Parents and Researchers Interested In Smith-Magenis Syndrome

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Roles of RAI1 in Translating the Histone Methylation Code into Synaptic Plasticity

Roles of RAI1 in Translating the Histone Methylation Code into Synaptic Plasticity

by PRISMS | May 26, 2020 | Research

Below is a summary of the research findings of PRISMS funded post-doctoral fellow, Takao Tsukahara D.D.S Ph.D. Takao was funded by PRISMS from January 2018 to March 2020. He will be continuing his work on RAI1 at the University of Michigan. We are excited to...

Birt-Hogg-Dubé and Smith-Magenis Syndrome: Separate Disorders Linked through 17p11.2

by PRISMS | Feb 7, 2020 | Education, Home Page, Research

Last Updated: 1/26/2023 Thank you to the PRISMS Professional Advisory Board for putting together this FAQ; to Laura S. Schmidt, Ph.D. at the National Cancer Institute for her expertise and additional review; and to SMS parent Jill Effron for championing this effort....
Rai1 Regulates Gene Expression Programs for Maintaining the “Homeostasis” of Neural Circuits

Rai1 Regulates Gene Expression Programs for Maintaining the “Homeostasis” of Neural Circuits

by PRISMS | Jan 5, 2020 | Research

A summary of findings from our post-doctoral fellow, Takao Tsukahara, as presented at the 10th SMS Research Symposium. Takao Tsukahara, DDS, PhD, University of Michigan, Iwase and Sutton Lab Knowledge gap. Smith-Magenis Syndrome (SMS) is a rare neurodevelopmental...
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PRISMS, Parents and Researchers Interested In Smith-Magenis syndrome, is dedicated to providing information and support to families of persons with Smith-Magenis syndrome, sponsoring research, and fostering partnerships with professionals to increase awareness, understanding, and treatment of SMS.

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