What happens if you have a GABAA receptor variant and clinical phenotype that doesn't quite fit into loss and gain of function? Our latest eBiomedicine paper by the awesome PhD student @NazaninAzarine1 and @FiladelfiaGene1 can tell you why!
https://t.co/Gy1LAeem2T
How to we predict whether GABA receptor variants are pathogenic and loss or gain of function? Follow the allosteric transitions, we argue in our latest letter to Brain. Thanks to our talented postdoc @SereneElkamand, @ChowHanChua and @Philip_K_Ahring,
https://t.co/tzocyaiRVY
Join us in supporting Beau (3), Keltie (7) and Harper (6) all with #GABRG2 deletion. Ranging from febrile seizures only to mild epilepsy to frequent seizures/types and delays, all within the same family.
https://t.co/EufjFxx11S
#epilepsy
A really original genetic study of its kind, presented by @Katrine92658231, shows the broad phenotypic spectrum of GABRA3 related disorders can be explained by sex and function effect of the #GABRA3 variants. @IlaeWeb#ILAE#IEC2023@FiladelfiaGene1 @Philip_K_Ahring
"Our warrior angel Zayden.
He survived 4 and half years battling GABRB2, before he could not fight it anymore.
Loved and missed every single day."
Visit https://t.co/CQj0fCf3dp for more information on GABA-A Receptor Related Disorders.
#epilepsy#GABRB2
Kinetics matter! How different kinetic properties can influence the severity of epilepsy in patients with GABA receptor variants. Great PhD work from Susan and collaboration @Vivian_WY_Liao @Philip_K_Ahring @AngeloKeramidas @MaryChebib@FiladelfiaGene1 https://t.co/u9Ag9zH0XV
Publication alert 📢 #GABRA1-related disorders: from genetic to functional pathways.
We expand the genetic and phenotypic spectrum and delineate specific sub-phenotypes for LoF and GoF variants.
Fantastic 🇩🇰🇦🇺🇮🇹 teamwork ‼️
@Elegardella @Philip_K_Ahring
https://t.co/Q9dLsqVtZH
Research led by the Institute's Dr @Charles_D_Cox published today in @ScienceMagazine identifies a critical molecule which could lead to the development of future drugs for obesity, osteoporosis, and inflammatory diseases: https://t.co/az88b1LiS5 #mechanobiology#ScienceTwitter
Delighted to share this out today in Lancet Neurology! Evaluation of the feasibility, diagnostic yield, and clinical utility of rapid genome sequencing in infantile epilepsy (Gene-STEPS): an international, multicentre, pilot cohort study - https://t.co/Stz0Exc101
Automated patch clamp was originally developed for the pharmaceutical industry, but Thompson et al. repurpose it to investigate functional properties of several sodium channel variants associated with neurodevelopmental disorders https://t.co/xu2T7Mwdlk
#SCN2A#epilepsy