Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32HD006875-01
Application #
3048239
Study Section
Clinical Sciences Subcommittee 1 (CLN)
Project Start
1986-03-05
Project End
Budget Start
1985-10-01
Budget End
1986-09-30
Support Year
1
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of California San Diego
Department
Type
Schools of Medicine
DUNS #
077758407
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Dahl, K D; Jia, X C; Hsueh, A J (1989) Granulosa cell aromatase bioassay for follicle-stimulating hormone. Methods Enzymol 168:414-22
Hsueh, A J; Liu, Y X; Cajander, S et al. (1988) Gonadotropin-releasing hormone induces ovulation in hypophysectomized rats: studies on ovarian tissue-type plasminogen activator activity, messenger ribonucleic acid content, and cellular localization. Endocrinology 122:1486-95
Dahl, K D; Bicsak, T A; Hsueh, A J (1988) Naturally occurring antihormones: secretion of FSH antagonists by women treated with a GnRH analog. Science 239:72-4
Dahl, K D; Czekala, N M; Lim, P et al. (1987) Monitoring the menstrual cycle of humans and lowland gorillas based on urinary profiles of bioactive follicle-stimulating hormone and steroid metabolites. J Clin Endocrinol Metab 64:486-93
Liu, Y X; Kasson, B G; Dahl, K D et al. (1987) Vasoactive intestinal peptide stimulates plasminogen activator activity by cultured rat granulosa cells and cumulus-oocyte complexes. Peptides 8:29-33
Dahl, K D; Hsueh, A J (1987) Use of the granulosa cell aromatase bioassay for measurement of bioactive follicle-stimulating hormone in urine and serum samples of diverse species. Steroids 50:375-92
Dahl, K D; Czekala, N M; Hsueh, A J (1987) Estrogen-producing ovarian granulosa cells: use of the granulosa cell aromatase bioassay (GAB) to monitor FSH levels in body fluids. Adv Exp Med Biol 219:275-98
Hsueh, A J; Dahl, K D; Vaughan, J et al. (1987) Heterodimers and homodimers of inhibin subunits have different paracrine action in the modulation of luteinizing hormone-stimulated androgen biosynthesis. Proc Natl Acad Sci U S A 84:5082-6