Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
7R01DK038855-06
Application #
3238418
Study Section
General Medicine B Study Section (GMB)
Project Start
1987-07-01
Project End
1992-06-30
Budget Start
1991-11-01
Budget End
1992-06-30
Support Year
6
Fiscal Year
1991
Total Cost
Indirect Cost
Name
University of Utah
Department
Type
Schools of Medicine
DUNS #
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
Nesbit, M Andrew; Hannan, Fadil M; Howles, Sarah A et al. (2013) Mutations affecting G-protein subunit ?11 in hypercalcemia and hypocalcemia. N Engl J Med 368:2476-2486
Hobbs, Maurine R; Rosen, Irving B; Jackson, Charles E (2002) Revised 14.7-cM locus for the hyperparathyroidism-jaw tumor syndrome gene, HRPT2. Am J Hum Genet 70:1376-7
Hobbs, M R; Pole, A R; Pidwirny, G N et al. (1999) Hyperparathyroidism-jaw tumor syndrome: the HRPT2 locus is within a 0.7-cM region on chromosome 1q. Am J Hum Genet 64:518-25
Health 3rd, H; Odelberg, S; Jackson, C E et al. (1996) Clustered inactivating mutations and benign polymorphisms of the calcium receptor gene in familial benign hypocalciuric hypercalcemia suggest receptor functional domains. J Clin Endocrinol Metab 81:1312-7
Szabo, J; Heath, B; Hill, V M et al. (1995) Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31. Am J Hum Genet 56:944-50
Thompson, D B; Samowitz, W S; Odelberg, S et al. (1995) Genetic abnormalities in sporadic parathyroid adenomas: loss of heterozygosity for chromosome 3q markers flanking the calcium receptor locus. J Clin Endocrinol Metab 80:3377-80
Heath 3rd, H (1994) Familial benign hypercalcemia--from clinical description to molecular genetics. West J Med 160:554-61
Khosla, S; Ebeling, P R; Firek, A F et al. (1993) Calcium infusion suggests a ""set-point"" abnormality of parathyroid gland function in familial benign hypercalcemia and more complex disturbances in primary hyperparathyroidism. J Clin Endocrinol Metab 76:715-20
Heath 3rd, H; Jackson, C E; Otterud, B et al. (1993) Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia: evidence for locus heterogeneity. Am J Hum Genet 53:193-200
Heath 3rd, H; Leppert, M F; Lifton, R P et al. (1992) Genetic linkage analysis in familial benign hypercalcemia using a candidate gene strategy. I. Studies in four families. J Clin Endocrinol Metab 75:846-51

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