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The sixth vital sign: what reproduction tells us about overall health. Proceedings from a NICHD/CDC workshop

Human reproduction open, 2017-01, Vol.2017 (2), p.hox008-hox008

2017

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Identification of a novel genetic locus for familial cardiac myxomas and Carney complex

Circulation (New York, N.Y.), 1998-12, Vol.98 (23), p.2560-2566

1998

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Mutations of the gene encoding the protein kinase A type I-α regulatory subunit in patients with the Carney complex

Nature genetics, 2000-09, Vol.26 (1), p.89-92

2000

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The Effects of Stress on Social Preferences are Sexually Dimorphic in Prairie Voles

Proceedings of the National Academy of Sciences - PNAS, 1996-10, Vol.93 (21), p.11980-11984

1996

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The Human Vitamin D Receptor Gene (VDR) Is Localized to Region 12cen‐q12 by Fluorescent In Situ Hybridization and Radiation Hybrid Mapping: Genetic and Physical VDR Map

Journal of bone and mineral research, 1999-07, Vol.14 (7), p.1163-1166

1999

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Ovarian Lesions in Carney Complex: Clinical Genetics and Possible Predisposition to Malignancy

The journal of clinical endocrinology and metabolism, 2000-11, Vol.85 (11), p.4359-4366

2000

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Human CYP11B2 (Aldosterone Synthase) Maps To Chromosome 8q24.3

The journal of clinical endocrinology and metabolism, 1998-03, Vol.83 (3), p.1033-1036

1998

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Role of social and endocrine factors in alloparental behavior of prairie voles (Microtus ochrogaster)

Canadian journal of zoology, 1998-10, Vol.76 (10), p.1862-1868

1998

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Carney Complex, Peutz-Jeghers Syndrome, Cowden Disease, and Bannayan-Zonana Syndrome Share Cutaneous and Endocrine Manifestations, But Not Genetic Loci

The journal of clinical endocrinology and metabolism, 1998-08, Vol.83 (8), p.2972-2976

1998

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Social Modulation of Corticosteroid Responses in Male Prairie Voles

Annals of the New York Academy of Sciences, 1997-01, Vol.807 (1), p.494-497

1997

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Mutational Analysis of the PRL Receptor Gene in Human Breast Tumors with Differential PRL Receptor Protein Expression

The journal of clinical endocrinology and metabolism, 2001-08, Vol.86 (8), p.3826-3832

2001

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A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22)

Journal of medical genetics, 2000-11, Vol.37 (11), p.831-835

2000

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Imbalanced Expression of the Glucocorticoid Receptor Isoforms in Cultured Lymphocytes from a Patient with Systemic Glucocorticoid Resistance and Chronic Lymphocytic Leukemia

Biochemical and biophysical research communications, 1999-01, Vol.254 (3), p.559-565

1999

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Anisomastia Associated with Interstitial Duplication of Chromosome 16, Mental Retardation, Obesity, Dysmorphic Facies, and Digital Anomalies: Molecular Mapping of a New Syndrome by Fluorescent in Situ Hybridization and Microsatellites to 16q13 (D16S419-D16S503)

The journal of clinical endocrinology and metabolism, 2000-09, Vol.85 (9), p.3396-3401

2000

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Familial hyperaldosteronism type II : Description of a large kindred and exclusion of the aldosterone synthase (CYP11B2) gene

The journal of clinical endocrinology and metabolism, 1998-09, Vol.83 (9), p.3214-3218

1998

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Anisomastia associated with interstitial duplication of chromosome 16, mental retardation, obesity, dysmorphic facies, and digital anomalies : Molecular mapping of a new syndrome by fluorescent in situ hybridization and microsatellites to 16q13 (D16S419-D16S503)

The journal of clinical endocrinology and metabolism, 2000-09, Vol.85 (9), p.3396-3401

2000

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Ovarian lesions in Carney complex : Clinical genetics and possible predisposition to malignancy

The journal of clinical endocrinology and metabolism, 2000-11, Vol.85 (11), p.4359-4366

2000

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The Hypothalamic–Pituitary–Adrenal Axis of Prairie Voles (Microtus ochrogaster): Evidence for Target Tissue Glucocorticoid Resistance

General and comparative endocrinology, 1997-04, Vol.106 (1), p.48-61

1997

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Mapping of the human genes (SLC23A2 andSLC23A1) coding for vitamin C transporters 1 and 2 (SVCT1 and SVCT2) to 5q23 and 20p12, respectively

Journal of medical genetics, 2000-09, Vol.37 (9), p.e20-20

2000

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Peptides, Steroids, and Pair Bonding

Annals of the New York Academy of Sciences, 1997-01, Vol.807 (1), p.260-272

1997

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Conditioned release of corticosterone by contextual stimuli associated with cocaine is mediated by corticotropin-releasing factor

Brain research, 1998-03, Vol.786 (1), p.39-46

1998

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Mutational analysis of the PRL receptor gene in human breast tumors with differential PRL receptor protein expression

The journal of clinical endocrinology and metabolism, 2001-08, Vol.86 (8), p.3826-3832

2001

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Segmental uniparental isodisomy (UPD) for 2p16 without clinical symptoms: implications for UPD and other genetic studies of chromosome 2

Journal of medical genetics, 2001-02, Vol.38 (2), p.106-109

2001

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Genomic Mapping of Chromosomal Region 2p15–p21 (D2S378–D2S391): Integration of Genemap'98 within a Framework of Yeast and Bacterial Artificial Chromosomes

Genomics (San Diego, Calif.), 1999-11, Vol.62 (1), p.21-33

1999

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Cloning and Characterization of a Novel Orphan G-Protein-Coupled Receptor Localized to Human Chromosome 2p16

Biochemical and biophysical research communications, 1999-06, Vol.260 (1), p.174-180

1999

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The sixth vital sign: what reproduction tells us about overall health. Proceedings from a NICHD/CDC workshop

Identification of a novel genetic locus for familial cardiac myxomas and Carney complex

Mutations of the gene encoding the protein kinase A type I-α regulatory subunit in patients with the Carney complex

The Effects of Stress on Social Preferences are Sexually Dimorphic in Prairie Voles

The Human Vitamin D Receptor Gene (VDR) Is Localized to Region 12cen‐q12 by Fluorescent In Situ Hybridization and Radiation Hybrid Mapping: Genetic and Physical VDR Map

Ovarian Lesions in Carney Complex: Clinical Genetics and Possible Predisposition to Malignancy

Human CYP11B2 (Aldosterone Synthase) Maps To Chromosome 8q24.3

Role of social and endocrine factors in alloparental behavior of prairie voles (Microtus ochrogaster)

Carney Complex, Peutz-Jeghers Syndrome, Cowden Disease, and Bannayan-Zonana Syndrome Share Cutaneous and Endocrine Manifestations, But Not Genetic Loci

Social Modulation of Corticosteroid Responses in Male Prairie Voles

Mutational Analysis of the PRL Receptor Gene in Human Breast Tumors with Differential PRL Receptor Protein Expression

A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22)

Imbalanced Expression of the Glucocorticoid Receptor Isoforms in Cultured Lymphocytes from a Patient with Systemic Glucocorticoid Resistance and Chronic Lymphocytic Leukemia

Anisomastia Associated with Interstitial Duplication of Chromosome 16, Mental Retardation, Obesity, Dysmorphic Facies, and Digital Anomalies: Molecular Mapping of a New Syndrome by Fluorescent in Situ Hybridization and Microsatellites to 16q13 (D16S419-D16S503)

Familial hyperaldosteronism type II : Description of a large kindred and exclusion of the aldosterone synthase (CYP11B2) gene

Anisomastia associated with interstitial duplication of chromosome 16, mental retardation, obesity, dysmorphic facies, and digital anomalies : Molecular mapping of a new syndrome by fluorescent in situ hybridization and microsatellites to 16q13 (D16S419-D16S503)

Ovarian lesions in Carney complex : Clinical genetics and possible predisposition to malignancy

The Hypothalamic–Pituitary–Adrenal Axis of Prairie Voles (Microtus ochrogaster): Evidence for Target Tissue Glucocorticoid Resistance

Mapping of the human genes (SLC23A2 andSLC23A1) coding for vitamin C transporters 1 and 2 (SVCT1 and SVCT2) to 5q23 and 20p12, respectively

Peptides, Steroids, and Pair Bonding

Conditioned release of corticosterone by contextual stimuli associated with cocaine is mediated by corticotropin-releasing factor

Mutational analysis of the PRL receptor gene in human breast tumors with differential PRL receptor protein expression

Segmental uniparental isodisomy (UPD) for 2p16 without clinical symptoms: implications for UPD and other genetic studies of chromosome 2

Genomic Mapping of Chromosomal Region 2p15–p21 (D2S378–D2S391): Integration of Genemap'98 within a Framework of Yeast and Bacterial Artificial Chromosomes

Cloning and Characterization of a Novel Orphan G-Protein-Coupled Receptor Localized to Human Chromosome 2p16

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