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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. Molecular and cell biology of lipids, 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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Expression of estrogen receptor alpha increases leptin‐induced STAT3 activity in breast cancer cells

International journal of cancer, 2010-07, Vol.127 (1), p.55-66

2010

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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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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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Steroid sulfatase (STS) expression in the human temporal lobe: enzyme activity, mRNA expression and immunohistochemistry study

Journal of neurochemistry, 2004-04, Vol.89 (2), p.403-417

2004

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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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Characterization of the dehydroepiandrosterone (DHEA) metabolism via oxysterol 7α‐hydroxylase and 17‐ketosteroid reductase activity in the human brain

Journal of neurochemistry, 2002-11, Vol.83 (3), p.713-726

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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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 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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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 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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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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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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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

Expression of estrogen receptor alpha increases leptin‐induced STAT3 activity in breast cancer cells

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

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

Steroid sulfatase (STS) expression in the human temporal lobe: enzyme activity, mRNA expression and immunohistochemistry study

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

Characterization of the dehydroepiandrosterone (DHEA) metabolism via oxysterol 7α‐hydroxylase and 17‐ketosteroid reductase activity in the human brain

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

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 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

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 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

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

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

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