
RubinsteinLab
@LabRubinstein
We are located in @TelAvivUni. We study the neuronal and molecular basis for severe epilepsy and autism.
你可能会喜欢
📢 A novel gene therapy for #Dravet. jci.org/articles/view/…. Using Canine adenovirus-2 (CAV-2) we delivered the full SCN1A coding sequence into the hippocampus and thalamus of juvenile Dravet mice.

Excited to share our new paper in @FEBSJournal! 🎉 We show how a #MYELOMA-linked GGPPS mutation tweaks hexamerization, substrate binding and product inhibition, revealing an unexpected layer of protein prenylation regulation 🔗 doi.org/10.1111/febs.7… @peterslab1 @TAUMedFaculty
🚨New preprint alert! Wonder how a cancer-associated mutation in GGPPS impacts hexameric stoichiometry, substrate affinity, and product inhibition? Our results shed light on a novel regulatory mechanism in protein prenylation bit.ly/3ZR7w47 #MultipleMyeloma
Congratulations!! 🥳🥳
How does a cytoplasmic enzyme make a membrane product? 🤔🧬 We found that a hydrophobic residue cluster helps the human cis-prenyltransferase feed its product into the ER membrane! MD simulations + fluorescence = mechanistic insight 👇 🔗doi.org/10.1002/pro.70…
Stop the doom scrolling! A new 🗞️ from my lab, describing one of our flagship projects of many years we are super excited to share: "Inducible formation of fusion transcripts upregulates haploinsufficient CHD2 gene expression". A 🧵biorxiv.org/content/early/…

💖Love, Science & the Brain💖 This #ValentinesDay, meet Profs. Moran Rubinstein & Yoni Haitin - a couple bonded by love & a passion for #neuroscience. From BSc to leading labs, their journey is proof that great discoveries are made together. 🔬 Read more: linkedin.com/feed/update/ur…

Congratulations 🎊🎈🎉!
The New Dravet syndrome mouse model sheds light on the disease! This research by Prof. Rubinstein & collaborators uses a more accurate mutation to study Dravet & its causes: frontiersin.org/articles/10.33… #epilepsyAwarenessDay #DravetSyndrome @FrontiersIn #EpilepsyAwareness
Happy to share our new collaborative paper exploring the molecular basis of DEE-related #SCN8A mutation 🍾 | Work led by @QuinnShir with Yuanyuan Liu, @roybensh, @HaitinLab 🥰, Haim Bassan #epilepsy surl.li/rvzbw

Have you ever thought that chloride intracellular channel (CLIC) proteins function as fusogens? 🫧 From 🧪&💎 to 🪱 we're happy to share our recent paper showing just that! nature.com/articles/s4146…
I am sad to report that Bill Catterall has died. He was an enormous presence @UW.
Three days full of sodium channel talks. Cant wait for it to start! See many of you in Grindelwald!
Very soon, we will start the first and unique Worldwide Sodium Channel Conference in the Alps #Grindelwald #Switzerland. The final program is out sodiumchannelseminars.org/Sodium-Channel… Want to know how much snow we have? Here is the webcam: jungfrau.ch/fr-ch/live/web… #IonChannels #SodiumChannels

Dravet syndrome is a devastating form of epilepsy that can strike before an infant’s first birthday. Researchers at the Allen Institute and @SeattleChildren are developing a precise gene replacement therapy that has shown promising results in mouse models. biorxiv.org/content/10.110…
United States 趋势
- 1. #KaneAI N/A
- 2. $CHA 1,187 posts
- 3. #VSFashionShow 84.1K posts
- 4. Nancy 97.3K posts
- 5. jihyo 57K posts
- 6. Supreme Court 133K posts
- 7. #TWICExVictoriasSecret 50.6K posts
- 8. Argentina 471K posts
- 9. Waddle 5,467 posts
- 10. #TORQSports N/A
- 11. Pelosi 74.5K posts
- 12. TWICE LIGHTS UP VSFS 47.4K posts
- 13. #PokemonGO 4,141 posts
- 14. Banish 1,612 posts
- 15. SCOTUS 42K posts
- 16. Malcolm Brogdon 5,258 posts
- 17. Big Balls 33.5K posts
- 18. Olave 4,286 posts
- 19. Biker Boyz N/A
- 20. UTEP 2,257 posts
你可能会喜欢
-
Dravet Syndrome Foundation
@curedravet -
Sagol School of Neuroscience
@of_sagol -
Pablo Blinder
@PBNeuroVascLab -
TavorLab
@LabTavor -
Ido Tavor
@IdoTavor -
Yuval Nir 💔
@LabNir -
Inna Slutsky
@inna_slutsky -
HaitinLab
@HaitinLab -
Avraham Ashkenazi Lab
@AvrahamLab -
Tal Laviv
@LavivTal -
Mark Shein-Idelson
@EvoNeuralCode -
Shiri Shoob
@ShiriShoob
Something went wrong.
Something went wrong.