Sentences with phrase «rare diseases research funding»

You will find here the information about the opportunities of rare diseases research funding at the national level in «National RD funding initiatives» and «Next generation sequencing facilities database» that groups sequencing platforms from Europe and Associated countires.

Since 2006, E-Rare has become one of the major contributors to transnational rare diseases research funding.

Next to performing Joint Transnational Calls and assessment of the funding mechanisms and results of the funded research projects the E-Rare-1 and E-Rare-2 programmes paid attention to deepening the cooperation and coordination among the E-Rare partners by systematic exchange of information on the national programmes and by strategic activities aimed at a sustainable development and extension of the network of rare disease research funders.

Not exact matches

Because this form of cancer is rare, even the Complaint acknowledged that it was difficult for Dr. Taub to get funding to conduct research on a disease that causes so much pain and suffering.

Congressman Chris Collins, along with local medical experts and families living with rare diseases, urged members of the U.S. Senate to pass legislation that boosts funds for research.

And in the United States, the National Human Genome Research Institute in Bethesda, Maryland, recently funded three Mendelian Disorders Sequencing Centers that will apply genome sequencing to diagnosing thousands of patients with a wider range of rare diseases, including intellectual disability and developmental delay.

«Steep funding cuts for the federal health agencies are counterproductive at a time when innovative research is moving us closer to identifying solutions for rare diseases, new prevention strategies to protect Americans from deadly and costly conditions, advances in gene therapy, new technologies for understanding the brain, and treatments that harness the ability of our immune system to fight cancer.»

The researchers conducted a survey of 210 patients with physician - diagnosed mitochondrial disease recruited through the National Institutes of Health - funded Rare Diseases Clinical Research Network.

European Journal of Human Genetics has published a key publication describing the achievements of three flagship EU - funded projects — RD - Connect, NeurOmics and EURenOmics — and how they are shaping the rare disease research environment in Europe and globally.

Funding organizations (i.e., funding bodies, groups of funders (for small funders), companies) investing more than 10 million USD over 5 years in rare disease rFunding organizations (i.e., funding bodies, groups of funders (for small funders), companies) investing more than 10 million USD over 5 years in rare disease rfunding bodies, groups of funders (for small funders), companies) investing more than 10 million USD over 5 years in rare disease research

Survey and Strategic Analysis on Future Themes and Needs for Rare Diseases Research Funding In the European Council recommendation on rare diseases (RD), Member States arRare Diseases Research Funding In the European Council recommendation on rare diseases (RD), Member States arrare diseases (RD), Member States are...

EURenOmics is collaborating with E-Rare, a consortium built to link responsible funding bodies that combine the scarce resources and fund rare disease research via Joint Transnational Calls.

Her current research is focused on the identification of genes and molecular pathways for rare disorders and she is the Lead Investigator of the Genome Canada, CIHR funded «Finding of Rare Disease Genes in Canada» (FORGE Canada) and «Enhanced CARE for RARE Genetic Diseases in Canada» initiatirare disorders and she is the Lead Investigator of the Genome Canada, CIHR funded «Finding of Rare Disease Genes in Canada» (FORGE Canada) and «Enhanced CARE for RARE Genetic Diseases in Canada» initiatirare disorders and she is the Lead Investigator of the Genome Canada, CIHR funded «Finding of Rare Disease Genes in Canada» (FORGE Canada) and «Enhanced CARE for RARE Genetic Diseases in Canada» initiatiRare Disease Genes in Canada» (FORGE Canada) and «Enhanced CARE for RARE Genetic Diseases in Canada» initiatiRare Disease Genes in Canada» (FORGE Canada) and «Enhanced CARE for RARE Genetic Diseases in Canada» initiatiRARE Genetic Diseases in Canada» initiatiRARE Genetic Diseases in Canada» initiatives.

This tool is one of the main outcomes of RD - Connect, the EU - funded project that has built a community of patients, clinicians, researchers and bioinformaticians in Europe and beyond, and has advanced collaboration and data sharing to facilitate and accelerate research for rare diseases.

Summary: A two day meeting to demonstrate to the wider scientific community where the IMPC is trying to go and how to include clinical scientists, geneticists and the rare disease research community, followed by two simultaneous one day workshops (phenotyping and EUCOMMTOOLS) to plan for Phase II phenotyping and discuss production technology development Attended by: IMPC members, corporate sponsors, external delegates, EUCOMMTOOLS members and IKMC members Hosted / funded by: Infrafrontier, EUCOMMTOOLS, CNR Monterotondo

That quick turnaround is particularly important for rare and orphan diseases, those that affect fewer than 200,000 people nationwide, because families and family - run foundations typically fund that research and they do so against a ticking clock — the life of their loved one.

The goal of IRDiRC is to team up researchers and funding organizations across the world that are strongly involved in rare diseases research in order to achieve two main and ambitious objectives: deliver 200 new therapies for rare diseases and means to diagnose most rare diseases by the year 2020.

About the International Rare Diseases Research Consortium (IRDiRC): IRDiRC was formed to unite public and private sector funders of research, patient advocacy groups, and scientific researchers to advance rare diseases research worldwRare Diseases Research Consortium (IRDiRC): IRDiRC was formed to unite public and private sector funders of research, patient advocacy groups, and scientific researchers to advance rare diseases research woResearch Consortium (IRDiRC): IRDiRC was formed to unite public and private sector funders of research, patient advocacy groups, and scientific researchers to advance rare diseases research woresearch, patient advocacy groups, and scientific researchers to advance rare diseases research worldwrare diseases research woresearch worldwide.

The successful linking of research funding organizations in E-Rare-1 and the subsequent exemplary joint funding activities have attested the need of, and the acknowledgment from, the research community for transnational funding of collaborative, multidisciplinary and ambitious projects on rare diseases.

Funded as part of the EU's commitment to the International Rare Diseases Research Consortium (IRDiRC), RD - Connect is a global infrastructure project that links omics data with databases, registries, biobanks, and clinical bioinformatics tools into a central research resource for rare diseaRare Diseases Research Consortium (IRDiRC), RD - Connect is a global infrastructure project that links omics data with databases, registries, biobanks, and clinical bioinformatics tools into a central research resource for rare dResearch Consortium (IRDiRC), RD - Connect is a global infrastructure project that links omics data with databases, registries, biobanks, and clinical bioinformatics tools into a central research resource for rare dresearch resource for rare disearare diseases.