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Recombinant CYP11B genes encode enzymes that can catalyze conversion of 11-deoxycortisol to cortisol, 18-hydroxycortisol, and 18-oxocortisol

The journal of clinical endocrinology and metabolism, 1998-11, Vol.83 (11), p.3996-4001

1998

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Isolated aldosterone synthase deficiency caused by simultaneous E198D and V386A mutations in the CYP11B2 gene

The journal of clinical endocrinology and metabolism, 1998-11, Vol.83 (11), p.4156-4161

1998

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Mutations in the Human CYP11B2 (Aldosterone Synthase) Gene Causing Corticosterone Methyloxidase II Deficiency

Proceedings of the National Academy of Sciences - PNAS, 1992-06, Vol.89 (11), p.4996-5000

1992

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Mutations in the CYP11B1 Gene Causing Congenital Adrenal Hyperplasia and Hypertension Cluster in Exons 6, 7, and 8

Proceedings of the National Academy of Sciences - PNAS, 1993-05, Vol.90 (10), p.4552-4556

1993

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Angiotensin II receptors: protein and gene structures, expression and potential pathological involvements

European journal of endocrinology, 1996-04, Vol.134 (4), p.403-411

1996

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Glucocorticoid-Suppressible Hyperaldosteronism Results from Hybrid Genes Created by Unequal Crossovers between CYP11B1 and CYP11B2

Proceedings of the National Academy of Sciences - PNAS, 1992-09, Vol.89 (17), p.8327-8331

1992

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The product of the CYP11B2 gene is required for aldosterone biosynthesis in the human adrenal cortex

Molecular endocrinology (Baltimore, Md.), 1991-10, Vol.5 (10), p.1513-1522

1991

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Genetic analysis of the human type-1 angiotensin II receptor

Molecular endocrinology (Baltimore, Md.), 1992-07, Vol.6 (7), p.1113-1118

1992

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Glucocorticoid-suppressible hyperaldosteronism and adrenal tumors occurring in a single French pedigree

The Journal of clinical investigation, 1995-11, Vol.96 (5), p.2236-2246

1995

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The amino acid substitutions Ser288Gly and Val320Ala convert the cortisol producing enzyme, CYP11B1, into an aldosterone producing enzyme

Nature structural & molecular biology, 1997-01, Vol.4 (1), p.32-35

1997

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Scaling Up the Ligase Chain Reaction-Based Approach to Gene Synthesis

BioTechniques, 2001-02, Vol.30 (2), p.249-252

2001

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The L10F mutation of angiotensinogen is rare in pre-eclampsia

Journal of hypertension, 2000-02, Vol.18 (2), p.173-178

2000

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Aldosterone Secretion: A Molecular Perspective

Trends in endocrinology and metabolism, 1997-11, Vol.8 (9), p.346-354

1997

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Polar residues in the transmembrane domains of the type 1 angiotensin II receptor are required for binding and coupling. Reconstitution of the binding site by co-expression of two deficient mutants

The Journal of biological chemistry, 1996-01, Vol.271 (3), p.1507-1513

1996

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Glucocorticoid-suppressible hyperaldosteronism and adrenal tumors occurring in a single French pedigree

The Journal of clinical investigation, 1995-11, Vol.96 (5), p.2236-2246

1995

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Genetic recombination as a cause of inherited disorders of aldosterone and cortisol biosynthesis and a contributor to genetic variation in blood pressure

Steroids, 1995, Vol.60 (1), p.22-27

1995

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Alternatively spliced human type 1 angiotensin II receptor mRNAs are translated at different efficiencies and encode two receptor isoforms

Molecular endocrinology (Baltimore, Md.), 1995-09, Vol.9 (9), p.1250-1262

1995

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Sequence similarities between a novel putative G protein-coupled receptor and Na+/Ca2+ exchangers define a cation binding domain

Molecular endocrinology (Baltimore, Md.), 2000-09, Vol.14 (9), p.1351-1364

2000

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Molecular biology of 11β-hydroxylase and 11β-hydroxysteroid dehydrogenase enzymes

Journal of steroid biochemistry and molecular biology, 1992-12, Vol.43 (8), p.827-835

1992

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Human type-1 angiotensin II (AT1) receptor gene structure and function

Clinical and experimental pharmacology & physiology, 1996-09, Vol.23 Suppl 3, p.S67-S73

Curnow, K M

1996

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Mapping of the mouse Ly-6, Xp-14 and Gdc-1 loci to chromosome 15

Immunogenetics (New York), 1987, Vol.25 (1), p.21-27

1987

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Transcripts originating in intron 1 of the HSD11 (11 beta-hydroxysteroid dehydrogenase) gene encode a truncated polypeptide that is enzymatically inactive

Molecular endocrinology (Baltimore, Md.), 1993-02, Vol.7 (2), p.154-160

1993

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Disorders of steroid 11β-hydroxylase isozymes

Endocrine reviews, 1994-08, Vol.15 (4), p.421-438

1994

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Disorders of steroid 11 beta-hydroxylase isozymes

Endocrine reviews, 1994-08, Vol.15 (4), p.421-438

White, P. C.

1994

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Prenatal Diagnosis and Treatment of 11β-Hydroxylase Deficiency Congenital Adrenal Hyperplasia Resulting in Normal Female Genitalia

The journal of clinical endocrinology and metabolism, 1999-09, Vol.84 (9), p.3129-3134

1999

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Recombinant CYP11B genes encode enzymes that can catalyze conversion of 11-deoxycortisol to cortisol, 18-hydroxycortisol, and 18-oxocortisol

Isolated aldosterone synthase deficiency caused by simultaneous E198D and V386A mutations in the CYP11B2 gene

Mutations in the Human CYP11B2 (Aldosterone Synthase) Gene Causing Corticosterone Methyloxidase II Deficiency

Mutations in the CYP11B1 Gene Causing Congenital Adrenal Hyperplasia and Hypertension Cluster in Exons 6, 7, and 8

Angiotensin II receptors: protein and gene structures, expression and potential pathological involvements

Glucocorticoid-Suppressible Hyperaldosteronism Results from Hybrid Genes Created by Unequal Crossovers between CYP11B1 and CYP11B2

The product of the CYP11B2 gene is required for aldosterone biosynthesis in the human adrenal cortex

Genetic analysis of the human type-1 angiotensin II receptor

Glucocorticoid-suppressible hyperaldosteronism and adrenal tumors occurring in a single French pedigree

The amino acid substitutions Ser288Gly and Val320Ala convert the cortisol producing enzyme, CYP11B1, into an aldosterone producing enzyme

Scaling Up the Ligase Chain Reaction-Based Approach to Gene Synthesis

The L10F mutation of angiotensinogen is rare in pre-eclampsia

Aldosterone Secretion: A Molecular Perspective

Polar residues in the transmembrane domains of the type 1 angiotensin II receptor are required for binding and coupling. Reconstitution of the binding site by co-expression of two deficient mutants

Glucocorticoid-suppressible hyperaldosteronism and adrenal tumors occurring in a single French pedigree

Genetic recombination as a cause of inherited disorders of aldosterone and cortisol biosynthesis and a contributor to genetic variation in blood pressure

Alternatively spliced human type 1 angiotensin II receptor mRNAs are translated at different efficiencies and encode two receptor isoforms

Sequence similarities between a novel putative G protein-coupled receptor and Na+/Ca2+ exchangers define a cation binding domain

Molecular biology of 11β-hydroxylase and 11β-hydroxysteroid dehydrogenase enzymes

Human type-1 angiotensin II (AT1) receptor gene structure and function

Mapping of the mouse Ly-6, Xp-14 and Gdc-1 loci to chromosome 15

Transcripts originating in intron 1 of the HSD11 (11 beta-hydroxysteroid dehydrogenase) gene encode a truncated polypeptide that is enzymatically inactive

Disorders of steroid 11β-hydroxylase isozymes

Disorders of steroid 11 beta-hydroxylase isozymes

Prenatal Diagnosis and Treatment of 11β-Hydroxylase Deficiency Congenital Adrenal Hyperplasia Resulting in Normal Female Genitalia

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