Proof-of-Concept: Antisense Oligonucleotide Mediated Skipping of Fibrillin-1 Exon 52. mdpi.com/1422-0067/22/7… #Morpholino

Very proud moment for one of our #PhD candidates who has published her first, first author paper! Congratulations Dr Jessica Cale Check out her paper on a possible therapy for a #raredisease #marfansyndrome bit.ly/2PC5RzD

Congratulations to PhD Candidate Di Huang who has taken out Murdoch University 3MT Competition with her project 'Stargardt disease and its therapeutics'. Along with the Perron Institute, we are incredibly proud of Di and her efforts. #3MT #PhD #PhDChat #PhDLife #Stargardt

@cmmit_mu Dr Jessica Cale Congratulations! 🎉

Thank you to my amazing supervisors and the CMMIT team 🎉

The Honourable Stephen Dawson MLC - Minister for Medical Research - had a first hand look at the innovative technology @cmmit_mu researchers use in the plight to find treatments for conditions such as #MuscularDystrophy #MND #Parkinsons #MS #Covid #Sepsis #Diabetes #HeartDisease

Just a few of the #RareDiseases we research into here at @cmmit_mu with the support of Murdoch University & Perron Institute. We believe no one should be left behind, everyone deserves the chance to receive a diagnosis & access potential treatments #RareDiseaseDay #RareDiseaseDay2023

Members of the Molecular Therapy team attended the @ConnectGroupsWA Rare Disease Day Exhibit showcasing photos & stories of local individuals & families living with rare, genetic & undiagnosed conditions #RareDiseaseDay #RareDiseaseDay2023 #RareDiseases

Thanks A Current Affair for raising awareness of #ChildhoodDementia New research led by University of Tasmania involves @cmmit_mu exploring if genetic ‘whiteout’ might be an effective therapy. 🎥@cmmit_mu Murdoch University + Perron Institute's Dr May Thandar Aung-Htut in story nine.social/c58

@cmmit_mu FACE it to make #ChildhoodDementia impossible to ignore. Over 70 genetic conditions cause childhood dementia, most won't live to adulthood. More research & better is support needed. @cmmit_mu @UTAS Childhood Dementia Initiative exploring if our genetic white out can help #faceit

A sobering reminder why we decided to #FaceIt for #ChildhoodDementia and why we are helping to develop therapies with University of Tasmania Childhood Dementia Initiative

Read my latest #research, published with Springer Nature in Scientific Reports rdcu.be/dq18G

CMMIT researchers @Jessica_Cale and Kristin Ham  recently published with Springer Nature in Scientific Reports. Read and share here: rdcu.be/dq18G

Thank you Malan Syndrome Foundation for your generous support, we look forward to continuing this important research.

We are delighted to continue our work on a potential ASO Therapeutic for Malan Syndrome. Thank you to Malan Syndrome Foundation for their continued support.

Today, on FACEIt Day, we are raising awareness for childhood dementia. Our lab is developing innovative treatments that could one day offer hope to those affected. Join us in spreading awareness & pushing for change. #FACEIt #ChildhoodDementia Childhood Dementia Initiative

Thanks Oligonucleotide Therapeutics Society for the opportunity to present my work through a poster at #ots24

Congratulations Professor Steve Wilton AO, who has been inducted as a Fellow of the Australian Academy of Health and Medical Sciences Australian Academy of Health and Medical Sciences in recognition of his work as an early pioneer in the use of antisense oligomers to treat #Duchenne #MuscularDystrophy

The Molecular Therapy Laboratory at Murdoch University would like to hear from people with a lived experience of a #rare #genetic #condition at this Community Conversation on the 9 April. Find out more & submit an EOI to attend - bit.ly/4aQl2Kw A $70 honorarium offered.

Yesterday, we welcomed WA Governor Chris Dawson AC APM, Science & Medical Research Minister Stephen Dawson MLC, and other VIPs for the official launch of the Personalised Medicine Centre - a joint Murdoch University & Perron Institute initiative reshaping rare disease treatment 🧬