Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Research Program Projects (P01)
Project #
5P01HG000834-04
Application #
2345199
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
4
Fiscal Year
1996
Total Cost
Indirect Cost
Name
University of California Irvine
Department
Type
DUNS #
161202122
City
Irvine
State
CA
Country
United States
Zip Code
92697
Church, D M; Yang, J; Bocian, M et al. (1997) A high-resolution physical and transcript map of the Cri du chat region of human chromosome 5p. Genome Res 7:787-801
McPherson, J D; Krane, M C; Wagner-McPherson, C B et al. (1997) High resolution mapping of the renal sodium-phosphate cotransporter gene (NPT2) confirms its localization to human chromosome 5q35. Pediatr Res 41:632-4
Gladwin, A J; Dixon, J; Loftus, S K et al. (1996) Treacher Collins syndrome may result from insertions, deletions or splicing mutations, which introduce a termination codon into the gene. Hum Mol Genet 5:1533-8
(1996) Positional cloning of a gene involved in the pathogenesis of Treacher Collins syndrome. The Treacher Collins Syndrome Collaborative Group. Nat Genet 12:130-6
Her, C; Aksoy, I A; Kimura, S et al. (1995) Human estrogen sulfotransferase gene (STE): cloning, structure, and chromosomal localization. Genomics 29:16-23
Bermingham, N; Hillermann, R; Gilmour, F et al. (1995) Human glial cell line-derived neurotrophic factor (GDNF) maps to chromosome 5. Hum Genet 96:671-3
Vamvakopoulos, N C; Sioutopoulou, T O; Durkin, S A et al. (1995) Mapping the human corticotropin releasing hormone binding protein gene (CRHBP) to the long arm of chromosome 5 (5q11.2-q13.3). Genomics 25:325-7
Church, D M; Bengtsson, U; Nielsen, K V et al. (1995) Molecular definition of deletions of different segments of distal 5p that result in distinct phenotypic features. Am J Hum Genet 56:1162-72
Del Mastro, R G; Wang, L; Simmons, A D et al. (1995) Human chromosome-specific cDNA libraries: new tools for gene identification and genome annotation. Genome Res 5:185-94
Tijssen, M A; Shiang, R; van Deutekom, J et al. (1995) Molecular genetic reevaluation of the Dutch hyperekplexia family. Arch Neurol 52:578-82

Showing the most recent 10 out of 15 publications