gnao1research (@gnao1research) 's Twitter Profile
gnao1research

@gnao1research

Developing a cure for GNAO1 mutation disorders: patient advocacy + research + collaboration

ID: 1315302889884127233

calendar_today11-10-2020 14:47:21

255 Tweet

96 Followers

343 Following

New Scientist (@newscientist) 's Twitter Profile Photo

Gene-replacement therapy means some children who once would have died at an early age or required a gruelling stem cell transplant are now having typical life experiences, such as attending school and living at home with their families x.com/i/events/15302…

MIT Technology Review (@techreview) 's Twitter Profile Photo

The European Union is planning new legislation aimed at curbing the worst harms associated with artificial intelligence. trib.al/Erh2G5F

gnao1research (@gnao1research) 's Twitter Profile Photo

Like my son, who just turned 11, Samuel Habib has a #GNAO1 disorder. Our families are part of a global alliance of patient family orgs supporting each other + research to find a cure. Ale is navigating the journey to adulthood with little guidance, so 🙏 Samuel & @_danhabib.

gnao1research (@gnao1research) 's Twitter Profile Photo

#GNAO1 International Research Updates, Jun 6, 2022 10am-1:30pm EDT, 4pm-7:30pm CEST Moderator: K Martemyanov Kirill Martemyanov Lab Speakers: F Baas/H Mikkers (NL) S Martinelli (IT) V Katanaev (CH) J Valnohova (CH) I Shomer (IL) X Chen (US) M Sena-Esteves (US) R Neubig Rick Neubig (US)

Jacky Ganguly (@jackyganguly) 's Twitter Profile Photo

Genetic Landscape of Childhood-Onset Hyperkinetic Movement Disorders from Prof Kurian et al. #neurotwitter Parkinsonism-dystonia : DDC, DHPR, PTPS, SLC6A3, SPR, TH Chorea: ADCY5, ATP1A3, FOXG1, NKX2.1, SLC2A1, GNAO1, PDE10A Stereotypies: FOXG1, GNAO1 doi.org/10.1002/mds.29…

Genetic Landscape of Childhood-Onset Hyperkinetic Movement Disorders from Prof Kurian et al. #neurotwitter
Parkinsonism-dystonia : DDC, DHPR, PTPS, SLC6A3, SPR, TH
Chorea: ADCY5, ATP1A3, FOXG1, NKX2.1, SLC2A1, GNAO1, PDE10A
Stereotypies: FOXG1, GNAO1
doi.org/10.1002/mds.29…
DUKΞ (@thedukekim) 's Twitter Profile Photo

GM is a grinder’s mindset. While you’re participating in Blur’s 48th airdrop challenge, I’m making sure I’ll dance with my daughter one day.

GM is a grinder’s mindset. 

While you’re participating in Blur’s 48th airdrop challenge, I’m making sure I’ll dance with my daughter one day.
Ethan Perlstein bio/acc (@eperlste) 's Twitter Profile Photo

Data hot off the presses! We performed a screen to assess the activation of a GPCR signaling pathway in a GNAO1/GPA1 yeast avatar with reduced pathway activity at baseline. Hit 1 (left) versus untreated control (right)

Data hot off the presses!

We performed a screen to assess the activation of a GPCR signaling pathway in a GNAO1/GPA1 yeast avatar with reduced pathway activity at baseline.

Hit 1 (left) versus untreated control (right)
GNAO1 España (@gnao1espana) 's Twitter Profile Photo

Tres años de sonrisas y lágrimas, ilusión y desilusiones,pero sobre todo tres años de esperanza🤞🤞🤞. Gracias por acompañarnos en este viaje! #GNAO1 #EERR #FebreroRaro

Tres años de sonrisas y lágrimas, ilusión y desilusiones,pero sobre todo tres años de esperanza🤞🤞🤞.

Gracias por acompañarnos en este viaje!

#GNAO1 #EERR #FebreroRaro
The Orphan Disease Center @ UPenn (@odc_upenn) 's Twitter Profile Photo

🚨🚨🚨Funding Opportunity! The Bow Foundation & The Orphan Disease Center @ UPenn are seeking #grant applications to support research related to #GNAO1 Neurodevelopmental Disorder. LOIs are due March 3, 2023; APPLY TODAY!! Follow the link to learn more: ow.ly/zLRs50MMxu2 #RareDisease #rare

Perlara (@perlarapbc) 's Twitter Profile Photo

GNAO1 yeast avatars update: The G203R variant (left) acts as both gain-of-function and loss-of-function. The G204A variant (right) behaves like a classic loss-of-function. GNAO1 Action

Sarepta Therapeutics (@sarepta) 's Twitter Profile Photo

Today’s FDA approval of our new treatment for Duchenne muscular dystrophy represents an important moment for Sarepta and the Duchenne community. Watch to hear a message from our CEO, Doug Ingram:

gnao1research (@gnao1research) 's Twitter Profile Photo

Happy to share that our multidisciplinary team from 10 countries (IT, CH, DE, FR, IL, TR; ES, NL, HR, UK) has been awarded >1.6M€ for a #GNAO1 natural history study under the @EJPRareDiseases Joint Transnational Call 2023. Our aim is to enrol 90 patients ages 0-18 over 3 years.

gnao1research (@gnao1research) 's Twitter Profile Photo

See the abstract + partners of our winning project for @EJPRareDiseases Joint Transnational Call 2023: #GNAO1-EU: European Natural History Study* and search for novel biomarkers in GNAO1-associated disorders. ejprarediseases.org/gnao1-eu/ *including setup of an international registry

gnao1research (@gnao1research) 's Twitter Profile Photo

Reminder — 2025 Famiglie GNAO1 grant deadline Wed, 30 April Potential areas of the #GNAO1 study: • Genetic/molecular studies • Development of therapies • Pre-clinical/clinical trials Eligibility and details: gnao1.it/research-grant…

gnao1research (@gnao1research) 's Twitter Profile Photo

-1 month to the 2025 GNAO European Conference (20-21 June) at Univ. of Cologne, Germany Speakers from CA, CH, CN, DE, ES, IT, KR, NL, US Day 1: Basic science, preclinical & clinical research Day 2: Clinical & caregiver aspects Program + registration @ gnao1.aey-congresse.de/start/program.….