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INFRAFRONTIER: a European resource for studying the functional basis of human disease

Authors :
Ana Ambrosio de Castro
Martin Hrabě de Angelis
Sabine Fessele
Michael Raess
Valerie Gailus-Durner
Source :
Mammalian genome (Internet) 27 (2016): 445–450. doi:10.1007/s00335-016-9642-y, info:cnr-pdr/source/autori:Raess M.1, de Castro A.A.1, Gailus-Durner V.2, Fessele S.1, Hrab? de Angelis M.3,4; INFRAFRONTIER Consortium/titolo:INFRAFRONTIER: a European resource for studying the functional basis of human disease/doi:10.1007%2Fs00335-016-9642-y/rivista:Mammalian genome (Internet)/anno:2016/pagina_da:445/pagina_a:450/intervallo_pagine:445–450/volume:27, Mammalian Genome, Mamm. Genome 27, 445-450 (2016)
Publisher :
Springer Nature

Abstract

Ageing research and more generally the study of the functional basis of human diseases profit enormously from the large-scale approaches and resources in mouse functional genomics: systematic targeted mutation of the mouse genome, systemic phenotyping in mouse clinics, and the archiving and distribution of the mouse resources in public repositories. INFRAFRONTIER, the European research infrastructure for the development, systemic phenotyping, archiving and distribution of mammalian models, offers access to sustainable mouse resources for biomedical research. INFRAFRONTIER promotes the global sharing of high-quality resources and data and thus contributes to data reproducibility and animal welfare. INFRAFRONTIER puts great effort into international standardisation and quality control and into technology development to improve and expand experimental protocols, reduce the use of animals in research and increase the reproducibility of results. In concert with the research community and the International Mouse Phenotyping Consortium (IMPC), INFRAFRONTIER is currently developing new pilot platforms and services for the research on ageing and age-related diseases.

Details

Language :
English
ISSN :
09388990
Volume :
27
Issue :
7-8
Database :
OpenAIRE
Journal :
Mammalian Genome
Accession number :
edsair.doi.dedup.....f294cd34f42edfd88e35c6360d412a54
Full Text :
https://doi.org/10.1007/s00335-016-9642-y