Peter John Houweling
@houweling_peter
Skeletal muscle researcher @mcri_for_kids. Working on the genetics of muscle performance in health and disease #DMD. tweets are my own.
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Australia has an amazing opportunity to use its Medical Research Future Fund to immediately supercharge healthcare innovation - to develop new medicines, new therapies, new cures. The economic and social potential for our country is huge.
‘Making cancer treatment worth it’ - Join ABC’s @natashamitchell in conversation with top cancer and stem cell scientists at a FREE public event in Adelaide (IRL, livestreamed and broadcast on Radio National Big Ideas) events.humanitix.com/making-cancer-… @abcnews @UniofAdelaide @the_ASSCR
A huge thanks to the Gillin Boys Foundation, who've made it possible for #MCRI to acquire Australia's first Mantarray™ machine from @Curi_Bio for rare #muscledisease research. | #MedicalResearch #DMD #Fundraising @houweling_peter Read more 👉 direc.to/mhNH
Today is World Duchenne Awareness Day. Raise your voices to support young people living with DMD and their families living around the world 🎈🎈🎈 #DMD #WDAD
Duchenne muscular dystrophy is a genetic disorder causing progressive muscle degeneration & weakness. This Saturday marks the first #WorldDuchenneAwarenessDay - a moment to foster understanding and empathy towards those affected by rare diseases. un.org/observances/du…
alpha-Actinin-3 deficiency protects from the effects of acute cold exposure through altered skeletal muscle Ca2+ and OXPHOS signaling. biorxiv.org/cgi/content/sh… #biorxiv_cellbio
Our Developing Therapies in Rare Neuromuscular Disease Symposium offers a unique opportunity to learn directly from the most experienced and knowledgeable members of the TACT committee. Each expert will bring their unique perspective and expertise, enriching our collective…
Modern Insights into Muscle Glycogen Phosphorylase Activity biorxiv.org/content/10.110…
Living with a progressive neuromuscular disease such as limb-girdle muscular dystrophy (LGMD) can be financially challenging at times. 💚Visit our website for some resources that may be able to provide assistance to help offset the financial burden. lgmd-info.org/knowledge-base…
lgmd-info.org
LGMD Grant Opportunities - LGMD Awareness Foundation
Living with limb-girdle muscular dystrophy (LGMD) presents unique challenges, both physically and financially. The LGMD Grant Opportunities page serves as a valuable resource, offering detailed...
We've heard your requests, and we're extending the registration and abstract submission deadlines for the Victorian Muscle Network Symposium by one more week! 🗓️ Register by Friday 13th October 👻🎃🦇 victorianmusclenetwork.wordpress.com A sneak peak of submissions so far:
🚨 Last call! 🚨Today's the day! 📢 Abstract submissions and registration for #VMN2023 are DUE TODAY! victorianmusclenetwork.wordpress.com
New #NewArticleInPress Targeting #LungInjury in #PretermInfant. Impact of tidal volume strategy at birth on initiating lung injury in preterm 🐑(Pereira-Fantini et al) @dr_prue @DavidTingay @ArunSett @MFatmous ow.ly/qvVT50PS7XG #resuscitation #tidalvolume #proteomics
Our latest paper understanding the functional consequence of #COPD GWAS variants is out @AJHGNews. Using #CRISPRi and #iPSC models we find that ADGRG6 exerts pleiotropic effects on type 2 alveolar epithelial cells, which is exacerbated by cigarette smoke exposure.
📢New @AJHGNews 📰The #COPD GWAS gene ADGRG6 instructs function and injury response in human iPSC-derived type II alveolar epithelial cells 🧑🤝🧑@RhiannonWerder @Awilsonlab & colleagues 👇 cell.com/ajhg/fulltext/…
The Novo Nordisk Foundation Cellerator has a bold vision: to advance the cell therapy ecosystem and enable transformative treatments. In this video, we look at why this new initiative is needed and how it could help change the lives of people living with chronic or…
Great to see this collaborative project between so many institutions get off the ground.
An Australian first biobank will be established to improve & discover new treatments for children with genetic #musclediseases. Housed at Murdoch Children’s, the #biobank will advance #research into why children develop these diseases. @Houweling_Peter 🔗👉mcri.edu.au/news-stories/b…
An Australian first biobank will be established to improve & discover new treatments for children with genetic #musclediseases. Housed at Murdoch Children’s, the #biobank will advance #research into why children develop these diseases. @Houweling_Peter 🔗👉mcri.edu.au/news-stories/b…
Attn @AFGNetwork: Pipeline Accelerator scheme open now to support access to @phenomics Australia (PA) & @TIA_Aust facilities, inc. generation of genetically modified in vivo and in vitro models, new iPSC lines, organoids, & screening facilities. Apply now! phenomicsaustralia.org.au/voucher-scheme/
Pipeline accelerator grants open now! These provide funds to access gene editing in cell and animal models, drug screening, iPSC and organoid generation, CRISPR screening and more provided by @phenomics Australia & @TIA_Aust nodes.
Congratulations to Dr Julie Moreau @JMoreau83 from the Combes lab @MonashBDI for winning the @ANZSCDB movie award with this captivating timelapse of nephron progenitor cell dynamics and differentiation (magenta) over 72 hours of kidney development.
Murdoch Children's recognises the positive impact #TheVoice can have on Aboriginal and Torres Strait Islander children and families. We're proudly voting Yes on October 14! #VoiceToParliament @UluruStatement #Referendum2023 #Australia
Today, Australia’s largest child health research institute, @MCRI_for_kids, announced their support for the Voice. By voting Yes, Indigenous children will be happier and healthier.
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