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11β-Hydroxysteroid Dehydrogenase Type 1 Activity in Lean and Obese Males with Type 2 Diabetes Mellitus

The journal of clinical endocrinology and metabolism, 2004-09, Vol.89 (9), p.4755-4761

2004

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Congenital Hypopituitarism as a Cause of Undetectable Estriol Levels in the Maternal Triple-Marker Screen

The journal of clinical endocrinology and metabolism, 2003-09, Vol.88 (9), p.4144-4148

2003

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The corticosteroid metabolic profile of the mouse

Steroids, 2008-10, Vol.73 (11), p.1066-1076

2008

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Cortisol metabolism in human obesity : Impaired cortisone→cortisol conversion in subjects with central adiposity

The journal of clinical endocrinology and metabolism, 1999-03, Vol.84 (3), p.1022-1027

1999

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Congenital deficiency of 11β-hydroxysteroid dehydrogenase (apparent mineralocorticoid excess syndrome) : Diagnostic value of urinary free cortisol and cortisone

Journal of endocrinological investigation, 2001, Vol.24 (1), p.17-23

2001

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Mechanisms of fructose-induced hypertriglyceridaemia in the rat : activation of hepatic pyruvate dehydrogenase through inhibition of pyruvate dehydrogenase kinase

Biochemical journal, 1992-03, Vol.282 (3), p.753-757

1992

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Mass spectrometry in the diagnosis of steroid-related disorders and in hypertension research

Journal of steroid biochemistry and molecular biology, 1993-04, Vol.45 (1-3), p.127-140

Shackleton, Cedric H.L.

1993

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Examination of genotype and phenotype relationships in 14 patients with apparent mineralocorticoid excess

The journal of clinical endocrinology and metabolism, 1998-07, Vol.83 (7), p.2244-2254

1998

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Confirming testosterone administration by isotope ratio mass spectrometric analysis of urinary androstanediols

Steroids, 1997-04, Vol.62 (4), p.379-387

1997

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Measuring synthesis rates of muscle creatine kinase and myosin with stable isotopes and mass spectrometry

Analytical biochemistry, 2002-10, Vol.309 (1), p.1-10

2002

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A mutation in the HSD11B2 gene in a family with apparent mineralocorticoid excess

The journal of clinical endocrinology and metabolism, 1995-07, Vol.80 (7), p.2263-2266

1995

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Increased Vasoconstrictor Sensitivity to Glucocorticoids in Essential Hypertension

Hypertension (Dallas, Tex. 1979), 1996-02, Vol.27 (2), p.190-196

1996

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Expediting Rare Variant Hemoglobin Characterization by Combined HPLC/Electrospray Mass Spectrometry

Hemoglobin, 1993-01, Vol.17 (3), p.227-242

1993

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Electrospray mass spectrometry of testosterone esters: Potential for use in doping control

Steroids, 1997-07, Vol.62 (7), p.523-529

1997

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Licorice-induced hypermineralocorticoidism

The New England journal of medicine, 1991-10, Vol.325 (17), p.1223-1227

1991

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Androstanediol and 5-androstenediol profiling for detecting exogenously administered dihydrotestosterone, epitestosterone, and dehydroepiandrosterone: Potential use in gas chromatography isotope ratio mass spectrometry

Steroids, 1997-10, Vol.62 (10), p.665-673

1997

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Profiling steroid hormones and urinary steroids

Journal of Chromatography B: Biomedical Sciences and Applications, 1986-06, Vol.379, p.91-156

Shackleton, C.H.L.

1986

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Several homozygous mutations in the gene for 11β-hydroxysteroid dehydrogenase type 2 in patients with apparent mineralocorticoid excess

The journal of clinical endocrinology and metabolism, 1995-11, Vol.80 (11), p.3145-3150

1995

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CONGENITAL 11β-HYDROXYSTEROID DEHYDROGENASE DEFICIENCY ASSOCIATED WITH JUVENILE HYPERTENSION: CORTICOSTEROID METABOLITE PROFILES OF FOUR PATIENTS AND THEIR FAMILIES

Clinical endocrinology (Oxford), 1985-06, Vol.22 (6), p.701-712

1985

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11β-Hydroxysteroid dehydrogenase activity in Cushing's syndrome : explaining the mineralocorticoid excess state of the ectopic adrenocorticotropin syndrome

The journal of clinical endocrinology and metabolism, 1995, Vol.80 (12), p.3617-3620

1995

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Apparent cortisone reductase deficiency : A unique form of hypercortisolism

The journal of clinical endocrinology and metabolism, 1996-11, Vol.81 (11), p.3855-3860

1996

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Neonatal urinary steroids in Smith-Lemli-Opitz syndrome associated with 7-dehydrocholesterol reductase deficiency

Steroids, 1999-07, Vol.64 (7), p.481-490

1999

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Increased De novo hepatic lipogenesis in human immunodeficiency virus infection

The journal of clinical endocrinology and metabolism, 1993-03, Vol.76 (3), p.559-565

1993

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The identification of 5α-reductase-2 and 17β-hydroxysteroid dehydrogenase-3 gene defects in male pseudohermaphrodites from a Turkish kindred

The journal of clinical endocrinology and metabolism, 1998-02, Vol.83 (2), p.560-569

1998

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Measurement of de novo hepatic lipogenesis in humans using stable isotopes

The Journal of clinical investigation, 1991-05, Vol.87 (5), p.1841-1852

1991

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11β-Hydroxysteroid Dehydrogenase Type 1 Activity in Lean and Obese Males with Type 2 Diabetes Mellitus

Congenital Hypopituitarism as a Cause of Undetectable Estriol Levels in the Maternal Triple-Marker Screen

The corticosteroid metabolic profile of the mouse

Cortisol metabolism in human obesity : Impaired cortisone→cortisol conversion in subjects with central adiposity

Congenital deficiency of 11β-hydroxysteroid dehydrogenase (apparent mineralocorticoid excess syndrome) : Diagnostic value of urinary free cortisol and cortisone

Mechanisms of fructose-induced hypertriglyceridaemia in the rat : activation of hepatic pyruvate dehydrogenase through inhibition of pyruvate dehydrogenase kinase

Mass spectrometry in the diagnosis of steroid-related disorders and in hypertension research

Examination of genotype and phenotype relationships in 14 patients with apparent mineralocorticoid excess

Confirming testosterone administration by isotope ratio mass spectrometric analysis of urinary androstanediols

Measuring synthesis rates of muscle creatine kinase and myosin with stable isotopes and mass spectrometry

A mutation in the HSD11B2 gene in a family with apparent mineralocorticoid excess

Increased Vasoconstrictor Sensitivity to Glucocorticoids in Essential Hypertension

Expediting Rare Variant Hemoglobin Characterization by Combined HPLC/Electrospray Mass Spectrometry

Electrospray mass spectrometry of testosterone esters: Potential for use in doping control

Licorice-induced hypermineralocorticoidism

Androstanediol and 5-androstenediol profiling for detecting exogenously administered dihydrotestosterone, epitestosterone, and dehydroepiandrosterone: Potential use in gas chromatography isotope ratio mass spectrometry

Profiling steroid hormones and urinary steroids

Several homozygous mutations in the gene for 11β-hydroxysteroid dehydrogenase type 2 in patients with apparent mineralocorticoid excess

CONGENITAL 11β-HYDROXYSTEROID DEHYDROGENASE DEFICIENCY ASSOCIATED WITH JUVENILE HYPERTENSION: CORTICOSTEROID METABOLITE PROFILES OF FOUR PATIENTS AND THEIR FAMILIES

11β-Hydroxysteroid dehydrogenase activity in Cushing's syndrome : explaining the mineralocorticoid excess state of the ectopic adrenocorticotropin syndrome

Apparent cortisone reductase deficiency : A unique form of hypercortisolism

Neonatal urinary steroids in Smith-Lemli-Opitz syndrome associated with 7-dehydrocholesterol reductase deficiency

Increased De novo hepatic lipogenesis in human immunodeficiency virus infection

The identification of 5α-reductase-2 and 17β-hydroxysteroid dehydrogenase-3 gene defects in male pseudohermaphrodites from a Turkish kindred

Measurement of de novo hepatic lipogenesis in humans using stable isotopes

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