Epigenetics and Genomics LaboratoryGenetic DiseaseMedia ReleasesMusclesNews & EventsRare Disease Genetics and Functional GenomicsResearch
Support needed for doctors offering couples genetic testing
By Richard Schoonraad | Epigenetics and Genomics Laboratory, Genetic Disease, Media Releases, Muscles, News & Events, Rare Disease Genetics and Functional Genomics, ResearchAs the number of genetic abnormalities that can be identified in pre and post pregnancy tests reaches the thousands, a national project has been launched to assist doctors as they…
Development of Improved Diagnostics for Genetic DiseaseDevelopment of Therapies for Selected Genetic Muscle DiseasesDisease AreaFundingGenesGenetic DiseaseGenetic DiseaseGenetic Neuromuscular DisordersGeneticsMedia ReleasesMusclesMuscular DystrophyNeurological DisordersNews & EventsRare Disease Genetics and Functional Genomics
WA scientists win Hearts and Minds
By Richard Schoonraad | Development of Improved Diagnostics for Genetic Disease, Development of Therapies for Selected Genetic Muscle Diseases, Disease Area, Funding, Genes, Genetic Disease, Genetic Disease, Genetic Neuromuscular Disorders, Genetics, Media Releases, Muscles, Muscular Dystrophy, Neurological Disorders, News & Events, Rare Disease Genetics and Functional GenomicsFirst West Australian team to attract unique listed investment company funds One of Australia's Top 30 Corporate Philanthropists, Hearts and Minds Investments Limited (ASX: HM1) has made its first donation…
Cancer and Cell BiologyDisease AreaGenesLabMolecular MedicineMusclesNews & EventsRare Disease Genetics and Functional GenomicsResearchResearch AreaSystems Biology and Genomics
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…
Disease AreaGenesLabMolecular MedicineMusclesNews & EventsRare Disease Genetics and Functional GenomicsResearchResearch Area
Perkins researchers decipher world-first muscle disorder cases
By Marlin Communications | Disease Area, Genes, Lab, Molecular Medicine, Muscles, News & Events, Rare Disease Genetics and Functional Genomics, Research, Research AreaDuring their investigation the multi-national team of researchers studied a muscle protein that is strongly influenced by calcium. The protein, known as tropomyosin-3 (TPM3), is vital for skeletal muscle development…
Disease AreaGenesLabMolecular MedicineMusclesNews & EventsRare Disease Genetics and Functional GenomicsResearchResearch Area
Sharpening the focus on muscle diseases
By Marlin Communications | Disease Area, Genes, Lab, Molecular Medicine, Muscles, News & Events, Rare Disease Genetics and Functional Genomics, Research, Research AreaDr Gina Ravenscroft, who is lead author of the review published by the prestigious journal Brain, works in the Neurogenetic Diseases Laboratory at the Harry Perkins Institute of Medical Research; one of the world's…
