Thanks, Dave! Stay tuned!
21.01.2025 01:01 — 👍 0 🔁 0 💬 0 📌 0
JCI -
Impaired hydrogen sulfide biosynthesis underlies eccentric contraction-induced force loss in dystrophin-deficient skeletal muscle
Excited to share new work from the Ervasti Lab, published last week in JCI, which will inform the foundation of my thesis research. Check it out below! 🐁 💪🏼 #myoblue
20.01.2025 03:50 — 👍 5 🔁 0 💬 2 📌 0
:)
20.01.2025 03:37 — 👍 0 🔁 0 💬 0 📌 0
Hi Mattia! Glad you enjoyed the work!
20.01.2025 03:34 — 👍 1 🔁 0 💬 0 📌 0
Rare & neuromuscular disease researcher at UWA & the Harry Perkins Institute, Perth 🇦🇺
Passionate about #sciencefunding, #womeninSTEM, #EMCRs
Mum of 👦👧🐶
Posting about genomics, rare disease, PI life & wine
https://www.ravenscroftlab.com
Professor of Neuromuscular Diseases at the John Walton Muscular Dystrophy Research Centre of the Newcastle University and Honorary Consultant in Genetics at the NHS Newcastle Hospital Trust. Member of the Neuromuscular diseases lab of Sant Pau Hospital.
Scientist and mum. Ikerbasque Professor @ Biobizkaia HRI
Interested in #RNAtherapy for #neuromuscular disorders. De Bilbao de toda la vida and adopted Londoner.
https://www.linkedin.com/in/virginia-arechavala-gomeza-a482509/
The European Reference Network for Rare Hereditary Metabolic Disorders (MetabERN). A better future for Rare Inherited Metabolic Disease patients.
Visit us 🔗 https://metab.ern-net.eu/
Canadian network connecting clinicians, scientists, patients, and industry to improve neuromuscular disease outcomes.
Funded through CIHR-IMHA and Muscular Dystrophy Canada
Visit us at: https://neuromuscularnetwork.ca/
No one should face FSHD alone.
Our Mission: Find treatments and a cure for FSHD while empowering families.
#CureFSHD
We share Chicago stories. Currently on view: #Chicago1871, #DesignForChange, #DressedInHistory. In the works: #AquíEnChicago.
William S. Adams Professor, Chair and Executive Medical Director, @DOMUCLA.bsky.social, @dgsomucla.bsky.social, @uclahealth.bsky.social via @intmedatiowa.bsky.social
Scientists | Molecular biologist playing bioengineering to fight muscular dystrophies at IBEC 🦾🧬⚙️💊🏳️🌈
Rare Genomics Institute (RG) is a 501(c)3 non-profit organization committed to filling the unmet needs of patients and families affected by rare diseases.
https://www.raregenomics.org/
National Institute for Health and Care Research - we fund, enable and deliver world-leading health and social care research that improves people's health and wellbeing, and promotes economic growth.
Impact, Innovation, Investment, Inclusion
The BMJ is patient centred, evidence based, and independent. Help us improve the health of our world with the best science, journalism, education, and comment.
Welcome to The Lancet, one of the world’s leading medical journals, published weekly since 1823.
🌐 thelancet.com
Skeletal muscle physiologist, University of Windsor
Professor of Neuromuscular & Skeletal Disorders, Keele University. I research pathologies and new treatments in rare neuromuscular & skeletal disorders.
www.thebowermanlab.com
Director: Muscle Health Research Centre
Professor: muscle disorders and the metabolic basis of muscle fitness. Translating mitochondrial bioenergetics and redox biology to health/disease
http://health.yorku.ca/health-profiles/index.php?mid=1068349
Instructor| Harvard Med| Research: Aging, Critical Illness, Musculoskeletal, ADRD, Geroscience, and Exercise Phys
🧬 We research the various aspects of hereditary myopathies and muscular dystrophies
📍 @folkhalsanresearch.bsky.social , Helsinki, Finland
https://linktr.ee/myofin
PhD candidate in Exercise Physiology. MSc in Cell and Molecular Biology. Interested in metabolism, regulation of muscle size, and bioanalytics (e.g. metabolomics).
Orcid: https://orcid.org/0000-0002-2313-0735
Performing world-class translational research to bring diagnosis, care and therapy to people with neuromuscular disease
