Search Results - "Byam, Courtney E."

Gene profiling links SCA1 pathophysiology to glutamate signaling in Purkinje cells of transgenic mice by Serra, Heliane G., Byam, Courtney E., Lande, Jeffrey D., Tousey, Susan K., Zoghbi, Huda Y., Orr, Harry T.

“…Spinocerebellar ataxia type 1 (SCA1) is a neurodegenerative disease caused by the expansion of a polyglutamine repeat within the disease protein, ataxin 1. To…”
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Availability of Cord Blood Extends Allogeneic Hematopoietic Stem Cell Transplant Access to Racial and Ethnic Minorities by Barker, Juliet N, Byam, Courtney E, Kernan, Nancy A, Lee, Sinda S, Hawke, Rebecca M, Doshi, Kathleen A, Wells, Deborah S, Heller, Glenn, Papadopoulos, Esperanza B, Scaradavou, Andromachi, Young, James W, van den Brink, Marcel R.M

“…Allogeneic transplant access can be severely limited for patients of racial and ethnic minorities without suitable sibling donors. Whether cord blood (CB)…”
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A cell-based screen for modulators of ataxin-1 phosphorylation by Kaytor, Michael D., Byam, Courtney E., Tousey, Susan K., Stevens, Samuel D., Zoghbi, Huda Y., Orr, Harry T.

“…Spinocerebellar ataxia type 1 (SCA1) is an autosomal dominant neurodegenerative disorder caused by the expansion of a glutamine repeat within the SCA1-encoded…”
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Phosphorylation of ATXN1 at Ser776 in the cerebellum by Jorgensen, Nathan D, Andresen, J. Michael, Lagalwar, Sara, Armstrong, Ben, Stevens, Sam, Byam, Courtney E, Duvick, Lisa A, Lai, Shaojuan, Jafar-Nejad, Paymaan, Zoghbi, Huda Y, Clark, H. Brent, Orr, Harry T

“…Spinocerebellar ataxia type 1 (SCA1) is one of nine inherited neurodegenerative disorders caused by a mutant protein with an expanded polyglutamine tract…”
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