The mission of The PolG Foundation is to support and accelerate research to find effective treatments and a cure for PolG-related mitochondrial disorders.
United States
Joined September 2021
- Tweets190
- Following373
- Followers410
- Likes51
PolG Foundation retweeted
Excellent Bologna workshop on DNA polymerase gamma diseases, organized and facilitated by the new vibrant @PolGFoundation. Action plans, brainstorms. A stimulating global effort to make a difference for the devastating disease group. #mitochondrialdisease #ResearchBringsHope
Our Founder, Julie de Luxembourg, interviewed by @4Lilyfoundation on their partnership and the importance of collaboration to drive research forward.
thelilyfoundation.org.uk/new…
PolG Foundation retweeted
Pleased to have shared some of my #Alpers and #POLG neuropathology findings with other mito researchers at the #MitoMed22 conference yesterday. It was also great to meet members of the @PolGFoundation and @4Lilyfoundation 💚🦋
@Ryanstanfordapp @MitoResearch
PolG Foundation retweeted
Proud to have been a part of today's panel discussion 'Putting Patients at the Heart of Clinical Trials' at #MitoMed22 alongside colleagues @PolGFoundation @UMDF #patientvoice #mitochondrialdisease
PolG Foundation retweeted
What an inspirational, comprehensive, mission-driven @PolGFoundation board meeting. For patients with #mitochondrialdisease & #polg-we won’t stop until we find better treatments & cures. Check out polgfoundation.org for our research grant program happening now!! #MedTwitter – at Geneva, Switzerland
PolG Foundation retweeted
The @PolGFoundation 2023 research call is open. The Foundation seeks to fund research projects of up to $250.000 p/y (max 5 year research projects) that will have direct impact on drug discovery and clinical development of PolG therapeutics. Full details: polgfoundation.org/call-for-…
ALT The image has a black background with large capital letters P, O and L in white and a large capital letter G in green. This is the POLG Foundation logo.
The mission of The PolG Foundation is to support and accelerate research to find effective treatments and a cure for PolG mitochondrial disorders.
To advance this mission, we are announcing our first Call for Proposals.
polgfoundation.org
#polg #mitochondrialdisease
PolG Foundation retweeted
The @PolGFoundation 2023 research call is open. The Foundation seeks to fund research projects of up to $250.000 p/y (max 5 year research projects) that will have direct impact on drug discovery and clinical development of PolG therapeutics. Full details: polgfoundation.org/call-for-…
ALT The image has a black background with large capital letters P, O and L in white and a large capital letter G in green. This is the POLG Foundation logo.
PolG Foundation retweeted
The only way I haven’t expressed my #Gratitude…(yet 🤪) is by running 🏃♀️ 26.2 miles— @cindypricegavin YOU ARE MY HERO ALWAYS @nycmarathon @letswinpc @PolGFoundation @EHTPnyc – at Manhattan, NY
PolG Foundation retweeted
Very proud to see our latest story and my art work in the cover of @Cell_Metabolism picturing the damaged, leaky #mitochondria due to oxidative stress and #ferroptosis
cell.com/cell-metabolism/ful…
PolG Foundation retweeted
Can we just take a moment to appreciate how crazy cool this is?
Dietary lipids inhibit mitochondria transfer to macrophages to divert adipocyte-derived mitochondria into the blood
cell.com/cell-metabolism/ful…
PolG Foundation retweeted
Pieces of the mitochondrial genome jump and are integrated into the nuclear DNA
nature.com/articles/s41586-0…
PolG Foundation retweeted
Hello from The PolG Foundation!
Our story starts with the journey of one family and, more particularly, one young man, Frederik. Inspired by Frederik's example of sheer determination, they set out to transform hardship into deep resolve and find a cure for a devastating disease.
ALT #WMDW
PolG Foundation retweeted
The disease comes from a mutation in POLG and POLG2 genes. These mutations impair efficient replication of the mitochondria DNA, causing symptoms that can start from early childhood to adulthood. Symptoms often include ophthalmoplegia, muscle weakness, epilepsy and liver failure.
ALT @polgfoundation #WMDW
PolG Foundation retweeted
We already have a few ongoing research projects.
Mouse model 1, Generating and investigating in vivo PolG mouse models to unravel the mechanistic pathogenesis of PolG disorders.
Mouse Model 2, Development and preclinical validation in mice of gene therapy treatment.
ALT @polgfoundation
PolG Foundation retweeted
Huge thanks to everyone who helped raise the profile of #mito during World @MitoAware Week for the benefit of the whole community💚@AusMito @LeighNetwork @PolGFoundation @4Lilyfoundation @MyMitoMission @MitoCanada @GeneticAll_UK @MDUK_News @AgmAssociation @UMDF #WMDW #curemito
PolG Foundation retweeted
Happy to have played a small part in the Acipimox Trial @MitoResearch the design of which has just been published in Trials tinyurl.com/2ych8wez
#mitoaware @mitomusclelab @jwmdrc
PolG Foundation retweeted
With 166 tweets seen by >31K people, thanks to everyone who took part in our #twitter takeover during @MitoAware Week to raise the profile of #mito💚
@ausmito @LeighNetwork @PolGFoundation @4Lilyfoundation @MyMitoMission @MitoCanada @GeneticAll_UK @MDUK_News @AgmAssociation @UMDF
PolG Foundation retweeted
What an amazing day! The WCMR team would like to say THANK YOU to those who took part in our #Twitter Takeover today💚
@AusMito #internationalmitopatients @LeighNetwork @4Lilyfoundation @PolGFoundation @MitoCanada @UMDF @GeneticAll_UK @MDUK_News @AgmAssociation @MyMitoMission
PolG Foundation retweeted
The @PolGFoundation teamed up with the Wellcome Centre for Mitochondrial Research & @4Lilyfoundation to complete a review of the published scientific literature to improve our understanding of PolG disease. The review was guided by clinical assessment of a male aged 18 years.
ALT #WMDW