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FRAXA Research Foundation – Finding a Cure for Fragile X Syndrome

FRAXA Research Foundation – Finding a Cure for Fragile X Syndrome

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FRAXA Funded Research

Research Type

Researcher

Research Organization

Grant Year

University of Edinburgh, Scotland

Oligodendrocytes: a Potential Route to Treat Fragile X Syndrome

FRAXA Research Foundation August 15, 2025August 15, 2025
Lida Zoupi and Laura Oliviera with myelin

This project explores the role of oligodendrocytes in Fragile X. The team will test if improving these support cells’ function can restore normal brain activity to treat Fragile X.

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Somatosensory Processing as a Therapeutic Target for Fragile X Syndrome

FRAXA Research Foundation September 7, 2023November 19, 2024

Awarded a FRAXA Research grant, Dr. Andrew Stanfield, Dr. Leena E. Williams, and Dr. Damien Wright are set to explore somatosensory processing (sense of touch) in Fragile X syndrome at the University of Edinburgh. Their aim? A noninvasive touch test that could set the stage for future clinical trials in FXS.

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Enhancement of NMDA Receptor Signaling for the Treatment of Fragile X Syndrome

Theodore Coutilish August 15, 2016February 27, 2025
Emily Osterweil

FRAXA Research Foundation funded a 2016-2017 Fellowship for Dr. Stephanie Barnes in the University of Edinburgh lab of Dr. Emily Osterweil. With this $90,000 award, the team is investigating NMDA signaling in fragile X syndrome mice.

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Development of the Fragile X Brain: Cellular Processes Regulated by FMRP During Development

FRAXA Research Foundation February 14, 2008March 25, 2025
Peter Kind, PhD, of University of Edinburgh, FRAXA research grant

With a $120,000 grant from FRAXA Research Foundation over 2 years, Dr. Peter Kind and his team at the University of Edinburgh will study the way FMRP affects and is affected by cortical development.

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