Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Physician Scientist Award (K11)
Project #
5K11HD000824-03
Application #
3087002
Study Section
Mental Retardation Research and Training Committee (HDMR)
Project Start
1987-09-30
Project End
1989-12-31
Budget Start
1989-09-01
Budget End
1989-12-31
Support Year
3
Fiscal Year
1989
Total Cost
Indirect Cost
Name
Eunice Kennedy Shriver Center Mtl Retardatn
Department
Type
DUNS #
City
Waltham
State
MA
Country
United States
Zip Code
02254
Sims, K B; Lebo, R V; Benson, G et al. (1992) The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3. Hum Mol Genet 1:83-9
Murphy, D L; Sims, K B; Karoum, F et al. (1991) Plasma amine oxidase activities in Norrie disease patients with an X-chromosomal deletion affecting monoamine oxidase. J Neural Transm Gen Sect 83:1-12
Murphy, D L; Sims, K B; Karoum, F et al. (1990) Marked amine and amine metabolite changes in Norrie disease patients with an X-chromosomal deletion affecting monoamine oxidase. J Neurochem 54:242-7
Sims, K B; Ozelius, L; Corey, T et al. (1989) Norrie disease gene is distinct from the monoamine oxidase genes. Am J Hum Genet 45:424-34
Hsu, Y P; Powell, J F; Sims, K B et al. (1989) Molecular genetics of the monoamine oxidases. J Neurochem 53:12-8
Diergaarde, P J; Wieringa, B; Bleeker-Wagemakers, E M et al. (1989) Physical fine-mapping of a deletion spanning the Norrie gene. Hum Genet 84:22-6
Sims, K B; de la Chapelle, A; Norio, R et al. (1989) Monoamine oxidase deficiency in males with an X chromosome deletion. Neuron 2:1069-76
Hsu, Y P; Weyler, W; Chen, S et al. (1988) Structural features of human monoamine oxidase A elucidated from cDNA and peptide sequences. J Neurochem 51:1321-4