Model matchmaking via the Solve-RD Rare Disease Models & Mechanisms Network (RDMM-Europe)

  • Kornelia Ellwanger*
  • , Julie A. Brill
  • , Elke de Boer
  • , Stephanie Efthymiou
  • , Ype Elgersma
  • , Marynelle Icmat
  • , François Lecoquierre
  • , Amanda G. Lobato
  • , Manuela Morleo
  • , Michela Ori
  • , Ashleigh E. Schaffer
  • , Antonio Vitobello
  • , Sara Wells
  • , Binnaz Yalcin
  • , R. Grace Zhai
  • , Marc Sturm
  • , Birte Zurek
  • , Holm Graessner
  • , Eva Bermejo-Sánchez
  • , Teresinha Evangelista
  • Nicoline Hoogerbrugge, Vincenzo Nigro, Rebecca Schüle, Alain Verloes, Han Brunner, Philippe M. Campeau, Paul Lasko, Olaf Riess*
*Corresponding author for this work

Research output: Contribution to journalComment/Letter to the editorAcademicpeer-review

4 Citations (Scopus)
34 Downloads (Pure)

Abstract

In biomedical research, particularly for rare diseases (RDs), there is a critical need for model organisms to unravel the mechanistic basis of diseases, perform biomarker studies and develop potential therapeutic interventions. Within Solve-RD, an EU-funded research project with the aim of solving large numbers of previously unsolved RDs, the European Rare Disease Models & Mechanisms Network (RDMM-Europe) has been established.

Original languageEnglish
Pages (from-to)161-165
Number of pages5
JournalLab Animal
Volume53
Issue number7
DOIs
Publication statusPublished - Jul 2024

Bibliographical note

Publisher Copyright:
© The Author(s) 2024.

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