Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
3R01HD028458-01A1S1
Application #
3330089
Study Section
Mammalian Genetics Study Section (MGN)
Project Start
1992-04-01
Project End
1996-03-31
Budget Start
1992-05-01
Budget End
1993-03-31
Support Year
1
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Baylor College of Medicine
Department
Type
Schools of Medicine
DUNS #
074615394
City
Houston
State
TX
Country
United States
Zip Code
77030
Lucas, R E; Vlangos, C N; Das, P et al. (2001) Genomic organisation of the approximately 1.5 Mb Smith-Magenis syndrome critical interval: transcription map, genomic contig, and candidate gene analysis. Eur J Hum Genet 9:892-902
Vlangos, C N; Das, P; Patel, P I et al. (2000) Assignment of developmentally regulated GTP-binding protein (DRG2) to human chromosome band 17p11.2 with somatic cell hybrids and localization to the Smith-Magenis syndrome critical interval. Cytogenet Cell Genet 88:283-5
Elsea, S H; Clark, I B; Juyal, R C et al. (1999) Assignment of beta-centractin (CTRN2) to human chromosome 2 bands q11.1-->q11.2 with somatic cell hybrids and in situ hybridization. Cytogenet Cell Genet 84:48-9
Elsea, S H; Fritz, E; Schoener-Scott, R et al. (1998) Gene for topoisomerase III maps within the Smith-Magenis syndrome critical region: analysis of cell-cycle distribution and radiation sensitivity. Am J Med Genet 75:104-8
Sun, D; Elsea, S H; Patel, P I et al. (1998) Cloning of a human ""epidermal-type"" 12-lipoxygenase-related gene and chromosomal localization to 17p13. Cytogenet Cell Genet 81:79-82
Fritz, E; Elsea, S H; Patel, P I et al. (1997) Overexpression of a truncated human topoisomerase III partially corrects multiple aspects of the ataxia-telangiectasia phenotype. Proc Natl Acad Sci U S A 94:4538-42
Elsea, S H; Purandare, S M; Adell, R A et al. (1997) Definition of the critical interval for Smith-Magenis syndrome. Cytogenet Cell Genet 79:276-81
Yang, S P; Bidichandani, S I; Figuera, L E et al. (1997) Molecular analysis of deletion (17)(p11.2p11.2) in a family segregating a 17p paracentric inversion: implications for carriers of paracentric inversions. Am J Hum Genet 60:1184-93
Trask, B J; Mefford, H; van den Engh, G et al. (1996) Quantification by flow cytometry of chromosome-17 deletions in Smith-Magenis syndrome patients. Hum Genet 98:710-8
Juyal, R C; Kuwano, A; Kondo, I et al. (1996) Mosaicism for del(17)(p11.2p11.2) underlying the Smith-Magenis syndrome. Am J Med Genet 66:193-6

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