Many human genes are regulated through alternative promoter utilisation, some examples of which can be induced by experiment, and many of which occur in diseases such as cancer. Read more
Asia is a center of bee evolution and its crops and native vegetation depend on bee pollination. However, relatively little is known about the life history, biogeography, and conservation status of regional pollinators (Warrit et al. Read more
Project Description. Prokaryotes, the microscopic architects of our biosphere, harbor intricate immune systems that stand as the guardians of their genetic sanctity against the incessant assault of phages and other mobile genetic elements. Read more
I am interested in students with experience in quantitative methods and a passion for ecology and conservation. Quantitative methods include mathematical analysis and computer simulation. Read more
Using molecular techniques such as RADseq, population genomics seeks to use the unparalleled resolution that several thousand Single Nucleotide Polymorphisms (SNPs) can provide. Read more
Digital media is central to our engagement with public information, news, government services, healthcare, finance, education, culture and entertainment, and facilitates communication and social interaction. Read more
PhD in Chemistry - Developing innovative organofluorine chemistry. Dr Matthew Tredwell is looking for a PhD student to develop innovative organofluorine chemistry. Read more
Signaling transduction at membrane interface plays an essential role in human health and diseases. The Sun lab combines structural biology, cell biology, pharmacology and biochemistry approaches to characterize important cell signaling events in atomic details. Read more
The Rousseau lab is interested in decoding how protein degradation by the proteasome is regulated in cells so that accumulation of unfolded, misfolded, or damaged proteins can be cleared before they become deleterious. Read more
Translation of mRNA into proteins is a critical cellular biological process. We recently described a novel human disorder, now called Faundes-Banka Syndrome (FABAS), caused by heterozygous variants in EIF5A1 that encodes a translation factor. Read more
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