Top Tweets for #Syt1
๐ฌ๐ซง๐ง NEW: Targeting luminal #Syt1 with flexible readouts powered by the #ALFAsystem! Meet our new sdAb anti-Syt1 Luminal Domain ALFA-tag fusion (N4843) โ combine it with different #NbALFA-based reagents for fluorescence imaging or EM.
๐ Explore more: https://t.co/tSPoGKT8Qb
๐ฃ Neuroscientists โ something NEW for you!
NanoTag expands its portfolio of neurobiological #rHcAbs ๐ง . Nanobodies targeting #SYT1 and #CNPase are now available as Mouse or Rabbit IgG Fc fusions โ ideal for ICC and IHC๐ฌ.
Learn more๐ https://t.co/58acWHHeV5
#RecombinantAntibody
Our first paper on BAGOS. Check it out Super excited! https://t.co/iVKrTCRTG4 #Drosophila #SYT1 #BAGOS #RareDisease
This work adds to the #SNAREopathies. @curestxbp1 @stxbp1 #STX1B, #PRRT2, #SNAP25, #VAMP2, #SYT1, etc.
If you are into #SNAREopathies, follow the work of @IngoHelbig @JulieXXian @SWeckhuysen @HannahStamberg1 @SynapticHolly @SteffenSyrbe @KimThalwitzer @FiladelfiaGene1 & others.
๐ฌExtensive scientific collaboration underpins research on #SYT1 gene variants causing rare #neurodevelopmental disorder, #BakerGordonSyndrome.
๐https://t.co/uUZyzway2K
@GIMJournal ๐ https://t.co/ZBnLDuAmVX
@TheGordonLab @SynapticHolly @KBGenesBrains @mrccbu #RareDisease
Thank you especially to @KBGenesBrains, @TheGordonLab, @amkolesnik, and twitterless Fabian Bumbak, as well as all the researchers, clinicians, geneticists, and importantly patients and families that were involved from across the globe. #SYT1 Connected.
THIS ๐ by @SynapticHolly! Working with the #SYT1 Connected community alongside @KBGenesBrains has been the most important work of my career. #RareDisease needs funding to provide resources, treatments and personalised care to the people and their families who are affected.
It is a priviledge to work to provide answers for the #SYT1 Connected community. @RareConnect is a fantastic resource to help bring families affected by #RareDisease (and also clinicians and researchers) together across the globe. ๐๐ค
It is a priviledge to work to provide answers for the #SYT1 Connected community. @RareConnect is a fantastic resource to help bring families affected by #RareDisease (and also clinicians and researchers) together across the globe. ๐๐ค
#SYT1 - Associated Neurodevelopmental Disorder families are waiting for you! Share your story & connect with others worldwide in the international SYT1 Connected RareConnect community. #raredisease
๐ https://t.co/l9BB8RIw63
#SYT1 - Associated Neurodevelopmental Disorder families are waiting for you! Share your story & connect with others worldwide in the international SYT1 Connected RareConnect community. #raredisease
๐ https://t.co/l9BB8RIw63
Mutations in the protein #syt1 led scientists to a possible treatment option for a rare neurodevelopmental disorder: https://t.co/oP7lmxJoW2
There's a new @RareConnect online community for #SYT1 associated #neurodevelopmental disorder. Join the community today to exchange information and support https://t.co/BqEf94dRuo
Check out the 1st international case series describing the #neurodevelopmental disorder associated w/ SYT1 de novo missense mutations. #HudsonAlpha is proud to participate in the #SYT1 connected movement @KBGenesBrains @MRCCBU @Brain1878
https://t.co/1kWBzeERU3
A research paper describing eleven individuals diagnosed with #SYT1 mutation has been published. This is the beginning of understanding SYT1 associated disorders. https://t.co/zYiVbAvF7s
@KBGenesBrains @TheFlorey contingent on publication day. Sarah Gordon (@TheGordonLab) and @SynapticHolly performed the functional studies of mutant #SYT1 while Fabian Bumbak (absent) and @Danscooter ran the molecular dynamics simulations.
Amazing to think you were working on the same gene @TheGordonLab in #Melbourne and it took a global network to connect us! @KBGenesBrains @MCRI_for_kids #UDPVic #SYT1
First paper from the lab is officially out! Collaborating with @KBGenesBrains, to uncover the mechanisms underlying synaptic dysfunction in a novel neurodevelopmental disorder. https://t.co/Nqb8olGBmy @TheFlorey
Delighted to have been part of this amazing collaboration #SYT1 Connected @TeamVCGS @MCRI_for_kids: solving #RareDisease is a global effort!
The Cousin lab is very proud to be part of this - huge thanks to @KBGenesBrains @TheGordonLab for all of their hard work! #SYT1 Connected
International #SYT1 case series links #presynaptic vesicle release speed to #cognitive #development: https://t.co/dsXHoNnfcx @mrccbu @KBGenesBrains @florey
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