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Potential, pitfalls, and prospects of food allergy diagnostics with recombinant allergens or synthetic sequential epitopes

Journal of allergy and clinical immunology, 2008-06, Vol.121 (6), p.1323-1330

2008

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Transcript Profiling of the Androgen Signal in Normal Prostate, Benign Prostatic Hyperplasia, and Prostate Cancer

Endocrinology (Philadelphia), 2006-12, Vol.147 (12), p.5806-5816

2006

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Aldo-keto reductase (AKR) 1C3: Role in prostate disease and the development of specific inhibitors

Molecular and cellular endocrinology, 2006-03, Vol.248 (1), p.182-191

2006

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Characterization of a monoclonal antibody for human aldo-keto reductase AKR1C3 (type 2 3α-hydroxysteroid dehydrogenase/type 5 17β-hydroxysteroid dehydrogenase); immunohistochemical detection in breast and prostate

Steroids, 2004-12, Vol.69 (13), p.795-801

2004

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Dithioerythritol (DTE) prevents inhibitory effects of triphenyltin (TPT) on the key enzymes of the human sex steroid hormone metabolism

The Journal of steroid biochemistry and molecular biology, 2003-04, Vol.84 (5), p.569-576

2003

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Non-stereo-selective cytosolic human brain tissue 3-ketosteroid reductase is refractory to inhibition by AKR1C inhibitors

Biochimica et biophysica acta, 2010-11, Vol.1801 (11), p.1221-1231

2010

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An indomethacin analogue, N-(4-chlorobenzoyl)-melatonin, is a selective inhibitor of aldo-keto reductase 1C3 (type 2 3α-HSD, type 5 17β-HSD, and prostaglandin F synthase), a potential target for the treatment of hormone dependent and hormone independent malignancies

Biochemical pharmacology, 2008-01, Vol.75 (2), p.484-493

2008

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Identification of the Major Oxidative 3α-Hydroxysteroid Dehydrogenase in Human Prostate That Converts 5α-Androstane-3α,17β-diol to 5α-Dihydrotestosterone: A Potential Therapeutic Target for Androgen-Dependent Disease

Molecular endocrinology (Baltimore, Md.), 2006-02, Vol.20 (2), p.444-458

2006

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Tibolone Metabolism in Human Liver Is Catalyzed by 3α/3β-Hydroxysteroid Dehydrogenase Activities of the Four Isoforms of the Aldo-Keto Reductase (AKR)1C Subfamily

The Journal of pharmacology and experimental therapeutics, 2006-03, Vol.316 (3), p.1300-1309

2006

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Human Type 3 3α-Hydroxysteroid Dehydrogenase (Aldo-Keto Reductase 1C2) and Androgen Metabolism in Prostate Cells

Endocrinology (Philadelphia), 2003-07, Vol.144 (7), p.2922-2932

2003

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Inhibition of human cytochrome P450 aromatase activity by butyltins

Steroids, 2001-10, Vol.66 (10), p.763-769

2001

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Reviews and feature article: Potential, pitfalls, and prospects of food allergy diagnostics with recombinant allergens or synthetic sequential epitopes

Journal of allergy and clinical immunology, 2008-06, Vol.121 (6), p.1323-1330

2008

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Effects of butyltins on human 5α-reductase type 1 and type 2 activity

Steroids, 2002-09, Vol.67 (10), p.859-867

2002

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Allopregnanolone serum levels and expression of 5α-reductase and 3α-hydroxysteroid dehydrogenase isoforms in hippocampal and temporal cortex of patients with epilepsy

Epilepsy research, 2003-04, Vol.54 (1), p.11-19

2003

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Characterization of aromatase cytochrome P450 activity in the human temporal lobe

The journal of clinical endocrinology and metabolism, 1999-08, Vol.84 (8), p.2795-2801

1999

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Characterization of the 5α-reductase-3α-hydroxysteroid dehydrogenase complex in the human brain

The journal of clinical endocrinology and metabolism, 2001-03, Vol.86 (3), p.1324-1331

2001

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Tibolone metabolism in human liver is catalyzed by 3alpha/3beta-hydroxysteroid dehydrogenase activities of the four isoforms of the aldo-keto reductase (AKR)1C subfamily

The Journal of pharmacology and experimental therapeutics, 2006-03, Vol.316 (3), p.1300

2006

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Identification of the major oxidative 3alpha-hydroxysteroid dehydrogenase in human prostate that converts 5alpha-androstane-3alpha,17beta-diol to 5alpha-dihydrotestosterone: a potential therapeutic target for androgen-dependent disease

Molecular endocrinology (Baltimore, Md.), 2006-02, Vol.20 (2), p.444-458

2006

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Characterisation of estrogenic 17β-hydroxysteroid dehydrogenase (17β-HSD) activity in the human brain

The Journal of steroid biochemistry and molecular biology, 2003-07, Vol.86 (1), p.79-92

2003

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Tibolone is metabolized by the 3alpha/3beta-hydroxysteroid dehydrogenase activities of the four human isozymes of the aldo-keto reductase 1C subfamily: inversion of stereospecificity with a delta5(10)-3-ketosteroid

Molecular pharmacology, 2004-12, Vol.66 (6), p.1702-1711

2004

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Tibolone Is Metabolized by the 3α/3β-Hydroxysteroid Dehydrogenase Activities of the Four Human Isozymes of the Aldo-Keto Reductase 1C Subfamily: Inversion of Stereospecificity with a Δ 5(10) -3-Ketosteroid

Molecular pharmacology, 2004-12, Vol.66 (6), p.1702-1711

2004

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Tibolone Is Metabolized by the 3Î±/3Î²-Hydroxysteroid Dehydrogenase Activities of the Four Human Isozymes of the Aldo-Keto Reductase 1C Subfamily: Inversion of Stereospecificity with a Î5(10)-3-Ketosteroid

Molecular pharmacology, 2004-12, Vol.66 (6), p.1702

2004

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Human Cytosolic 3Î±-Hydroxysteroid Dehydrogenases of the Aldo-keto Reductase Superfamily Display Significant 3Î²-Hydroxysteroid Dehydrogenase Activity

The Journal of biological chemistry, 2004-03, Vol.279 (11), p.10784

2004

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Human Cytosolic 3α-Hydroxysteroid Dehydrogenases of the Aldo-keto Reductase Superfamily Display Significant 3β-Hydroxysteroid Dehydrogenase Activity

The Journal of biological chemistry, 2004-03, Vol.279 (11), p.10784-10795

2004

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Human cytosolic 3alpha-hydroxysteroid dehydrogenases of the aldo-keto reductase superfamily display significant 3beta-hydroxysteroid dehydrogenase activity: implications for steroid hormone metabolism and action

The Journal of biological chemistry, 2004-03, Vol.279 (11), p.10784-10795

2004

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Potential, pitfalls, and prospects of food allergy diagnostics with recombinant allergens or synthetic sequential epitopes

Transcript Profiling of the Androgen Signal in Normal Prostate, Benign Prostatic Hyperplasia, and Prostate Cancer

Aldo-keto reductase (AKR) 1C3: Role in prostate disease and the development of specific inhibitors

Characterization of a monoclonal antibody for human aldo-keto reductase AKR1C3 (type 2 3α-hydroxysteroid dehydrogenase/type 5 17β-hydroxysteroid dehydrogenase); immunohistochemical detection in breast and prostate

Dithioerythritol (DTE) prevents inhibitory effects of triphenyltin (TPT) on the key enzymes of the human sex steroid hormone metabolism

Non-stereo-selective cytosolic human brain tissue 3-ketosteroid reductase is refractory to inhibition by AKR1C inhibitors

An indomethacin analogue, N-(4-chlorobenzoyl)-melatonin, is a selective inhibitor of aldo-keto reductase 1C3 (type 2 3α-HSD, type 5 17β-HSD, and prostaglandin F synthase), a potential target for the treatment of hormone dependent and hormone independent malignancies

Identification of the Major Oxidative 3α-Hydroxysteroid Dehydrogenase in Human Prostate That Converts 5α-Androstane-3α,17β-diol to 5α-Dihydrotestosterone: A Potential Therapeutic Target for Androgen-Dependent Disease

Tibolone Metabolism in Human Liver Is Catalyzed by 3α/3β-Hydroxysteroid Dehydrogenase Activities of the Four Isoforms of the Aldo-Keto Reductase (AKR)1C Subfamily

Human Type 3 3α-Hydroxysteroid Dehydrogenase (Aldo-Keto Reductase 1C2) and Androgen Metabolism in Prostate Cells

Inhibition of human cytochrome P450 aromatase activity by butyltins

Reviews and feature article: Potential, pitfalls, and prospects of food allergy diagnostics with recombinant allergens or synthetic sequential epitopes

Effects of butyltins on human 5α-reductase type 1 and type 2 activity

Allopregnanolone serum levels and expression of 5α-reductase and 3α-hydroxysteroid dehydrogenase isoforms in hippocampal and temporal cortex of patients with epilepsy

Characterization of aromatase cytochrome P450 activity in the human temporal lobe

Characterization of the 5α-reductase-3α-hydroxysteroid dehydrogenase complex in the human brain

Tibolone metabolism in human liver is catalyzed by 3alpha/3beta-hydroxysteroid dehydrogenase activities of the four isoforms of the aldo-keto reductase (AKR)1C subfamily

Identification of the major oxidative 3alpha-hydroxysteroid dehydrogenase in human prostate that converts 5alpha-androstane-3alpha,17beta-diol to 5alpha-dihydrotestosterone: a potential therapeutic target for androgen-dependent disease

Characterisation of estrogenic 17β-hydroxysteroid dehydrogenase (17β-HSD) activity in the human brain

Tibolone is metabolized by the 3alpha/3beta-hydroxysteroid dehydrogenase activities of the four human isozymes of the aldo-keto reductase 1C subfamily: inversion of stereospecificity with a delta5(10)-3-ketosteroid

Tibolone Is Metabolized by the 3α/3β-Hydroxysteroid Dehydrogenase Activities of the Four Human Isozymes of the Aldo-Keto Reductase 1C Subfamily: Inversion of Stereospecificity with a Δ 5(10) -3-Ketosteroid

Tibolone Is Metabolized by the 3Î±/3Î²-Hydroxysteroid Dehydrogenase Activities of the Four Human Isozymes of the Aldo-Keto Reductase 1C Subfamily: Inversion of Stereospecificity with a Î5(10)-3-Ketosteroid

Human Cytosolic 3Î±-Hydroxysteroid Dehydrogenases of the Aldo-keto Reductase Superfamily Display Significant 3Î²-Hydroxysteroid Dehydrogenase Activity

Human Cytosolic 3α-Hydroxysteroid Dehydrogenases of the Aldo-keto Reductase Superfamily Display Significant 3β-Hydroxysteroid Dehydrogenase Activity

Human cytosolic 3alpha-hydroxysteroid dehydrogenases of the aldo-keto reductase superfamily display significant 3beta-hydroxysteroid dehydrogenase activity: implications for steroid hormone metabolism and action

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