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Gene Mutation Linked to Childhood Blindness
The findings shed light on childhood blindness and help to explain how genes contribute to the development of the eye.
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The Origin of RNA – A Simple Chemical Solution for Developing Purines and Pyrimidines
A single process for how a group of molecules called nucleotides were made on the early Earth, before life began, has been suggested by a UCL-led team of researchers.
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Liver Scarring Protein Identified in Breakthrough Study
The team analysed liver samples from 2000 patients with Hepatitis C, using state-of-the-art genetic and functional analysis, to determine the specific IFNL protein responsible for liver fibrosis.
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BMS, Nordic Bioscience Collaborate on Fibrosis Biomarker Tech
Collaboration to develop translational biomarkers for fibrotic diseases, including non-alcoholic steatohepatitis (NASH).
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Making Big Data More Accessible
Database tool provides a new strategy for compiling big data in a human-centric way.
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Inhibiting Tumor Suppression Gene Could Present Counter-intuitive Cancer Therapy
Ludwig researchers have shown that one way to override the growth-promoting effects of PTEN deletion is, surprisingly, to inhibit a separate tumor suppressor gene.
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Novel Epigenetic Changes Play Role in 20 Percent of AML Cases
Research adds to understanding of cancers that carry IDH mutation.
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Cat Genomics Study Reveals Rare Genetic Disorders
Findings could help feline preservationists implement breeding strategies for rare species.
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Eye-targeting Virus Could Be a Useful Tool for Gene Delivery
New understanding of structural details could be key to using viruses for gene therapies.
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Gene Variant on Chromosome 12 Implicated in Anorexia
UNC researchers led the most powerful genomic study of anorexia nervosa conducted to date to identify the common roots anorexia shares with psychiatric and metabolic traits.
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