NINDS Neuroscience Funding Announcements

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Basic and Clinical Research on Rett Syndrome and MECP2 (R01)
Release Date: December 18, 2006
Announcement Number: PAS-07-192
Application Receipt Date:
February 5, 2007
June 5, 2007
October 5, 2007   

Funding Contact: Laura Mamounas, Ph.D.
Program Area: Neurogenetics

Brief Description:
invite research grant applications aimed at understanding and/or treating Rett Syndrome (RTT). The recent demonstration that mutations in the MECP2 gene cause most cases of RTT has created new opportunities for both basic and clinical research. Included within the scope of this Program Announcement with set-aside funds (PAS) are developmental, neuroanatomical, molecular genetic, and pathophysiological research, therapy development projects and clinical studies. Studies of the role of MeCP2 in basic biological processes or in the etiology of other neurological or neurobehavioral disorders are also appropriate.

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