Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK020630-17
Application #
2137522
Study Section
Hematology Subcommittee 2 (HEM)
Project Start
1979-07-01
Project End
1998-03-31
Budget Start
1996-04-01
Budget End
1997-03-31
Support Year
17
Fiscal Year
1996
Total Cost
Indirect Cost
Name
University of Utah
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
Toomajian, Christopher; Ajioka, Richard S; Jorde, Lynn B et al. (2003) A method for detecting recent selection in the human genome from allele age estimates. Genetics 165:287-97
Ajioka, Richard S; Levy, Joanne E; Andrews, Nancy C et al. (2002) Regulation of iron absorption in Hfe mutant mice. Blood 100:1465-9
Bulaj, Z J; Franklin, M R; Phillips, J D et al. (2000) Transdermal estrogen replacement therapy in postmenopausal women previously treated for porphyria cutanea tarda. J Lab Clin Med 136:482-8
Bulaj, Z J; Ajioka, R S; Phillips, J D et al. (2000) Disease-related conditions in relatives of patients with hemochromatosis. N Engl J Med 343:1529-35
Lonjou, C; Collins, A; Ajioka, R S et al. (1998) Allelic association under map error and recombinational heterogeneity: a tale of two sites. Proc Natl Acad Sci U S A 95:11366-70
Bernard, P S; Ajioka, R S; Kushner, J P et al. (1998) Homogeneous multiplex genotyping of hemochromatosis mutations with fluorescent hybridization probes. Am J Pathol 153:1055-61
Edwards, C Q; Griffen, L M; Ajioka, R S et al. (1998) Screening for hemochromatosis: phenotype versus genotype. Semin Hematol 35:72-6
Ajioka, R S; Jorde, L B; Gruen, J R et al. (1997) Haplotype analysis of hemochromatosis: evaluation of different linkage-disequilibrium approaches and evolution of disease chromosomes. Am J Hum Genet 60:1439-47
Ajioka, R S; Yu, P; Gruen, J R et al. (1997) Recombinations defining centromeric and telomeric borders for the hereditary haemochromatosis locus. J Med Genet 34:28-33
Bulaj, Z J; Griffen, L M; Jorde, L B et al. (1996) Clinical and biochemical abnormalities in people heterozygous for hemochromatosis. N Engl J Med 335:1799-805

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