Matthew Williams(@MattWilliamsIT) 's Twitter Profile Photo

We’re super proud of Macsen’s progress since November so we’re treating him to a new pop to celebrate every time he invites a new Disney friend


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Lorena Tejera(@Lorenatv507) 's Twitter Profile Photo

Omar Danoun, MD Doc, an 11 yr with Pathogenic variant, c.2357-2A>T (Splice acceptor) in GRIN2A what type of medicine should be used instead?

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Johannes Lemke(@lemke_johannes) 's Twitter Profile Photo

Have a look at our 2022 achievements on :
uniklinikum-leipzig.de/einrichtungen/…

Thanks to the research groups of Tim Benke, Steve Traynelis and Dennis Lal

Join our registry grin-portal.broadinstitute.org
CureGRIN GRIN2Bsyndrome

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dazzle4rare(@dazzle4rare) 's Twitter Profile Photo

CureGRIN We have down the whole of March is GRIN Awareness Month. We shared this in out most recent podcast. Were we inaccurate on that?

Happy to pop a correction in th3 show notes if so.

podfollow.com/signalise-a-da…

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Ingo Helbig(@IngoHelbig) 's Twitter Profile Photo

5/

...but we can do better than this

...we can comb through medical records of 52K+ individuals

...to see which genetic diagnoses are identified in various speech disorders

...we find known associations for (not communicating verbally) and (speech apraxia)

5/

...but we can do better than this

...we can comb through medical records of 52K+ individuals

...to see which genetic diagnoses are identified in various speech disorders 

...we find known associations for #STXBP1 (not communicating verbally) and #GRIN2A (speech apraxia)
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Krzysztof Potempa(@BRAINCURES) 's Twitter Profile Photo

Out of 1320 nsSNPs retrieved from the NCBI database, initially 16 were predicted as deleterious by 9 tools. Further assessment & Molecular Dynamic Simulation revealed that the variant I463S is likely to be the most deleterious in GRIN2A-associated diseases
journals.plos.org/plosone/articl…

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Johannes Lemke(@lemke_johannes) 's Twitter Profile Photo

We investigate potentially recognisable features of   with a facial recognition tool.

You can support our research with a photograph. 
This is how: uniklinikum-leipzig.de/einrichtungen/…
CureGRIN GRIN2Bsyndrome
Thanks you!

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Halgrim(@Randomn13357688) 's Twitter Profile Photo

'[...]in schizophrenia, but the SCHEMA study provides the first solid genetic evidence of this. Additionally, GRIN2A activity in the brain peaks during adolescence, around the time people suffering schizophrenia begin to experience symptoms.[...]'

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FamilieSCN2A(@FamilieSCN2A) 's Twitter Profile Photo

GRIN Disorder is part of a more prominent family of related to ionotropic glutamate receptors and is caused by a change in 1 of 7 GRIN genes: GRIN1, GRIN2A, GRIN2B, and GRIN2D. These genes code are essential for learning and memory. Learn more here at: curegrin.org/resources/

GRIN Disorder is part of a more prominent family of related to ionotropic glutamate receptors and is caused by a change in 1 of 7 GRIN genes: GRIN1, GRIN2A, GRIN2B, and GRIN2D. These genes code are essential for learning and memory. Learn more here at: curegrin.org/resources/
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Jane(@JJanerwcarter) 's Twitter Profile Photo

Lisa 💙 Just looked up grin2A online what a shocking and rare condition, sending love and prayers to you and your family through the interweb

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Halgrim(@Randomn13357688) 's Twitter Profile Photo

'[...]Insights into two of the 10 genes from the SCHEMA study, GRIN2A and GRIA3, further implicate the synapse as a key part of schizophrenia's mechanistic roots[...]

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Neel Fotedar(@neelmed) 's Twitter Profile Photo

Ken Myers Brain Fascinating. I was just teaching our fellows today about potential role of Memantine in DEEs, especially GRIN2A.

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Paul McCullough(@ThePostsynaptic) 's Twitter Profile Photo

Mouse mutants in schizophrenia risk genes GRIN2A and AKAP11 show EEG abnormalities in common with schizophrenia patients dlvr.it/SlRNKN

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