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SUMMARY:Rare Disease Models and Mechanisms-Europe registry open for regist
 ration
DTSTART;VALUE=DATE:20190219
DTSTAMP:20260428T082542Z
UID:0536a807a379550513200f1dc22fee6c82013a2cd18cf69e6d4d385d
CATEGORIES:Call for proposal
DESCRIPTION:Rare Disease Models and Mechanisms-Europe registry open for re
 gistration\n“Solve-RD – Solving the unsolved Rare Diseases” is a lar
 ge European research project funded by the EU for five years (2018-2022) u
 nder Horizon 2020. The consortium is collaborating with European reference
  networks (ERNs) to improve the diagnosis of rare diseases.\nSolve-RD is a
 bout to establish a European Rare Disease Models & Mechanisms Network (RDM
 M-Europe) using the successful Canadian blueprint as a role model.\nThe go
 al of RDMM-Europe is to link clinicians discovering new genes in patients 
 with rare diseases with basic scientists\, who can functionally analyze eq
 uivalent genes and pathways in model organisms. Solve-RD will provide 50 S
 eeding Grants (20.000 EUR each) to fund projects that will allow rapid con
 firmation of potentially disease-causing genes and elucidation of the unde
 rlying molecular disease mechanisms. For more information please check the
  Solve-RD website or contact Sanja Hermanns (sanja.hermanns@med.uni-tuebin
 gen.de).\n 
LOCATION:
STATUS:CONFIRMED
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