04/06/2020
Free mouse model development service
Call information and application form
Open call for development of one novel mouse model of human disease to the biomedical research community based in Greece. The novel mouse line should advance knowledge of human disease and should be of widespread use in biomedical science.
04/06/2020
Free mouse model development service
Call information and application form
Open call for development of one novel mouse model of human disease to the biomedical research community based in Greece. The novel mouse line should advance knowledge of human disease and should be of widespread use in biomedical science.
Mouse Phenotyping
Mouse Phenotyping
Mouse Phenotyping
INFRAFRONTIER/IMPC Stakeholder Meeting 2018
INFRAFRONTIER/IMPC Stakeholder Meeting 2018
Advancing Rare Disease Research and Gene Therapy Applications with Animal Models, 3-4 Dec 2018, Munich
The second Stakeholder Meeting of INFRAFRONTIER, the European Research Infrastructure for phenotyping and archiving of model mammalian genomes, will be jointly organized with the International Mouse Phenotyping Consortium (IMPC). The thematic focus of the meeting is on advancing Rare Disease research and gene therapy applications with animal models.
The Stakeholder Meeting provides an excellent opportunity to support a better alignment of INFRAFRONTIER / IMPC platforms with current Rare Disease research and personalised medicine initiatives and supports interactions with human genetics centers and clinical consortia. New partnerships can support the rapid impact of mouse functional genomics analyses on the understanding of human genetic variation and disease, and the translation into diagnostic and therapeutic approaches.
The Stakeholder Meeting will be structured into three main parts:
- Advancing Rare Disease research with animal models
- Gene therapy applications using animal models
- Young Investigator / Stakeholder presentations
Meeting aims are to:
- Raise awareness of INFRAFRONTIER / IMPC platforms among the Rare Disease community
- Present use cases for the utility of animal models to advance Rare Disease research
- Share advances in gene therapy applications, including gene-editing approaches to cure human diseases
- Strengthen interactions with Rare Disease and clinical research consortia
- Support presentation of use cases by Young Investigators
Programme outline
Session topics
Monday, December 3
- Model organisms facilitate Rare Disease diagnosis and therapeutic research
- Genomic Medicine and EU collaborative initiatives targeting Rare Diseases
- Funder and regulator perspectives on Rare Disease modeling and gene therapy applications
- Poster session
- Young investigator presentations
- Panel discussion: Advancing Rare Disease diagnosis and therapeutic research with model organisms - building bridges between basic and clinical research
Tuesday, December 4
- Animal models for human gene therapy applications
- Gene editing in gene therapy of human (rare) diseases
- Optimising gene editing for therapeutics
- Gene editing for advanced therapies – Ethics, governance, policy, and society
- Young investigator presentations
Meeting venue
Hilton Munich Park Hotel
Meeting venue
Hilton Munich Park Hotel