Double hit of new appointments for Head of Molecular Endocrinology and Pharmacology
By Alicia Bienkowski | Molecular Endocrinology and Pharmacology, Molecular Medicine, News & EventsPerkins’ Head of Molecular Endocrinology and Pharmacology, Professor Kevin Pfleger, was appointed President of the Australasian Society of Clinical and Experimental Pharmacologists and Toxicologists (ASCEPT) earlier this month. Coincidentally, on…
$20M for biopharm DIMERIX to fund phase 3 trials for rare kidney disease
By Alicia Bienkowski | Chronic Kidney Disease, Funding, Kidney Disease, Kidneys, Media Releases, Molecular Endocrinology and Pharmacology, Molecular Medicine, News & Events, Research AreaBiopharmaceutical company, Dimerix (ASX: DXB), which is developing new treatments for types of inflammatory kidney and respiratory diseases, announced it has successfully raised $20 million to fund Phase 3 trials…
One in twenty five couples found to be at high risk of having a baby with a recessive genetic condition
By Alicia Bienkowski | DNA, Genes, Genetic Disease, Genetic Disease, Genetic Neuromuscular Disorders, Genetics, Lab, Media Releases, Molecular Medicine, Motor Neurone Disease, Muscular Dystrophy, News & Events, Rare Disease Genetics and Functional Genomics, ResearchWA’s first pre-pregnancy study finishing screening for more than 200 couples The first major pre-pregnancy screening study in WA found around 4% of couples were at risk of having a…
Changing view of Muscular Dystrophy
By Marlin Communications | Disease Area, Lab, Molecular Medicine, Muscular Dystrophy, News & Events, Rare Disease Genetics and Functional Genomics, Research, Research AreaPerkins PhD student, Dr Macarena Cabrera-Serrano, from the Laboratory for Neurogenetic Diseases, was lead author on the paper, Expanding the phenotype of GMPPB mutations. Although Congenital Muscular Dystrophy has several…
Perth team solve forty-year genetic mystery
By Marlin Communications | Cancer and Cell Biology, Disease Area, Genes, Lab, Molecular Medicine, Muscles, News & Events, Rare Disease Genetics and Functional Genomics, Research, Research Area, Systems Biology and GenomicsResearch involving teams in Perth, Spain and Sweden identified the genetic mutation for the late-onset muscle weakening disease. Professor Nigel Laing AO, Head of the Neurogenetic Disease Laboratory at the…
Perkins scientists celebrate international women’s day
By Marlin Communications | Lab, Media Releases, Mitochondrial Medicine and Biology, Molecular Medicine, News & Events, Research AreaScientific research and discovery are highly stimulating and rewarding careers that many women are frequently drawn to, most often as a result of a positive role model that piqued their…
Perth scientists part of international hunt for disease genes
By Marlin Communications | Disease Area, Genes, Lab, Molecular Medicine, News & Events, Rare Disease Genetics and Functional Genomics, Research, Research AreaHaving conducted genetic sequencing on Australian and NZ samples at the Harry Perkins Institute of Medical Research, it’s now time to take her samples to a team in London to…
Revolutionary new view of how living cells make energy
By Marlin Communications | Cancer, Diabetes, Disease Area, Heart, Lab, Mitochondrial Medicine and Biology, Molecular Medicine, News & Events, Research, Research AreaJust as cars need fossil fuels to power their engines, the living cells that make up our bodies use food as a fuel source. To harness the energy in food…