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Induction of vitellogenesis by 17-hydroxyprogesterone and methyl farnesoate during post-reproductive period, in the estuarine crab Neohelice granulata
(Int Science Services/Balaban Publishers, 2015-04)
Adult female crabs (Neohelice granulata) were treated during the post-reproductive period with both 17-hydroxyprogesterone (17PG) and methyl farnesoate (MF). During the 4-week in vivo assay, animals were fed hormone-enriched ...
Generation of monoclonal antibodies against 17α-hydroxyprogesterone for newborn screening of congenital adrenal hyperplasia
(Elsevier B.V., 2018)
© 2018 Elsevier B.V. Congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder caused by the deficiency of one of the five enzymes involved in the biosynthesis of corticosteroids. The most common form of the ...
Aluminum as an endocrine disruptor in female Nile tilapia (Oreochromis niloticus)
(ELSEVIER SCIENCE INC, 2010)
The effects of aluminum on plasma ion, lipid, protein and steroid hormone concentration were evaluated in Oreochromis niloticus broodstock females. Lipid and protein concentrations from the gonads and liver were also ...
Astyanax altiparanae Ovarian maturation after spawning in water recycling systems*Maturação ovariana de astyanax altiparanae após desova em sistema de recirculação de água
(2018-01-01)
In this study, we evaluated the possibility of obtaining successive Astyanax altiparanae spawns under laboratory conditions. In order to do so, 104 specimens were randomly distributed into four boxes (10 females and 16 ...
INVITRO BIOTRANSFORMATION OF PROGESTERONE-4-C-14 IN 17 HYDROXY-PROGESTERONE AND TESTOSTERONE IN HUMAN SKIN
(INST MEXICANO SEGURO, 1989)
INVITRO BIOTRANSFORMATION OF PROGESTERONE-4-C-14 IN 17 HYDROXY-PROGESTERONE AND TESTOSTERONE IN HUMAN SKIN
(INST MEXICANO SEGURO, 1989)
21-hydroxylase deficiency transiently mimicking combined 21- and 11 beta-hydroxylase deficiency
(Walter De Gruyter Gmbh, 2008-05-01)
21-Hydroxylase deficiency (21OHD) is the commonest form of congenital adrenal hyperplasia, while 11 beta OHD represents 5% of cases. Although both result from mutations in distinct genes, cases of 'apparent' combined 210HD ...