Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Institutional National Research Service Award (T32)
Project #
5T32DK007116-21
Application #
2134609
Study Section
Diabetes, Endocrinology and Metabolic Diseases B Subcommittee (DDK)
Project Start
1975-07-01
Project End
1995-12-31
Budget Start
1995-01-01
Budget End
1995-12-31
Support Year
21
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Pediatrics
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Sher, E S; Migeon, C J; Berkovitz, G D (1998) Evaluation of boys with marked breast development at puberty. Clin Pediatr (Phila) 37:367-71
Sher, E S; Addelston, M B; Plotnick, L et al. (1998) Molecular investigation of two male subjects with short stature and a 45,X/46,X,ring(Y) karyotype. Horm Res 49:46-50
Rogers, S A; Padanilam, B J; Hruska, K A et al. (1997) Metanephric osteopontin regulates nephrogenesis in vitro. Am J Physiol 272:F469-76
Fuqua, J S; Sher, E S; Perlman, E J et al. (1996) Abnormal gonadal differentiation in two subjects with ambiguous genitalia, Mullerian structures, and normally developed testes: evidence for a defect in gonadal ridge development. Hum Genet 97:506-11
Fuqua, J S; Sher, E S; Migeon, C J et al. (1995) Assay of plasma testosterone during the first six months of life: importance of chromatographic purification of steroids. Clin Chem 41:1146-9
Turner, B; Fechner, P Y; Fuqua, J S et al. (1995) Combined Leydig cell and Sertoli cell dysfunction in 46,XX males lacking the sex determining region Y gene. Am J Med Genet 57:440-3
Fechner, P Y; Rosenberg, C; Stetten, G et al. (1994) Nonrandom inactivation of the Y-bearing X chromosome in a 46,XX individual: evidence for the etiology of 46,XX true hermaphroditism. Cytogenet Cell Genet 66:22-6
Marcantonio, S M; Fechner, P Y; Migeon, C J et al. (1994) Embryonic testicular regression sequence: a part of the clinical spectrum of 46,XY gonadal dysgenesis. Am J Med Genet 49:1-5
Casella, S J; Reiner, B J; Chen, T C et al. (1994) A possible genetic defect in 25-hydroxylation as a cause of rickets. J Pediatr 124:929-32
Fechner, P Y; Marcantonio, S M; Ogata, T et al. (1993) Report of a kindred with X-linked (or autosomal dominant sex-limited) 46,XY partial gonadal dysgenesis. J Clin Endocrinol Metab 76:1248-53

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