Adelaide Medical School, The University of Adelaide, Adelaide, Australia
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Adelaide Medical School, The University of Adelaide, Adelaide, Australia
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GH in non-pregnant female mice and throughout murine pregnancy. Methods Animals Experimental procedures were approved by the University of Adelaide Animal Ethics Committee (M-2014-167) and carried out in accordance with the Australian code
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Departments of, Clinical Biochemistry, Medicine, Department of Endocrinology and Internal Medicine, King's College Hospital, London SE5 9RS, UK
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Pharma, Paris, France) and oral hydrocortisone (six males: range 26–66 years, median 50 years and 11 females: range 20–76 years, median 47 years (six of premenopausal age)) and patients receiving hydrocortisone only after surgery in the period before
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1 syndrome in patients. However, the frequency of tumour development and age of onset depended on the background strain and sex of the mice. Thus, overall, more pituitary tumours developed in female C57BL/6 Men1 +/- mice than in female 129S6/SvEv
School of Medicine, Ningbo University, Ningbo, China
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School of Medicine, Ningbo University, Ningbo, China
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School of Medicine, Ningbo University, Ningbo, China
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School of Medicine, Ningbo University, Ningbo, China
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School of Medicine, Ningbo University, Ningbo, China
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combination with the actual situation of WC in the Chinese population ( 1 , 16 ). For each component, the diagnostic criteria were as follows: (i) central obesity (WC ≥ 90 cm in males and ≥ 85 cm in females), (ii) hypertriglyceridemia (TGs ≥ 1.7 mmol/L (150
Frontier Science Research Center, Circulatory and Body Fluid Regulation, AIA Research Group, Department of Internal Medicine, Faculty of Medicine, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki 889-1692, Japan
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2013, were randomly selected for this study (172 males and 174 females; 62.0±8.9 years, mean± s.d .). Upon visiting the community center of Kiyotake Town, the medical history of the residents, which included the questionnaire of whether or not they have
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Division of Interventional Cognitive Neurology, Department of Neurology, Berenson-Allen Center for Noninvasive Brain Stimulation, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA
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Introduction Patients with primary aldosteronism (PA) are thought to be a natural model for chronic aldosterone excess, showing significantly higher scores for depression and anxiety compared to the general population, with females being more
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). The Leydig cell also produces insulin-like factor 3, an important component acting in concert with testosterone to promote testicular descent ( 21 ). The female fetus lacks AMH, permitting the Müllerian structures to remain, and lacks the
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Hospices Civils de Lyon, Hôpital Femme-Mère-Enfant, Service de psychopathologie du développement, Bron, France
Hospices Civils de Lyon, Hôpital Femme-Mère-Enfant, Centre de biologie et pathologie Est, Service d’hormonologie, d’endocrinologie moléculaire et des maladies rares, Bron, France
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Hospices Civils de Lyon, Hôpital Femme-Mère-Enfant, Centre de biologie et pathologie Est, Service d’hormonologie, d’endocrinologie moléculaire et des maladies rares, Bron, France
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Hospices Civils de Lyon, Hôpital Femme-Mère-Enfant, Service Endocrinologie Moléculaire et Maladies Rares, Bron, France
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Hospices Civils de Lyon, Hôpital Femme-Mère-Enfant, Service de chirurgie Uro-viscérale et de Transplantation de l’Enfant, Bron, France
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Hospices Civils de Lyon, Groupement Hospitalier Est, Service d’endocrinologie, Bron, France
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Centre National de Référence Maladies Rares du développement génital du fœtus à l’adulte DEV-GEN, Hospices Civils de Lyon, Bron, France
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Université Claude Bernard, Lyon, France
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Centre National de Référence Maladies Rares du développement génital du fœtus à l’adulte DEV-GEN, Hospices Civils de Lyon, Bron, France
Université Claude Bernard, Lyon, France
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Hospices Civils de Lyon, Hôpital Femme-Mère-Enfant, Service de chirurgie Uro-viscérale et de Transplantation de l’Enfant, Bron, France
Université Claude Bernard, Lyon, France
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Hospices Civils de Lyon, Hôpital Femme-Mère-Enfant, Service de chirurgie Uro-viscérale et de Transplantation de l’Enfant, Bron, France
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Centre National de Référence Maladies Rares du développement génital du fœtus à l’adulte DEV-GEN, Hospices Civils de Lyon, Bron, France
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deficiency (HSD17B3). These two rare autosomal recessive conditions display a great heterogeneity at both the genotypic and phenotypic levels ( 1 , 2 , 3 , 4 , 5 , 6 ). Clinical presentations of external genitalia at birth range from a female appearance
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of gestational diabetes as early as 11–13 weeks of gestation ( 15 ). Of note, several studies have shown that the relationship between SHBG levels and diabetes is independent of sex hormones, in both female and male subjects ( 16 , 17 , 18 ). In a
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, males and females express different CYP profiles. In some cases, the isoforms may be sex exclusive as is the case of CYP2C12, only expressed in female rats ( 1 , 2 ). More commonly, isoforms are sex predominant: for example, women express greater levels