Tetrahydro-11-deoxycortisol

Tetrahydro-11-deoxycortisol is a lipid of Sterol Lipids (ST) class.

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There are no associated biomedical information in the current reference collection.

Current reference collection contains 42 references associated with Tetrahydro-11-deoxycortisol in LipidPedia. Due to lack of full text of references or no associated biomedical terms are recognized in our current text-mining method, we cannot extract any biomedical terms related to diseases, pathways, locations, functions, genes, lipids, and animal models from the associated reference collection.

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Authors Title Published Journal PubMed Link
Gröndal S et al. Steroid profile in urine: a useful tool in the diagnosis and follow up of adrenocortical carcinoma. 1990 Acta Endocrinol. pmid:2141212
Canario AV and Scott AP Identification of, and development of radioimmunoassays for 17 alpha, 21-dihydroxy-4-pregnene-3,20-dione and 3 alpha,17 alpha, 21-trihydroxy-5 beta-pregnan-20-one in the ovaries of mature plaice (Pleuronectes platessa). 1990 Gen. Comp. Endocrinol. pmid:2354767
Canario AV and Scott AP Conjugates of ovarian steroids, including 17 alpha,20 beta-dihydroxy-4-pregnen-3-one (maturation-inducing steroid), accumulate in the urine of a marine teleost (plaice; Pleuronectes platessa). 1989 J. Endocrinol. pmid:2809483
Rösler A et al. 11 Beta-hydroxylase deficiency congenital adrenal hyperplasia: update of prenatal diagnosis. 1988 J. Clin. Endocrinol. Metab. pmid:3346360
Hughes IA et al. Early diagnosis of 11 beta-hydroxylase deficiency in two siblings confirmed by analysis of a novel steroid metabolite in newborn urine. 1986 Acta Endocrinol. pmid:3515819
Tucker WS et al. Reversible adrenal insufficiency induced by ketoconazole. 1985 JAMA pmid:3981770
Masi AT et al. Low adrenal androgenic-anabolic steroids in women with rheumatoid arthritis (RA): gas-liquid chromatographic studies of RA patients and matched normal control women indicating decreased 11-deoxy-17-ketosteroid excretion. 1984 Semin. Arthritis Rheum. pmid:6091273
Zachmann M et al. Clinical and biochemical variability of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency. A study of 25 patients. 1983 J. Clin. Endocrinol. Metab. pmid:6296182
Knorr D et al. Diagnosis and monitoring of therapy of the various enzymatic defects causing congenital adrenal hyperplasia by semiautomatic capillary gas-liquid chromatography. 1982 Jul-Aug Horm. Res. pmid:6982215
Zachmann M et al. Transient impairment or delay of urinary trihydroxypregnanone (THS) response to metyrapone in boys with delayed adolescence and in patients with isolated growth hormone deficiency. 1982 Acta Endocrinol. pmid:7058680