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Adrenal and Hypertension
Contributing journals to this collection:
Journal of Clinical Endocrinology & Metabolism,
Molecular Endocrinology,
Endocrinology,
Endocrine Reviews,
and Endocrine Society Journals
Citations 441-450 of 496 total displayed.
- Other Original Articles
Exogenous Corticosteroids and in Utero Oxygenation Modulate Indices of Fetal Insulin Secretion
- Johan Verhaeghe, Rita van Bree, Erik van Herck, and Willy Coopmans
J. Clin. Endocrinol. Metab. 90: 3449 -3453; published online before print as doi:10.1210/jc.2004-2512
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- Other Original Articles
Germline Homozygous Mutations at Codon 804 in the RET Protooncogene in Medullary Thyroid Carcinoma/Multiple Endocrine Neoplasia Type 2A Patients
- F. Lesueur, A. Cebrian, A. Cranston, J. Leyland, T. M. Faid, M. R. Clements, M. Robledo, J. Whittaker, and B. A. J. Ponder
J. Clin. Endocrinol. Metab. 90: 3454 -3457; published online before print as doi:10.1210/jc.2004-1622
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- Other Original Articles
G Protein Receptors 7 and 8 Are Expressed in Human Adrenocortical Cells, and Their Endogenous Ligands Neuropeptides B and W Enhance Cortisol Secretion by Activating Adenylate Cyclase- and Phospholipase C-Dependent Signaling Cascades
- G. Mazzocchi, P. Rebuffat, A. Ziolkowska, G. P. Rossi, L. K. Malendowicz, and G. G. Nussdorfer
J. Clin. Endocrinol. Metab. 90: 3466 -3471; published online before print as doi:10.1210/jc.2004-2132
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- Other Original Articles
The Human Glucocorticoid Receptor (GR) Isoform ß Differentially Suppresses GR -Induced Transactivation Stimulated by Synthetic Glucocorticoids
- Oren Fruchter, Tomoshige Kino, Emmanouil Zoumakis, Salvatore Alesci, Massimo De Martino, George Chrousos, and Ze’ev Hochberg
J. Clin. Endocrinol. Metab. 90: 3505 -3509; published online before print as doi:10.1210/jc.2004-1646
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- Other Original Articles
Preproorexin and Orexin Receptors Are Expressed in Cortisol-Secreting Adrenocortical Adenomas, and Orexins Stimulate in Vitro Cortisol Secretion and Growth of Tumor Cells
- R. Spinazzi, M. Rucinski, G. Neri, L. K. Malendowicz, and G. G. Nussdorfer
J. Clin. Endocrinol. Metab. 90: 3544 -3549; published online before print as doi:10.1210/jc.2004-2385
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- Other Original Articles
A Novel Point Mutation in the Ligand-Binding Domain (LBD) of the Human Glucocorticoid Receptor (hGR) Causing Generalized Glucocorticoid Resistance: The Importance of the C Terminus of hGR LBD in Conferring Transactivational Activity
- Evangelia Charmandari, Annaswamy Raji, Tomoshige Kino, Takamasa Ichijo, Anatoly Tiulpakov, Keith Zachman, and George P. Chrousos
J. Clin. Endocrinol. Metab. 90: 3696 -3705; published online before print as doi:10.1210/jc.2004-1920
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- Other Original Articles
Congenital Adrenal Hyperplasia Due to 11-Hydroxylase Deficiency: Functional Characterization of Two Novel Point Mutations and a Three-Base Pair Deletion in the CYP11B1 Gene
- Nils Krone, Felix G. Riepe, Dorothea Götze, Eckhard Korsch, Manfred Rister, Jens Commentz, Carl-Joachim Partsch, Joachim Grötzinger, Michael Peter, and Wolfgang G. Sippell
J. Clin. Endocrinol. Metab. 90: 3724 -3730; published online before print as doi:10.1210/jc.2005-0089
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- Other Original Articles
Differential Expression of Erythropoietin and Its Receptor in von Hippel-Lindau-Associated and Multiple Endocrine Neoplasia Type 2-Associated Pheochromocytomas
- Timothy W. A. Vogel, Frederieke M. Brouwers, Irina A. Lubensky, Alexander O. Vortmeyer, Robert J. Weil, McClellan M. Walther, Edward H. Oldfield, W. Marston Linehan, Karel Pacak, and Zhengping Zhuang
J. Clin. Endocrinol. Metab. 90: 3747 -3751; published online before print as doi:10.1210/jc.2004-1899
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- Special Features
Hereditary Leiomyomatosis Associated with Bilateral, Massive, Macronodular Adrenocortical Disease and Atypical Cushing Syndrome: A Clinical and Molecular Genetic Investigation
- Ludmila Matyakhina, Reneé J. Freedman, Isabelle Bourdeau, Ming-Hui Wei, Sotirios G. Stergiopoulos, Aaron Chidakel, McClellan Walther, Mones Abu-Asab, Maria Tsokos, Meg Keil, Jorge Toro, W. Marston Linehan, and Constantine A. Stratakis
J. Clin. Endocrinol. Metab. 90: 3773 -3779; published online before print as doi:10.1210/jc.2004-2377
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- Endocrine Care
Subtle 17-Hydroxylase/17,20-Lyase Deficiency with Homozygous Y201N Mutation in an Infertile Woman
- Matsuo Taniyama, Makito Tanabe, Hiroshi Saito, Yoshio Ban, Hajime Nawata, and Toshihiko Yanase
J. Clin. Endocrinol. Metab. 90: 2508 -2511; published online before print as doi:10.1210/jc.2004-2067
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