
gnao1research
@gnao1research
Developing a cure for GNAO1 mutation disorders: patient advocacy + research + collaboration
ID: 1315302889884127233
11-10-2020 14:47:21
255 Tweet
96 Followers
343 Following



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.

#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)





🚨🚨🚨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

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



On our project team: Istituto Neurologico Carlo Besta, Hospital Sant Joan de Déu Barcelona ES, Université de Genève, Fondazione Santa Lucia, Sheba Medical Center, CHU de Montpellier, Uniklinik Köln, Gazi Üniversitesi, Ricerca Sapienza, Bambino Gesù, Amsterdam Neuroscience | Amsterdam UMC, UHC Sestre Milosrdnice, Evelina London Famiglie GNAO1, GNAO1 España, Stichting GNAO1 NL




-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.….