protein homeostasis might be compensated for by boosting protein quality control and how this may help delaying disease onset. It is the aim of this project to investigate whether such events may be prevented by boosting the expression levels of (specific) heat shock proteins in cells derived from juvenile DCM patients. 
Financing:  Stichting Hartdroom, Dutch Heart Foundation, post-doc
Start:   01-09-2014
End: 01-09-2017

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Mutations in HSPB5, HSPB7 and BAG3 lead to juvenile DCM.
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