This proposal describes the renewal of the New England Huntington's Disease Center Without Walls. The objective of this proposal is to continue clinical and basic research directed toward an understanding of an autosomal dominant disorder which serves as an important model of regional programmed nerve cell death. It is proposed to continue to collect data on the pedigrees, clinical findings and autopsy observations of patients seen in the New England area. Medical clinics at the Massachusetts General Hospital and Boston University School of Medicine, together with chronic care facilities at local V.A. Hospitals (West Roxbury and Brockton) and the Middlesex Community Hospital will function to collect neurological, genetic, neuropsychological and epidemiological data. Other projects described in this proposal include: continued work to develop additional probes located close to the Huntington's Disease gene on chromosome 4 and to develop strategies to find and clone the defective gene as outlined by Dr. James Gusella; further studies on the neuropathology of Huntington's Disease described by E.P. Richardson, M.D. using material obtained and stored in the McLean Hospital Brain Tissue Bank; investigations of the function of somatostatin and other neuropeptides in the basal ganglia as described in the proposal by Joseph Martin and Flint Beal; studies on the anatomy and function of the basal ganglia as outlined by Marion DiFiglia; studies on neurotransmitter and neuropeptide receptors using new approaches to the identification and characterization of these receptors as described by Linda Chun and Ann Graybiel. These research efforts of the Center Without Walls are coordinated through an executive committee responsible for the activities of the Center. Important research advances accomplished over the last four years are anticipated to continue during the period for which funding is requested.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Program Projects (P01)
Project #
2P01NS016367-06
Application #
3099613
Study Section
Neurological Disorders Program Project Review B Committee (NSPB)
Project Start
1980-07-01
Project End
1990-06-30
Budget Start
1985-07-01
Budget End
1986-06-30
Support Year
6
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
City
Boston
State
MA
Country
United States
Zip Code
Keum, Jae Whan; Shin, Aram; Gillis, Tammy et al. (2016) The HTT CAG-Expansion Mutation Determines Age at Death but Not Disease Duration in Huntington Disease. Am J Hum Genet 98:287-98
Ramos, Eliana Marisa; Gillis, Tammy; Mysore, Jayalakshmi S et al. (2015) Haplotype analysis of the 4p16.3 region in Portuguese families with Huntington's disease. Am J Med Genet B Neuropsychiatr Genet 168B:135-43
Ramos, Eliana Marisa; Gillis, Tammy; Mysore, Jayalakshmi S et al. (2015) Prevalence of Huntington's disease gene CAG trinucleotide repeat alleles in patients with bipolar disorder. Bipolar Disord 17:403-8
Galkina, Ekaterina I; Shin, Aram; Coser, Kathryn R et al. (2014) HD CAGnome: a search tool for huntingtin CAG repeat length-correlated genes. PLoS One 9:e95556
Ramos, Eliana Marisa; Latourelle, Jeanne C; Gillis, Tammy et al. (2013) Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset. Neurogenetics 14:173-9
Lee, Jong-Min; Galkina, Ekaterina I; Levantovsky, Rachel M et al. (2013) Dominant effects of the Huntington's disease HTT CAG repeat length are captured in gene-expression data sets by a continuous analysis mathematical modeling strategy. Hum Mol Genet 22:3227-38
Ramos, Eliana Marisa; Latourelle, Jeanne C; Lee, Ji-Hyun et al. (2012) Population stratification may bias analysis of PGC-1? as a modifier of age at Huntington disease motor onset. Hum Genet 131:1833-40
Chiang, Colby; Jacobsen, Jessie C; Ernst, Carl et al. (2012) Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration. Nat Genet 44:390-7, S1
Lee, Jong-Min; Gillis, Tammy; Mysore, Jayalakshmi Srinidhi et al. (2012) Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region. Am J Hum Genet 90:434-44
Lee, Ji-Hyun; Lee, Jong-Min; Ramos, Eliana Marisa et al. (2012) TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease. Biochem Biophys Res Commun 424:404-8

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