In a global study led by Dr Brian Chung Hong-yin (left), the HKUMed research team identifies a novel gene, DDX39B, for a rare ...
Biologists have discovered a new type of RNA-splicing regulation that helps to determine which protein-coding exons will be included in messenger RNA transcripts.
Rett syndrome is a rare genetic disease affecting 1 in 10,000 newborn girls, characterized by sudden regression around 1 year ...
Roche's innovative sequencing by expansion (SBX) technology represents a leap forward in next-generation sequencing (NGS), ...
Highly valued economically, ecologically and culturally, the white oak (Quercus alba) is a keystone forest species and is one ...
Researchers from the Bellvitge Biomedical Research Institute (IDIBELL) and the Germans Trias i Pujol Research Institute (IGTP) have studied variations in mRNA length during the progression of ...
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