Funding is key when it comes to developing an idea or research result. Every year, KTH Innovation helps KTH projects secure over 40 million SEK in funding.
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The Fondation Maladies Rares is pleased to announce the launch of its “GenOmics” 2024 call for projects.
The aim of this AAP is to support hypothesis-driven research projects aimed at exploring the genetic and molecular basis of rare diseases using NGS approaches (WES, WGS, RNA-seq, small RNA-seq, ChIP-seq, Methyl-seq, etc.).
Support from the Fondation Maladies Rares will give project leaders access to innovative high-throughput sequencing technologies for the analysis of exomes, genomes, transcriptomes or epigenomes.
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Towards a Concrete Improvement in the Quality of Life of Patients with Autoimmune Myasthenia
Published by FONDATION MALADIES RARES
Autoimmune MyastheniaThe Fondation Maladies Rares and UCB have joined forces to offer a €30, 000 research grant to a humanities and social sciences (HSS) research project focused on findingconcrete, short-term ways ofimproving the life course of patients suffering from generalized autoimmune myasthenia gravis.
The grant will be awarded to a research project focusing on the individual, family and/or social consequences specifically linked to generalized autoimmune myasthenia gravis, in order to gain a better understanding of the impact of this disease, and in particular muscular fatigability, on quality of life at the level of the individual, couple or family, for example.
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Sanofi iAwards Europe
Published by SANOFI
Cell and Gene TherapiesOncologyImmunologyInflammatory DiseasesRare and Neurological DiseasesA booster to transform groundbreaking ideas in the field of target identification, disease knowledge and translational science into innovative therapeutic solutions. We partner with best-in-class academics to serve a common goal: accelerating innovation for patients.
View this resource Bookmark this resourceIn addition to traditional grantmaking to support people and organizations working toward our missions in Science, Education, and within our communities, the Chan Zuckerberg Initiative makes venture investments in impact-focused companies, builds tools and products that we can scale and give away for free, and supports capacity building to achieve progress across our work.
View this resource Bookmark this resourceThis scheme provides funding for established researchers and teams from any discipline who want to pursue bold and creative research ideas to deliver significant shifts in understanding that could improve human life, health and wellbeing.
View this resource Bookmark this resourceOIF will invest in early stage technology projects in order to make a return which is funnelled back into this self-sustaining “evergreen” fund. The OIF is endowed by charitable donors to the University as part of the Oxford Thinking campaign. It supports early-stage, proof-of-concept activity.
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Path to a Cure — Collaborative Research Grant
Published by Cystic Fibrosis Foundation
GrantCystic FibrosisThis program is intended to facilitate research that will contribute to the development of new therapies or therapeutic strategies to treat cystic fibrosis with an emphasis on advancing CFTR gene repair and replacement approaches.
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Primary Bone Cancer Consortium Funding Support
Published by Bone Cancer Research Trust
GrantBone CancerThe Primary Bone Cancer Consortium Funding Support from the Bone Cancer Research Trust provides funding for UK and international consortium working on bone sarcoma clinical and translational research. The consortium must include researchers from at least 5 countries and at least one group must be based in the UK. Applicants may apply for up to 240,000 GBP for projects spanning at least 3 years. Applications close on July 1, 2022.
View this resource Bookmark this resourceThe Society’s Board of Directors is pleased to announce the approval of $725,000 in new funding to be awarded as part of the Society’s competitive research grants program for 2022. These funds are made available through the great generosity of friends of the Society and especially through the efforts of our membership families. This year, the funds are dedicated to be used to further the research needs of syndromes as described below.
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