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For better diagnosis of rare/genetic diseases
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For better diagnosis of rare/genetic diseases

RESEARCH ORGANIZATION OF INFORMATION AND SYSTEMS IMAGE: RESEARCH TEAM UPGRADED CLINICAL DECISION SUPPORT SYSTEM PUBCASEFINDER TO PROVIDE BETTER DIAGNOSIS WITH RARE/GENETIC DISEASE CREDIT: © 2022 FUJIWARA ET AL. HUMAN MUTATION PUBLISHED BY WILEY PERIODICALS LLC Even trained experts can spend hours looking for trusted medical sources (e.g., textbooks, literature, and databases) for candidate diseases to...

Single test for more than 50 genetic diseases will cut diagnosis from decades to days
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Single test for more than 50 genetic diseases will cut diagnosis from decades to days

by Garvan Institute of Medical Research Dr Ira Deveson of the Garvan Institute of Medical Research. Credit: Garvan Institute of Medical Research A new DNA test, developed by researchers at the Garvan Institute of Medical Research in Sydney and collaborators from Australia, UK and Israel, has been shown to identify a range of hard-to-diagnose neurological...

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Simplifying RNA editing for treating genetic diseases

UNIVERSITY OF CALIFORNIA – SAN DIEGO New research led by bioengineers at the University of California San Diego could make it much simpler to repair disease-causing mutations in RNA without compromising precision or efficiency. The new RNA editing technology holds promise as a gene therapy for treating genetic diseases. In a proof of concept, UC...

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How mRNA and DNA vaccines could soon treat cancers, HIV, autoimmune disorders and genetic diseases

January 24, 2022 8.31am EST Author Deborah FullerProfessor of Microbiology, School of Medicine, University of Washington The two most successful coronavirus vaccines developed in the U.S. – the Pfizer and Moderna vaccines – are both mRNA vaccines. The idea of using genetic material to produce an immune response has opened up a world of research...

Innovative drug delivery system offers hope for treating genetic diseases
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Innovative drug delivery system offers hope for treating genetic diseases

HARVARD UNIVERSITY IMAGE: POSTDOCTORAL FELLOW SAMAGYA BANSKOTA (LEFT) AND GRADUATE STUDENT ADITYA RAGURAM (RIGHT), CO-LEAD AUTHORS, INVESTIGATE IN VIVO DELIVERY OF THERAPEUTIC PROTEINS AT THE LIU LAB. CREDIT: JULIA MCCREARY/ HARVARD GRADUATE STUDENT. A team of researchers led by Harvard and Broad Institute scientists has developed a new drug delivery system using engineered DNA-free virus-like...

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Super-precise new CRISPR tool could tackle a plethora of genetic diseases

The system allows researchers more control over DNA changes, potentially opening up conditions that have challenged gene-editors. Heidi Ledford For all the ease with which the wildly popular CRISPR–Cas9 gene-editing tool alters genomes, it’s still somewhat clunky and prone to errors and unintended effects. Now, a recently developed alternative offers greater control over genome edits — an advance...

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Common genetic variant explains why immunotherapy often fails in Crohn’s disease

By Lois Zoppi, BAReviewed by Kate Anderton, B.Sc. (Editor) The reason why a commonly used range of drugs is not effective in some patients living with Crohn’s disease has so far not been identified. However, a collaboration between the University of Exeter, Royal Devon & Exeter NHS Foundation Trust and the Wellcome Sanger Institute has discovered a genetic marker...

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