GRI Genes Roundtable – Oct 2021
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GRI Genes Research Roundtable Summary
CureGRIN Foundation hosted our tenth GRI Genes Roundtable on October 21, 2021. Our goal is to promote collaboration so that we can accelerate the path to treatments and cures for GRI Disorders.
We brought together researchers and clinicians studying GRI Disorders, GRIN genes, GRIA genes, GRIK genes, NMDA receptors, and other ionotropic receptors (AMPARs, kainate receptors, and delta receptors) to discuss and exchange ideas.
We asked Bobbie Couch to share her family story about her son with a variant in GRIN1. A panel of two researchers presented their work on NMDAR functioning. Keith McArthur also shared more information about the GRI Connect Platform. This document summarizes these presentations.
Our next GRI Genes Research Roundtable is scheduled for: Thursday, December 2, 2021.
If you are a GRIN / NMDAR researcher and/or a GRIA genes/AMPAR researcher or clinician, please reach out to meagan@curegrin.org to be added to the next meeting invitation.
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Serve as Treasurer on the CureGRIN Board
Do you know our next Treasurer? CureGRIN Foundation is looking for a Treasurer located in the United States to join our Voluntary Board of Directors. This person does not need to be a family member of someone with GRI Disorder but they must be committed to our mission. If you know anyone with finance or accounting experience interested in serving the global GRI community, please nominate them by providing their contact information to heather@curegrin.org by May 3, 2022.
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